Table
11 Data transformed
using the language of templates |
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Gene |
0MIN - 30MIN |
0MIN - 1H |
0MIN - 2H |
0MIN - 4H |
0MIN - 6H |
0MIN - 8H |
0MIN - 12H |
0MIN - 16H |
0MIN - 20H |
0MIN - 24H |
15MIN - 1H |
15MIN - 2H |
15MIN - 4H |
15MIN - 6H |
15MIN - 8H |
15MIN - 12H |
15MIN - 16H |
15MIN - 20H |
15MIN - 24H |
30MIN - 2H |
30MIN - 4H |
30MIN - 6H |
30MIN - 8H |
30MIN - 12H |
30MIN - 16H |
30MIN - 20H |
30MIN - 24H |
1H - 4H |
1H - 6H |
1H - 8H |
1H - 12H |
1H - 16H |
1H - 20H |
1H - 24H |
2H - 6H |
2H - 8H |
2H - 12H |
2H - 16H |
2H - 20H |
2H - 24H |
4H - 8H |
4H - 12H |
4H - 16H |
4H - 20H |
4H - 24H |
6H - 12H |
6H - 16H |
6H - 20H |
6H - 24H |
8H - 16H |
8H - 20H |
8H - 24H |
12H - 20H |
12H - 24H |
16H - 24H |
Annotation |
LOC80298 |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
SEPP1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
transport |
SEPP1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
stress response |
NO SYMBOL 3 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
unknown |
EPB41L2 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
cell proliferation |
OA48-18 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
cell proliferation |
NO SYMBOL 6 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
unknown |
NO SYMBOL 7 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
unknown |
CTSK |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
protein metabolism and modification |
CPT1B |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
lipid metabolism |
KIAA0455 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
CLDN11 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell motility |
CLDN11 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell proliferation |
CLDN11 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell adhesion |
CLDN11 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
developmental processes |
RPL5 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
protein metabolism and modification |
RPL5 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
cell organization and biogenesis |
NO SYMBOL 13 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 14 |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Constant |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
cell adhesion |
NO SYMBOL 15 |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell surface receptor linked signal transduction |
KIAA1391 |
NoMatch |
Constant |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 17 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 18 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
CCNG1 |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
cell death |
CCNG1 |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
cell cycle |
NO SYMBOL 20 |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
unknown |
CDKN1C |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
cell proliferation |
CDKN1C |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
cell cycle |
GRIA1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell death |
GRIA1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell surface receptor linked signal transduction |
NO SYMBOL 23 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 24 |
NoMatch |
Constant |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 25 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
transport |
NO SYMBOL 26 |
NoMatch |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 27 |
NoMatch |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 28 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 29 |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
KIAA1628 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 31 |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 32 |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
FMOD |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell adhesion |
FLJ20643 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
KIAA0993 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
CDK5R1 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell proliferation |
CDK5R1 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell cycle |
CAT |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
stress response |
NO SYMBOL 38 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
LOC55977 |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
unknown |
FLJ10849 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
unknown |
KIAA0451 |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
unknown |
NO SYMBOL 42 |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 43 |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
unknown |
FLJ00026 |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 45 |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 46 |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 47 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
transport |
NO SYMBOL 47 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
intracellular signalling cascade |
NO SYMBOL 48 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
energy pathways |
NO SYMBOL 48 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
lipid metabolism |
ULK2 |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
GBAS |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
cell surface receptor linked signal transduction |
NO SYMBOL 51 |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 52 |
NoMatch |
Constant |
Constant |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
unknown |
MME |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
protein metabolism and modification |
MME |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell motility |
MME |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
defense (immune) response |
MME |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell proliferation |
NO SYMBOL 54 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
unknown |
DPP4 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
protein metabolism and modification |
DPP4 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
cell motility |
NO SYMBOL 56 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
unknown |
NO SYMBOL 57 |
NoMatch |
Constant |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
FLJ11273 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
FBN2 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
cell motility |
FBN2 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
cell adhesion |
NO SYMBOL 60 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell adhesion |
NO SYMBOL 60 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
developmental processes |
ANXA3 |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
blood coagulation |
PP5395 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 63 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
unknown |
HFL1 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Constant |
Constant |
Constant |
Constant |
Decreasing |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
stress response |
HFL1 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Constant |
Constant |
Constant |
Constant |
Decreasing |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
defense (immune) response |
NO SYMBOL 65 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
SQLE |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
lipid metabolism |
NO SYMBOL 67 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
unknown |
AD036 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
unknown |
FLJ10217 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
unknown |
WNT2 |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
developmental processes |
NO SYMBOL 71 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
unknown |
ASNS |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
amino-acid and derivative metabolism |
SMARCB1 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
DNA metabolism |
SMARCB1 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
transcription |
SMARCB1 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
cell proliferation |
DHCR24 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
lipid metabolism |
NO SYMBOL 75 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
unknown |
OSBP2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
lipid metabolism |
OSBP2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
cell death |
KIAA0878 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
unknown |
TAX1BP1 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
transcription |
TAX1BP1 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell death |
MAC30 |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
SC5DL |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
lipid metabolism |
NO SYMBOL 81 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
unknown |
NO SYMBOL 82 |
NoMatch |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
transport |
NO SYMBOL 83 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
LOC57100 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
unknown |
HMGCR |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
lipid metabolism |
CYP1B1 |
NoMatch |
Constant |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
lipid metabolism |
NO SYMBOL 87 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
unknown |
NO SYMBOL 88 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
unknown |
MID1 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
cell organization and biogenesis |
MID1 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
developmental processes |
NO SYMBOL 90 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
unknown |
NO SYMBOL 91 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
ELF2 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
transcription |
ELF2 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
cell proliferation |
HBP1 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
DNA metabolism |
HBP1 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
transcription |
HBP1 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
oncogenesis |
NO SYMBOL 94 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
unknown |
NO SYMBOL 95 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Constant |
Increasing |
NoMatch |
NoMatch |
Increasing |
transcription |
NO SYMBOL 95 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Constant |
Increasing |
NoMatch |
NoMatch |
Increasing |
transport |
PDE8A |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
intracellular signalling cascade |
FLJ14525 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 98 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
SSPN |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Increasing |
NoMatch |
oncogenesis |
SSPN |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Increasing |
NoMatch |
cell adhesion |
PGRMC2 |
NoMatch |
Constant |
Constant |
Constant |
Constant |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
ZNF161 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
transcription |
ZNF161 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
defense (immune) response |
VDUP1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell death |
VDUP1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
stress response |
VDUP1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell proliferation |
RABIF |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
transport |
TRIP7 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
transcription |
BM-002 |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
unknown |
FLJ22794 |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
unknown |
FPGT |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
unknown |
KIAA1376 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 109 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell cycle |
SMARCA3 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
DNA metabolism |
SMARCA3 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
transcription |
SMARCA3 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
cell motility |
SMARCA3 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
defense (immune) response |
SMARCA3 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
blood coagulation |
NO SYMBOL 111 |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
DKFZP586D2223 |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
unknown |
RAP140 |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
unknown |
FLJ10971 |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
unknown |
NO SYMBOL 115 |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
unknown |
ZNF302 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 117 |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
P38IP |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
FLJ20008 |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
unknown |
NO SYMBOL 120 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
unknown |
KIAA0643 |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
NO SYMBOL 122 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
unknown |
NO SYMBOL 123 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
cell organization and biogenesis |
ALDH3A2 |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
lipid metabolism |
MEIS1 |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
transcription |
MEIS1 |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
oncogenesis |
NEDD4L |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
FLJ10283 |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
Constant |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
unknown |
F2R |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell surface receptor linked signal transduction |
F2R |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
blood coagulation |
NO SYMBOL 129 |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
unknown |
THBS3 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell death |
THBS3 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell proliferation |
THBS3 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell adhesion |
THBS3 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
circulation |
NO SYMBOL 131 |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
KIT |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell death |
KIT |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell motility |
KIT |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
defense (immune) response |
KIT |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
oncogenesis |
KIT |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell proliferation |
KIT |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell surface receptor linked signal transduction |
FLJ10287 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
SULT4A1 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
ECM2 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell proliferation |
ECM2 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell adhesion |
BBS2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
unknown |
NO SYMBOL 137 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
unknown |
DMWD |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
HMG2 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
DNA metabolism |
HMG2 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
transcription |
HMG2 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell organization and biogenesis |
HMG2 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell cycle |
KIAA0447 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
GTF2I |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
transcription |
B4-2 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell motility |
B4-2 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
defense (immune) response |
NO SYMBOL 143 |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
unknown |
WW45 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
unknown |
TGFBR3 |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
cell death |
TGFBR3 |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
defense (immune) response |
TGFBR3 |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
cell proliferation |
TGFBR3 |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
cell surface receptor linked signal transduction |
FYN |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
oncogenesis |
FYN |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
cell proliferation |
FYN |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
intracellular signalling cascade |
MGC12904 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
PRKCL2 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
intracellular signalling cascade |
LPIN1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
unknown |
DDIT3 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Increasing |
Increasing |
transcription |
DDIT3 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Increasing |
Increasing |
cell cycle |
NO SYMBOL 151 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
ACF7 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
transport |
ACF7 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
cell organization and biogenesis |
ACF7 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
cell cycle |
TAX1BP1 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
transcription |
TAX1BP1 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell death |
KIAA0977 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
PDE8B |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
intracellular signalling cascade |
DKFZP564D0764 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
transcription |
AHR |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
transcription |
AHR |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
lipid metabolism |
ACACA |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
lipid metabolism |
CAMK2D |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell cycle |
CAMK2D |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
intracellular signalling cascade |
CAMK2D |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell cycle |
CAMK2D |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
intracellular signalling cascade |
NO SYMBOL 161 |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
unknown |
MGC16169 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
unknown |
KIAA0456 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
cell organization and biogenesis |
KIAA0456 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
cell cycle |
KIAA0456 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
intracellular signalling cascade |
DPYD |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 165 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
BBS2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
DDB2 |
NoMatch |
Constant |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
DNA metabolism |
KIAA0203 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
cell organization and biogenesis |
NO SYMBOL 169 |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
Rab11-FIP2 |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
NO SYMBOL 171 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
AHRR |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
ADD3 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
cell organization and biogenesis |
NO SYMBOL 174 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
unknown |
NO SYMBOL 175 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 176 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
unknown |
DDX17 |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
transcription |
NO SYMBOL 178 |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
unknown |
KIAA1536 |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
DNA metabolism |
KIAA1536 |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
transcription |
KIAA1536 |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
oncogenesis |
NO SYMBOL 180 |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 181 |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
DKFZP434P0721 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
LOC58486 |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
NO SYMBOL 184 |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
unknown |
NO SYMBOL 185 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
NO SYMBOL 186 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
KIAA0786 |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
unknown |
CLCN3 |
NoMatch |
Constant |
Constant |
Constant |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
transport |
TIA1 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
cell death |
TIA1 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
defense (immune) response |
HCGVIII-1 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
unknown |
NO SYMBOL 191 |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
unknown |
CDKN1B |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell cycle |
DKFZP434E2318 |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 194 |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
NO SYMBOL 195 |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
HSF2 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
transcription |
NO SYMBOL 197 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
SIAH1 |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
NO SYMBOL 199 |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
unknown |
WW45 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
FLJ22054 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
unknown |
KIAA0923 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
KIAA0923 |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
CDKN2C |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell proliferation |
CDKN2C |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell cycle |
KIAA0923 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
TFDP2 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
transcription |
OXR1 |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
stress response |
HNMT |
NoMatch |
Constant |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
amino-acid and derivative metabolism |
FLJ11896 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
unknown |
KIAA0923 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
RFX5 |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
transcription |
RFX5 |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
defense (immune) response |
NO SYMBOL 212 |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
unknown |
NO SYMBOL 213 |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
FLJ11040 |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
NDR |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
protein metabolism and modification |
KIAA0602 |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
unknown |
ROR2 |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell surface receptor linked signal transduction |
CEBPG |
NoMatch |
Constant |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
transcription |
KIAA0092 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
cell motility |
PLSCR1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
lipid metabolism |
PLSCR1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell death |
PLSCR1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
blood coagulation |
DDX17 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
transcription |
KIAA1799 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
unknown |
NO SYMBOL 223 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
unknown |
NO SYMBOL 224 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
UACA |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
NO SYMBOL 226 |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
unknown |
NO SYMBOL 227 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
unknown |
PIST |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
unknown |
ATRX |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
DNA metabolism |
ATRX |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
transcription |
KIAA0355 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
NARS |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
protein metabolism and modification |
AUTL1 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
unknown |
SDC3 |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell motility |
SDC3 |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell adhesion |
SDC3 |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell surface receptor linked signal transduction |
NR1D2 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
transcription |
NO SYMBOL 235 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
unknown |
NO SYMBOL 236 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
unknown |
FOXF2 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
transcription |
ZFP36L2 |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
cell proliferation |
NO SYMBOL 239 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
unknown |
DC8 |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
unknown |
PPM1B |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
protein metabolism and modification |
GARP |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell surface receptor linked signal transduction |
TMOD |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
cell organization and biogenesis |
IFIT1 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
PSPH |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
amino-acid and derivative metabolism |
KIAA1462 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
DAPK1 |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
cell death |
TRABID |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
intracellular signalling cascade |
PTGFRN |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
D5S346 |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
oncogenesis |
NO SYMBOL 251 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
CDA08 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
CPT1A |
NoMatch |
Constant |
Constant |
Constant |
Constant |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
lipid metabolism |
NO SYMBOL 254 |
NoMatch |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Constant |
Increasing |
NoMatch |
NoMatch |
NoMatch |
unknown |
FBN1 |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell motility |
FBN1 |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell adhesion |
NO SYMBOL 256 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
PBX3 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
transcription |
EPS15 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
cell proliferation |
EPS15 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
cell surface receptor linked signal transduction |
PLA2R1 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
defense (immune) response |
PLA2R1 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell surface receptor linked signal transduction |
PACE4 |
NoMatch |
Constant |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
protein metabolism and modification |
NO SYMBOL 261 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 262 |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Constant |
NoMatch |
unknown |
ANGPTL2 |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
unknown |
PDGFRB |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
oncogenesis |
PDGFRB |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
cell proliferation |
PDGFRB |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
cell surface receptor linked signal transduction |
NO SYMBOL 265 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
MEG3 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
unknown |
PAPPA |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
protein metabolism and modification |
PAPPA |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell proliferation |
CYP2C9 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
lipid metabolism |
CYP2C9 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
developmental processes |
FADS2 |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
lipid metabolism |
SCD |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
lipid metabolism |
NO SYMBOL 271 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
oncogenesis |
NO SYMBOL 271 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
developmental processes |
C1S |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
cell motility |
C1S |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
defense (immune) response |
C1R |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
cell motility |
C1R |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
defense (immune) response |
NO SYMBOL 274 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
unknown |
H-l(3)mbt-l |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
unknown |
LPL |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
lipid metabolism |
LPL |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
transport |
LPL |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
cell adhesion |
NO SYMBOL 277 |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
cell motility |
NO SYMBOL 277 |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
cell cycle |
SPR |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
unknown |
P8 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
cell proliferation |
SCD |
NoMatch |
Constant |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
lipid metabolism |
NO SYMBOL 281 |
NoMatch |
Constant |
Constant |
Constant |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
unknown |
PSA |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
protein metabolism and modification |
PSA |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
amino-acid and derivative metabolism |
PSA |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell organization and biogenesis |
FDFT1 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
lipid metabolism |
NO SYMBOL 284 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 285 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
GJB1 |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
unknown |
MLN64 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
lipid metabolism |
MLN64 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
transport |
RPL39 |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
protein metabolism and modification |
RPL39 |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
cell organization and biogenesis |
IDI1 |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
lipid metabolism |
OSR1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
stress response |
INSIG1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
cell proliferation |
INSIG1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
cell cycle |
ARG99 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
unknown |
LOC57018 |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
unknown |
NO SYMBOL 294 |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
unknown |
SCD |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
lipid metabolism |
NO SYMBOL 296 |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
unknown |
PPAP2B |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
lipid metabolism |
NO SYMBOL 298 |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
unknown |
AKAP12 |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
cell motility |
AKAP12 |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
cell organization and biogenesis |
AKAP12 |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
cell cycle |
AKAP12 |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
intracellular signalling cascade |
HEF1 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
cell organization and biogenesis |
HEF1 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
cell cycle |
HEF1 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
cell adhesion |
HEF1 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
cell surface receptor linked signal transduction |
SMC2L1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
ANKT |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
DC8 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
unknown |
PRIM2A |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
DNA metabolism |
PRIM2A |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell cycle |
CIC |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
defense (immune) response |
CIC |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell surface receptor linked signal transduction |
LBR |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell organization and biogenesis |
LBR |
NoMatch |
Constant |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell cycle |
NO SYMBOL 307 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
unknown |
CENPE |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
cell organization and biogenesis |
CENPE |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
cell cycle |
KIAA0175 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
unknown |
NO SYMBOL 310 |
NoMatch |
Constant |
Constant |
Constant |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
MSH2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
DNA metabolism |
MSH2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
oncogenesis |
MSH2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell cycle |
XPO1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
transcription |
XPO1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
protein targeting |
XPO1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
transport |
POLD3 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
DNA metabolism |
POLD3 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
cell cycle |
FAF1 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
cell death |
FAF1 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
intracellular signalling cascade |
ADAMTS1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
defense (immune) response |
ADAMTS1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell proliferation |
ADAMTS1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell adhesion |
ADAMTS1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
circulation |
ARF4L |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
protein metabolism and modification |
ARF4L |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
transport |
ARF4L |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
stress response |
ARF4L |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
intracellular signalling cascade |
KIAA1382 |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
unknown |
NO SYMBOL 318 |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
unknown |
CNAP1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
unknown |
BMP1 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
protein metabolism and modification |
BMP1 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell death |
BMP1 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell motility |
BMP1 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell proliferation |
BMP1 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
developmental processes |
BMP1 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
circulation |
PCNA |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
DNA metabolism |
PCNA |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Constant |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell cycle |
LOC51053 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
DNA metabolism |
LOC51053 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
transcription |
LOC51053 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
cell cycle |
LOC51053 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
developmental processes |
NO SYMBOL 323 |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
developmental processes |
GPC1 |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
protein metabolism and modification |
GPC1 |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell proliferation |
GPC1 |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell adhesion |
TOP2A |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
DNA metabolism |
TOP2A |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
transcription |
TOP2A |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell cycle |
CKAP2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
ANLN |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
cell cycle |
MAD2L1 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell cycle |
C20orf1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
cell proliferation |
C20orf1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
cell cycle |
HSPC150 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
unknown |
CENPF |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell organization and biogenesis |
CENPF |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell cycle |
RRM1 |
NoMatch |
Constant |
Constant |
Constant |
Constant |
Constant |
Constant |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
DNA metabolism |
RRM1 |
NoMatch |
Constant |
Constant |
Constant |
Constant |
Constant |
Constant |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell cycle |
CCNA2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell cycle |
PMSCL1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell organization and biogenesis |
FEN1 |
NoMatch |
Constant |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
DNA metabolism |
FEN1 |
NoMatch |
Constant |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell cycle |
KPNA2 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
protein targeting |
KPNA2 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
transport |
ARL6IP |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
unknown |
RRM2 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
DNA metabolism |
RRM2 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
cell cycle |
CDC2 |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
DNA metabolism |
CDC2 |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
cell cycle |
OCLN |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
cell adhesion |
CKS2 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
transcription |
CKS2 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
cell cycle |
CCNB1 |
NoMatch |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
cell cycle |
NO SYMBOL 343 |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
transcription |
NO SYMBOL 344 |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
PPP4C |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
protein metabolism and modification |
PPP4C |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
intracellular signalling cascade |
NO SYMBOL 346 |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
unknown |
NO SYMBOL 347 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
FOS |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
transcription |
FOS |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
oncogenesis |
FOS |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Constant |
NoMatch |
cell proliferation |
EGR1 |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
transcription |
EGR1 |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
cell proliferation |
NR4A2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Increasing |
NoMatch |
NoMatch |
transcription |
NR4A2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Increasing |
NoMatch |
NoMatch |
cell cycle |
GRO2 |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
cell motility |
GRO2 |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
defense (immune) response |
GEM |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
intracellular signalling cascade |
NO SYMBOL 353 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
PBEF |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
defense (immune) response |
PBEF |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
cell proliferation |
ZNF295 |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
transcription |
DUSP6 |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
protein metabolism and modification |
DUSP6 |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
intracellular signalling cascade |
TNFAIP3 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
transcription |
TNFAIP3 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
cell death |
TNFAIP3 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
defense (immune) response |
HIVEP2 |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
transcription |
HIVEP2 |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
defense (immune) response |
FLJ21661 |
NoMatch |
Constant |
Constant |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
unknown |
SCYA2 |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
cell motility |
SCYA2 |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
defense (immune) response |
KIAA0157 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
unknown |
IL1B |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
defense (immune) response |
IL1B |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
cell proliferation |
IL8 |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
cell motility |
IL8 |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
defense (immune) response |
ETS2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
transcription |
ETS2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell death |
ETS2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
oncogenesis |
ETS2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell proliferation |
ETS2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
developmental processes |
ETS2 |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
transcription |
ETS2 |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
cell death |
ETS2 |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
oncogenesis |
ETS2 |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
cell proliferation |
ETS2 |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
developmental processes |
MGC5627 |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
unknown |
CLDN4 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
cell adhesion |
CLDN4 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
circulation |
NO SYMBOL 368 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
DNA metabolism |
NO SYMBOL 368 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
transcription |
TMEPAI |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
unknown |
VEGF |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
cell proliferation |
VEGF |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
developmental processes |
VEGF |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
circulation |
NO SYMBOL 371 |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
cell surface receptor linked signal transduction |
NO SYMBOL 371 |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
circulation |
MAT2A |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
amino-acid and derivative metabolism |
NO SYMBOL 373 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
unknown |
KIAA1552 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
unknown |
THBD |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
defense (immune) response |
THBD |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
cell surface receptor linked signal transduction |
THBD |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
blood coagulation |
BMPR2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
cell proliferation |
BMPR2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
developmental processes |
BMPR2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
circulation |
NO SYMBOL 377 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
unknown |
STC1 |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
transport |
STC1 |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
ion homeostasis |
STC1 |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
circulation |
RGS4 |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
cell surface receptor linked signal transduction |
FCGR2B |
NoMatch |
Constant |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
defense (immune) response |
FCGR2B |
NoMatch |
Constant |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
cell surface receptor linked signal transduction |
NO SYMBOL 381 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
unknown |
ICAM1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
cell motility |
ICAM1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
defense (immune) response |
ICAM1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
cell adhesion |
FLJ23476 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
unknown |
DUSP6 |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
protein metabolism and modification |
DUSP6 |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
intracellular signalling cascade |
HMGE |
NoMatch |
Constant |
Constant |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
TMEM2 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
transcription |
FGF7 |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
cell proliferation |
FGF7 |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
circulation |
NO SYMBOL 388 |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
unknown |
FGF2 |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
cell motility |
FGF2 |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
cell proliferation |
FGF2 |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
circulation |
NO SYMBOL 390 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
ADRA2C |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
cell surface receptor linked signal transduction |
FOSL1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
transcription |
FOSL1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
cell proliferation |
SDC2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
cell proliferation |
SDC2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
cell adhesion |
MKI67 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Increasing |
NoMatch |
NoMatch |
Increasing |
cell proliferation |
MKI67 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Increasing |
NoMatch |
NoMatch |
Increasing |
cell cycle |
RPS2 |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
protein metabolism and modification |
SDF1 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell motility |
SDF1 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
defense (immune) response |
SDF1 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell proliferation |
RAN |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
transcription |
RAN |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
protein targeting |
RAN |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
transport |
RAN |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
cell organization and biogenesis |
RAN |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
oncogenesis |
RAN |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
cell cycle |
RAN |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
intracellular signalling cascade |
ITGA6 |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell motility |
ITGA6 |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell organization and biogenesis |
ITGA6 |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell adhesion |
ITGA6 |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
cell surface receptor linked signal transduction |
ACP1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
protein metabolism and modification |
ACP1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
intracellular signalling cascade |
CDK7 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
DNA metabolism |
CDK7 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
transcription |
CDK7 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
cell proliferation |
CDK7 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
cell cycle |
FLJ10830 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
unknown |
SLC25A5 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
energy pathways |
SLC25A5 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
transport |
RANBP1 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
transcription |
RANBP1 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
protein targeting |
RANBP1 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
transport |
RANBP1 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell organization and biogenesis |
RANBP1 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell cycle |
RANBP1 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
intracellular signalling cascade |
FKBP1A |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
protein metabolism and modification |
FKBP1A |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
transport |
NOP56 |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
cell organization and biogenesis |
NO SYMBOL 406 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
protein metabolism and modification |
HSPA8 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
protein metabolism and modification |
HSPA8 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
stress response |
CKAP1 |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
protein metabolism and modification |
CKAP1 |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
cell organization and biogenesis |
CKAP1 |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
cell cycle |
B4GALT1 |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
protein metabolism and modification |
B4GALT1 |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
lipid metabolism |
C21orf25 |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
unknown |
G2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
unknown |
ESM1 |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
defense (immune) response |
ESM1 |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
cell adhesion |
DSP |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell organization and biogenesis |
HNT |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell adhesion |
HNT |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell surface receptor linked signal transduction |
HNT |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
cell adhesion |
HNT |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
cell surface receptor linked signal transduction |
DNAJB9 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
circulation |
DKFZp667O2416 |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
unknown |
NO SYMBOL 418 |
NoMatch |
Constant |
Constant |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
Constant |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 419 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Constant |
NoMatch |
unknown |
NO SYMBOL 420 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
OXTR |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell motility |
OXTR |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell proliferation |
OXTR |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell surface receptor linked signal transduction |
LOC51660 |
NoMatch |
Constant |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Increasing |
NoMatch |
Constant |
Constant |
NoMatch |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
stress response |
EBNA1BP2 |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell organization and biogenesis |
EBNA1BP2 |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
cell proliferation |
COL4A1 |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
cell motility |
COL4A1 |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
cell adhesion |
NO SYMBOL 425 |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
unknown |
HSPB7 |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
protein metabolism and modification |
HSPB7 |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
stress response |
GCH1 |
NoMatch |
Constant |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
unknown |
TIMP3 |
NoMatch |
Constant |
Constant |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
protein metabolism and modification |
TIMP3 |
NoMatch |
Constant |
Constant |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
cell motility |
TIMP3 |
NoMatch |
Constant |
Constant |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
cell adhesion |
DDX21 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
transcription |
DDX21 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
cell organization and biogenesis |
DDX21 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
cell proliferation |
ANPEP |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
protein metabolism and modification |
ANPEP |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell motility |
ANPEP |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
circulation |
NO SYMBOL 431 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
PPIF |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
protein metabolism and modification |
CTPS |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
unknown |
FDPS |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
lipid metabolism |
TM4SF1 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
transport |
TM4SF1 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
stress response |
HXB |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
cell motility |
HXB |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
oncogenesis |
HXB |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
cell adhesion |
NO SYMBOL 437 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
unknown |
FLJ21079 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
unknown |
DSCR1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
transcription |
DSCR1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
intracellular signalling cascade |
DSCR1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
developmental processes |
DSCR1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
circulation |
HSPA1A |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
protein metabolism and modification |
HSPA1A |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
protein targeting |
HSPA1A |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
stress response |
HSPA1A |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
intracellular signalling cascade |
MYO10 |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
transport |
MYO10 |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
cell motility |
MYO10 |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
cell organization and biogenesis |
MYO10 |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
cell adhesion |
NO SYMBOL 442 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
unknown |
TGM2 |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
protein metabolism and modification |
TGM2 |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
stress response |
SSR3 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
protein targeting |
EDG1 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
cell surface receptor linked signal transduction |
SDF1 |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
cell motility |
SDF1 |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
defense (immune) response |
SDF1 |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
cell proliferation |
NO SYMBOL 447 |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
unknown |
WDR1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Constant |
NoMatch |
cell adhesion |
PLOD2 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
protein metabolism and modification |
ATP5G1 |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
energy pathways |
ATP5G1 |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
lipid metabolism |
NO SYMBOL 451 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
unknown |
PFKP |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
energy pathways |
SLC20A1 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
transport |
SLC20A1 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
circulation |
HCS |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
unknown |
NO SYMBOL 455 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
unknown |
MT1L |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
ion homeostasis |
MT1L |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
stress response |
MT2A |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
ion homeostasis |
MT2A |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
stress response |
ACY1 |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
amino-acid and derivative metabolism |
CCND1 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
oncogenesis |
CCND1 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
cell proliferation |
CCND1 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
cell cycle |
GPM6B |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
Constant |
NoMatch |
developmental processes |
NO SYMBOL 461 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
unknown |
NO SYMBOL 462 |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
unknown |
MT1H |
NoMatch |
Constant |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
Constant |
NoMatch |
ion homeostasis |
MT1H |
NoMatch |
Constant |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Constant |
NoMatch |
NoMatch |
Constant |
NoMatch |
stress response |
NO SYMBOL 464 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
unknown |
KIAA0165 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
cell organization and biogenesis |
KIAA0165 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
cell cycle |
KIAA0368 |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
unknown |
CDH2 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
cell adhesion |
SERPIND1 |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
cell motility |
SERPIND1 |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
defense (immune) response |
SERPIND1 |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Constant |
Constant |
Constant |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
blood coagulation |
KIAA0186 |
NoMatch |
Constant |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
unknown |
GPD1 |
NoMatch |
Constant |
Constant |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
energy pathways |
NO SYMBOL 471 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
unknown |
FLJ20727 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
unknown |
TFPI2 |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
defense (immune) response |
TFPI2 |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
cell proliferation |
TFPI2 |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
cell adhesion |
TFPI2 |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
blood coagulation |
PKM2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
energy pathways |
CCT5 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
protein metabolism and modification |
CCT5 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
cell organization and biogenesis |
CCT5 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
cell cycle |
CLTC |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
transport |
CLTC |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
cell organization and biogenesis |
RGS12 |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
cell surface receptor linked signal transduction |
ACLY |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
lipid metabolism |
FLNB |
NoMatch |
Constant |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
cell organization and biogenesis |
FLNB |
NoMatch |
Constant |
Constant |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
cell cycle |
TPM1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
cell motility |
SERPINE1 |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
cell motility |
SERPINE1 |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
defense (immune) response |
SERPINE1 |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
cell adhesion |
SERPINE1 |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
blood coagulation |
FLNA |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
cell organization and biogenesis |
FLNA |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
cell cycle |
MAP2K3 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
defense (immune) response |
MAP2K3 |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
intracellular signalling cascade |
NET1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
defense (immune) response |
NET1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
cell organization and biogenesis |
NET1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
oncogenesis |
NET1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
cell proliferation |
NET1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
cell cycle |
NET1 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
intracellular signalling cascade |
UAP1 |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
unknown |
PLAUR |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
defense (immune) response |
PLAUR |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
cell adhesion |
PLAUR |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
blood coagulation |
NDRG2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 488 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
unknown |
ZNF222 |
NoMatch |
Constant |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
transcription |
F3 |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
defense (immune) response |
F3 |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
cell surface receptor linked signal transduction |
F3 |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
blood coagulation |
PTGS2 |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
lipid metabolism |
PTGS2 |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
defense (immune) response |
PTGS2 |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
cell proliferation |
PTGS2 |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
intracellular signalling cascade |
ID3 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
transcription |
NR4A1 |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
transcription |
NR4A1 |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
cell proliferation |
NR4A1 |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
intracellular signalling cascade |
TIEG |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
transcription |
TIEG |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
cell proliferation |
TIEG |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
cell surface receptor linked signal transduction |
TIEG |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
Constant |
NoMatch |
developmental processes |
MGC5469 |
NoMatch |
Constant |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Increasing |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
unknown |
CTGF |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
cell motility |
CTGF |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
cell proliferation |
CTGF |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
cell surface receptor linked signal transduction |
ARV1 |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
unknown |
NO SYMBOL 498 |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
unknown |
CDKN1A |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
stress response |
CDKN1A |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell proliferation |
CDKN1A |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
cell cycle |
RPS5 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
protein metabolism and modification |
RPS5 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
cell organization and biogenesis |
NR4A3 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
transcription |
NR4A3 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
cell proliferation |
BHLHB2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
transcription |
DKFZP564B167 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
unknown |
JUNB |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
transcription |
JUNB |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
oncogenesis |
JUNB |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
cell proliferation |
JUNB |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
intracellular signalling cascade |
MCL1 |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
cell death |
MCL1 |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
defense (immune) response |
MCL1 |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
intracellular signalling cascade |
MCL1 |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
cell death |
MCL1 |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
defense (immune) response |
MCL1 |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
intracellular signalling cascade |
PBEF |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
defense (immune) response |
PBEF |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
cell proliferation |
EDN1 |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
circulation |
IL6 |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
defense (immune) response |
IL6 |
Increasing |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
cell proliferation |
CRIP2 |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
unknown |
SGK |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
protein metabolism and modification |
SGK |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
defense (immune) response |
SGK |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
intracellular signalling cascade |
COPEB |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Constant |
NoMatch |
transcription |
SV2B |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Constant |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
KIAA1409 |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
unknown |
UROS |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Constant |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
NoMatch |
Decreasing |
NoMatch |
NoMatch |
unknown |
NO SYMBOL 516 |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
Constant |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
unknown |
RCL |
Increasing |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
Increasing |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Increasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
NoMatch |
NoMatch |
NoMatch |
NoMatch |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
Decreasing |
unknown |
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