Classical antibody-mediated complement activation |
10 |
1.44e-06 |
1.11e-04 |
0.94200 |
0.864000 |
-0.375000 |
2.25e-06 |
0.039900 |
FCGR activation |
15 |
3.17e-05 |
1.35e-03 |
0.67500 |
0.626000 |
-0.253000 |
2.71e-05 |
0.089400 |
Creation of C4 and C2 activators |
14 |
7.72e-05 |
2.51e-03 |
0.66900 |
0.643000 |
-0.185000 |
3.13e-05 |
0.230000 |
Initial triggering of complement |
20 |
2.62e-06 |
1.80e-04 |
0.65300 |
0.638000 |
-0.139000 |
7.95e-07 |
0.281000 |
Digestion |
12 |
5.74e-04 |
1.04e-02 |
0.64300 |
-0.636000 |
0.095000 |
1.38e-04 |
0.569000 |
Na+/Cl- dependent neurotransmitter transporters |
11 |
1.37e-03 |
1.95e-02 |
0.63000 |
-0.617000 |
0.129000 |
3.95e-04 |
0.460000 |
Digestion and absorption |
13 |
7.45e-04 |
1.26e-02 |
0.60600 |
-0.593000 |
0.127000 |
2.16e-04 |
0.428000 |
Cholesterol biosynthesis |
16 |
3.56e-04 |
7.58e-03 |
0.57600 |
-0.575000 |
-0.036400 |
6.87e-05 |
0.801000 |
Signal regulatory protein family interactions |
11 |
3.99e-03 |
3.84e-02 |
0.57400 |
0.427000 |
-0.384000 |
1.41e-02 |
0.027500 |
GABA synthesis, release, reuptake and degradation |
11 |
7.32e-03 |
5.90e-02 |
0.54500 |
-0.543000 |
0.049000 |
1.82e-03 |
0.778000 |
Regulation of IFNA signaling |
10 |
1.31e-02 |
8.73e-02 |
0.54100 |
0.455000 |
0.293000 |
1.26e-02 |
0.109000 |
eNOS activation |
10 |
1.20e-02 |
8.24e-02 |
0.54100 |
0.161000 |
-0.516000 |
3.78e-01 |
0.004710 |
SRP-dependent cotranslational protein targeting to membrane |
42 |
2.00e-08 |
2.24e-06 |
0.53300 |
0.517000 |
0.131000 |
6.94e-09 |
0.143000 |
Regulation of Complement cascade |
30 |
2.80e-06 |
1.82e-04 |
0.53100 |
0.490000 |
-0.203000 |
3.40e-06 |
0.054100 |
Citric acid cycle (TCA cycle) |
13 |
4.29e-03 |
4.00e-02 |
0.53100 |
-0.519000 |
-0.112000 |
1.20e-03 |
0.486000 |
Metabolism of nitric oxide: NOS3 activation and regulation |
14 |
2.61e-03 |
3.15e-02 |
0.53000 |
0.169000 |
-0.502000 |
2.72e-01 |
0.001140 |
Retrograde neurotrophin signalling |
12 |
6.51e-03 |
5.38e-02 |
0.52600 |
0.214000 |
-0.481000 |
2.00e-01 |
0.003940 |
HDMs demethylate histones |
15 |
2.19e-03 |
2.79e-02 |
0.52100 |
-0.521000 |
0.026100 |
4.79e-04 |
0.861000 |
HIV elongation arrest and recovery |
15 |
3.51e-03 |
3.49e-02 |
0.50500 |
-0.374000 |
-0.340000 |
1.22e-02 |
0.022600 |
Pausing and recovery of HIV elongation |
15 |
3.51e-03 |
3.49e-02 |
0.50500 |
-0.374000 |
-0.340000 |
1.22e-02 |
0.022600 |
Pausing and recovery of Tat-mediated HIV elongation |
15 |
3.51e-03 |
3.49e-02 |
0.50500 |
-0.374000 |
-0.340000 |
1.22e-02 |
0.022600 |
Tat-mediated HIV elongation arrest and recovery |
15 |
3.51e-03 |
3.49e-02 |
0.50500 |
-0.374000 |
-0.340000 |
1.22e-02 |
0.022600 |
Regulation of FZD by ubiquitination |
11 |
1.45e-02 |
9.48e-02 |
0.50400 |
-0.242000 |
0.442000 |
1.64e-01 |
0.011200 |
NS1 Mediated Effects on Host Pathways |
25 |
8.97e-05 |
2.84e-03 |
0.50100 |
-0.477000 |
-0.152000 |
3.61e-05 |
0.188000 |
Peptide chain elongation |
27 |
4.43e-05 |
1.66e-03 |
0.50000 |
0.467000 |
0.181000 |
2.71e-05 |
0.104000 |
Viral mRNA Translation |
27 |
5.58e-05 |
1.96e-03 |
0.49400 |
0.478000 |
0.123000 |
1.69e-05 |
0.269000 |
Activation of Matrix Metalloproteinases |
18 |
1.31e-03 |
1.92e-02 |
0.49400 |
0.472000 |
-0.146000 |
5.29e-04 |
0.284000 |
Downregulation of SMAD2/3:SMAD4 transcriptional activity |
14 |
5.90e-03 |
5.12e-02 |
0.49300 |
-0.473000 |
0.137000 |
2.18e-03 |
0.374000 |
Activation of gene expression by SREBF (SREBP) |
35 |
4.11e-06 |
2.42e-04 |
0.48800 |
-0.475000 |
-0.114000 |
1.18e-06 |
0.243000 |
Interferon gamma signaling |
53 |
5.09e-09 |
7.84e-07 |
0.48800 |
0.447000 |
-0.195000 |
1.78e-08 |
0.014100 |
Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) |
19 |
1.25e-03 |
1.85e-02 |
0.48800 |
-0.209000 |
-0.441000 |
1.15e-01 |
0.000888 |
TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain |
14 |
6.54e-03 |
5.38e-02 |
0.48700 |
-0.459000 |
0.163000 |
2.94e-03 |
0.290000 |
Interleukin-35 Signalling |
11 |
2.39e-02 |
1.26e-01 |
0.47800 |
0.174000 |
0.446000 |
3.17e-01 |
0.010500 |
Pyruvate metabolism and Citric Acid (TCA) cycle |
35 |
7.08e-06 |
3.80e-04 |
0.47800 |
-0.455000 |
-0.146000 |
3.20e-06 |
0.136000 |
Antimicrobial peptides |
21 |
7.61e-04 |
1.27e-02 |
0.47700 |
0.469000 |
-0.084300 |
1.99e-04 |
0.504000 |
Common Pathway of Fibrin Clot Formation |
12 |
1.79e-02 |
1.05e-01 |
0.47600 |
0.390000 |
0.274000 |
1.94e-02 |
0.101000 |
Transport of Ribonucleoproteins into the Host Nucleus |
22 |
6.37e-04 |
1.14e-02 |
0.47400 |
-0.460000 |
-0.114000 |
1.87e-04 |
0.355000 |
Processing of Intronless Pre-mRNAs |
11 |
2.63e-02 |
1.30e-01 |
0.46900 |
-0.467000 |
0.047400 |
7.39e-03 |
0.786000 |
Selenocysteine synthesis |
29 |
9.24e-05 |
2.85e-03 |
0.46400 |
0.449000 |
0.119000 |
2.90e-05 |
0.267000 |
Transcriptional regulation by small RNAs |
29 |
1.03e-04 |
3.11e-03 |
0.46100 |
-0.454000 |
-0.078100 |
2.31e-05 |
0.467000 |
ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression |
13 |
1.72e-02 |
1.04e-01 |
0.46000 |
-0.225000 |
-0.401000 |
1.60e-01 |
0.012400 |
Viral Messenger RNA Synthesis |
25 |
4.15e-04 |
8.33e-03 |
0.45800 |
-0.437000 |
-0.139000 |
1.59e-04 |
0.231000 |
Interferon alpha/beta signaling |
37 |
9.90e-06 |
5.09e-04 |
0.45700 |
0.453000 |
0.059100 |
1.85e-06 |
0.534000 |
Biosynthesis of specialized proresolving mediators (SPMs) |
11 |
3.50e-02 |
1.56e-01 |
0.45000 |
0.444000 |
-0.072300 |
1.08e-02 |
0.678000 |
Deposition of new CENPA-containing nucleosomes at the centromere |
16 |
8.35e-03 |
6.32e-02 |
0.45000 |
-0.246000 |
-0.376000 |
8.81e-02 |
0.009160 |
Nucleosome assembly |
16 |
8.35e-03 |
6.32e-02 |
0.45000 |
-0.246000 |
-0.376000 |
8.81e-02 |
0.009160 |
TNFR1-induced proapoptotic signaling |
12 |
2.64e-02 |
1.30e-01 |
0.45000 |
0.004140 |
-0.450000 |
9.80e-01 |
0.007020 |
Transport of Mature mRNAs Derived from Intronless Transcripts |
29 |
1.64e-04 |
4.51e-03 |
0.44900 |
-0.439000 |
-0.098200 |
4.38e-05 |
0.360000 |
Eukaryotic Translation Termination |
29 |
1.74e-04 |
4.66e-03 |
0.44800 |
0.442000 |
0.068100 |
3.76e-05 |
0.526000 |
Export of Viral Ribonucleoproteins from Nucleus |
23 |
1.15e-03 |
1.75e-02 |
0.44400 |
-0.442000 |
-0.046200 |
2.47e-04 |
0.701000 |
Regulation of TP53 Activity through Acetylation |
22 |
1.82e-03 |
2.41e-02 |
0.44100 |
-0.331000 |
-0.291000 |
7.27e-03 |
0.018000 |
Resolution of D-Loop Structures |
23 |
1.41e-03 |
1.97e-02 |
0.44000 |
-0.250000 |
-0.362000 |
3.81e-02 |
0.002680 |
Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) |
20 |
3.14e-03 |
3.49e-02 |
0.43900 |
-0.438000 |
-0.035200 |
7.03e-04 |
0.786000 |
Regulation of Glucokinase by Glucokinase Regulatory Protein |
20 |
3.14e-03 |
3.49e-02 |
0.43900 |
-0.438000 |
-0.035200 |
7.03e-04 |
0.786000 |
Transport of Mature mRNA Derived from an Intronless Transcript |
28 |
3.51e-04 |
7.58e-03 |
0.43700 |
-0.430000 |
-0.076600 |
8.27e-05 |
0.483000 |
FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes |
20 |
3.27e-03 |
3.49e-02 |
0.43500 |
-0.420000 |
0.115000 |
1.15e-03 |
0.375000 |
Interactions of Rev with host cellular proteins |
25 |
8.80e-04 |
1.43e-02 |
0.43500 |
-0.424000 |
-0.097200 |
2.44e-04 |
0.400000 |
Complement cascade |
37 |
2.59e-05 |
1.14e-03 |
0.43500 |
0.413000 |
-0.135000 |
1.38e-05 |
0.154000 |
Deadenylation of mRNA |
16 |
1.09e-02 |
7.62e-02 |
0.43200 |
-0.418000 |
0.109000 |
3.77e-03 |
0.450000 |
ER Quality Control Compartment (ERQC) |
11 |
4.65e-02 |
1.89e-01 |
0.43200 |
-0.034400 |
-0.431000 |
8.43e-01 |
0.013400 |
Pyruvate metabolism |
21 |
3.05e-03 |
3.48e-02 |
0.43100 |
-0.412000 |
-0.127000 |
1.08e-03 |
0.316000 |
Activation of the pre-replicative complex |
23 |
1.76e-03 |
2.38e-02 |
0.43100 |
-0.416000 |
-0.112000 |
5.56e-04 |
0.353000 |
Transport of the SLBP Dependant Mature mRNA |
24 |
1.34e-03 |
1.95e-02 |
0.43100 |
-0.413000 |
-0.122000 |
4.60e-04 |
0.303000 |
Abortive elongation of HIV-1 transcript in the absence of Tat |
12 |
3.73e-02 |
1.62e-01 |
0.43000 |
-0.376000 |
-0.210000 |
2.42e-02 |
0.209000 |
mRNA Capping |
16 |
1.28e-02 |
8.61e-02 |
0.43000 |
-0.269000 |
-0.335000 |
6.27e-02 |
0.020300 |
TP53 Regulates Transcription of Death Receptors and Ligands |
10 |
6.51e-02 |
2.25e-01 |
0.42900 |
-0.185000 |
-0.387000 |
3.10e-01 |
0.034000 |
Budding and maturation of HIV virion |
15 |
1.51e-02 |
9.73e-02 |
0.42900 |
0.277000 |
-0.327000 |
6.29e-02 |
0.028600 |
Formation of a pool of free 40S subunits |
33 |
1.42e-04 |
3.97e-03 |
0.42500 |
0.415000 |
0.091300 |
3.72e-05 |
0.364000 |
SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion |
12 |
4.07e-02 |
1.71e-01 |
0.42500 |
0.361000 |
0.223000 |
3.03e-02 |
0.181000 |
RNA Pol II CTD phosphorylation and interaction with CE |
15 |
1.91e-02 |
1.10e-01 |
0.42300 |
-0.235000 |
-0.351000 |
1.16e-01 |
0.018500 |
RNA Pol II CTD phosphorylation and interaction with CE during HIV infection |
15 |
1.91e-02 |
1.10e-01 |
0.42300 |
-0.235000 |
-0.351000 |
1.16e-01 |
0.018500 |
TNFs bind their physiological receptors |
19 |
6.35e-03 |
5.34e-02 |
0.42100 |
0.419000 |
-0.041900 |
1.58e-03 |
0.752000 |
FOXO-mediated transcription of cell death genes |
13 |
3.03e-02 |
1.42e-01 |
0.42000 |
-0.294000 |
0.301000 |
6.66e-02 |
0.060500 |
Nuclear import of Rev protein |
23 |
2.41e-03 |
2.95e-02 |
0.42000 |
-0.410000 |
-0.088500 |
6.64e-04 |
0.463000 |
Rev-mediated nuclear export of HIV RNA |
24 |
1.84e-03 |
2.41e-02 |
0.42000 |
-0.415000 |
-0.061600 |
4.34e-04 |
0.602000 |
NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 |
10 |
7.15e-02 |
2.37e-01 |
0.41900 |
0.053200 |
-0.415000 |
7.71e-01 |
0.023000 |
Formation of the beta-catenin:TCF transactivating complex |
29 |
4.53e-04 |
8.73e-03 |
0.41900 |
-0.376000 |
0.184000 |
4.57e-04 |
0.087100 |
Eukaryotic Translation Elongation |
30 |
4.19e-04 |
8.33e-03 |
0.41800 |
0.385000 |
0.165000 |
2.67e-04 |
0.119000 |
FGFR2 alternative splicing |
13 |
3.42e-02 |
1.55e-01 |
0.41800 |
-0.386000 |
-0.162000 |
1.60e-02 |
0.313000 |
Resolution of D-loop Structures through Holliday Junction Intermediates |
22 |
3.40e-03 |
3.49e-02 |
0.41800 |
-0.232000 |
-0.348000 |
6.02e-02 |
0.004700 |
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) |
29 |
5.63e-04 |
1.04e-02 |
0.41700 |
0.389000 |
0.152000 |
2.93e-04 |
0.158000 |
NEP/NS2 Interacts with the Cellular Export Machinery |
22 |
3.29e-03 |
3.49e-02 |
0.41700 |
-0.417000 |
-0.006840 |
7.20e-04 |
0.956000 |
Heme degradation |
11 |
6.05e-02 |
2.17e-01 |
0.41400 |
0.397000 |
0.118000 |
2.27e-02 |
0.497000 |
Transport of the SLBP independent Mature mRNA |
23 |
2.92e-03 |
3.40e-02 |
0.41300 |
-0.402000 |
-0.096200 |
8.58e-04 |
0.425000 |
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
11 |
6.44e-02 |
2.24e-01 |
0.41100 |
0.335000 |
0.238000 |
5.45e-02 |
0.172000 |
PKMTs methylate histone lysines |
32 |
3.23e-04 |
7.38e-03 |
0.41000 |
-0.410000 |
-0.018400 |
6.14e-05 |
0.857000 |
Other interleukin signaling |
16 |
1.93e-02 |
1.10e-01 |
0.40800 |
0.145000 |
0.381000 |
3.16e-01 |
0.008300 |
Vpr-mediated nuclear import of PICs |
23 |
3.36e-03 |
3.49e-02 |
0.40800 |
-0.400000 |
-0.077500 |
8.92e-04 |
0.520000 |
Gluconeogenesis |
21 |
5.53e-03 |
4.87e-02 |
0.40600 |
-0.404000 |
0.038000 |
1.35e-03 |
0.763000 |
Thromboxane signalling through TP receptor |
14 |
3.30e-02 |
1.51e-01 |
0.40500 |
0.392000 |
0.101000 |
1.11e-02 |
0.512000 |
Surfactant metabolism |
13 |
4.20e-02 |
1.75e-01 |
0.40100 |
0.208000 |
-0.343000 |
1.95e-01 |
0.032500 |
Diseases of carbohydrate metabolism |
22 |
5.71e-03 |
4.99e-02 |
0.39800 |
0.373000 |
0.140000 |
2.50e-03 |
0.256000 |
Glutamate Neurotransmitter Release Cycle |
15 |
2.85e-02 |
1.37e-01 |
0.39500 |
-0.261000 |
0.297000 |
8.07e-02 |
0.046600 |
Receptor-type tyrosine-protein phosphatases |
10 |
9.55e-02 |
2.84e-01 |
0.39300 |
0.339000 |
-0.200000 |
6.37e-02 |
0.274000 |
SUMOylation of SUMOylation proteins |
22 |
6.38e-03 |
5.34e-02 |
0.39200 |
-0.390000 |
-0.045600 |
1.56e-03 |
0.712000 |
GTP hydrolysis and joining of the 60S ribosomal subunit |
38 |
1.79e-04 |
4.70e-03 |
0.39100 |
0.375000 |
0.113000 |
6.49e-05 |
0.230000 |
Glucuronidation |
10 |
1.02e-01 |
2.93e-01 |
0.39100 |
0.387000 |
0.060000 |
3.43e-02 |
0.743000 |
ADP signalling through P2Y purinoceptor 1 |
17 |
2.17e-02 |
1.17e-01 |
0.39000 |
0.361000 |
0.147000 |
9.95e-03 |
0.294000 |
Prostacyclin signalling through prostacyclin receptor |
11 |
8.08e-02 |
2.57e-01 |
0.39000 |
0.386000 |
-0.053000 |
2.66e-02 |
0.761000 |
L13a-mediated translational silencing of Ceruloplasmin expression |
37 |
2.40e-04 |
5.87e-03 |
0.38900 |
0.377000 |
0.096000 |
7.16e-05 |
0.313000 |
Interactions of Vpr with host cellular proteins |
25 |
3.62e-03 |
3.57e-02 |
0.38900 |
-0.382000 |
-0.072400 |
9.55e-04 |
0.531000 |
Regulation of TP53 Activity through Association with Co-factors |
10 |
1.04e-01 |
2.95e-01 |
0.38800 |
0.015800 |
-0.388000 |
9.31e-01 |
0.033800 |
FOXO-mediated transcription of cell cycle genes |
13 |
5.16e-02 |
2.02e-01 |
0.38800 |
-0.346000 |
0.176000 |
3.09e-02 |
0.273000 |
Attenuation phase |
15 |
3.68e-02 |
1.62e-01 |
0.38400 |
-0.381000 |
-0.046100 |
1.06e-02 |
0.757000 |
Glutathione synthesis and recycling |
10 |
1.12e-01 |
3.02e-01 |
0.38200 |
0.025600 |
-0.381000 |
8.88e-01 |
0.037000 |
Misspliced GSK3beta mutants stabilize beta-catenin |
13 |
5.80e-02 |
2.10e-01 |
0.38200 |
-0.380000 |
0.035300 |
1.77e-02 |
0.826000 |
S33 mutants of beta-catenin aren't phosphorylated |
13 |
5.80e-02 |
2.10e-01 |
0.38200 |
-0.380000 |
0.035300 |
1.77e-02 |
0.826000 |
S37 mutants of beta-catenin aren't phosphorylated |
13 |
5.80e-02 |
2.10e-01 |
0.38200 |
-0.380000 |
0.035300 |
1.77e-02 |
0.826000 |
S45 mutants of beta-catenin aren't phosphorylated |
13 |
5.80e-02 |
2.10e-01 |
0.38200 |
-0.380000 |
0.035300 |
1.77e-02 |
0.826000 |
T41 mutants of beta-catenin aren't phosphorylated |
13 |
5.80e-02 |
2.10e-01 |
0.38200 |
-0.380000 |
0.035300 |
1.77e-02 |
0.826000 |
phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex |
13 |
5.80e-02 |
2.10e-01 |
0.38200 |
-0.380000 |
0.035300 |
1.77e-02 |
0.826000 |
Diseases associated with glycosylation precursor biosynthesis |
15 |
3.82e-02 |
1.65e-01 |
0.38200 |
0.381000 |
0.026700 |
1.07e-02 |
0.858000 |
Regulation of cholesterol biosynthesis by SREBP (SREBF) |
45 |
6.34e-05 |
2.17e-03 |
0.38000 |
-0.369000 |
-0.091500 |
1.85e-05 |
0.289000 |
Fertilization |
10 |
1.16e-01 |
3.10e-01 |
0.37600 |
0.279000 |
-0.252000 |
1.27e-01 |
0.167000 |
Regulation of pyruvate dehydrogenase (PDH) complex |
11 |
9.89e-02 |
2.87e-01 |
0.37500 |
-0.375000 |
-0.006250 |
3.15e-02 |
0.971000 |
Interleukin-10 signaling |
29 |
2.32e-03 |
2.92e-02 |
0.37500 |
0.370000 |
0.056200 |
5.57e-04 |
0.601000 |
SUMOylation of ubiquitinylation proteins |
25 |
5.35e-03 |
4.78e-02 |
0.37500 |
-0.371000 |
-0.049900 |
1.32e-03 |
0.666000 |
Formation of Fibrin Clot (Clotting Cascade) |
23 |
8.41e-03 |
6.32e-02 |
0.37400 |
0.358000 |
0.109000 |
2.99e-03 |
0.365000 |
Postmitotic nuclear pore complex (NPC) reformation |
20 |
1.65e-02 |
1.03e-01 |
0.37100 |
-0.367000 |
-0.057100 |
4.56e-03 |
0.659000 |
ROS and RNS production in phagocytes |
22 |
1.01e-02 |
7.25e-02 |
0.37100 |
0.245000 |
-0.279000 |
4.71e-02 |
0.023700 |
Translesion Synthesis by POLH |
10 |
1.25e-01 |
3.23e-01 |
0.37000 |
-0.188000 |
0.319000 |
3.04e-01 |
0.080700 |
Signaling by Leptin |
10 |
1.25e-01 |
3.24e-01 |
0.37000 |
-0.211000 |
0.303000 |
2.47e-01 |
0.097000 |
Interleukin-7 signaling |
14 |
5.62e-02 |
2.09e-01 |
0.36900 |
-0.362000 |
0.074400 |
1.91e-02 |
0.630000 |
Regulation of TP53 Degradation |
27 |
4.34e-03 |
4.02e-02 |
0.36900 |
-0.325000 |
-0.175000 |
3.46e-03 |
0.116000 |
Regulation of HSF1-mediated heat shock response |
50 |
4.05e-05 |
1.61e-03 |
0.36800 |
-0.368000 |
-0.005950 |
6.88e-06 |
0.942000 |
Triglyceride metabolism |
19 |
2.15e-02 |
1.16e-01 |
0.36600 |
-0.357000 |
0.080700 |
7.06e-03 |
0.542000 |
Class I peroxisomal membrane protein import |
10 |
1.30e-01 |
3.31e-01 |
0.36600 |
0.244000 |
-0.273000 |
1.81e-01 |
0.135000 |
G0 and Early G1 |
21 |
1.43e-02 |
9.46e-02 |
0.36600 |
-0.352000 |
0.098800 |
5.20e-03 |
0.433000 |
Cell recruitment (pro-inflammatory response) |
18 |
2.61e-02 |
1.30e-01 |
0.36500 |
0.317000 |
-0.182000 |
2.00e-02 |
0.182000 |
Purinergic signaling in leishmaniasis infection |
18 |
2.61e-02 |
1.30e-01 |
0.36500 |
0.317000 |
-0.182000 |
2.00e-02 |
0.182000 |
NOTCH2 intracellular domain regulates transcription |
10 |
1.40e-01 |
3.39e-01 |
0.36500 |
-0.214000 |
-0.296000 |
2.42e-01 |
0.106000 |
VLDLR internalisation and degradation |
10 |
1.34e-01 |
3.32e-01 |
0.36500 |
0.112000 |
-0.347000 |
5.41e-01 |
0.057400 |
Transcription of E2F targets under negative control by DREAM complex |
16 |
3.98e-02 |
1.69e-01 |
0.36400 |
-0.300000 |
0.207000 |
3.81e-02 |
0.152000 |
G1/S-Specific Transcription |
23 |
1.03e-02 |
7.40e-02 |
0.36300 |
-0.354000 |
0.080300 |
3.28e-03 |
0.505000 |
DNA Damage/Telomere Stress Induced Senescence |
20 |
2.14e-02 |
1.16e-01 |
0.36100 |
-0.314000 |
-0.177000 |
1.50e-02 |
0.171000 |
CS/DS degradation |
11 |
1.17e-01 |
3.11e-01 |
0.36000 |
0.353000 |
-0.069000 |
4.25e-02 |
0.692000 |
Condensation of Prophase Chromosomes |
10 |
1.43e-01 |
3.43e-01 |
0.35900 |
-0.355000 |
0.056300 |
5.20e-02 |
0.758000 |
Metabolism of steroid hormones |
22 |
1.49e-02 |
9.62e-02 |
0.35900 |
0.340000 |
0.115000 |
5.77e-03 |
0.352000 |
Antigen Presentation: Folding, assembly and peptide loading of class I MHC |
11 |
1.24e-01 |
3.23e-01 |
0.35900 |
0.296000 |
0.203000 |
8.94e-02 |
0.244000 |
CD28 dependent PI3K/Akt signaling |
19 |
2.74e-02 |
1.33e-01 |
0.35800 |
-0.160000 |
-0.320000 |
2.28e-01 |
0.015800 |
Presynaptic depolarization and calcium channel opening |
11 |
1.23e-01 |
3.23e-01 |
0.35700 |
-0.356000 |
-0.018600 |
4.09e-02 |
0.915000 |
Cellular response to heat stress |
66 |
3.74e-06 |
2.31e-04 |
0.35600 |
-0.355000 |
0.024200 |
6.29e-07 |
0.735000 |
RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known |
30 |
3.18e-03 |
3.49e-02 |
0.35600 |
-0.307000 |
0.180000 |
3.64e-03 |
0.089000 |
Platelet Adhesion to exposed collagen |
11 |
1.30e-01 |
3.31e-01 |
0.35500 |
0.263000 |
0.238000 |
1.31e-01 |
0.171000 |
Striated Muscle Contraction |
30 |
3.49e-03 |
3.49e-02 |
0.35400 |
-0.353000 |
0.035900 |
8.34e-04 |
0.734000 |
Collagen degradation |
27 |
6.41e-03 |
5.34e-02 |
0.35400 |
0.350000 |
0.054700 |
1.65e-03 |
0.623000 |
Miscellaneous transport and binding events |
16 |
5.21e-02 |
2.02e-01 |
0.35300 |
-0.311000 |
-0.167000 |
3.12e-02 |
0.247000 |
Downregulation of ERBB2 signaling |
17 |
4.07e-02 |
1.71e-01 |
0.35300 |
0.089900 |
-0.342000 |
5.21e-01 |
0.014800 |
RORA activates gene expression |
16 |
5.18e-02 |
2.02e-01 |
0.35300 |
-0.342000 |
-0.087800 |
1.80e-02 |
0.543000 |
Depolymerisation of the Nuclear Lamina |
13 |
8.73e-02 |
2.69e-01 |
0.35100 |
-0.299000 |
0.185000 |
6.20e-02 |
0.249000 |
Glucagon-type ligand receptors |
15 |
6.40e-02 |
2.23e-01 |
0.35100 |
0.338000 |
0.096500 |
2.36e-02 |
0.518000 |
ADP signalling through P2Y purinoceptor 12 |
13 |
9.06e-02 |
2.73e-01 |
0.35000 |
0.345000 |
-0.058900 |
3.12e-02 |
0.713000 |
Metabolism of Angiotensinogen to Angiotensins |
11 |
1.30e-01 |
3.31e-01 |
0.34900 |
0.244000 |
-0.250000 |
1.62e-01 |
0.152000 |
TP53 Regulates Transcription of DNA Repair Genes |
38 |
1.11e-03 |
1.72e-02 |
0.34800 |
-0.280000 |
-0.207000 |
2.81e-03 |
0.027400 |
Cap-dependent Translation Initiation |
44 |
3.63e-04 |
7.58e-03 |
0.34800 |
0.338000 |
0.083800 |
1.06e-04 |
0.337000 |
Eukaryotic Translation Initiation |
44 |
3.63e-04 |
7.58e-03 |
0.34800 |
0.338000 |
0.083800 |
1.06e-04 |
0.337000 |
AMER1 mutants destabilize the destruction complex |
12 |
1.12e-01 |
3.02e-01 |
0.34800 |
-0.347000 |
0.033200 |
3.77e-02 |
0.842000 |
APC truncation mutants have impaired AXIN binding |
12 |
1.12e-01 |
3.02e-01 |
0.34800 |
-0.347000 |
0.033200 |
3.77e-02 |
0.842000 |
AXIN missense mutants destabilize the destruction complex |
12 |
1.12e-01 |
3.02e-01 |
0.34800 |
-0.347000 |
0.033200 |
3.77e-02 |
0.842000 |
AXIN mutants destabilize the destruction complex, activating WNT signaling |
12 |
1.12e-01 |
3.02e-01 |
0.34800 |
-0.347000 |
0.033200 |
3.77e-02 |
0.842000 |
Truncations of AMER1 destabilize the destruction complex |
12 |
1.12e-01 |
3.02e-01 |
0.34800 |
-0.347000 |
0.033200 |
3.77e-02 |
0.842000 |
truncated APC mutants destabilize the destruction complex |
12 |
1.12e-01 |
3.02e-01 |
0.34800 |
-0.347000 |
0.033200 |
3.77e-02 |
0.842000 |
NOTCH3 Activation and Transmission of Signal to the Nucleus |
16 |
5.60e-02 |
2.09e-01 |
0.34800 |
-0.057400 |
-0.343000 |
6.91e-01 |
0.017600 |
Formation of the ternary complex, and subsequently, the 43S complex |
17 |
4.84e-02 |
1.94e-01 |
0.34600 |
0.338000 |
0.071500 |
1.57e-02 |
0.610000 |
EGFR downregulation |
19 |
3.70e-02 |
1.62e-01 |
0.34300 |
-0.172000 |
-0.296000 |
1.95e-01 |
0.025400 |
Regulation of TP53 Expression and Degradation |
28 |
7.82e-03 |
6.11e-02 |
0.34300 |
-0.284000 |
-0.192000 |
9.34e-03 |
0.079300 |
Amino acid transport across the plasma membrane |
26 |
1.08e-02 |
7.60e-02 |
0.34300 |
-0.328000 |
-0.099200 |
3.82e-03 |
0.382000 |
Triglyceride catabolism |
13 |
1.00e-01 |
2.88e-01 |
0.34200 |
-0.326000 |
0.103000 |
4.16e-02 |
0.521000 |
PKA activation |
15 |
7.30e-02 |
2.40e-01 |
0.34100 |
0.013500 |
0.341000 |
9.28e-01 |
0.022200 |
Repression of WNT target genes |
11 |
1.44e-01 |
3.44e-01 |
0.34000 |
-0.234000 |
0.247000 |
1.80e-01 |
0.155000 |
Signaling by WNT in cancer |
26 |
1.07e-02 |
7.55e-02 |
0.33900 |
-0.277000 |
0.196000 |
1.46e-02 |
0.084100 |
SUMOylation of DNA replication proteins |
32 |
4.18e-03 |
3.96e-02 |
0.33900 |
-0.336000 |
-0.040700 |
9.96e-04 |
0.691000 |
Regulation of glycolysis by fructose 2,6-bisphosphate metabolism |
11 |
1.51e-01 |
3.51e-01 |
0.33900 |
-0.338000 |
0.017500 |
5.22e-02 |
0.920000 |
Regulation of TNFR1 signaling |
24 |
1.71e-02 |
1.04e-01 |
0.33800 |
-0.125000 |
-0.314000 |
2.88e-01 |
0.007770 |
Glucose metabolism |
63 |
2.29e-05 |
1.05e-03 |
0.33700 |
-0.336000 |
-0.027700 |
3.99e-06 |
0.704000 |
PINK1-PRKN Mediated Mitophagy |
13 |
1.10e-01 |
3.02e-01 |
0.33700 |
-0.057600 |
-0.332000 |
7.19e-01 |
0.038000 |
Formation of HIV elongation complex in the absence of HIV Tat |
23 |
2.14e-02 |
1.16e-01 |
0.33700 |
-0.250000 |
-0.226000 |
3.82e-02 |
0.061200 |
Formation of HIV-1 elongation complex containing HIV-1 Tat |
23 |
2.14e-02 |
1.16e-01 |
0.33700 |
-0.250000 |
-0.226000 |
3.82e-02 |
0.061200 |
HIV Transcription Elongation |
23 |
2.14e-02 |
1.16e-01 |
0.33700 |
-0.250000 |
-0.226000 |
3.82e-02 |
0.061200 |
Tat-mediated elongation of the HIV-1 transcript |
23 |
2.14e-02 |
1.16e-01 |
0.33700 |
-0.250000 |
-0.226000 |
3.82e-02 |
0.061200 |
Late endosomal microautophagy |
17 |
5.42e-02 |
2.06e-01 |
0.33600 |
0.287000 |
-0.175000 |
4.05e-02 |
0.212000 |
Nucleotide-like (purinergic) receptors |
10 |
1.90e-01 |
4.08e-01 |
0.33500 |
0.308000 |
0.132000 |
9.18e-02 |
0.471000 |
Signal amplification |
22 |
2.54e-02 |
1.29e-01 |
0.33500 |
0.331000 |
0.045600 |
7.14e-03 |
0.712000 |
Inhibition of replication initiation of damaged DNA by RB1/E2F1 |
12 |
1.39e-01 |
3.37e-01 |
0.33400 |
-0.242000 |
-0.230000 |
1.46e-01 |
0.168000 |
Kinesins |
29 |
8.47e-03 |
6.33e-02 |
0.33400 |
-0.177000 |
-0.283000 |
1.00e-01 |
0.008310 |
Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell |
61 |
4.26e-05 |
1.64e-03 |
0.33300 |
0.330000 |
0.045800 |
8.48e-06 |
0.537000 |
Cytosolic sulfonation of small molecules |
14 |
9.80e-02 |
2.87e-01 |
0.33300 |
0.332000 |
0.019900 |
3.13e-02 |
0.898000 |
E2F mediated regulation of DNA replication |
18 |
5.25e-02 |
2.02e-01 |
0.33300 |
-0.276000 |
-0.186000 |
4.25e-02 |
0.172000 |
Regulation of IFNG signaling |
10 |
1.92e-01 |
4.10e-01 |
0.33100 |
0.321000 |
-0.078700 |
7.85e-02 |
0.667000 |
Homologous DNA Pairing and Strand Exchange |
28 |
1.09e-02 |
7.62e-02 |
0.33000 |
-0.159000 |
-0.290000 |
1.46e-01 |
0.007980 |
EGR2 and SOX10-mediated initiation of Schwann cell myelination |
23 |
2.37e-02 |
1.26e-01 |
0.33000 |
-0.328000 |
-0.036700 |
6.47e-03 |
0.761000 |
Endogenous sterols |
18 |
5.55e-02 |
2.08e-01 |
0.33000 |
0.217000 |
0.249000 |
1.11e-01 |
0.067900 |
Glycolysis |
51 |
2.58e-04 |
6.01e-03 |
0.33000 |
-0.328000 |
-0.031500 |
5.08e-05 |
0.698000 |
RNA polymerase II transcribes snRNA genes |
47 |
5.39e-04 |
1.01e-02 |
0.33000 |
-0.266000 |
-0.195000 |
1.64e-03 |
0.020700 |
Removal of the Flap Intermediate |
11 |
1.69e-01 |
3.79e-01 |
0.32900 |
-0.319000 |
-0.083100 |
6.72e-02 |
0.633000 |
Regulation of beta-cell development |
19 |
4.79e-02 |
1.93e-01 |
0.32900 |
-0.298000 |
-0.138000 |
2.44e-02 |
0.297000 |
HSF1 activation |
18 |
5.35e-02 |
2.05e-01 |
0.32800 |
-0.310000 |
0.107000 |
2.28e-02 |
0.432000 |
Intrinsic Pathway of Fibrin Clot Formation |
14 |
1.07e-01 |
2.97e-01 |
0.32800 |
0.315000 |
0.092000 |
4.14e-02 |
0.551000 |
Smooth Muscle Contraction |
26 |
1.57e-02 |
1.00e-01 |
0.32800 |
0.317000 |
0.082100 |
5.11e-03 |
0.469000 |
Selenoamino acid metabolism |
39 |
2.01e-03 |
2.58e-02 |
0.32800 |
0.316000 |
0.086000 |
6.42e-04 |
0.353000 |
Response of EIF2AK4 (GCN2) to amino acid deficiency |
32 |
6.32e-03 |
5.34e-02 |
0.32700 |
0.302000 |
0.126000 |
3.14e-03 |
0.219000 |
G beta:gamma signalling through PLC beta |
12 |
1.46e-01 |
3.46e-01 |
0.32600 |
0.324000 |
-0.038700 |
5.21e-02 |
0.817000 |
Translesion synthesis by REV1 |
10 |
2.03e-01 |
4.18e-01 |
0.32400 |
-0.294000 |
0.137000 |
1.07e-01 |
0.453000 |
Circadian Clock |
53 |
2.30e-04 |
5.79e-03 |
0.32300 |
-0.297000 |
0.129000 |
1.89e-04 |
0.105000 |
Positive epigenetic regulation of rRNA expression |
32 |
7.27e-03 |
5.90e-02 |
0.32300 |
-0.260000 |
-0.192000 |
1.11e-02 |
0.059800 |
Gap junction trafficking |
13 |
1.27e-01 |
3.27e-01 |
0.32300 |
0.208000 |
-0.247000 |
1.93e-01 |
0.124000 |
Interleukin-6 family signaling |
17 |
7.33e-02 |
2.40e-01 |
0.32300 |
0.237000 |
0.220000 |
9.15e-02 |
0.117000 |
Erythropoietin activates Phosphoinositide-3-kinase (PI3K) |
10 |
2.05e-01 |
4.22e-01 |
0.32300 |
-0.195000 |
0.257000 |
2.86e-01 |
0.159000 |
SUMOylation of transcription cofactors |
32 |
7.11e-03 |
5.80e-02 |
0.32200 |
-0.317000 |
-0.059600 |
1.94e-03 |
0.560000 |
Scavenging by Class A Receptors |
10 |
2.07e-01 |
4.25e-01 |
0.32200 |
0.284000 |
-0.151000 |
1.19e-01 |
0.408000 |
Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer |
30 |
9.71e-03 |
7.04e-02 |
0.32100 |
-0.321000 |
-0.004610 |
2.33e-03 |
0.965000 |
B-WICH complex positively regulates rRNA expression |
21 |
3.97e-02 |
1.69e-01 |
0.32100 |
-0.315000 |
-0.062400 |
1.25e-02 |
0.621000 |
Processive synthesis on the lagging strand |
12 |
1.60e-01 |
3.65e-01 |
0.31900 |
-0.319000 |
0.002730 |
5.55e-02 |
0.987000 |
Oncogene Induced Senescence |
24 |
2.58e-02 |
1.30e-01 |
0.31900 |
-0.319000 |
-0.010000 |
6.85e-03 |
0.932000 |
VEGFR2 mediated vascular permeability |
24 |
2.62e-02 |
1.30e-01 |
0.31900 |
-0.031100 |
-0.317000 |
7.92e-01 |
0.007160 |
Rap1 signalling |
14 |
1.16e-01 |
3.10e-01 |
0.31900 |
-0.133000 |
0.290000 |
3.90e-01 |
0.060600 |
Interleukin-20 family signaling |
12 |
1.65e-01 |
3.73e-01 |
0.31900 |
0.172000 |
0.268000 |
3.02e-01 |
0.108000 |
Dissolution of Fibrin Clot |
10 |
2.23e-01 |
4.36e-01 |
0.31700 |
0.316000 |
0.017300 |
8.32e-02 |
0.924000 |
HDR through Single Strand Annealing (SSA) |
26 |
2.15e-02 |
1.16e-01 |
0.31600 |
-0.157000 |
-0.274000 |
1.65e-01 |
0.015500 |
Interleukin-12 family signaling |
40 |
2.76e-03 |
3.31e-02 |
0.31600 |
0.237000 |
0.209000 |
9.48e-03 |
0.022300 |
Glycosphingolipid metabolism |
27 |
1.75e-02 |
1.04e-01 |
0.31400 |
0.264000 |
-0.170000 |
1.75e-02 |
0.126000 |
Amine ligand-binding receptors |
14 |
1.25e-01 |
3.23e-01 |
0.31300 |
-0.144000 |
0.278000 |
3.52e-01 |
0.071700 |
Antigen processing-Cross presentation |
65 |
7.43e-05 |
2.48e-03 |
0.31100 |
0.284000 |
-0.128000 |
7.71e-05 |
0.075200 |
TP53 Regulates Transcription of Cell Cycle Genes |
38 |
4.07e-03 |
3.89e-02 |
0.31100 |
-0.311000 |
0.015500 |
9.30e-04 |
0.869000 |
Role of phospholipids in phagocytosis |
25 |
2.60e-02 |
1.30e-01 |
0.31100 |
0.098400 |
-0.295000 |
3.95e-01 |
0.010700 |
G beta:gamma signalling through CDC42 |
11 |
2.01e-01 |
4.17e-01 |
0.31100 |
0.293000 |
-0.102000 |
9.20e-02 |
0.558000 |
Processive synthesis on the C-strand of the telomere |
13 |
1.50e-01 |
3.50e-01 |
0.31000 |
-0.261000 |
0.168000 |
1.04e-01 |
0.295000 |
Class B/2 (Secretin family receptors) |
45 |
1.70e-03 |
2.33e-02 |
0.30900 |
0.289000 |
0.111000 |
8.12e-04 |
0.197000 |
Hyaluronan metabolism |
11 |
2.11e-01 |
4.25e-01 |
0.30900 |
0.296000 |
0.087300 |
8.92e-02 |
0.616000 |
SUMO E3 ligases SUMOylate target proteins |
117 |
7.29e-08 |
6.91e-06 |
0.30900 |
-0.298000 |
-0.079900 |
2.72e-08 |
0.137000 |
Signaling by cytosolic FGFR1 fusion mutants |
16 |
9.94e-02 |
2.88e-01 |
0.30800 |
-0.173000 |
0.255000 |
2.31e-01 |
0.077500 |
Detoxification of Reactive Oxygen Species |
19 |
6.59e-02 |
2.26e-01 |
0.30800 |
0.298000 |
-0.076000 |
2.44e-02 |
0.566000 |
HDR through Homologous Recombination (HRR) |
42 |
2.92e-03 |
3.40e-02 |
0.30700 |
-0.213000 |
-0.222000 |
1.71e-02 |
0.013100 |
Signal transduction by L1 |
15 |
1.24e-01 |
3.23e-01 |
0.30700 |
0.157000 |
0.263000 |
2.93e-01 |
0.077400 |
SUMOylation |
122 |
4.80e-08 |
4.93e-06 |
0.30600 |
-0.293000 |
-0.087600 |
2.33e-08 |
0.095800 |
Beta-catenin phosphorylation cascade |
15 |
1.19e-01 |
3.15e-01 |
0.30600 |
-0.276000 |
0.131000 |
6.42e-02 |
0.378000 |
Signaling by FGFR2 in disease |
21 |
5.56e-02 |
2.08e-01 |
0.30400 |
-0.298000 |
-0.059900 |
1.81e-02 |
0.635000 |
Nuclear Pore Complex (NPC) Disassembly |
25 |
3.12e-02 |
1.45e-01 |
0.30400 |
-0.303000 |
0.025500 |
8.79e-03 |
0.825000 |
Gene Silencing by RNA |
44 |
2.37e-03 |
2.95e-02 |
0.30400 |
-0.303000 |
-0.019800 |
5.14e-04 |
0.820000 |
G-protein activation |
15 |
1.26e-01 |
3.26e-01 |
0.30300 |
0.303000 |
0.000711 |
4.20e-02 |
0.996000 |
Signaling by Erythropoietin |
19 |
7.06e-02 |
2.35e-01 |
0.30300 |
-0.265000 |
0.147000 |
4.55e-02 |
0.267000 |
Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal |
67 |
1.14e-04 |
3.26e-03 |
0.30300 |
-0.284000 |
-0.104000 |
5.79e-05 |
0.141000 |
Amplification of signal from the kinetochores |
67 |
1.14e-04 |
3.26e-03 |
0.30300 |
-0.284000 |
-0.104000 |
5.79e-05 |
0.141000 |
Synthesis of Prostaglandins (PG) and Thromboxanes (TX) |
10 |
2.59e-01 |
4.71e-01 |
0.30200 |
0.162000 |
0.255000 |
3.75e-01 |
0.163000 |
PKA activation in glucagon signalling |
14 |
1.47e-01 |
3.46e-01 |
0.30200 |
-0.033000 |
0.300000 |
8.31e-01 |
0.052200 |
ERBB2 Activates PTK6 Signaling |
10 |
2.55e-01 |
4.69e-01 |
0.30100 |
0.048600 |
-0.297000 |
7.90e-01 |
0.104000 |
Presynaptic function of Kainate receptors |
13 |
1.69e-01 |
3.79e-01 |
0.30100 |
0.285000 |
-0.094700 |
7.51e-02 |
0.555000 |
Constitutive Signaling by EGFRvIII |
12 |
2.01e-01 |
4.17e-01 |
0.30000 |
-0.278000 |
-0.114000 |
9.58e-02 |
0.496000 |
Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants |
12 |
2.01e-01 |
4.17e-01 |
0.30000 |
-0.278000 |
-0.114000 |
9.58e-02 |
0.496000 |
Signaling by EGFRvIII in Cancer |
12 |
2.01e-01 |
4.17e-01 |
0.30000 |
-0.278000 |
-0.114000 |
9.58e-02 |
0.496000 |
Signaling by Ligand-Responsive EGFR Variants in Cancer |
12 |
2.01e-01 |
4.17e-01 |
0.30000 |
-0.278000 |
-0.114000 |
9.58e-02 |
0.496000 |
N-Glycan antennae elongation |
10 |
2.63e-01 |
4.75e-01 |
0.29900 |
0.065200 |
0.292000 |
7.21e-01 |
0.110000 |
Processing of Capped Intronless Pre-mRNA |
17 |
1.04e-01 |
2.95e-01 |
0.29900 |
-0.288000 |
-0.081700 |
4.01e-02 |
0.560000 |
Activation of ATR in response to replication stress |
23 |
4.77e-02 |
1.93e-01 |
0.29900 |
-0.285000 |
-0.089800 |
1.82e-02 |
0.456000 |
mRNA decay by 5' to 3' exoribonuclease |
12 |
2.00e-01 |
4.17e-01 |
0.29800 |
-0.276000 |
0.112000 |
9.79e-02 |
0.503000 |
Recognition of DNA damage by PCNA-containing replication complex |
17 |
1.08e-01 |
2.99e-01 |
0.29600 |
-0.296000 |
0.007710 |
3.49e-02 |
0.956000 |
Resolution of Sister Chromatid Cohesion |
76 |
5.46e-05 |
1.96e-03 |
0.29600 |
-0.284000 |
-0.082400 |
1.94e-05 |
0.215000 |
Signaling by EGFR |
34 |
1.27e-02 |
8.57e-02 |
0.29500 |
-0.230000 |
-0.185000 |
2.02e-02 |
0.062300 |
Telomere Extension By Telomerase |
15 |
1.38e-01 |
3.36e-01 |
0.29500 |
-0.212000 |
0.205000 |
1.55e-01 |
0.170000 |
ATF4 activates genes in response to endoplasmic reticulum stress |
17 |
1.06e-01 |
2.97e-01 |
0.29500 |
-0.242000 |
0.168000 |
8.40e-02 |
0.230000 |
Estrogen-dependent gene expression |
65 |
2.43e-04 |
5.87e-03 |
0.29500 |
-0.267000 |
-0.124000 |
1.99e-04 |
0.083500 |
Endosomal Sorting Complex Required For Transport (ESCRT) |
17 |
1.07e-01 |
2.97e-01 |
0.29500 |
0.254000 |
-0.150000 |
7.03e-02 |
0.285000 |
Signaling by FGFR3 in disease |
13 |
1.84e-01 |
3.98e-01 |
0.29400 |
-0.292000 |
0.034500 |
6.82e-02 |
0.829000 |
Signaling by FGFR3 point mutants in cancer |
13 |
1.84e-01 |
3.98e-01 |
0.29400 |
-0.292000 |
0.034500 |
6.82e-02 |
0.829000 |
DNA strand elongation |
23 |
5.17e-02 |
2.02e-01 |
0.29400 |
-0.289000 |
-0.051600 |
1.63e-02 |
0.669000 |
Branched-chain amino acid catabolism |
19 |
8.82e-02 |
2.69e-01 |
0.29400 |
-0.121000 |
-0.268000 |
3.63e-01 |
0.043300 |
Deactivation of the beta-catenin transactivating complex |
27 |
2.98e-02 |
1.42e-01 |
0.29300 |
-0.262000 |
0.131000 |
1.84e-02 |
0.241000 |
Zinc transporters |
11 |
2.44e-01 |
4.57e-01 |
0.29300 |
-0.017300 |
-0.292000 |
9.21e-01 |
0.093500 |
FGFR2 mutant receptor activation |
13 |
1.93e-01 |
4.13e-01 |
0.29300 |
-0.194000 |
-0.219000 |
2.25e-01 |
0.172000 |
Transcriptional regulation of pluripotent stem cells |
18 |
1.03e-01 |
2.93e-01 |
0.29300 |
0.222000 |
0.191000 |
1.04e-01 |
0.161000 |
Translesion synthesis by POLK |
11 |
2.42e-01 |
4.55e-01 |
0.29200 |
-0.270000 |
0.111000 |
1.21e-01 |
0.523000 |
Resolution of AP sites via the multiple-nucleotide patch replacement pathway |
17 |
1.11e-01 |
3.02e-01 |
0.29100 |
-0.238000 |
0.168000 |
8.91e-02 |
0.231000 |
Disassembly of the destruction complex and recruitment of AXIN to the membrane |
24 |
4.52e-02 |
1.86e-01 |
0.29100 |
-0.193000 |
0.218000 |
1.02e-01 |
0.064100 |
PKA-mediated phosphorylation of CREB |
16 |
1.32e-01 |
3.31e-01 |
0.29100 |
-0.008000 |
0.291000 |
9.56e-01 |
0.044200 |
Activation of G protein gated Potassium channels |
16 |
1.34e-01 |
3.32e-01 |
0.29000 |
0.284000 |
0.059100 |
4.92e-02 |
0.682000 |
G protein gated Potassium channels |
16 |
1.34e-01 |
3.32e-01 |
0.29000 |
0.284000 |
0.059100 |
4.92e-02 |
0.682000 |
Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits |
16 |
1.34e-01 |
3.32e-01 |
0.29000 |
0.284000 |
0.059100 |
4.92e-02 |
0.682000 |
RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function |
32 |
1.77e-02 |
1.05e-01 |
0.29000 |
-0.290000 |
0.008730 |
4.55e-03 |
0.932000 |
Regulation of TP53 Activity |
114 |
8.02e-07 |
6.59e-05 |
0.29000 |
-0.233000 |
-0.172000 |
1.80e-05 |
0.001510 |
Formation of RNA Pol II elongation complex |
33 |
1.73e-02 |
1.04e-01 |
0.28900 |
-0.246000 |
-0.151000 |
1.46e-02 |
0.133000 |
RNA Polymerase II Transcription Elongation |
33 |
1.73e-02 |
1.04e-01 |
0.28900 |
-0.246000 |
-0.151000 |
1.46e-02 |
0.133000 |
Collagen biosynthesis and modifying enzymes |
46 |
3.46e-03 |
3.49e-02 |
0.28700 |
0.287000 |
0.009830 |
7.63e-04 |
0.908000 |
TRAF6 mediated NF-kB activation |
18 |
1.10e-01 |
3.02e-01 |
0.28700 |
-0.054700 |
-0.282000 |
6.88e-01 |
0.038700 |
Downstream signaling of activated FGFR3 |
15 |
1.59e-01 |
3.65e-01 |
0.28600 |
-0.286000 |
-0.017000 |
5.54e-02 |
0.909000 |
Ribosomal scanning and start codon recognition |
20 |
8.86e-02 |
2.69e-01 |
0.28600 |
0.272000 |
0.088300 |
3.54e-02 |
0.495000 |
Translation initiation complex formation |
20 |
8.86e-02 |
2.69e-01 |
0.28600 |
0.272000 |
0.088300 |
3.54e-02 |
0.495000 |
Regulation of signaling by CBL |
15 |
1.59e-01 |
3.64e-01 |
0.28500 |
-0.088100 |
0.271000 |
5.55e-01 |
0.069300 |
Synthesis, secretion, and deacylation of Ghrelin |
10 |
2.96e-01 |
5.05e-01 |
0.28400 |
0.280000 |
-0.050100 |
1.26e-01 |
0.784000 |
Pre-NOTCH Transcription and Translation |
29 |
3.16e-02 |
1.46e-01 |
0.28400 |
-0.129000 |
-0.253000 |
2.30e-01 |
0.018500 |
ER-Phagosome pathway |
52 |
1.79e-03 |
2.39e-02 |
0.28400 |
0.260000 |
-0.114000 |
1.19e-03 |
0.157000 |
Insulin processing |
16 |
1.42e-01 |
3.41e-01 |
0.28300 |
-0.191000 |
0.209000 |
1.85e-01 |
0.148000 |
Cross-presentation of soluble exogenous antigens (endosomes) |
35 |
1.47e-02 |
9.55e-02 |
0.28200 |
0.248000 |
-0.135000 |
1.12e-02 |
0.169000 |
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane |
10 |
3.04e-01 |
5.11e-01 |
0.28200 |
0.005110 |
0.282000 |
9.78e-01 |
0.123000 |
TNFR1-induced NFkappaB signaling pathway |
22 |
7.61e-02 |
2.48e-01 |
0.28200 |
-0.184000 |
-0.213000 |
1.35e-01 |
0.083400 |
Downstream signaling of activated FGFR4 |
15 |
1.68e-01 |
3.78e-01 |
0.28100 |
-0.279000 |
0.032100 |
6.12e-02 |
0.830000 |
Inwardly rectifying K+ channels |
19 |
1.07e-01 |
2.97e-01 |
0.28100 |
0.280000 |
0.027800 |
3.50e-02 |
0.834000 |
SUMOylation of DNA damage response and repair proteins |
49 |
3.28e-03 |
3.49e-02 |
0.28000 |
-0.274000 |
-0.059700 |
9.16e-04 |
0.471000 |
Presynaptic phase of homologous DNA pairing and strand exchange |
25 |
5.46e-02 |
2.06e-01 |
0.28000 |
-0.118000 |
-0.254000 |
3.06e-01 |
0.027900 |
PI-3K cascade:FGFR1 |
11 |
2.72e-01 |
4.83e-01 |
0.28000 |
-0.272000 |
0.067000 |
1.18e-01 |
0.700000 |
Chondroitin sulfate biosynthesis |
16 |
1.53e-01 |
3.56e-01 |
0.28000 |
0.280000 |
0.004670 |
5.28e-02 |
0.974000 |
Interleukin-12 signaling |
32 |
2.50e-02 |
1.28e-01 |
0.28000 |
0.209000 |
0.185000 |
4.05e-02 |
0.069600 |
Carnitine metabolism |
11 |
2.80e-01 |
4.91e-01 |
0.27900 |
-0.267000 |
-0.081700 |
1.25e-01 |
0.639000 |
Plasma lipoprotein clearance |
25 |
5.29e-02 |
2.03e-01 |
0.27900 |
0.256000 |
-0.111000 |
2.70e-02 |
0.337000 |
N-glycan antennae elongation in the medial/trans-Golgi |
16 |
1.57e-01 |
3.62e-01 |
0.27900 |
0.061200 |
0.272000 |
6.72e-01 |
0.059800 |
PERK regulates gene expression |
19 |
1.06e-01 |
2.97e-01 |
0.27800 |
-0.203000 |
0.191000 |
1.26e-01 |
0.150000 |
HSF1-dependent transactivation |
24 |
6.41e-02 |
2.23e-01 |
0.27600 |
-0.276000 |
0.013500 |
1.93e-02 |
0.909000 |
Cyclin A/B1/B2 associated events during G2/M transition |
12 |
2.58e-01 |
4.69e-01 |
0.27600 |
-0.253000 |
-0.111000 |
1.30e-01 |
0.505000 |
Removal of the Flap Intermediate from the C-strand |
12 |
2.53e-01 |
4.67e-01 |
0.27500 |
-0.255000 |
0.103000 |
1.26e-01 |
0.538000 |
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S |
21 |
9.86e-02 |
2.87e-01 |
0.27300 |
0.248000 |
0.115000 |
4.97e-02 |
0.362000 |
VEGFR2 mediated cell proliferation |
18 |
1.33e-01 |
3.32e-01 |
0.27300 |
-0.270000 |
0.036600 |
4.71e-02 |
0.788000 |
Synthesis of PC |
19 |
1.17e-01 |
3.12e-01 |
0.27200 |
-0.164000 |
0.218000 |
2.17e-01 |
0.101000 |
Leading Strand Synthesis |
12 |
2.72e-01 |
4.83e-01 |
0.27100 |
-0.218000 |
-0.162000 |
1.92e-01 |
0.333000 |
Polymerase switching |
12 |
2.72e-01 |
4.83e-01 |
0.27100 |
-0.218000 |
-0.162000 |
1.92e-01 |
0.333000 |
Mitophagy |
17 |
1.55e-01 |
3.58e-01 |
0.27100 |
0.006160 |
-0.271000 |
9.65e-01 |
0.053500 |
Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 |
13 |
2.39e-01 |
4.53e-01 |
0.27000 |
-0.255000 |
0.088000 |
1.11e-01 |
0.583000 |
Signaling by ERBB2 ECD mutants |
13 |
2.47e-01 |
4.59e-01 |
0.26900 |
-0.265000 |
-0.040200 |
9.75e-02 |
0.802000 |
Diseases associated with N-glycosylation of proteins |
14 |
2.25e-01 |
4.39e-01 |
0.26800 |
0.239000 |
0.121000 |
1.21e-01 |
0.432000 |
Regulation of TP53 Activity through Phosphorylation |
62 |
1.38e-03 |
1.95e-02 |
0.26800 |
-0.244000 |
-0.111000 |
8.94e-04 |
0.130000 |
DAG and IP3 signaling |
34 |
2.44e-02 |
1.27e-01 |
0.26800 |
-0.187000 |
0.192000 |
5.92e-02 |
0.052600 |
PCNA-Dependent Long Patch Base Excision Repair |
15 |
1.95e-01 |
4.15e-01 |
0.26800 |
-0.239000 |
0.121000 |
1.08e-01 |
0.419000 |
Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells |
11 |
3.11e-01 |
5.18e-01 |
0.26800 |
-0.137000 |
-0.231000 |
4.33e-01 |
0.186000 |
Nuclear Envelope Breakdown |
38 |
1.65e-02 |
1.03e-01 |
0.26800 |
-0.261000 |
0.061600 |
5.47e-03 |
0.512000 |
Lagging Strand Synthesis |
16 |
1.80e-01 |
3.93e-01 |
0.26800 |
-0.267000 |
-0.020900 |
6.47e-02 |
0.885000 |
Regulation of gene expression by Hypoxia-inducible Factor |
10 |
3.43e-01 |
5.54e-01 |
0.26700 |
-0.004690 |
0.267000 |
9.80e-01 |
0.144000 |
Binding and Uptake of Ligands by Scavenger Receptors |
27 |
5.41e-02 |
2.06e-01 |
0.26700 |
0.233000 |
-0.130000 |
3.60e-02 |
0.243000 |
Defective CFTR causes cystic fibrosis |
37 |
1.86e-02 |
1.08e-01 |
0.26700 |
0.242000 |
-0.111000 |
1.08e-02 |
0.242000 |
ZBP1(DAI) mediated induction of type I IFNs |
18 |
1.52e-01 |
3.53e-01 |
0.26600 |
-0.078800 |
-0.254000 |
5.63e-01 |
0.062500 |
FOXO-mediated transcription |
49 |
5.49e-03 |
4.87e-02 |
0.26500 |
-0.252000 |
0.084900 |
2.34e-03 |
0.304000 |
PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases |
11 |
3.12e-01 |
5.19e-01 |
0.26500 |
-0.071200 |
0.255000 |
6.83e-01 |
0.143000 |
Mitotic Spindle Checkpoint |
82 |
2.25e-04 |
5.77e-03 |
0.26400 |
-0.231000 |
-0.128000 |
3.11e-04 |
0.045200 |
Aberrant regulation of mitotic exit in cancer due to RB1 defects |
18 |
1.56e-01 |
3.59e-01 |
0.26400 |
-0.081600 |
-0.251000 |
5.49e-01 |
0.065500 |
RIP-mediated NFkB activation via ZBP1 |
15 |
2.12e-01 |
4.25e-01 |
0.26400 |
-0.079000 |
-0.252000 |
5.96e-01 |
0.091600 |
WNT ligand biogenesis and trafficking |
14 |
2.38e-01 |
4.52e-01 |
0.26400 |
0.187000 |
0.186000 |
2.25e-01 |
0.229000 |
Apoptotic execution phase |
35 |
2.74e-02 |
1.33e-01 |
0.26300 |
-0.248000 |
-0.089400 |
1.12e-02 |
0.360000 |
Cellular hexose transport |
12 |
2.89e-01 |
4.97e-01 |
0.26300 |
0.011900 |
0.263000 |
9.43e-01 |
0.115000 |
Energy dependent regulation of mTOR by LKB1-AMPK |
20 |
1.28e-01 |
3.27e-01 |
0.26300 |
-0.259000 |
-0.045700 |
4.51e-02 |
0.724000 |
Regulation of expression of SLITs and ROBOs |
78 |
3.41e-04 |
7.58e-03 |
0.26200 |
0.262000 |
0.017600 |
6.58e-05 |
0.789000 |
CLEC7A (Dectin-1) induces NFAT activation |
10 |
3.55e-01 |
5.63e-01 |
0.26200 |
-0.258000 |
0.048100 |
1.58e-01 |
0.792000 |
Transcription of the HIV genome |
43 |
1.30e-02 |
8.73e-02 |
0.26200 |
-0.180000 |
-0.191000 |
4.17e-02 |
0.030800 |
Metabolism of non-coding RNA |
34 |
3.04e-02 |
1.42e-01 |
0.26200 |
-0.261000 |
0.022800 |
8.54e-03 |
0.818000 |
snRNP Assembly |
34 |
3.04e-02 |
1.42e-01 |
0.26200 |
-0.261000 |
0.022800 |
8.54e-03 |
0.818000 |
Assembly of active LPL and LIPC lipase complexes |
15 |
2.12e-01 |
4.25e-01 |
0.26100 |
0.120000 |
-0.232000 |
4.22e-01 |
0.120000 |
WNT5A-dependent internalization of FZD2, FZD5 and ROR2 |
11 |
3.21e-01 |
5.29e-01 |
0.26100 |
0.232000 |
-0.120000 |
1.83e-01 |
0.490000 |
Effects of PIP2 hydrolysis |
19 |
1.47e-01 |
3.46e-01 |
0.26100 |
-0.236000 |
-0.112000 |
7.52e-02 |
0.400000 |
Synthesis of very long-chain fatty acyl-CoAs |
15 |
2.21e-01 |
4.36e-01 |
0.26100 |
-0.221000 |
-0.139000 |
1.39e-01 |
0.350000 |
Synaptic adhesion-like molecules |
14 |
2.35e-01 |
4.51e-01 |
0.26100 |
0.206000 |
-0.160000 |
1.83e-01 |
0.300000 |
EML4 and NUDC in mitotic spindle formation |
70 |
8.96e-04 |
1.44e-02 |
0.26100 |
-0.244000 |
-0.090200 |
4.13e-04 |
0.193000 |
Mitochondrial biogenesis |
60 |
2.42e-03 |
2.95e-02 |
0.26000 |
-0.256000 |
-0.046700 |
6.17e-04 |
0.532000 |
Meiotic synapsis |
23 |
9.73e-02 |
2.87e-01 |
0.26000 |
-0.259000 |
0.016700 |
3.14e-02 |
0.889000 |
SUMOylation of RNA binding proteins |
34 |
3.22e-02 |
1.48e-01 |
0.26000 |
-0.260000 |
0.005960 |
8.81e-03 |
0.952000 |
Calnexin/calreticulin cycle |
14 |
2.44e-01 |
4.57e-01 |
0.26000 |
-0.012700 |
-0.259000 |
9.34e-01 |
0.093200 |
Formation of tubulin folding intermediates by CCT/TriC |
15 |
2.25e-01 |
4.39e-01 |
0.25900 |
-0.217000 |
-0.142000 |
1.45e-01 |
0.341000 |
Nucleobase catabolism |
22 |
1.08e-01 |
3.00e-01 |
0.25800 |
0.235000 |
-0.107000 |
5.63e-02 |
0.385000 |
Ubiquitin-dependent degradation of Cyclin D |
34 |
3.35e-02 |
1.52e-01 |
0.25700 |
0.240000 |
-0.092900 |
1.56e-02 |
0.349000 |
Mitochondrial translation initiation |
55 |
4.40e-03 |
4.02e-02 |
0.25700 |
0.257000 |
-0.001060 |
9.89e-04 |
0.989000 |
TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest |
11 |
3.43e-01 |
5.54e-01 |
0.25600 |
-0.218000 |
-0.136000 |
2.12e-01 |
0.436000 |
Synthesis of glycosylphosphatidylinositol (GPI) |
10 |
3.78e-01 |
5.78e-01 |
0.25600 |
0.113000 |
0.230000 |
5.37e-01 |
0.208000 |
Translation |
148 |
6.22e-07 |
5.48e-05 |
0.25500 |
0.255000 |
0.010100 |
9.06e-08 |
0.833000 |
Cleavage of the damaged purine |
10 |
3.71e-01 |
5.74e-01 |
0.25500 |
-0.123000 |
0.224000 |
5.00e-01 |
0.220000 |
Depurination |
10 |
3.71e-01 |
5.74e-01 |
0.25500 |
-0.123000 |
0.224000 |
5.00e-01 |
0.220000 |
Recognition and association of DNA glycosylase with site containing an affected purine |
10 |
3.71e-01 |
5.74e-01 |
0.25500 |
-0.123000 |
0.224000 |
5.00e-01 |
0.220000 |
Hedgehog ligand biogenesis |
40 |
1.92e-02 |
1.10e-01 |
0.25500 |
0.210000 |
-0.145000 |
2.15e-02 |
0.113000 |
Regulation of MECP2 expression and activity |
23 |
1.07e-01 |
2.97e-01 |
0.25400 |
-0.249000 |
0.052800 |
3.91e-02 |
0.661000 |
RUNX3 regulates NOTCH signaling |
13 |
2.88e-01 |
4.97e-01 |
0.25400 |
-0.095400 |
-0.235000 |
5.52e-01 |
0.142000 |
DNA Double Strand Break Response |
32 |
4.75e-02 |
1.93e-01 |
0.25400 |
-0.137000 |
-0.214000 |
1.81e-01 |
0.036100 |
activated TAK1 mediates p38 MAPK activation |
15 |
2.31e-01 |
4.47e-01 |
0.25400 |
-0.207000 |
0.146000 |
1.65e-01 |
0.328000 |
Apoptotic cleavage of cellular proteins |
29 |
6.41e-02 |
2.23e-01 |
0.25200 |
-0.248000 |
-0.044400 |
2.07e-02 |
0.679000 |
Laminin interactions |
22 |
1.21e-01 |
3.18e-01 |
0.25200 |
-0.225000 |
0.113000 |
6.79e-02 |
0.360000 |
TNF signaling |
31 |
5.59e-02 |
2.09e-01 |
0.25100 |
-0.138000 |
-0.210000 |
1.84e-01 |
0.043500 |
Mitotic Prometaphase |
139 |
2.63e-06 |
1.80e-04 |
0.25100 |
-0.240000 |
-0.071000 |
1.06e-06 |
0.150000 |
Neutrophil degranulation |
315 |
2.23e-13 |
2.75e-10 |
0.25100 |
0.242000 |
-0.066200 |
2.26e-13 |
0.044900 |
JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 |
15 |
2.43e-01 |
4.57e-01 |
0.25000 |
-0.061900 |
0.242000 |
6.78e-01 |
0.104000 |
Constitutive Signaling by AKT1 E17K in Cancer |
21 |
1.42e-01 |
3.41e-01 |
0.25000 |
-0.243000 |
-0.060400 |
5.44e-02 |
0.632000 |
Inhibition of DNA recombination at telomere |
12 |
3.30e-01 |
5.39e-01 |
0.25000 |
-0.220000 |
-0.118000 |
1.86e-01 |
0.480000 |
SUMOylation of chromatin organization proteins |
39 |
2.71e-02 |
1.33e-01 |
0.24900 |
-0.246000 |
-0.041200 |
7.91e-03 |
0.656000 |
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) |
44 |
1.75e-02 |
1.04e-01 |
0.24900 |
0.236000 |
0.081300 |
6.91e-03 |
0.351000 |
Nonsense-Mediated Decay (NMD) |
44 |
1.75e-02 |
1.04e-01 |
0.24900 |
0.236000 |
0.081300 |
6.91e-03 |
0.351000 |
Signaling by NOTCH2 |
21 |
1.47e-01 |
3.46e-01 |
0.24900 |
-0.162000 |
-0.189000 |
2.00e-01 |
0.133000 |
Gap junction trafficking and regulation |
15 |
2.45e-01 |
4.57e-01 |
0.24800 |
0.188000 |
-0.162000 |
2.08e-01 |
0.276000 |
Chromosome Maintenance |
56 |
6.21e-03 |
5.34e-02 |
0.24800 |
-0.230000 |
-0.091500 |
2.90e-03 |
0.237000 |
FRS-mediated FGFR1 signaling |
10 |
3.97e-01 |
6.00e-01 |
0.24800 |
-0.247000 |
0.022800 |
1.77e-01 |
0.901000 |
Synthesis of bile acids and bile salts |
18 |
1.96e-01 |
4.17e-01 |
0.24800 |
0.187000 |
0.162000 |
1.69e-01 |
0.234000 |
Signaling by FGFR1 in disease |
26 |
8.88e-02 |
2.69e-01 |
0.24800 |
-0.156000 |
0.193000 |
1.70e-01 |
0.089400 |
SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription |
21 |
1.48e-01 |
3.47e-01 |
0.24700 |
-0.246000 |
-0.008160 |
5.07e-02 |
0.948000 |
Deadenylation-dependent mRNA decay |
38 |
3.08e-02 |
1.43e-01 |
0.24600 |
-0.235000 |
0.073900 |
1.22e-02 |
0.431000 |
Synthesis of PIPs at the Golgi membrane |
11 |
3.65e-01 |
5.72e-01 |
0.24600 |
-0.235000 |
0.073400 |
1.77e-01 |
0.673000 |
Lewis blood group biosynthesis |
10 |
4.00e-01 |
6.01e-01 |
0.24600 |
0.227000 |
-0.093900 |
2.13e-01 |
0.607000 |
Homology Directed Repair |
70 |
1.99e-03 |
2.58e-02 |
0.24600 |
-0.178000 |
-0.170000 |
1.00e-02 |
0.014300 |
Synthesis of IP2, IP, and Ins in the cytosol |
12 |
3.41e-01 |
5.54e-01 |
0.24600 |
0.077500 |
0.233000 |
6.42e-01 |
0.162000 |
Downstream signal transduction |
25 |
1.01e-01 |
2.91e-01 |
0.24600 |
-0.153000 |
0.192000 |
1.85e-01 |
0.096900 |
Translesion synthesis by POLI |
11 |
3.67e-01 |
5.72e-01 |
0.24500 |
-0.205000 |
0.134000 |
2.39e-01 |
0.442000 |
TP53 Regulates Transcription of Cell Death Genes |
30 |
7.04e-02 |
2.35e-01 |
0.24500 |
-0.148000 |
-0.195000 |
1.60e-01 |
0.064700 |
Thrombin signalling through proteinase activated receptors (PARs) |
22 |
1.38e-01 |
3.37e-01 |
0.24500 |
0.245000 |
-0.008450 |
4.70e-02 |
0.945000 |
Tie2 Signaling |
14 |
2.81e-01 |
4.91e-01 |
0.24400 |
-0.209000 |
0.126000 |
1.75e-01 |
0.413000 |
Late Phase of HIV Life Cycle |
83 |
7.09e-04 |
1.23e-02 |
0.24400 |
-0.162000 |
-0.182000 |
1.08e-02 |
0.004150 |
Glutamate binding, activation of AMPA receptors and synaptic plasticity |
23 |
1.32e-01 |
3.31e-01 |
0.24400 |
-0.236000 |
-0.058900 |
4.99e-02 |
0.625000 |
Trafficking of AMPA receptors |
23 |
1.32e-01 |
3.31e-01 |
0.24400 |
-0.236000 |
-0.058900 |
4.99e-02 |
0.625000 |
WNT5A-dependent internalization of FZD4 |
11 |
3.83e-01 |
5.83e-01 |
0.24300 |
-0.117000 |
-0.213000 |
5.02e-01 |
0.222000 |
Formation of the Early Elongation Complex |
19 |
1.92e-01 |
4.10e-01 |
0.24300 |
-0.204000 |
-0.132000 |
1.25e-01 |
0.319000 |
Formation of the HIV-1 Early Elongation Complex |
19 |
1.92e-01 |
4.10e-01 |
0.24300 |
-0.204000 |
-0.132000 |
1.25e-01 |
0.319000 |
p38MAPK events |
11 |
3.76e-01 |
5.75e-01 |
0.24300 |
-0.062700 |
0.234000 |
7.19e-01 |
0.178000 |
Negative regulators of DDX58/IFIH1 signaling |
20 |
1.76e-01 |
3.87e-01 |
0.24200 |
-0.117000 |
-0.212000 |
3.66e-01 |
0.101000 |
HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) |
66 |
3.38e-03 |
3.49e-02 |
0.24200 |
-0.172000 |
-0.171000 |
1.60e-02 |
0.016500 |
Pre-NOTCH Expression and Processing |
42 |
2.63e-02 |
1.30e-01 |
0.24200 |
-0.105000 |
-0.218000 |
2.38e-01 |
0.014500 |
Bile acid and bile salt metabolism |
20 |
1.76e-01 |
3.87e-01 |
0.24200 |
0.229000 |
0.079300 |
7.67e-02 |
0.539000 |
TRP channels |
16 |
2.47e-01 |
4.59e-01 |
0.24100 |
0.241000 |
-0.009890 |
9.48e-02 |
0.945000 |
Glyoxylate metabolism and glycine degradation |
21 |
1.61e-01 |
3.67e-01 |
0.24100 |
-0.241000 |
-0.017000 |
5.63e-02 |
0.893000 |
Gap-filling DNA repair synthesis and ligation in GG-NER |
17 |
2.26e-01 |
4.40e-01 |
0.24100 |
-0.240000 |
0.028400 |
8.73e-02 |
0.839000 |
Heme biosynthesis |
10 |
4.14e-01 |
6.10e-01 |
0.24100 |
-0.217000 |
0.105000 |
2.35e-01 |
0.565000 |
Diseases associated with the TLR signaling cascade |
18 |
2.10e-01 |
4.25e-01 |
0.24100 |
-0.001830 |
-0.241000 |
9.89e-01 |
0.077200 |
Diseases of Immune System |
18 |
2.10e-01 |
4.25e-01 |
0.24100 |
-0.001830 |
-0.241000 |
9.89e-01 |
0.077200 |
Integration of energy metabolism |
83 |
7.22e-04 |
1.24e-02 |
0.24100 |
-0.225000 |
0.085000 |
3.99e-04 |
0.182000 |
Other semaphorin interactions |
18 |
2.14e-01 |
4.28e-01 |
0.24100 |
0.117000 |
0.211000 |
3.92e-01 |
0.122000 |
Hh mutants that don't undergo autocatalytic processing are degraded by ERAD |
34 |
5.08e-02 |
2.00e-01 |
0.24000 |
0.201000 |
-0.132000 |
4.27e-02 |
0.184000 |
TGF-beta receptor signaling activates SMADs |
18 |
2.15e-01 |
4.29e-01 |
0.24000 |
-0.209000 |
-0.119000 |
1.25e-01 |
0.383000 |
HIV Life Cycle |
91 |
4.51e-04 |
8.73e-03 |
0.24000 |
-0.167000 |
-0.173000 |
5.91e-03 |
0.004530 |
Signaling by Hippo |
17 |
2.35e-01 |
4.51e-01 |
0.23800 |
0.000184 |
0.238000 |
9.99e-01 |
0.088900 |
HCMV Early Events |
44 |
2.47e-02 |
1.27e-01 |
0.23800 |
-0.224000 |
-0.082100 |
1.03e-02 |
0.346000 |
Extension of Telomeres |
35 |
4.94e-02 |
1.97e-01 |
0.23800 |
-0.215000 |
0.104000 |
2.81e-02 |
0.289000 |
Negative regulation of NOTCH4 signaling |
35 |
4.96e-02 |
1.97e-01 |
0.23800 |
0.188000 |
-0.146000 |
5.43e-02 |
0.137000 |
Vif-mediated degradation of APOBEC3G |
32 |
6.54e-02 |
2.26e-01 |
0.23700 |
0.183000 |
-0.151000 |
7.36e-02 |
0.141000 |
IL-6-type cytokine receptor ligand interactions |
12 |
3.71e-01 |
5.74e-01 |
0.23700 |
0.199000 |
0.128000 |
2.33e-01 |
0.442000 |
SLC transporter disorders |
64 |
4.66e-03 |
4.19e-02 |
0.23600 |
-0.228000 |
0.063100 |
1.66e-03 |
0.384000 |
Plasma lipoprotein assembly, remodeling, and clearance |
48 |
1.74e-02 |
1.04e-01 |
0.23600 |
0.193000 |
-0.136000 |
2.10e-02 |
0.103000 |
HSP90 chaperone cycle for steroid hormone receptors (SHR) |
28 |
9.78e-02 |
2.87e-01 |
0.23600 |
-0.235000 |
-0.016300 |
3.13e-02 |
0.881000 |
Response of Mtb to phagocytosis |
17 |
2.40e-01 |
4.54e-01 |
0.23600 |
-0.223000 |
0.075800 |
1.11e-01 |
0.589000 |
DNA Double-Strand Break Repair |
90 |
6.66e-04 |
1.17e-02 |
0.23500 |
-0.175000 |
-0.158000 |
4.22e-03 |
0.009870 |
Transcriptional activation of mitochondrial biogenesis |
45 |
2.44e-02 |
1.27e-01 |
0.23500 |
-0.233000 |
-0.030200 |
6.78e-03 |
0.726000 |
PI-3K cascade:FGFR4 |
11 |
3.98e-01 |
6.00e-01 |
0.23500 |
-0.216000 |
0.093800 |
2.16e-01 |
0.590000 |
SHC1 events in ERBB2 signaling |
17 |
2.47e-01 |
4.59e-01 |
0.23500 |
-0.039700 |
-0.232000 |
7.77e-01 |
0.098500 |
Gap-filling DNA repair synthesis and ligation in TC-NER |
41 |
3.51e-02 |
1.56e-01 |
0.23400 |
-0.232000 |
-0.033600 |
1.03e-02 |
0.710000 |
EPHB-mediated forward signaling |
24 |
1.39e-01 |
3.38e-01 |
0.23400 |
0.234000 |
-0.010500 |
4.75e-02 |
0.929000 |
Uptake and actions of bacterial toxins |
26 |
1.21e-01 |
3.17e-01 |
0.23300 |
-0.233000 |
-0.009800 |
3.97e-02 |
0.931000 |
GAB1 signalosome |
12 |
3.74e-01 |
5.74e-01 |
0.23300 |
0.059600 |
-0.225000 |
7.21e-01 |
0.177000 |
RAB geranylgeranylation |
36 |
5.22e-02 |
2.02e-01 |
0.23300 |
0.218000 |
-0.082300 |
2.37e-02 |
0.393000 |
Mitochondrial translation termination |
55 |
1.16e-02 |
7.97e-02 |
0.23300 |
0.231000 |
-0.030900 |
3.14e-03 |
0.692000 |
CASP8 activity is inhibited |
10 |
4.43e-01 |
6.33e-01 |
0.23200 |
0.054900 |
-0.226000 |
7.64e-01 |
0.217000 |
Dimerization of procaspase-8 |
10 |
4.43e-01 |
6.33e-01 |
0.23200 |
0.054900 |
-0.226000 |
7.64e-01 |
0.217000 |
Regulation by c-FLIP |
10 |
4.43e-01 |
6.33e-01 |
0.23200 |
0.054900 |
-0.226000 |
7.64e-01 |
0.217000 |
Activated NOTCH1 Transmits Signal to the Nucleus |
19 |
2.22e-01 |
4.36e-01 |
0.23100 |
-0.109000 |
-0.204000 |
4.12e-01 |
0.123000 |
GRB2 events in ERBB2 signaling |
11 |
4.14e-01 |
6.10e-01 |
0.23100 |
0.029500 |
-0.229000 |
8.65e-01 |
0.189000 |
Arachidonic acid metabolism |
32 |
8.09e-02 |
2.57e-01 |
0.23100 |
0.207000 |
0.102000 |
4.29e-02 |
0.320000 |
p130Cas linkage to MAPK signaling for integrins |
10 |
4.56e-01 |
6.44e-01 |
0.23000 |
0.200000 |
0.115000 |
2.75e-01 |
0.529000 |
Glucagon signaling in metabolic regulation |
21 |
1.93e-01 |
4.13e-01 |
0.23000 |
0.132000 |
0.188000 |
2.94e-01 |
0.135000 |
Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation |
25 |
1.42e-01 |
3.41e-01 |
0.23000 |
0.149000 |
0.176000 |
1.99e-01 |
0.128000 |
Downstream signaling of activated FGFR2 |
17 |
2.57e-01 |
4.69e-01 |
0.23000 |
-0.224000 |
0.052200 |
1.10e-01 |
0.709000 |
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks |
31 |
8.93e-02 |
2.70e-01 |
0.23000 |
-0.129000 |
-0.190000 |
2.15e-01 |
0.066700 |
Prolactin receptor signaling |
10 |
4.52e-01 |
6.40e-01 |
0.22900 |
-0.047300 |
0.224000 |
7.96e-01 |
0.219000 |
Transcriptional Regulation by TP53 |
247 |
7.01e-09 |
9.60e-07 |
0.22900 |
-0.201000 |
-0.109000 |
5.93e-08 |
0.003330 |
Glycogen breakdown (glycogenolysis) |
11 |
4.16e-01 |
6.12e-01 |
0.22900 |
-0.159000 |
0.164000 |
3.61e-01 |
0.345000 |
DDX58/IFIH1-mediated induction of interferon-alpha/beta |
43 |
3.60e-02 |
1.60e-01 |
0.22900 |
-0.098900 |
-0.206000 |
2.62e-01 |
0.019300 |
Downregulation of TGF-beta receptor signaling |
16 |
2.89e-01 |
4.97e-01 |
0.22900 |
-0.212000 |
-0.087000 |
1.43e-01 |
0.547000 |
Sema4D in semaphorin signaling |
19 |
2.26e-01 |
4.40e-01 |
0.22800 |
0.228000 |
-0.006550 |
8.49e-02 |
0.961000 |
Growth hormone receptor signaling |
18 |
2.51e-01 |
4.64e-01 |
0.22800 |
0.094400 |
0.207000 |
4.88e-01 |
0.128000 |
Chemokine receptors bind chemokines |
31 |
8.73e-02 |
2.69e-01 |
0.22800 |
0.169000 |
-0.152000 |
1.03e-01 |
0.143000 |
Oxidative Stress Induced Senescence |
51 |
2.00e-02 |
1.13e-01 |
0.22700 |
-0.223000 |
-0.044700 |
5.96e-03 |
0.581000 |
TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest |
16 |
2.92e-01 |
5.00e-01 |
0.22700 |
-0.223000 |
-0.043000 |
1.23e-01 |
0.766000 |
Mitochondrial translation elongation |
55 |
1.45e-02 |
9.48e-02 |
0.22700 |
0.227000 |
-0.006200 |
3.65e-03 |
0.937000 |
Telomere C-strand (Lagging Strand) Synthesis |
25 |
1.44e-01 |
3.44e-01 |
0.22600 |
-0.214000 |
0.073300 |
6.38e-02 |
0.526000 |
Hh mutants abrogate ligand secretion |
36 |
6.10e-02 |
2.18e-01 |
0.22600 |
0.187000 |
-0.128000 |
5.29e-02 |
0.184000 |
Peptide ligand-binding receptors |
75 |
3.04e-03 |
3.48e-02 |
0.22600 |
0.202000 |
-0.102000 |
2.52e-03 |
0.128000 |
PI-3K cascade:FGFR3 |
11 |
4.30e-01 |
6.21e-01 |
0.22600 |
-0.224000 |
0.026900 |
1.98e-01 |
0.877000 |
Recruitment of NuMA to mitotic centrosomes |
64 |
8.04e-03 |
6.24e-02 |
0.22600 |
-0.211000 |
-0.081100 |
3.58e-03 |
0.262000 |
TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway |
12 |
4.02e-01 |
6.03e-01 |
0.22600 |
0.027500 |
0.224000 |
8.69e-01 |
0.179000 |
Epigenetic regulation of gene expression |
59 |
1.23e-02 |
8.38e-02 |
0.22500 |
-0.196000 |
-0.110000 |
9.20e-03 |
0.145000 |
Ubiquitin Mediated Degradation of Phosphorylated Cdc25A |
32 |
8.78e-02 |
2.69e-01 |
0.22400 |
0.191000 |
-0.117000 |
6.17e-02 |
0.253000 |
p53-Independent DNA Damage Response |
32 |
8.78e-02 |
2.69e-01 |
0.22400 |
0.191000 |
-0.117000 |
6.17e-02 |
0.253000 |
p53-Independent G1/S DNA damage checkpoint |
32 |
8.78e-02 |
2.69e-01 |
0.22400 |
0.191000 |
-0.117000 |
6.17e-02 |
0.253000 |
Negative regulation of MET activity |
13 |
3.82e-01 |
5.82e-01 |
0.22400 |
-0.151000 |
-0.165000 |
3.45e-01 |
0.303000 |
G beta:gamma signalling through PI3Kgamma |
15 |
3.23e-01 |
5.31e-01 |
0.22400 |
0.220000 |
-0.038700 |
1.40e-01 |
0.795000 |
IRS-mediated signalling |
31 |
9.82e-02 |
2.87e-01 |
0.22400 |
-0.224000 |
0.005200 |
3.13e-02 |
0.960000 |
Activation of kainate receptors upon glutamate binding |
21 |
2.10e-01 |
4.25e-01 |
0.22300 |
0.223000 |
0.015900 |
7.75e-02 |
0.900000 |
Signaling by EGFR in Cancer |
14 |
3.59e-01 |
5.67e-01 |
0.22300 |
-0.152000 |
-0.162000 |
3.24e-01 |
0.293000 |
Centrosome maturation |
65 |
8.59e-03 |
6.34e-02 |
0.22300 |
-0.205000 |
-0.086700 |
4.28e-03 |
0.227000 |
Recruitment of mitotic centrosome proteins and complexes |
65 |
8.59e-03 |
6.34e-02 |
0.22300 |
-0.205000 |
-0.086700 |
4.28e-03 |
0.227000 |
Mitochondrial protein import |
44 |
3.90e-02 |
1.67e-01 |
0.22200 |
-0.019600 |
-0.222000 |
8.22e-01 |
0.011100 |
Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models |
17 |
2.82e-01 |
4.91e-01 |
0.22200 |
-0.110000 |
0.193000 |
4.35e-01 |
0.169000 |
Neurodegenerative Diseases |
17 |
2.82e-01 |
4.91e-01 |
0.22200 |
-0.110000 |
0.193000 |
4.35e-01 |
0.169000 |
Chromatin modifying enzymes |
150 |
1.87e-05 |
8.89e-04 |
0.22200 |
-0.221000 |
-0.008910 |
3.09e-06 |
0.851000 |
Chromatin organization |
150 |
1.87e-05 |
8.89e-04 |
0.22200 |
-0.221000 |
-0.008910 |
3.09e-06 |
0.851000 |
APC-Cdc20 mediated degradation of Nek2A |
19 |
2.51e-01 |
4.65e-01 |
0.22100 |
-0.065900 |
-0.211000 |
6.19e-01 |
0.111000 |
ESR-mediated signaling |
116 |
2.48e-04 |
5.89e-03 |
0.22100 |
-0.174000 |
-0.137000 |
1.25e-03 |
0.011200 |
Regulation of PLK1 Activity at G2/M Transition |
62 |
1.06e-02 |
7.55e-02 |
0.22100 |
-0.218000 |
0.034600 |
2.98e-03 |
0.638000 |
Autodegradation of Cdh1 by Cdh1:APC/C |
44 |
3.86e-02 |
1.67e-01 |
0.22100 |
0.137000 |
-0.173000 |
1.16e-01 |
0.047200 |
TNFR2 non-canonical NF-kB pathway |
66 |
7.72e-03 |
6.11e-02 |
0.22100 |
0.190000 |
-0.113000 |
7.75e-03 |
0.113000 |
Formation of the cornified envelope |
20 |
2.36e-01 |
4.51e-01 |
0.22100 |
-0.079200 |
-0.206000 |
5.40e-01 |
0.111000 |
EPH-ephrin mediated repulsion of cells |
37 |
6.72e-02 |
2.28e-01 |
0.22000 |
0.218000 |
-0.034700 |
2.21e-02 |
0.715000 |
TRAF6 mediated IRF7 activation |
14 |
3.66e-01 |
5.72e-01 |
0.22000 |
-0.112000 |
-0.190000 |
4.70e-01 |
0.219000 |
Retrograde transport at the Trans-Golgi-Network |
35 |
8.21e-02 |
2.59e-01 |
0.22000 |
-0.174000 |
-0.134000 |
7.43e-02 |
0.169000 |
AURKA Activation by TPX2 |
57 |
1.62e-02 |
1.02e-01 |
0.22000 |
-0.220000 |
0.000611 |
4.08e-03 |
0.994000 |
RUNX1 regulates transcription of genes involved in differentiation of HSCs |
49 |
2.74e-02 |
1.33e-01 |
0.22000 |
0.170000 |
-0.140000 |
4.00e-02 |
0.090300 |
Regulation of activated PAK-2p34 by proteasome mediated degradation |
32 |
9.60e-02 |
2.85e-01 |
0.22000 |
0.195000 |
-0.102000 |
5.67e-02 |
0.319000 |
Selective autophagy |
43 |
4.60e-02 |
1.89e-01 |
0.22000 |
-0.058900 |
-0.212000 |
5.05e-01 |
0.016400 |
Iron uptake and transport |
36 |
7.71e-02 |
2.50e-01 |
0.22000 |
0.185000 |
0.119000 |
5.55e-02 |
0.216000 |
NIK-->noncanonical NF-kB signaling |
37 |
6.66e-02 |
2.27e-01 |
0.22000 |
0.132000 |
-0.176000 |
1.65e-01 |
0.064700 |
Autodegradation of the E3 ubiquitin ligase COP1 |
34 |
8.29e-02 |
2.61e-01 |
0.22000 |
0.170000 |
-0.139000 |
8.57e-02 |
0.162000 |
Synthesis of Leukotrienes (LT) and Eoxins (EX) |
13 |
3.88e-01 |
5.87e-01 |
0.21900 |
0.195000 |
-0.101000 |
2.24e-01 |
0.530000 |
Telomere Maintenance |
42 |
4.97e-02 |
1.97e-01 |
0.21800 |
-0.217000 |
0.022100 |
1.49e-02 |
0.805000 |
Post-translational protein phosphorylation |
59 |
1.58e-02 |
1.00e-01 |
0.21800 |
0.201000 |
0.085400 |
7.68e-03 |
0.257000 |
Transport of Mature Transcript to Cytoplasm |
59 |
1.59e-02 |
1.01e-01 |
0.21800 |
-0.193000 |
-0.101000 |
1.03e-02 |
0.180000 |
FCGR3A-mediated IL10 synthesis |
36 |
7.93e-02 |
2.55e-01 |
0.21800 |
0.209000 |
0.063200 |
3.05e-02 |
0.512000 |
Fatty acyl-CoA biosynthesis |
22 |
2.08e-01 |
4.25e-01 |
0.21800 |
-0.216000 |
0.030900 |
8.02e-02 |
0.802000 |
Estrogen-dependent nuclear events downstream of ESR-membrane signaling |
17 |
3.04e-01 |
5.11e-01 |
0.21800 |
-0.103000 |
-0.192000 |
4.64e-01 |
0.171000 |
Phase 2 - plateau phase |
17 |
2.98e-01 |
5.05e-01 |
0.21800 |
-0.214000 |
0.038400 |
1.27e-01 |
0.784000 |
Golgi Cisternae Pericentriolar Stack Reorganization |
11 |
4.65e-01 |
6.53e-01 |
0.21700 |
0.153000 |
0.154000 |
3.80e-01 |
0.377000 |
AUF1 (hnRNP D0) binds and destabilizes mRNA |
35 |
8.24e-02 |
2.60e-01 |
0.21700 |
0.140000 |
-0.165000 |
1.51e-01 |
0.090900 |
Cobalamin (Cbl, vitamin B12) transport and metabolism |
10 |
4.93e-01 |
6.77e-01 |
0.21700 |
0.029300 |
-0.215000 |
8.73e-01 |
0.240000 |
Purine catabolism |
12 |
4.25e-01 |
6.21e-01 |
0.21700 |
0.185000 |
-0.113000 |
2.68e-01 |
0.498000 |
Transport of inorganic cations/anions and amino acids/oligopeptides |
68 |
8.33e-03 |
6.32e-02 |
0.21700 |
-0.211000 |
0.048900 |
2.66e-03 |
0.486000 |
Interleukin-4 and Interleukin-13 signaling |
78 |
4.23e-03 |
3.98e-02 |
0.21600 |
0.213000 |
-0.039200 |
1.19e-03 |
0.551000 |
APC/C:Cdc20 mediated degradation of Securin |
48 |
3.35e-02 |
1.52e-01 |
0.21600 |
0.137000 |
-0.167000 |
1.02e-01 |
0.045300 |
RNA Polymerase I Transcription |
33 |
1.04e-01 |
2.94e-01 |
0.21600 |
-0.110000 |
-0.185000 |
2.73e-01 |
0.065400 |
Interferon Signaling |
114 |
3.84e-04 |
7.88e-03 |
0.21500 |
0.206000 |
-0.060500 |
1.51e-04 |
0.266000 |
LDL clearance |
13 |
4.05e-01 |
6.04e-01 |
0.21400 |
0.091000 |
-0.194000 |
5.70e-01 |
0.226000 |
G2/M DNA damage checkpoint |
43 |
5.48e-02 |
2.06e-01 |
0.21400 |
-0.136000 |
-0.165000 |
1.22e-01 |
0.061100 |
Loss of Nlp from mitotic centrosomes |
55 |
2.34e-02 |
1.25e-01 |
0.21400 |
-0.214000 |
-0.006240 |
6.15e-03 |
0.936000 |
Loss of proteins required for interphase microtubule organization from the centrosome |
55 |
2.34e-02 |
1.25e-01 |
0.21400 |
-0.214000 |
-0.006240 |
6.15e-03 |
0.936000 |
RHO GTPases Activate Formins |
87 |
2.82e-03 |
3.35e-02 |
0.21400 |
-0.209000 |
-0.045400 |
7.85e-04 |
0.465000 |
RNA Polymerase II Pre-transcription Events |
51 |
3.27e-02 |
1.50e-01 |
0.21300 |
-0.174000 |
-0.124000 |
3.20e-02 |
0.126000 |
Cell Cycle Checkpoints |
181 |
6.82e-06 |
3.80e-04 |
0.21300 |
-0.151000 |
-0.150000 |
4.83e-04 |
0.000543 |
Processing of DNA double-strand break ends |
41 |
6.59e-02 |
2.26e-01 |
0.21200 |
-0.131000 |
-0.167000 |
1.47e-01 |
0.064500 |
DNA Damage Bypass |
29 |
1.39e-01 |
3.38e-01 |
0.21200 |
-0.199000 |
0.073400 |
6.39e-02 |
0.494000 |
Signaling by FGFR2 |
39 |
7.63e-02 |
2.48e-01 |
0.21100 |
-0.199000 |
-0.070000 |
3.16e-02 |
0.450000 |
Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters |
15 |
3.72e-01 |
5.74e-01 |
0.21100 |
-0.192000 |
-0.088300 |
1.99e-01 |
0.554000 |
Synthesis of IP3 and IP4 in the cytosol |
20 |
2.68e-01 |
4.81e-01 |
0.21100 |
0.072500 |
0.198000 |
5.75e-01 |
0.126000 |
Cellular Senescence |
100 |
1.48e-03 |
2.06e-02 |
0.21100 |
-0.180000 |
-0.110000 |
1.95e-03 |
0.057700 |
PI3K Cascade |
29 |
1.46e-01 |
3.45e-01 |
0.21000 |
-0.210000 |
0.016300 |
5.07e-02 |
0.879000 |
PD-1 signaling |
11 |
4.86e-01 |
6.71e-01 |
0.21000 |
-0.188000 |
-0.093600 |
2.79e-01 |
0.591000 |
Plasma lipoprotein remodeling |
19 |
2.79e-01 |
4.91e-01 |
0.21000 |
0.147000 |
-0.151000 |
2.68e-01 |
0.256000 |
KSRP (KHSRP) binds and destabilizes mRNA |
13 |
4.18e-01 |
6.13e-01 |
0.21000 |
-0.167000 |
0.128000 |
2.97e-01 |
0.426000 |
Insulin receptor signalling cascade |
37 |
8.73e-02 |
2.69e-01 |
0.21000 |
-0.210000 |
0.003310 |
2.73e-02 |
0.972000 |
BMAL1:CLOCK,NPAS2 activates circadian gene expression |
19 |
2.81e-01 |
4.91e-01 |
0.21000 |
-0.155000 |
0.141000 |
2.42e-01 |
0.288000 |
Negative epigenetic regulation of rRNA expression |
28 |
1.62e-01 |
3.69e-01 |
0.21000 |
-0.097200 |
-0.186000 |
3.74e-01 |
0.089100 |
Apoptotic factor-mediated response |
11 |
4.85e-01 |
6.70e-01 |
0.21000 |
0.209000 |
0.006050 |
2.29e-01 |
0.972000 |
Prolonged ERK activation events |
12 |
4.51e-01 |
6.39e-01 |
0.20900 |
-0.159000 |
0.136000 |
3.42e-01 |
0.414000 |
Synthesis of PA |
25 |
1.99e-01 |
4.17e-01 |
0.20900 |
-0.196000 |
-0.070500 |
8.94e-02 |
0.542000 |
Synthesis of active ubiquitin: roles of E1 and E2 enzymes |
18 |
3.09e-01 |
5.17e-01 |
0.20800 |
-0.193000 |
0.076200 |
1.56e-01 |
0.576000 |
RET signaling |
31 |
1.33e-01 |
3.32e-01 |
0.20700 |
-0.187000 |
0.089800 |
7.18e-02 |
0.387000 |
Inositol phosphate metabolism |
36 |
9.89e-02 |
2.87e-01 |
0.20700 |
-0.007070 |
0.207000 |
9.42e-01 |
0.031700 |
ERBB2 Regulates Cell Motility |
11 |
4.92e-01 |
6.76e-01 |
0.20700 |
0.048200 |
-0.201000 |
7.82e-01 |
0.248000 |
CD28 co-stimulation |
28 |
1.72e-01 |
3.83e-01 |
0.20600 |
-0.102000 |
-0.180000 |
3.52e-01 |
0.100000 |
Glycogen metabolism |
18 |
3.17e-01 |
5.24e-01 |
0.20600 |
-0.024700 |
0.205000 |
8.56e-01 |
0.133000 |
RNA Polymerase I Transcription Initiation |
29 |
1.63e-01 |
3.69e-01 |
0.20600 |
-0.095800 |
-0.182000 |
3.72e-01 |
0.089700 |
Dual incision in TC-NER |
42 |
7.16e-02 |
2.37e-01 |
0.20600 |
-0.198000 |
-0.054200 |
2.62e-02 |
0.544000 |
Termination of translesion DNA synthesis |
20 |
2.81e-01 |
4.91e-01 |
0.20500 |
-0.203000 |
0.029700 |
1.16e-01 |
0.818000 |
Inactivation of APC/C via direct inhibition of the APC/C complex |
18 |
3.27e-01 |
5.35e-01 |
0.20400 |
-0.042800 |
-0.200000 |
7.53e-01 |
0.143000 |
Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components |
18 |
3.27e-01 |
5.35e-01 |
0.20400 |
-0.042800 |
-0.200000 |
7.53e-01 |
0.143000 |
ABC transporter disorders |
45 |
5.88e-02 |
2.12e-01 |
0.20400 |
0.187000 |
-0.082600 |
3.04e-02 |
0.338000 |
Dectin-1 mediated noncanonical NF-kB signaling |
39 |
8.53e-02 |
2.66e-01 |
0.20400 |
0.121000 |
-0.164000 |
1.92e-01 |
0.076000 |
Chondroitin sulfate/dermatan sulfate metabolism |
37 |
9.98e-02 |
2.88e-01 |
0.20400 |
0.202000 |
-0.024300 |
3.34e-02 |
0.798000 |
Extra-nuclear estrogen signaling |
55 |
3.50e-02 |
1.56e-01 |
0.20300 |
-0.065500 |
-0.192000 |
4.01e-01 |
0.013800 |
CaM pathway |
28 |
1.74e-01 |
3.84e-01 |
0.20300 |
-0.124000 |
0.161000 |
2.58e-01 |
0.141000 |
Calmodulin induced events |
28 |
1.74e-01 |
3.84e-01 |
0.20300 |
-0.124000 |
0.161000 |
2.58e-01 |
0.141000 |
Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA |
11 |
5.03e-01 |
6.83e-01 |
0.20300 |
-0.113000 |
0.168000 |
5.15e-01 |
0.335000 |
Signaling by ERBB2 |
34 |
1.29e-01 |
3.30e-01 |
0.20200 |
-0.094700 |
-0.178000 |
3.39e-01 |
0.072200 |
Mismatch Repair |
13 |
4.50e-01 |
6.38e-01 |
0.20200 |
-0.192000 |
0.061300 |
2.31e-01 |
0.702000 |
Formation of Incision Complex in GG-NER |
27 |
1.90e-01 |
4.08e-01 |
0.20100 |
-0.107000 |
0.171000 |
3.37e-01 |
0.125000 |
Aberrant regulation of mitotic cell cycle due to RB1 defects |
30 |
1.66e-01 |
3.73e-01 |
0.20100 |
-0.092900 |
-0.179000 |
3.79e-01 |
0.090500 |
Diseases of mitotic cell cycle |
30 |
1.66e-01 |
3.73e-01 |
0.20100 |
-0.092900 |
-0.179000 |
3.79e-01 |
0.090500 |
Downstream signaling of activated FGFR1 |
18 |
3.37e-01 |
5.49e-01 |
0.20100 |
-0.200000 |
0.017000 |
1.42e-01 |
0.900000 |
RNA Polymerase I Promoter Clearance |
32 |
1.50e-01 |
3.50e-01 |
0.20000 |
-0.105000 |
-0.171000 |
3.04e-01 |
0.094900 |
Ovarian tumor domain proteases |
26 |
2.17e-01 |
4.31e-01 |
0.20000 |
-0.174000 |
-0.098200 |
1.25e-01 |
0.386000 |
Vpu mediated degradation of CD4 |
33 |
1.38e-01 |
3.37e-01 |
0.19900 |
0.176000 |
-0.092500 |
8.00e-02 |
0.358000 |
Purine ribonucleoside monophosphate biosynthesis |
11 |
5.17e-01 |
6.92e-01 |
0.19900 |
0.064800 |
-0.188000 |
7.10e-01 |
0.280000 |
Regulation of insulin secretion |
55 |
3.72e-02 |
1.62e-01 |
0.19900 |
-0.171000 |
0.102000 |
2.86e-02 |
0.192000 |
CDK-mediated phosphorylation and removal of Cdc6 |
50 |
5.02e-02 |
1.98e-01 |
0.19900 |
0.100000 |
-0.172000 |
2.20e-01 |
0.035900 |
Regulation of Apoptosis |
34 |
1.31e-01 |
3.31e-01 |
0.19900 |
0.175000 |
-0.093700 |
7.73e-02 |
0.345000 |
Stabilization of p53 |
37 |
1.10e-01 |
3.02e-01 |
0.19800 |
0.108000 |
-0.166000 |
2.54e-01 |
0.080600 |
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 |
53 |
4.29e-02 |
1.78e-01 |
0.19800 |
0.080600 |
-0.181000 |
3.11e-01 |
0.022600 |
MHC class II antigen presentation |
82 |
7.70e-03 |
6.11e-02 |
0.19800 |
0.102000 |
-0.170000 |
1.11e-01 |
0.007870 |
Cell Cycle, Mitotic |
353 |
2.98e-09 |
5.24e-07 |
0.19700 |
-0.180000 |
-0.078400 |
7.60e-09 |
0.012000 |
Mitochondrial translation |
61 |
2.96e-02 |
1.41e-01 |
0.19600 |
0.195000 |
-0.021800 |
8.48e-03 |
0.768000 |
FRS-mediated FGFR3 signaling |
10 |
5.64e-01 |
7.31e-01 |
0.19600 |
-0.195000 |
-0.021400 |
2.87e-01 |
0.907000 |
Ca2+ pathway |
47 |
6.57e-02 |
2.26e-01 |
0.19600 |
-0.125000 |
0.151000 |
1.40e-01 |
0.074100 |
Costimulation by the CD28 family |
48 |
6.78e-02 |
2.28e-01 |
0.19500 |
-0.127000 |
-0.148000 |
1.28e-01 |
0.075800 |
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein |
59 |
3.62e-02 |
1.60e-01 |
0.19500 |
0.186000 |
0.057300 |
1.34e-02 |
0.447000 |
Adherens junctions interactions |
13 |
4.76e-01 |
6.60e-01 |
0.19500 |
0.017800 |
-0.194000 |
9.11e-01 |
0.226000 |
Collagen formation |
60 |
3.48e-02 |
1.56e-01 |
0.19400 |
0.190000 |
0.038500 |
1.09e-02 |
0.606000 |
Signaling by TGF-beta Receptor Complex |
48 |
6.75e-02 |
2.28e-01 |
0.19400 |
-0.194000 |
-0.007330 |
2.03e-02 |
0.930000 |
Sphingolipid metabolism |
54 |
4.63e-02 |
1.89e-01 |
0.19400 |
0.167000 |
-0.098200 |
3.37e-02 |
0.212000 |
Cell Cycle |
439 |
6.62e-11 |
2.69e-08 |
0.19400 |
-0.169000 |
-0.094300 |
1.77e-09 |
0.000802 |
Platelet degranulation |
86 |
8.33e-03 |
6.32e-02 |
0.19400 |
0.193000 |
0.011700 |
1.99e-03 |
0.851000 |
Activation of GABAB receptors |
28 |
2.12e-01 |
4.25e-01 |
0.19300 |
0.178000 |
0.076200 |
1.04e-01 |
0.485000 |
GABA B receptor activation |
28 |
2.12e-01 |
4.25e-01 |
0.19300 |
0.178000 |
0.076200 |
1.04e-01 |
0.485000 |
Meiotic recombination |
19 |
3.49e-01 |
5.57e-01 |
0.19300 |
-0.056000 |
-0.185000 |
6.73e-01 |
0.163000 |
G-protein beta:gamma signalling |
20 |
3.23e-01 |
5.31e-01 |
0.19300 |
0.146000 |
-0.125000 |
2.57e-01 |
0.332000 |
Nucleobase biosynthesis |
13 |
4.82e-01 |
6.67e-01 |
0.19200 |
0.078300 |
-0.176000 |
6.25e-01 |
0.273000 |
RNA Polymerase III Chain Elongation |
11 |
5.46e-01 |
7.16e-01 |
0.19200 |
0.187000 |
0.044600 |
2.83e-01 |
0.798000 |
Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) |
36 |
1.37e-01 |
3.36e-01 |
0.19200 |
-0.192000 |
-0.015900 |
4.68e-02 |
0.869000 |
FRS-mediated FGFR4 signaling |
10 |
5.73e-01 |
7.38e-01 |
0.19200 |
-0.185000 |
0.052300 |
3.12e-01 |
0.775000 |
Metabolism of polyamines |
39 |
1.15e-01 |
3.07e-01 |
0.19200 |
0.183000 |
-0.058700 |
4.85e-02 |
0.526000 |
Signaling by KIT in disease |
16 |
4.09e-01 |
6.05e-01 |
0.19200 |
-0.158000 |
0.110000 |
2.75e-01 |
0.448000 |
Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants |
16 |
4.09e-01 |
6.05e-01 |
0.19200 |
-0.158000 |
0.110000 |
2.75e-01 |
0.448000 |
Glutamate and glutamine metabolism |
12 |
5.19e-01 |
6.93e-01 |
0.19200 |
0.182000 |
0.060500 |
2.75e-01 |
0.717000 |
Signaling by NTRK3 (TRKC) |
14 |
4.63e-01 |
6.51e-01 |
0.19200 |
-0.192000 |
-0.003690 |
2.14e-01 |
0.981000 |
Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects |
13 |
4.97e-01 |
6.79e-01 |
0.19100 |
-0.147000 |
-0.122000 |
3.60e-01 |
0.446000 |
Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) |
13 |
4.97e-01 |
6.79e-01 |
0.19100 |
-0.147000 |
-0.122000 |
3.60e-01 |
0.446000 |
Degradation of AXIN |
35 |
1.45e-01 |
3.44e-01 |
0.19100 |
0.110000 |
-0.156000 |
2.58e-01 |
0.111000 |
Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA |
11 |
5.48e-01 |
7.18e-01 |
0.19100 |
-0.006170 |
0.191000 |
9.72e-01 |
0.274000 |
ABC transporters in lipid homeostasis |
12 |
5.23e-01 |
6.95e-01 |
0.19100 |
-0.184000 |
-0.048700 |
2.69e-01 |
0.770000 |
Caspase-mediated cleavage of cytoskeletal proteins |
10 |
5.78e-01 |
7.44e-01 |
0.19000 |
-0.182000 |
0.054700 |
3.18e-01 |
0.765000 |
Regulation of PTEN stability and activity |
44 |
9.01e-02 |
2.72e-01 |
0.19000 |
0.090200 |
-0.167000 |
3.01e-01 |
0.055000 |
mRNA Splicing - Minor Pathway |
30 |
2.02e-01 |
4.18e-01 |
0.19000 |
-0.114000 |
-0.152000 |
2.78e-01 |
0.150000 |
Caspase activation via Death Receptors in the presence of ligand |
14 |
4.64e-01 |
6.52e-01 |
0.19000 |
0.104000 |
-0.159000 |
5.02e-01 |
0.303000 |
Diseases of programmed cell death |
18 |
3.74e-01 |
5.74e-01 |
0.19000 |
-0.078000 |
0.173000 |
5.67e-01 |
0.203000 |
Collagen chain trimerization |
32 |
1.78e-01 |
3.90e-01 |
0.19000 |
0.189000 |
-0.016000 |
6.45e-02 |
0.875000 |
Phosphorylation of CD3 and TCR zeta chains |
12 |
5.29e-01 |
7.01e-01 |
0.18900 |
-0.114000 |
-0.151000 |
4.94e-01 |
0.365000 |
Dopamine Neurotransmitter Release Cycle |
12 |
5.21e-01 |
6.94e-01 |
0.18900 |
-0.086400 |
0.168000 |
6.04e-01 |
0.312000 |
CDT1 association with the CDC6:ORC:origin complex |
38 |
1.27e-01 |
3.27e-01 |
0.18900 |
0.098900 |
-0.161000 |
2.92e-01 |
0.085600 |
PI-3K cascade:FGFR2 |
13 |
4.94e-01 |
6.77e-01 |
0.18900 |
-0.153000 |
0.111000 |
3.39e-01 |
0.490000 |
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) |
68 |
2.78e-02 |
1.34e-01 |
0.18900 |
0.183000 |
0.046100 |
9.18e-03 |
0.511000 |
MicroRNA (miRNA) biogenesis |
13 |
5.05e-01 |
6.84e-01 |
0.18900 |
-0.150000 |
-0.115000 |
3.50e-01 |
0.474000 |
Listeria monocytogenes entry into host cells |
13 |
5.05e-01 |
6.84e-01 |
0.18900 |
-0.089200 |
-0.166000 |
5.78e-01 |
0.300000 |
Nonhomologous End-Joining (NHEJ) |
24 |
2.86e-01 |
4.95e-01 |
0.18700 |
-0.054200 |
-0.179000 |
6.46e-01 |
0.128000 |
ISG15 antiviral mechanism |
46 |
9.20e-02 |
2.76e-01 |
0.18700 |
-0.174000 |
-0.068500 |
4.10e-02 |
0.422000 |
TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain |
10 |
5.91e-01 |
7.50e-01 |
0.18700 |
0.010400 |
-0.187000 |
9.55e-01 |
0.306000 |
Protein ubiquitination |
37 |
1.43e-01 |
3.43e-01 |
0.18600 |
-0.170000 |
0.076400 |
7.36e-02 |
0.422000 |
PIWI-interacting RNA (piRNA) biogenesis |
10 |
5.97e-01 |
7.54e-01 |
0.18600 |
-0.174000 |
-0.067100 |
3.41e-01 |
0.713000 |
Phase II - Conjugation of compounds |
63 |
3.81e-02 |
1.65e-01 |
0.18600 |
0.186000 |
-0.004480 |
1.06e-02 |
0.951000 |
Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template |
25 |
2.72e-01 |
4.83e-01 |
0.18500 |
-0.168000 |
0.077500 |
1.45e-01 |
0.502000 |
COPI-dependent Golgi-to-ER retrograde traffic |
57 |
5.47e-02 |
2.06e-01 |
0.18500 |
-0.016500 |
-0.184000 |
8.30e-01 |
0.016200 |
RNA Polymerase III Transcription Termination |
15 |
4.68e-01 |
6.55e-01 |
0.18500 |
0.162000 |
0.088900 |
2.77e-01 |
0.551000 |
Regulation of ornithine decarboxylase (ODC) |
34 |
1.73e-01 |
3.84e-01 |
0.18500 |
0.172000 |
-0.067300 |
8.25e-02 |
0.497000 |
RUNX2 regulates osteoblast differentiation |
17 |
4.19e-01 |
6.13e-01 |
0.18500 |
0.185000 |
-0.002900 |
1.87e-01 |
0.983000 |
DNA Damage Recognition in GG-NER |
24 |
2.89e-01 |
4.97e-01 |
0.18500 |
-0.084400 |
0.164000 |
4.74e-01 |
0.163000 |
TP53 Regulates Transcription of Genes Involved in Cytochrome C Release |
13 |
5.17e-01 |
6.92e-01 |
0.18500 |
-0.178000 |
-0.048600 |
2.66e-01 |
0.761000 |
CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling |
23 |
3.13e-01 |
5.19e-01 |
0.18500 |
-0.171000 |
-0.069700 |
1.56e-01 |
0.563000 |
FCGR3A-mediated phagocytosis |
54 |
6.28e-02 |
2.21e-01 |
0.18400 |
0.175000 |
-0.059200 |
2.66e-02 |
0.452000 |
Leishmania phagocytosis |
54 |
6.28e-02 |
2.21e-01 |
0.18400 |
0.175000 |
-0.059200 |
2.66e-02 |
0.452000 |
Parasite infection |
54 |
6.28e-02 |
2.21e-01 |
0.18400 |
0.175000 |
-0.059200 |
2.66e-02 |
0.452000 |
CD209 (DC-SIGN) signaling |
17 |
4.16e-01 |
6.12e-01 |
0.18400 |
-0.151000 |
0.105000 |
2.81e-01 |
0.452000 |
Aquaporin-mediated transport |
31 |
2.10e-01 |
4.25e-01 |
0.18400 |
0.026100 |
0.182000 |
8.02e-01 |
0.079500 |
Cell-extracellular matrix interactions |
14 |
4.87e-01 |
6.71e-01 |
0.18400 |
0.108000 |
-0.149000 |
4.84e-01 |
0.335000 |
mRNA Splicing - Major Pathway |
116 |
3.30e-03 |
3.49e-02 |
0.18300 |
-0.149000 |
-0.107000 |
5.58e-03 |
0.048000 |
Ca-dependent events |
30 |
2.18e-01 |
4.31e-01 |
0.18300 |
-0.089500 |
0.160000 |
3.96e-01 |
0.130000 |
Dual Incision in GG-NER |
30 |
2.22e-01 |
4.36e-01 |
0.18300 |
-0.178000 |
0.041100 |
9.21e-02 |
0.697000 |
Gamma carboxylation, hypusine formation and arylsulfatase activation |
21 |
3.47e-01 |
5.56e-01 |
0.18200 |
0.150000 |
-0.103000 |
2.33e-01 |
0.415000 |
FBXL7 down-regulates AURKA during mitotic entry and in early mitosis |
35 |
1.73e-01 |
3.84e-01 |
0.18200 |
0.161000 |
-0.085000 |
1.00e-01 |
0.385000 |
Trafficking of GluR2-containing AMPA receptors |
10 |
6.14e-01 |
7.64e-01 |
0.18200 |
-0.150000 |
-0.103000 |
4.12e-01 |
0.573000 |
NOTCH4 Intracellular Domain Regulates Transcription |
18 |
4.13e-01 |
6.10e-01 |
0.18100 |
-0.024200 |
-0.180000 |
8.59e-01 |
0.187000 |
FGFR1 mutant receptor activation |
21 |
3.55e-01 |
5.63e-01 |
0.18000 |
-0.078800 |
0.162000 |
5.32e-01 |
0.198000 |
PECAM1 interactions |
10 |
6.16e-01 |
7.66e-01 |
0.18000 |
0.052200 |
0.173000 |
7.75e-01 |
0.344000 |
Processing of Capped Intron-Containing Pre-mRNA |
160 |
4.96e-04 |
9.41e-03 |
0.18000 |
-0.163000 |
-0.077000 |
3.88e-04 |
0.094100 |
Cytochrome P450 - arranged by substrate type |
29 |
2.49e-01 |
4.61e-01 |
0.18000 |
0.104000 |
0.148000 |
3.35e-01 |
0.169000 |
NOTCH1 Intracellular Domain Regulates Transcription |
37 |
1.62e-01 |
3.68e-01 |
0.18000 |
-0.138000 |
0.116000 |
1.47e-01 |
0.223000 |
TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) |
10 |
6.18e-01 |
7.67e-01 |
0.18000 |
0.065100 |
0.168000 |
7.22e-01 |
0.358000 |
Transport of Mature mRNA derived from an Intron-Containing Transcript |
53 |
7.97e-02 |
2.56e-01 |
0.18000 |
-0.149000 |
-0.101000 |
6.03e-02 |
0.206000 |
Transcriptional regulation of white adipocyte differentiation |
65 |
4.46e-02 |
1.84e-01 |
0.18000 |
-0.169000 |
-0.060600 |
1.83e-02 |
0.399000 |
Signaling by FGFR in disease |
38 |
1.56e-01 |
3.59e-01 |
0.18000 |
-0.164000 |
0.073200 |
7.98e-02 |
0.435000 |
RNA Polymerase I Transcription Termination |
16 |
4.61e-01 |
6.49e-01 |
0.18000 |
-0.007040 |
-0.180000 |
9.61e-01 |
0.213000 |
Degradation of cysteine and homocysteine |
11 |
5.85e-01 |
7.48e-01 |
0.18000 |
-0.171000 |
0.054600 |
3.26e-01 |
0.754000 |
SUMOylation of transcription factors |
12 |
5.62e-01 |
7.30e-01 |
0.17900 |
-0.179000 |
-0.017200 |
2.84e-01 |
0.918000 |
Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) |
12 |
5.59e-01 |
7.29e-01 |
0.17900 |
-0.170000 |
0.057100 |
3.09e-01 |
0.732000 |
Elevation of cytosolic Ca2+ levels |
10 |
6.23e-01 |
7.71e-01 |
0.17900 |
-0.071700 |
-0.164000 |
6.95e-01 |
0.370000 |
Mitotic Prophase |
62 |
5.15e-02 |
2.02e-01 |
0.17900 |
-0.175000 |
0.034400 |
1.72e-02 |
0.640000 |
HATs acetylate histones |
58 |
6.73e-02 |
2.28e-01 |
0.17800 |
-0.162000 |
-0.071900 |
3.26e-02 |
0.345000 |
Separation of Sister Chromatids |
122 |
3.72e-03 |
3.64e-02 |
0.17700 |
-0.120000 |
-0.130000 |
2.22e-02 |
0.013400 |
Acyl chain remodelling of PS |
14 |
5.20e-01 |
6.94e-01 |
0.17700 |
0.175000 |
0.027900 |
2.57e-01 |
0.857000 |
Metabolism of cofactors |
17 |
4.46e-01 |
6.35e-01 |
0.17700 |
0.087900 |
-0.154000 |
5.31e-01 |
0.273000 |
Nuclear Receptor transcription pathway |
41 |
1.45e-01 |
3.44e-01 |
0.17700 |
-0.077400 |
0.159000 |
3.92e-01 |
0.079100 |
Polymerase switching on the C-strand of the telomere |
21 |
3.75e-01 |
5.74e-01 |
0.17700 |
-0.176000 |
0.010700 |
1.62e-01 |
0.932000 |
Interleukin-17 signaling |
54 |
7.92e-02 |
2.55e-01 |
0.17600 |
-0.164000 |
0.065300 |
3.75e-02 |
0.407000 |
The role of Nef in HIV-1 replication and disease pathogenesis |
22 |
3.54e-01 |
5.63e-01 |
0.17600 |
-0.083500 |
0.155000 |
4.98e-01 |
0.207000 |
Activation of RAC1 |
10 |
6.33e-01 |
7.77e-01 |
0.17600 |
-0.159000 |
-0.075000 |
3.85e-01 |
0.681000 |
MAP kinase activation |
50 |
9.80e-02 |
2.87e-01 |
0.17500 |
-0.164000 |
0.063600 |
4.57e-02 |
0.437000 |
Nephrin family interactions |
17 |
4.57e-01 |
6.44e-01 |
0.17500 |
-0.175000 |
0.008300 |
2.11e-01 |
0.953000 |
Nuclear signaling by ERBB4 |
23 |
3.42e-01 |
5.54e-01 |
0.17500 |
0.126000 |
-0.121000 |
2.94e-01 |
0.315000 |
Signaling by ERBB2 in Cancer |
20 |
4.08e-01 |
6.05e-01 |
0.17400 |
-0.117000 |
-0.129000 |
3.65e-01 |
0.317000 |
Keratan sulfate biosynthesis |
17 |
4.56e-01 |
6.44e-01 |
0.17400 |
-0.085900 |
0.152000 |
5.40e-01 |
0.279000 |
Negative regulation of MAPK pathway |
32 |
2.31e-01 |
4.47e-01 |
0.17400 |
-0.169000 |
0.044300 |
9.89e-02 |
0.664000 |
Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha |
41 |
1.55e-01 |
3.59e-01 |
0.17400 |
0.174000 |
0.000828 |
5.36e-02 |
0.993000 |
Nuclear Envelope (NE) Reassembly |
52 |
9.63e-02 |
2.85e-01 |
0.17400 |
-0.168000 |
-0.046100 |
3.62e-02 |
0.566000 |
Regulation of lipid metabolism by PPARalpha |
91 |
1.76e-02 |
1.05e-01 |
0.17400 |
-0.143000 |
-0.099500 |
1.89e-02 |
0.102000 |
TRAF6-mediated induction of TAK1 complex within TLR4 complex |
10 |
6.32e-01 |
7.77e-01 |
0.17400 |
-0.119000 |
0.127000 |
5.14e-01 |
0.488000 |
Signaling by NOTCH3 |
36 |
1.99e-01 |
4.17e-01 |
0.17400 |
-0.028300 |
-0.171000 |
7.69e-01 |
0.075500 |
MAPK targets/ Nuclear events mediated by MAP kinases |
27 |
2.97e-01 |
5.05e-01 |
0.17300 |
-0.173000 |
0.005650 |
1.20e-01 |
0.959000 |
Signaling by Retinoic Acid |
30 |
2.57e-01 |
4.69e-01 |
0.17300 |
-0.150000 |
0.086700 |
1.56e-01 |
0.411000 |
Regulation of actin dynamics for phagocytic cup formation |
55 |
8.33e-02 |
2.61e-01 |
0.17300 |
0.115000 |
-0.129000 |
1.41e-01 |
0.098700 |
The canonical retinoid cycle in rods (twilight vision) |
13 |
5.56e-01 |
7.26e-01 |
0.17200 |
-0.128000 |
0.116000 |
4.25e-01 |
0.470000 |
G2/M Checkpoints |
89 |
2.03e-02 |
1.14e-01 |
0.17200 |
-0.056600 |
-0.163000 |
3.57e-01 |
0.008060 |
Metal ion SLC transporters |
18 |
4.45e-01 |
6.35e-01 |
0.17200 |
0.130000 |
-0.112000 |
3.39e-01 |
0.410000 |
Generation of second messenger molecules |
21 |
4.01e-01 |
6.03e-01 |
0.17200 |
-0.148000 |
-0.087500 |
2.42e-01 |
0.488000 |
Neurotransmitter release cycle |
26 |
3.14e-01 |
5.20e-01 |
0.17200 |
-0.150000 |
0.083500 |
1.86e-01 |
0.461000 |
Mitotic Anaphase |
164 |
9.18e-04 |
1.45e-02 |
0.17100 |
-0.117000 |
-0.125000 |
9.74e-03 |
0.006130 |
MTOR signalling |
30 |
2.69e-01 |
4.81e-01 |
0.17100 |
-0.171000 |
0.004360 |
1.05e-01 |
0.967000 |
IGF1R signaling cascade |
35 |
2.18e-01 |
4.31e-01 |
0.17100 |
-0.169000 |
-0.023300 |
8.32e-02 |
0.811000 |
Glutathione conjugation |
27 |
3.08e-01 |
5.15e-01 |
0.17000 |
0.161000 |
-0.056100 |
1.49e-01 |
0.614000 |
Response to elevated platelet cytosolic Ca2+ |
90 |
2.12e-02 |
1.16e-01 |
0.17000 |
0.169000 |
0.016600 |
5.65e-03 |
0.786000 |
Mitotic Metaphase and Anaphase |
165 |
9.81e-04 |
1.53e-02 |
0.17000 |
-0.120000 |
-0.120000 |
8.09e-03 |
0.007940 |
Phosphorylation of the APC/C |
17 |
4.82e-01 |
6.67e-01 |
0.17000 |
-0.034800 |
-0.166000 |
8.04e-01 |
0.236000 |
Cdc20:Phospho-APC/C mediated degradation of Cyclin A |
51 |
1.09e-01 |
3.00e-01 |
0.17000 |
0.101000 |
-0.136000 |
2.11e-01 |
0.093600 |
Ion homeostasis |
37 |
2.04e-01 |
4.19e-01 |
0.16900 |
-0.169000 |
0.015400 |
7.60e-02 |
0.871000 |
TCF dependent signaling in response to WNT |
117 |
6.37e-03 |
5.34e-02 |
0.16900 |
-0.135000 |
0.102000 |
1.18e-02 |
0.057000 |
Signaling by FGFR4 |
23 |
3.79e-01 |
5.79e-01 |
0.16800 |
-0.164000 |
-0.038000 |
1.74e-01 |
0.753000 |
APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint |
52 |
1.09e-01 |
3.01e-01 |
0.16800 |
0.090200 |
-0.141000 |
2.61e-01 |
0.078200 |
Sulfur amino acid metabolism |
18 |
4.73e-01 |
6.58e-01 |
0.16800 |
-0.159000 |
-0.053500 |
2.44e-01 |
0.695000 |
Switching of origins to a post-replicative state |
62 |
7.46e-02 |
2.44e-01 |
0.16700 |
0.008590 |
-0.167000 |
9.07e-01 |
0.023000 |
Recycling pathway of L1 |
25 |
3.56e-01 |
5.63e-01 |
0.16700 |
-0.076300 |
-0.149000 |
5.09e-01 |
0.198000 |
Gastrin-CREB signalling pathway via PKC and MAPK |
13 |
5.82e-01 |
7.48e-01 |
0.16700 |
-0.031500 |
-0.164000 |
8.44e-01 |
0.306000 |
Signaling by NTRK2 (TRKB) |
18 |
4.70e-01 |
6.56e-01 |
0.16700 |
-0.047000 |
0.160000 |
7.30e-01 |
0.241000 |
Synthesis of substrates in N-glycan biosythesis |
47 |
1.46e-01 |
3.45e-01 |
0.16600 |
0.156000 |
0.058500 |
6.48e-02 |
0.488000 |
TICAM1, RIP1-mediated IKK complex recruitment |
12 |
6.06e-01 |
7.61e-01 |
0.16600 |
-0.163000 |
0.034700 |
3.29e-01 |
0.835000 |
IRS-related events triggered by IGF1R |
34 |
2.45e-01 |
4.57e-01 |
0.16600 |
-0.166000 |
0.000650 |
9.36e-02 |
0.995000 |
Post NMDA receptor activation events |
48 |
1.36e-01 |
3.35e-01 |
0.16600 |
-0.162000 |
0.037600 |
5.27e-02 |
0.653000 |
RHO GTPases Activate NADPH Oxidases |
18 |
4.71e-01 |
6.57e-01 |
0.16600 |
0.106000 |
-0.128000 |
4.38e-01 |
0.348000 |
M Phase |
255 |
4.04e-05 |
1.61e-03 |
0.16600 |
-0.140000 |
-0.088700 |
1.31e-04 |
0.015300 |
Basigin interactions |
21 |
4.23e-01 |
6.18e-01 |
0.16600 |
-0.002560 |
-0.165000 |
9.84e-01 |
0.189000 |
YAP1- and WWTR1 (TAZ)-stimulated gene expression |
11 |
6.41e-01 |
7.81e-01 |
0.16500 |
-0.056400 |
-0.155000 |
7.46e-01 |
0.373000 |
Notch-HLH transcription pathway |
22 |
4.13e-01 |
6.10e-01 |
0.16500 |
-0.112000 |
-0.121000 |
3.65e-01 |
0.324000 |
NoRC negatively regulates rRNA expression |
25 |
3.65e-01 |
5.72e-01 |
0.16500 |
-0.064900 |
-0.152000 |
5.75e-01 |
0.190000 |
HS-GAG degradation |
15 |
5.43e-01 |
7.14e-01 |
0.16500 |
0.164000 |
-0.012300 |
2.71e-01 |
0.934000 |
Telomere C-strand synthesis initiation |
11 |
6.37e-01 |
7.79e-01 |
0.16400 |
-0.142000 |
0.082900 |
4.15e-01 |
0.634000 |
RHO GTPases activate IQGAPs |
10 |
6.72e-01 |
8.10e-01 |
0.16400 |
0.084100 |
0.141000 |
6.45e-01 |
0.441000 |
PPARA activates gene expression |
89 |
2.99e-02 |
1.42e-01 |
0.16400 |
-0.133000 |
-0.095600 |
3.03e-02 |
0.120000 |
Factors involved in megakaryocyte development and platelet production |
80 |
4.14e-02 |
1.73e-01 |
0.16400 |
-0.162000 |
-0.023600 |
1.23e-02 |
0.716000 |
Interleukin-3, Interleukin-5 and GM-CSF signaling |
32 |
2.76e-01 |
4.87e-01 |
0.16300 |
-0.067400 |
0.149000 |
5.09e-01 |
0.146000 |
Role of LAT2/NTAL/LAB on calcium mobilization |
13 |
5.92e-01 |
7.50e-01 |
0.16300 |
-0.092700 |
0.134000 |
5.63e-01 |
0.403000 |
p53-Dependent G1 DNA Damage Response |
43 |
1.82e-01 |
3.95e-01 |
0.16200 |
0.052300 |
-0.153000 |
5.53e-01 |
0.082100 |
p53-Dependent G1/S DNA damage checkpoint |
43 |
1.82e-01 |
3.95e-01 |
0.16200 |
0.052300 |
-0.153000 |
5.53e-01 |
0.082100 |
Signaling by NOTCH4 |
59 |
9.71e-02 |
2.87e-01 |
0.16200 |
0.098400 |
-0.128000 |
1.92e-01 |
0.089000 |
Degradation of GLI1 by the proteasome |
37 |
2.32e-01 |
4.48e-01 |
0.16100 |
0.143000 |
-0.074900 |
1.33e-01 |
0.431000 |
TRAF3-dependent IRF activation pathway |
12 |
6.30e-01 |
7.77e-01 |
0.16100 |
-0.077400 |
-0.141000 |
6.42e-01 |
0.397000 |
Senescence-Associated Secretory Phenotype (SASP) |
37 |
2.39e-01 |
4.53e-01 |
0.16100 |
-0.021900 |
-0.160000 |
8.18e-01 |
0.093000 |
Regulation of necroptotic cell death |
12 |
6.24e-01 |
7.72e-01 |
0.16100 |
0.048600 |
-0.154000 |
7.71e-01 |
0.357000 |
Mitochondrial calcium ion transport |
16 |
5.39e-01 |
7.11e-01 |
0.16000 |
-0.006260 |
0.160000 |
9.65e-01 |
0.267000 |
S Phase |
115 |
1.32e-02 |
8.78e-02 |
0.16000 |
-0.115000 |
-0.112000 |
3.33e-02 |
0.039300 |
Signaling by ERBB4 |
35 |
2.62e-01 |
4.74e-01 |
0.16000 |
-0.001070 |
-0.160000 |
9.91e-01 |
0.102000 |
tRNA processing in the nucleus |
41 |
2.12e-01 |
4.25e-01 |
0.16000 |
-0.154000 |
-0.043100 |
8.85e-02 |
0.633000 |
Nucleotide Excision Repair |
74 |
5.84e-02 |
2.11e-01 |
0.16000 |
-0.149000 |
0.056400 |
2.65e-02 |
0.402000 |
Deubiquitination |
180 |
1.19e-03 |
1.78e-02 |
0.16000 |
-0.158000 |
-0.021500 |
2.68e-04 |
0.621000 |
GPCR ligand binding |
189 |
8.47e-04 |
1.39e-02 |
0.15900 |
0.159000 |
0.013100 |
1.75e-04 |
0.757000 |
Signalling to ERKs |
27 |
3.54e-01 |
5.63e-01 |
0.15900 |
-0.066800 |
0.145000 |
5.48e-01 |
0.194000 |
RHO GTPases activate CIT |
16 |
5.40e-01 |
7.11e-01 |
0.15900 |
-0.113000 |
0.112000 |
4.33e-01 |
0.439000 |
RAF-independent MAPK1/3 activation |
18 |
5.02e-01 |
6.83e-01 |
0.15900 |
-0.059900 |
0.147000 |
6.60e-01 |
0.280000 |
Synthesis of PIPs at the early endosome membrane |
14 |
5.86e-01 |
7.48e-01 |
0.15900 |
-0.153000 |
0.042300 |
3.21e-01 |
0.784000 |
Asymmetric localization of PCP proteins |
45 |
1.87e-01 |
4.03e-01 |
0.15800 |
0.158000 |
-0.009500 |
6.77e-02 |
0.912000 |
APC/C:Cdc20 mediated degradation of mitotic proteins |
54 |
1.31e-01 |
3.31e-01 |
0.15800 |
0.076800 |
-0.138000 |
3.29e-01 |
0.080100 |
Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins |
54 |
1.31e-01 |
3.31e-01 |
0.15800 |
0.076800 |
-0.138000 |
3.29e-01 |
0.080100 |
Innate Immune System |
651 |
1.09e-10 |
2.69e-08 |
0.15700 |
0.151000 |
-0.043400 |
9.02e-11 |
0.062700 |
Signaling by ERBB2 KD Mutants |
19 |
5.00e-01 |
6.83e-01 |
0.15700 |
-0.121000 |
-0.101000 |
3.63e-01 |
0.447000 |
Meiosis |
40 |
2.33e-01 |
4.49e-01 |
0.15700 |
-0.151000 |
-0.041000 |
9.81e-02 |
0.654000 |
Transcriptional regulation by RUNX2 |
77 |
5.73e-02 |
2.10e-01 |
0.15700 |
0.121000 |
-0.099400 |
6.64e-02 |
0.132000 |
ABC-family proteins mediated transport |
64 |
9.30e-02 |
2.78e-01 |
0.15700 |
0.121000 |
-0.099000 |
9.37e-02 |
0.172000 |
Cargo concentration in the ER |
18 |
5.12e-01 |
6.88e-01 |
0.15700 |
0.124000 |
-0.095200 |
3.62e-01 |
0.484000 |
Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors |
23 |
4.28e-01 |
6.21e-01 |
0.15600 |
-0.144000 |
0.061000 |
2.33e-01 |
0.613000 |
Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase |
18 |
5.22e-01 |
6.95e-01 |
0.15600 |
-0.057700 |
-0.145000 |
6.72e-01 |
0.287000 |
SCF-beta-TrCP mediated degradation of Emi1 |
36 |
2.66e-01 |
4.78e-01 |
0.15600 |
0.138000 |
-0.072800 |
1.53e-01 |
0.450000 |
G alpha (z) signalling events |
31 |
3.33e-01 |
5.43e-01 |
0.15500 |
0.104000 |
0.115000 |
3.16e-01 |
0.268000 |
HIV Transcription Initiation |
30 |
3.45e-01 |
5.54e-01 |
0.15500 |
-0.074900 |
-0.136000 |
4.78e-01 |
0.199000 |
RNA Polymerase II HIV Promoter Escape |
30 |
3.45e-01 |
5.54e-01 |
0.15500 |
-0.074900 |
-0.136000 |
4.78e-01 |
0.199000 |
RNA Polymerase II Promoter Escape |
30 |
3.45e-01 |
5.54e-01 |
0.15500 |
-0.074900 |
-0.136000 |
4.78e-01 |
0.199000 |
RNA Polymerase II Transcription Initiation |
30 |
3.45e-01 |
5.54e-01 |
0.15500 |
-0.074900 |
-0.136000 |
4.78e-01 |
0.199000 |
RNA Polymerase II Transcription Initiation And Promoter Clearance |
30 |
3.45e-01 |
5.54e-01 |
0.15500 |
-0.074900 |
-0.136000 |
4.78e-01 |
0.199000 |
RNA Polymerase II Transcription Pre-Initiation And Promoter Opening |
30 |
3.45e-01 |
5.54e-01 |
0.15500 |
-0.074900 |
-0.136000 |
4.78e-01 |
0.199000 |
EPHA-mediated growth cone collapse |
11 |
6.79e-01 |
8.14e-01 |
0.15400 |
0.139000 |
0.066700 |
4.25e-01 |
0.702000 |
Mitochondrial tRNA aminoacylation |
12 |
6.51e-01 |
7.91e-01 |
0.15400 |
0.143000 |
-0.056400 |
3.91e-01 |
0.735000 |
Chaperone Mediated Autophagy |
12 |
6.53e-01 |
7.93e-01 |
0.15300 |
0.044600 |
-0.147000 |
7.89e-01 |
0.379000 |
Intraflagellar transport |
33 |
3.10e-01 |
5.17e-01 |
0.15300 |
0.142000 |
-0.057100 |
1.57e-01 |
0.570000 |
Signaling by ROBO receptors |
112 |
1.95e-02 |
1.11e-01 |
0.15300 |
0.146000 |
-0.047200 |
7.88e-03 |
0.390000 |
APC/C:Cdc20 mediated degradation of Cyclin B |
18 |
5.34e-01 |
7.06e-01 |
0.15300 |
-0.044700 |
-0.147000 |
7.43e-01 |
0.282000 |
SCF(Skp2)-mediated degradation of p27/p21 |
38 |
2.60e-01 |
4.71e-01 |
0.15300 |
0.122000 |
-0.092800 |
1.95e-01 |
0.322000 |
GP1b-IX-V activation signalling |
10 |
7.01e-01 |
8.29e-01 |
0.15300 |
-0.081000 |
0.130000 |
6.57e-01 |
0.478000 |
FCERI mediated Ca+2 mobilization |
24 |
4.33e-01 |
6.25e-01 |
0.15200 |
-0.152000 |
0.006210 |
1.97e-01 |
0.958000 |
Signaling by FGFR1 |
30 |
3.60e-01 |
5.68e-01 |
0.15200 |
-0.117000 |
-0.096500 |
2.66e-01 |
0.361000 |
Regulation of RUNX3 expression and activity |
36 |
2.85e-01 |
4.94e-01 |
0.15200 |
0.088400 |
-0.123000 |
3.59e-01 |
0.201000 |
DARPP-32 events |
19 |
5.15e-01 |
6.90e-01 |
0.15200 |
-0.093800 |
0.119000 |
4.79e-01 |
0.369000 |
Gene expression (Transcription) |
857 |
1.93e-12 |
1.19e-09 |
0.15100 |
-0.149000 |
-0.024600 |
3.77e-13 |
0.231000 |
Transferrin endocytosis and recycling |
17 |
5.64e-01 |
7.31e-01 |
0.15100 |
0.140000 |
0.057100 |
3.19e-01 |
0.684000 |
Initiation of Nuclear Envelope (NE) Reformation |
15 |
6.02e-01 |
7.58e-01 |
0.15100 |
-0.145000 |
-0.040400 |
3.30e-01 |
0.786000 |
DAP12 interactions |
24 |
4.37e-01 |
6.27e-01 |
0.15100 |
0.121000 |
-0.090200 |
3.06e-01 |
0.445000 |
Major pathway of rRNA processing in the nucleolus and cytosol |
90 |
5.00e-02 |
1.98e-01 |
0.15100 |
0.088700 |
0.122000 |
1.47e-01 |
0.046300 |
Ub-specific processing proteases |
121 |
1.85e-02 |
1.08e-01 |
0.15000 |
-0.124000 |
-0.085300 |
1.93e-02 |
0.106000 |
HIV Infection |
148 |
7.73e-03 |
6.11e-02 |
0.15000 |
-0.082400 |
-0.125000 |
8.47e-02 |
0.008680 |
Syndecan interactions |
16 |
5.90e-01 |
7.50e-01 |
0.15000 |
0.114000 |
0.096600 |
4.29e-01 |
0.504000 |
Hedgehog 'on' state |
52 |
1.72e-01 |
3.84e-01 |
0.15000 |
0.121000 |
-0.087700 |
1.31e-01 |
0.274000 |
Metabolic disorders of biological oxidation enzymes |
20 |
5.10e-01 |
6.87e-01 |
0.14900 |
-0.118000 |
0.090200 |
3.60e-01 |
0.485000 |
Degradation of DVL |
36 |
3.02e-01 |
5.09e-01 |
0.14800 |
0.109000 |
-0.099700 |
2.57e-01 |
0.301000 |
Vasopressin regulates renal water homeostasis via Aquaporins |
28 |
4.06e-01 |
6.04e-01 |
0.14800 |
0.076900 |
0.126000 |
4.82e-01 |
0.248000 |
GABA receptor activation |
32 |
3.57e-01 |
5.65e-01 |
0.14800 |
0.132000 |
0.065300 |
1.96e-01 |
0.523000 |
Synthesis of DNA |
84 |
6.88e-02 |
2.31e-01 |
0.14700 |
-0.070300 |
-0.129000 |
2.66e-01 |
0.040800 |
G1/S DNA Damage Checkpoints |
44 |
2.38e-01 |
4.52e-01 |
0.14700 |
0.036400 |
-0.143000 |
6.76e-01 |
0.102000 |
MAP3K8 (TPL2)-dependent MAPK1/3 activation |
10 |
7.20e-01 |
8.40e-01 |
0.14700 |
-0.120000 |
0.085400 |
5.12e-01 |
0.640000 |
PLC beta mediated events |
43 |
2.45e-01 |
4.57e-01 |
0.14700 |
-0.078300 |
0.124000 |
3.75e-01 |
0.158000 |
Activation of HOX genes during differentiation |
39 |
2.83e-01 |
4.92e-01 |
0.14700 |
-0.143000 |
0.030400 |
1.21e-01 |
0.743000 |
Activation of anterior HOX genes in hindbrain development during early embryogenesis |
39 |
2.83e-01 |
4.92e-01 |
0.14700 |
-0.143000 |
0.030400 |
1.21e-01 |
0.743000 |
NOTCH2 Activation and Transmission of Signal to the Nucleus |
11 |
7.06e-01 |
8.32e-01 |
0.14700 |
-0.114000 |
-0.092200 |
5.13e-01 |
0.597000 |
RNA Polymerase II Transcription Termination |
45 |
2.44e-01 |
4.57e-01 |
0.14600 |
-0.078900 |
-0.123000 |
3.60e-01 |
0.155000 |
Acyl chain remodelling of PI |
12 |
6.83e-01 |
8.18e-01 |
0.14500 |
0.145000 |
-0.009330 |
3.84e-01 |
0.955000 |
Glycosaminoglycan metabolism |
81 |
7.91e-02 |
2.55e-01 |
0.14500 |
0.144000 |
0.023000 |
2.58e-02 |
0.721000 |
Signaling by FGFR |
49 |
2.17e-01 |
4.31e-01 |
0.14500 |
-0.129000 |
-0.066300 |
1.18e-01 |
0.423000 |
Nitric oxide stimulates guanylate cyclase |
18 |
5.63e-01 |
7.31e-01 |
0.14500 |
0.043700 |
-0.139000 |
7.49e-01 |
0.309000 |
FRS-mediated FGFR2 signaling |
12 |
6.82e-01 |
8.18e-01 |
0.14500 |
-0.122000 |
0.077400 |
4.63e-01 |
0.643000 |
Mitotic G2-G2/M phases |
127 |
2.06e-02 |
1.15e-01 |
0.14500 |
-0.120000 |
-0.081100 |
2.02e-02 |
0.116000 |
A tetrasaccharide linker sequence is required for GAG synthesis |
17 |
5.90e-01 |
7.50e-01 |
0.14500 |
-0.138000 |
-0.041900 |
3.24e-01 |
0.765000 |
Myogenesis |
22 |
5.08e-01 |
6.86e-01 |
0.14400 |
-0.084600 |
-0.117000 |
4.92e-01 |
0.342000 |
Anchoring of the basal body to the plasma membrane |
74 |
1.03e-01 |
2.93e-01 |
0.14400 |
-0.133000 |
-0.057000 |
4.89e-02 |
0.397000 |
RNA Polymerase II Transcription |
769 |
2.28e-10 |
4.69e-08 |
0.14400 |
-0.141000 |
-0.031100 |
6.74e-11 |
0.149000 |
Signaling by ERBB2 TMD/JMD mutants |
16 |
6.11e-01 |
7.64e-01 |
0.14400 |
-0.057600 |
-0.132000 |
6.90e-01 |
0.361000 |
DNA Replication |
91 |
6.33e-02 |
2.22e-01 |
0.14400 |
-0.095000 |
-0.108000 |
1.18e-01 |
0.075500 |
Signaling by PDGF |
44 |
2.54e-01 |
4.67e-01 |
0.14400 |
-0.037500 |
0.139000 |
6.67e-01 |
0.111000 |
Processing of SMDT1 |
11 |
7.15e-01 |
8.38e-01 |
0.14400 |
0.073400 |
0.123000 |
6.73e-01 |
0.479000 |
CRMPs in Sema3A signaling |
13 |
6.72e-01 |
8.10e-01 |
0.14400 |
0.138000 |
0.038800 |
3.88e-01 |
0.809000 |
mRNA Splicing |
123 |
2.46e-02 |
1.27e-01 |
0.14300 |
-0.122000 |
-0.076200 |
2.03e-02 |
0.145000 |
The role of GTSE1 in G2/M progression after G2 checkpoint |
39 |
2.97e-01 |
5.05e-01 |
0.14300 |
0.105000 |
-0.097700 |
2.59e-01 |
0.291000 |
Translocation of SLC2A4 (GLUT4) to the plasma membrane |
43 |
2.64e-01 |
4.75e-01 |
0.14300 |
-0.121000 |
0.075800 |
1.69e-01 |
0.390000 |
G2/M Transition |
125 |
2.42e-02 |
1.27e-01 |
0.14300 |
-0.118000 |
-0.079800 |
2.28e-02 |
0.125000 |
Translation of structural proteins |
18 |
5.83e-01 |
7.48e-01 |
0.14200 |
0.135000 |
0.044100 |
3.21e-01 |
0.746000 |
Pre-NOTCH Processing in Golgi |
14 |
6.54e-01 |
7.93e-01 |
0.14200 |
0.023800 |
-0.140000 |
8.77e-01 |
0.365000 |
Transcriptional Regulation by E2F6 |
27 |
4.48e-01 |
6.37e-01 |
0.14200 |
-0.122000 |
-0.072300 |
2.73e-01 |
0.516000 |
NOD1/2 Signaling Pathway |
25 |
4.67e-01 |
6.53e-01 |
0.14200 |
-0.123000 |
0.070700 |
2.88e-01 |
0.541000 |
PRC2 methylates histones and DNA |
11 |
7.22e-01 |
8.42e-01 |
0.14200 |
-0.102000 |
-0.097800 |
5.56e-01 |
0.575000 |
Integrin cell surface interactions |
52 |
2.17e-01 |
4.31e-01 |
0.14100 |
0.128000 |
0.058600 |
1.10e-01 |
0.466000 |
Incretin synthesis, secretion, and inactivation |
10 |
7.44e-01 |
8.49e-01 |
0.14100 |
-0.033000 |
-0.137000 |
8.57e-01 |
0.453000 |
Class A/1 (Rhodopsin-like receptors) |
137 |
1.72e-02 |
1.04e-01 |
0.14100 |
0.137000 |
-0.034400 |
5.89e-03 |
0.488000 |
Signaling by FGFR3 |
24 |
4.94e-01 |
6.77e-01 |
0.14100 |
-0.129000 |
-0.057500 |
2.75e-01 |
0.626000 |
Semaphorin interactions |
53 |
2.12e-01 |
4.25e-01 |
0.14100 |
0.131000 |
0.051100 |
9.89e-02 |
0.520000 |
Assembly of the pre-replicative complex |
45 |
2.63e-01 |
4.75e-01 |
0.14000 |
0.029700 |
-0.137000 |
7.31e-01 |
0.111000 |
Termination of O-glycan biosynthesis |
12 |
7.04e-01 |
8.30e-01 |
0.14000 |
-0.135000 |
-0.037200 |
4.17e-01 |
0.823000 |
Activation of NF-kappaB in B cells |
43 |
2.79e-01 |
4.91e-01 |
0.14000 |
0.058400 |
-0.127000 |
5.08e-01 |
0.148000 |
Regulation of RUNX2 expression and activity |
46 |
2.54e-01 |
4.67e-01 |
0.14000 |
0.097600 |
-0.101000 |
2.52e-01 |
0.238000 |
Heparan sulfate/heparin (HS-GAG) metabolism |
34 |
3.63e-01 |
5.72e-01 |
0.14000 |
0.111000 |
-0.084900 |
2.61e-01 |
0.392000 |
Degradation of the extracellular matrix |
69 |
1.36e-01 |
3.35e-01 |
0.13900 |
0.139000 |
-0.001520 |
4.57e-02 |
0.983000 |
Fanconi Anemia Pathway |
22 |
5.25e-01 |
6.97e-01 |
0.13900 |
-0.134000 |
0.038900 |
2.78e-01 |
0.752000 |
Global Genome Nucleotide Excision Repair (GG-NER) |
59 |
1.77e-01 |
3.89e-01 |
0.13900 |
-0.088400 |
0.107000 |
2.41e-01 |
0.154000 |
Signaling by Nuclear Receptors |
168 |
9.40e-03 |
6.90e-02 |
0.13800 |
-0.110000 |
-0.083400 |
1.42e-02 |
0.063100 |
BBSome-mediated cargo-targeting to cilium |
16 |
6.29e-01 |
7.76e-01 |
0.13800 |
0.115000 |
-0.076900 |
4.27e-01 |
0.594000 |
EPH-Ephrin signaling |
70 |
1.34e-01 |
3.32e-01 |
0.13800 |
0.125000 |
-0.058000 |
7.02e-02 |
0.403000 |
Regulation of PTEN gene transcription |
46 |
2.69e-01 |
4.81e-01 |
0.13800 |
-0.138000 |
0.010500 |
1.07e-01 |
0.902000 |
Generic Transcription Pathway |
684 |
1.18e-08 |
1.46e-06 |
0.13800 |
-0.137000 |
-0.018900 |
2.02e-09 |
0.407000 |
G1/S Transition |
90 |
7.99e-02 |
2.56e-01 |
0.13800 |
-0.132000 |
-0.040400 |
3.09e-02 |
0.509000 |
LGI-ADAM interactions |
13 |
6.88e-01 |
8.21e-01 |
0.13800 |
-0.040300 |
0.132000 |
8.01e-01 |
0.411000 |
Mitotic G1 phase and G1/S transition |
102 |
5.78e-02 |
2.10e-01 |
0.13800 |
-0.131000 |
-0.044100 |
2.31e-02 |
0.443000 |
Carboxyterminal post-translational modifications of tubulin |
24 |
5.11e-01 |
6.87e-01 |
0.13700 |
-0.012900 |
0.136000 |
9.13e-01 |
0.249000 |
NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux |
27 |
4.75e-01 |
6.59e-01 |
0.13600 |
0.125000 |
0.054400 |
2.61e-01 |
0.625000 |
FCERI mediated MAPK activation |
24 |
5.09e-01 |
6.87e-01 |
0.13600 |
-0.092400 |
0.099900 |
4.34e-01 |
0.397000 |
Regulation of RAS by GAPs |
46 |
2.83e-01 |
4.92e-01 |
0.13500 |
0.022900 |
-0.133000 |
7.88e-01 |
0.118000 |
Inactivation, recovery and regulation of the phototransduction cascade |
18 |
6.14e-01 |
7.64e-01 |
0.13500 |
-0.133000 |
-0.024400 |
3.30e-01 |
0.858000 |
The phototransduction cascade |
18 |
6.14e-01 |
7.64e-01 |
0.13500 |
-0.133000 |
-0.024400 |
3.30e-01 |
0.858000 |
Extracellular matrix organization |
202 |
4.57e-03 |
4.15e-02 |
0.13500 |
0.135000 |
0.002130 |
1.03e-03 |
0.959000 |
Cargo trafficking to the periciliary membrane |
33 |
4.04e-01 |
6.04e-01 |
0.13500 |
0.110000 |
-0.077800 |
2.75e-01 |
0.440000 |
PCP/CE pathway |
63 |
1.80e-01 |
3.93e-01 |
0.13400 |
0.125000 |
-0.050300 |
8.78e-02 |
0.491000 |
Hedgehog 'off' state |
69 |
1.61e-01 |
3.68e-01 |
0.13400 |
0.106000 |
0.081800 |
1.27e-01 |
0.241000 |
mRNA 3'-end processing |
39 |
3.56e-01 |
5.63e-01 |
0.13400 |
-0.097300 |
-0.092400 |
2.94e-01 |
0.318000 |
Cardiac conduction |
82 |
1.09e-01 |
3.01e-01 |
0.13400 |
-0.126000 |
0.046400 |
4.96e-02 |
0.468000 |
G-protein mediated events |
44 |
3.06e-01 |
5.13e-01 |
0.13300 |
-0.059800 |
0.119000 |
4.93e-01 |
0.171000 |
Lysosome Vesicle Biogenesis |
25 |
5.15e-01 |
6.90e-01 |
0.13300 |
-0.017700 |
-0.132000 |
8.79e-01 |
0.253000 |
Phase 0 - rapid depolarisation |
29 |
4.63e-01 |
6.51e-01 |
0.13300 |
0.009010 |
0.133000 |
9.33e-01 |
0.215000 |
tRNA Aminoacylation |
17 |
6.34e-01 |
7.77e-01 |
0.13300 |
0.079600 |
-0.106000 |
5.70e-01 |
0.448000 |
Intra-Golgi traffic |
34 |
4.04e-01 |
6.04e-01 |
0.13300 |
0.080200 |
-0.106000 |
4.19e-01 |
0.287000 |
PI3K events in ERBB2 signaling |
13 |
7.12e-01 |
8.38e-01 |
0.13200 |
-0.001160 |
-0.132000 |
9.94e-01 |
0.410000 |
NGF-stimulated transcription |
29 |
4.66e-01 |
6.53e-01 |
0.13200 |
-0.120000 |
0.054300 |
2.63e-01 |
0.613000 |
RHO GTPase Effectors |
185 |
9.58e-03 |
6.99e-02 |
0.13100 |
-0.116000 |
-0.062500 |
6.96e-03 |
0.145000 |
Interaction between L1 and Ankyrins |
22 |
5.68e-01 |
7.33e-01 |
0.13100 |
0.004560 |
0.131000 |
9.70e-01 |
0.287000 |
trans-Golgi Network Vesicle Budding |
48 |
2.88e-01 |
4.97e-01 |
0.13100 |
0.063100 |
-0.115000 |
4.50e-01 |
0.169000 |
Signaling by Insulin receptor |
47 |
3.02e-01 |
5.09e-01 |
0.13100 |
-0.130000 |
-0.018100 |
1.24e-01 |
0.830000 |
CTLA4 inhibitory signaling |
18 |
6.26e-01 |
7.74e-01 |
0.13100 |
0.103000 |
-0.080300 |
4.48e-01 |
0.555000 |
DNA Repair |
194 |
7.83e-03 |
6.11e-02 |
0.13100 |
-0.124000 |
-0.041000 |
2.97e-03 |
0.328000 |
Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) |
12 |
7.39e-01 |
8.46e-01 |
0.13100 |
0.108000 |
0.074100 |
5.19e-01 |
0.657000 |
Diseases of hemostasis |
12 |
7.39e-01 |
8.46e-01 |
0.13100 |
0.108000 |
0.074100 |
5.19e-01 |
0.657000 |
MyD88 cascade initiated on plasma membrane |
63 |
1.99e-01 |
4.17e-01 |
0.13000 |
-0.113000 |
0.065600 |
1.23e-01 |
0.369000 |
Toll Like Receptor 10 (TLR10) Cascade |
63 |
1.99e-01 |
4.17e-01 |
0.13000 |
-0.113000 |
0.065600 |
1.23e-01 |
0.369000 |
Toll Like Receptor 5 (TLR5) Cascade |
63 |
1.99e-01 |
4.17e-01 |
0.13000 |
-0.113000 |
0.065600 |
1.23e-01 |
0.369000 |
Golgi-to-ER retrograde transport |
83 |
1.24e-01 |
3.23e-01 |
0.13000 |
-0.011900 |
-0.130000 |
8.51e-01 |
0.041600 |
Caspase activation via extrinsic apoptotic signalling pathway |
21 |
5.85e-01 |
7.48e-01 |
0.13000 |
0.042900 |
-0.123000 |
7.34e-01 |
0.330000 |
The citric acid (TCA) cycle and respiratory electron transport |
95 |
9.39e-02 |
2.80e-01 |
0.13000 |
-0.123000 |
-0.040600 |
3.80e-02 |
0.495000 |
Downstream signaling events of B Cell Receptor (BCR) |
54 |
2.57e-01 |
4.69e-01 |
0.13000 |
-0.012000 |
-0.129000 |
8.79e-01 |
0.100000 |
Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) |
12 |
7.38e-01 |
8.46e-01 |
0.13000 |
-0.127000 |
0.024900 |
4.45e-01 |
0.881000 |
GLI3 is processed to GLI3R by the proteasome |
37 |
3.94e-01 |
5.96e-01 |
0.12900 |
0.125000 |
-0.031700 |
1.87e-01 |
0.739000 |
Orc1 removal from chromatin |
45 |
3.25e-01 |
5.34e-01 |
0.12900 |
0.031300 |
-0.125000 |
7.17e-01 |
0.147000 |
Cellular response to hypoxia |
49 |
2.97e-01 |
5.05e-01 |
0.12900 |
0.129000 |
0.002280 |
1.19e-01 |
0.978000 |
Antiviral mechanism by IFN-stimulated genes |
52 |
2.82e-01 |
4.91e-01 |
0.12900 |
-0.114000 |
-0.060200 |
1.57e-01 |
0.454000 |
N-glycan trimming in the ER and Calnexin/Calreticulin cycle |
21 |
5.91e-01 |
7.50e-01 |
0.12800 |
0.097300 |
-0.083800 |
4.40e-01 |
0.507000 |
Purine salvage |
11 |
7.64e-01 |
8.61e-01 |
0.12800 |
-0.037400 |
-0.123000 |
8.30e-01 |
0.481000 |
Negative regulation of NMDA receptor-mediated neuronal transmission |
15 |
6.90e-01 |
8.22e-01 |
0.12800 |
0.120000 |
-0.045000 |
4.22e-01 |
0.763000 |
Transport of vitamins, nucleosides, and related molecules |
28 |
5.10e-01 |
6.87e-01 |
0.12800 |
0.092500 |
0.088200 |
3.97e-01 |
0.420000 |
Translocation of ZAP-70 to Immunological synapse |
10 |
7.84e-01 |
8.74e-01 |
0.12700 |
-0.127000 |
0.005370 |
4.86e-01 |
0.977000 |
Sema4D induced cell migration and growth-cone collapse |
16 |
6.77e-01 |
8.14e-01 |
0.12700 |
0.116000 |
-0.051500 |
4.22e-01 |
0.721000 |
Metabolism of folate and pterines |
13 |
7.32e-01 |
8.46e-01 |
0.12700 |
0.013100 |
0.126000 |
9.35e-01 |
0.431000 |
TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation |
67 |
1.97e-01 |
4.17e-01 |
0.12700 |
-0.114000 |
0.055700 |
1.07e-01 |
0.431000 |
Signaling by MET |
52 |
2.93e-01 |
5.00e-01 |
0.12700 |
-0.090600 |
-0.088700 |
2.59e-01 |
0.269000 |
Acyl chain remodelling of PC |
19 |
6.33e-01 |
7.77e-01 |
0.12600 |
0.122000 |
-0.031200 |
3.56e-01 |
0.814000 |
CD28 dependent Vav1 pathway |
11 |
7.67e-01 |
8.63e-01 |
0.12600 |
0.121000 |
-0.037300 |
4.89e-01 |
0.831000 |
DNA Replication Pre-Initiation |
57 |
2.66e-01 |
4.78e-01 |
0.12600 |
-0.067600 |
-0.106000 |
3.78e-01 |
0.167000 |
Intra-Golgi and retrograde Golgi-to-ER traffic |
134 |
4.39e-02 |
1.82e-01 |
0.12600 |
-0.005880 |
-0.125000 |
9.07e-01 |
0.012400 |
mTORC1-mediated signalling |
17 |
6.69e-01 |
8.09e-01 |
0.12600 |
-0.009510 |
0.125000 |
9.46e-01 |
0.372000 |
RHO GTPases activate PAKs |
18 |
6.58e-01 |
7.97e-01 |
0.12500 |
0.056500 |
0.112000 |
6.78e-01 |
0.411000 |
Transcription-Coupled Nucleotide Excision Repair (TC-NER) |
52 |
2.99e-01 |
5.06e-01 |
0.12500 |
-0.115000 |
-0.049100 |
1.50e-01 |
0.540000 |
Synthesis of PIPs at the plasma membrane |
47 |
3.27e-01 |
5.35e-01 |
0.12500 |
-0.071400 |
0.103000 |
3.98e-01 |
0.223000 |
Base Excision Repair |
36 |
4.25e-01 |
6.21e-01 |
0.12500 |
-0.110000 |
0.060500 |
2.55e-01 |
0.531000 |
Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants |
42 |
3.74e-01 |
5.74e-01 |
0.12500 |
-0.122000 |
0.024800 |
1.71e-01 |
0.781000 |
Constitutive Signaling by NOTCH1 PEST Domain Mutants |
42 |
3.74e-01 |
5.74e-01 |
0.12500 |
-0.122000 |
0.024800 |
1.71e-01 |
0.781000 |
Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer |
42 |
3.74e-01 |
5.74e-01 |
0.12500 |
-0.122000 |
0.024800 |
1.71e-01 |
0.781000 |
Signaling by NOTCH1 PEST Domain Mutants in Cancer |
42 |
3.74e-01 |
5.74e-01 |
0.12500 |
-0.122000 |
0.024800 |
1.71e-01 |
0.781000 |
Signaling by NOTCH1 in Cancer |
42 |
3.74e-01 |
5.74e-01 |
0.12500 |
-0.122000 |
0.024800 |
1.71e-01 |
0.781000 |
Host Interactions of HIV factors |
88 |
1.36e-01 |
3.35e-01 |
0.12400 |
-0.098300 |
-0.076000 |
1.12e-01 |
0.219000 |
Signalling to RAS |
15 |
7.06e-01 |
8.32e-01 |
0.12400 |
-0.024700 |
0.122000 |
8.68e-01 |
0.415000 |
Leishmania infection |
157 |
2.75e-02 |
1.33e-01 |
0.12400 |
0.121000 |
-0.026500 |
9.05e-03 |
0.567000 |
RHO GTPases Activate ROCKs |
13 |
7.40e-01 |
8.47e-01 |
0.12400 |
0.122000 |
-0.023700 |
4.48e-01 |
0.882000 |
Degradation of GLI2 by the proteasome |
38 |
4.19e-01 |
6.13e-01 |
0.12400 |
0.123000 |
-0.011800 |
1.90e-01 |
0.900000 |
Protein localization |
108 |
8.63e-02 |
2.69e-01 |
0.12300 |
0.023900 |
-0.121000 |
6.69e-01 |
0.030400 |
Protein folding |
68 |
2.21e-01 |
4.36e-01 |
0.12300 |
0.097400 |
0.075000 |
1.65e-01 |
0.286000 |
Asparagine N-linked glycosylation |
202 |
1.14e-02 |
7.87e-02 |
0.12300 |
0.123000 |
0.003610 |
2.77e-03 |
0.930000 |
RAF activation |
27 |
5.46e-01 |
7.16e-01 |
0.12300 |
-0.122000 |
-0.016000 |
2.75e-01 |
0.886000 |
Signaling by NOTCH1 |
55 |
2.94e-01 |
5.03e-01 |
0.12200 |
-0.121000 |
0.011100 |
1.20e-01 |
0.887000 |
CLEC7A (Dectin-1) signaling |
68 |
2.24e-01 |
4.38e-01 |
0.12200 |
-0.001850 |
-0.121000 |
9.79e-01 |
0.083700 |
SUMOylation of intracellular receptors |
22 |
6.13e-01 |
7.64e-01 |
0.12100 |
-0.114000 |
0.042900 |
3.57e-01 |
0.728000 |
RIPK1-mediated regulated necrosis |
14 |
7.33e-01 |
8.46e-01 |
0.12100 |
0.117000 |
-0.032400 |
4.50e-01 |
0.834000 |
Regulated Necrosis |
14 |
7.33e-01 |
8.46e-01 |
0.12100 |
0.117000 |
-0.032400 |
4.50e-01 |
0.834000 |
Toll Like Receptor 3 (TLR3) Cascade |
73 |
2.01e-01 |
4.17e-01 |
0.12100 |
-0.116000 |
0.035600 |
8.81e-02 |
0.600000 |
DCC mediated attractive signaling |
12 |
7.69e-01 |
8.64e-01 |
0.12100 |
-0.002590 |
0.121000 |
9.88e-01 |
0.469000 |
Cleavage of the damaged pyrimidine |
14 |
7.37e-01 |
8.46e-01 |
0.12100 |
-0.002420 |
-0.121000 |
9.88e-01 |
0.435000 |
Depyrimidination |
14 |
7.37e-01 |
8.46e-01 |
0.12100 |
-0.002420 |
-0.121000 |
9.88e-01 |
0.435000 |
Recognition and association of DNA glycosylase with site containing an affected pyrimidine |
14 |
7.37e-01 |
8.46e-01 |
0.12100 |
-0.002420 |
-0.121000 |
9.88e-01 |
0.435000 |
Signaling by Non-Receptor Tyrosine Kinases |
39 |
4.37e-01 |
6.27e-01 |
0.12000 |
0.052400 |
0.108000 |
5.71e-01 |
0.244000 |
Signaling by PTK6 |
39 |
4.37e-01 |
6.27e-01 |
0.12000 |
0.052400 |
0.108000 |
5.71e-01 |
0.244000 |
Phase I - Functionalization of compounds |
56 |
3.02e-01 |
5.09e-01 |
0.12000 |
0.013500 |
0.119000 |
8.61e-01 |
0.124000 |
rRNA processing in the nucleus and cytosol |
96 |
1.32e-01 |
3.31e-01 |
0.12000 |
0.068400 |
0.098500 |
2.48e-01 |
0.096200 |
Ras activation upon Ca2+ influx through NMDA receptor |
15 |
7.26e-01 |
8.43e-01 |
0.12000 |
-0.119000 |
-0.006550 |
4.23e-01 |
0.965000 |
RMTs methylate histone arginines |
25 |
5.86e-01 |
7.48e-01 |
0.11900 |
-0.118000 |
0.019200 |
3.09e-01 |
0.868000 |
Fcgamma receptor (FCGR) dependent phagocytosis |
75 |
2.01e-01 |
4.17e-01 |
0.11900 |
0.094400 |
-0.072400 |
1.58e-01 |
0.279000 |
Acyl chain remodelling of PE |
17 |
6.99e-01 |
8.29e-01 |
0.11900 |
0.119000 |
0.005340 |
3.98e-01 |
0.970000 |
Toll Like Receptor 9 (TLR9) Cascade |
70 |
2.27e-01 |
4.40e-01 |
0.11800 |
-0.100000 |
0.063400 |
1.48e-01 |
0.360000 |
MyD88 dependent cascade initiated on endosome |
68 |
2.38e-01 |
4.52e-01 |
0.11800 |
-0.097600 |
0.066700 |
1.65e-01 |
0.343000 |
Toll Like Receptor 7/8 (TLR7/8) Cascade |
68 |
2.38e-01 |
4.52e-01 |
0.11800 |
-0.097600 |
0.066700 |
1.65e-01 |
0.343000 |
Platelet activation, signaling and aggregation |
183 |
2.33e-02 |
1.25e-01 |
0.11800 |
0.118000 |
-0.001380 |
6.12e-03 |
0.975000 |
VxPx cargo-targeting to cilium |
13 |
7.65e-01 |
8.61e-01 |
0.11700 |
0.117000 |
-0.005480 |
4.65e-01 |
0.973000 |
Transcriptional Regulation by MECP2 |
41 |
4.31e-01 |
6.22e-01 |
0.11700 |
-0.117000 |
0.005590 |
1.95e-01 |
0.951000 |
RUNX2 regulates bone development |
22 |
6.37e-01 |
7.79e-01 |
0.11700 |
0.117000 |
0.009440 |
3.43e-01 |
0.939000 |
Biological oxidations |
122 |
8.70e-02 |
2.69e-01 |
0.11700 |
0.101000 |
0.058800 |
5.46e-02 |
0.263000 |
Activation of BAD and translocation to mitochondria |
13 |
7.70e-01 |
8.65e-01 |
0.11700 |
0.102000 |
0.056100 |
5.23e-01 |
0.726000 |
Reduction of cytosolic Ca++ levels |
10 |
8.18e-01 |
8.95e-01 |
0.11600 |
-0.019300 |
0.114000 |
9.16e-01 |
0.532000 |
Glucagon-like Peptide-1 (GLP1) regulates insulin secretion |
26 |
5.92e-01 |
7.50e-01 |
0.11500 |
-0.043200 |
0.107000 |
7.03e-01 |
0.345000 |
Signaling by WNT |
188 |
2.41e-02 |
1.26e-01 |
0.11500 |
-0.074000 |
0.088200 |
8.17e-02 |
0.038000 |
Muscle contraction |
133 |
7.14e-02 |
2.37e-01 |
0.11500 |
-0.093900 |
0.066200 |
6.22e-02 |
0.189000 |
MET activates PTK2 signaling |
16 |
7.27e-01 |
8.44e-01 |
0.11500 |
-0.106000 |
0.043500 |
4.62e-01 |
0.763000 |
SUMOylation of DNA methylation proteins |
15 |
7.43e-01 |
8.48e-01 |
0.11400 |
-0.043400 |
0.106000 |
7.71e-01 |
0.478000 |
Immune System |
1332 |
9.66e-11 |
2.69e-08 |
0.11400 |
0.111000 |
-0.027300 |
5.00e-11 |
0.107000 |
Antigen activates B Cell Receptor (BCR) leading to generation of second messengers |
25 |
6.17e-01 |
7.66e-01 |
0.11400 |
-0.110000 |
-0.030100 |
3.41e-01 |
0.794000 |
Platelet homeostasis |
63 |
2.90e-01 |
4.98e-01 |
0.11400 |
0.089400 |
-0.070500 |
2.20e-01 |
0.334000 |
Signaling by NOTCH |
133 |
8.01e-02 |
2.56e-01 |
0.11300 |
-0.022200 |
-0.111000 |
6.60e-01 |
0.027100 |
Nucleotide salvage |
16 |
7.36e-01 |
8.46e-01 |
0.11300 |
-0.018800 |
-0.112000 |
8.96e-01 |
0.439000 |
Nuclear Events (kinase and transcription factor activation) |
49 |
3.87e-01 |
5.87e-01 |
0.11300 |
-0.106000 |
0.039200 |
1.99e-01 |
0.635000 |
TBC/RABGAPs |
33 |
5.36e-01 |
7.08e-01 |
0.11300 |
-0.089500 |
-0.069400 |
3.74e-01 |
0.491000 |
Insertion of tail-anchored proteins into the endoplasmic reticulum membrane |
12 |
7.94e-01 |
8.84e-01 |
0.11300 |
-0.010000 |
0.113000 |
9.52e-01 |
0.499000 |
mRNA decay by 3' to 5' exoribonuclease |
10 |
8.25e-01 |
8.95e-01 |
0.11300 |
0.109000 |
-0.028500 |
5.50e-01 |
0.876000 |
Signaling by Interleukins |
298 |
4.39e-03 |
4.02e-02 |
0.11200 |
0.098100 |
0.055000 |
3.82e-03 |
0.105000 |
Macroautophagy |
80 |
2.28e-01 |
4.42e-01 |
0.11200 |
-0.047000 |
-0.102000 |
4.68e-01 |
0.116000 |
Signaling by the B Cell Receptor (BCR) |
78 |
2.41e-01 |
4.55e-01 |
0.11100 |
-0.054600 |
-0.097100 |
4.06e-01 |
0.139000 |
SHC-mediated cascade:FGFR2 |
11 |
8.18e-01 |
8.95e-01 |
0.11100 |
-0.065000 |
-0.090300 |
7.09e-01 |
0.604000 |
Metabolism of nucleotides |
70 |
2.72e-01 |
4.83e-01 |
0.11100 |
0.096900 |
-0.054100 |
1.62e-01 |
0.434000 |
Cell surface interactions at the vascular wall |
93 |
1.81e-01 |
3.93e-01 |
0.11100 |
0.097100 |
-0.052800 |
1.06e-01 |
0.380000 |
Voltage gated Potassium channels |
21 |
6.86e-01 |
8.20e-01 |
0.11000 |
-0.102000 |
-0.041200 |
4.19e-01 |
0.744000 |
Activation of NMDA receptors and postsynaptic events |
54 |
3.80e-01 |
5.79e-01 |
0.10900 |
-0.109000 |
0.010400 |
1.67e-01 |
0.895000 |
rRNA modification in the nucleus and cytosol |
42 |
4.73e-01 |
6.58e-01 |
0.10900 |
-0.108000 |
-0.016200 |
2.25e-01 |
0.856000 |
Defective B4GALT7 causes EDS, progeroid type |
14 |
7.81e-01 |
8.72e-01 |
0.10900 |
-0.070700 |
-0.083500 |
6.47e-01 |
0.589000 |
Chaperonin-mediated protein folding |
62 |
3.38e-01 |
5.49e-01 |
0.10900 |
0.060100 |
0.091100 |
4.14e-01 |
0.216000 |
Interleukin receptor SHC signaling |
18 |
7.24e-01 |
8.42e-01 |
0.10900 |
-0.038600 |
0.102000 |
7.77e-01 |
0.454000 |
MyD88-independent TLR4 cascade |
76 |
2.58e-01 |
4.69e-01 |
0.10900 |
-0.104000 |
0.031800 |
1.17e-01 |
0.632000 |
TRIF(TICAM1)-mediated TLR4 signaling |
76 |
2.58e-01 |
4.69e-01 |
0.10900 |
-0.104000 |
0.031800 |
1.17e-01 |
0.632000 |
rRNA processing |
103 |
1.66e-01 |
3.74e-01 |
0.10900 |
0.043300 |
0.099900 |
4.49e-01 |
0.080400 |
Signaling by BMP |
21 |
6.88e-01 |
8.21e-01 |
0.10900 |
0.021400 |
-0.107000 |
8.65e-01 |
0.398000 |
Blood group systems biosynthesis |
12 |
8.10e-01 |
8.95e-01 |
0.10900 |
0.102000 |
0.036900 |
5.40e-01 |
0.825000 |
Transmission across Chemical Synapses |
152 |
6.90e-02 |
2.31e-01 |
0.10900 |
-0.104000 |
0.030200 |
2.69e-02 |
0.522000 |
Spry regulation of FGF signaling |
10 |
8.37e-01 |
8.98e-01 |
0.10900 |
0.020000 |
-0.107000 |
9.13e-01 |
0.559000 |
Influenza Infection |
67 |
3.17e-01 |
5.24e-01 |
0.10800 |
-0.064900 |
-0.086400 |
3.59e-01 |
0.222000 |
Interleukin-2 family signaling |
29 |
5.99e-01 |
7.55e-01 |
0.10800 |
-0.083000 |
0.069100 |
4.40e-01 |
0.520000 |
Regulation of APC/C activators between G1/S and early anaphase |
56 |
3.73e-01 |
5.74e-01 |
0.10800 |
0.057100 |
-0.091600 |
4.61e-01 |
0.236000 |
Golgi Associated Vesicle Biogenesis |
37 |
5.27e-01 |
6.98e-01 |
0.10700 |
0.024500 |
-0.104000 |
7.97e-01 |
0.272000 |
RHO GTPases Activate WASPs and WAVEs |
30 |
5.92e-01 |
7.50e-01 |
0.10700 |
0.087800 |
-0.061600 |
4.05e-01 |
0.560000 |
ERKs are inactivated |
12 |
8.16e-01 |
8.95e-01 |
0.10700 |
0.043800 |
0.097700 |
7.93e-01 |
0.558000 |
Reproduction |
50 |
4.39e-01 |
6.28e-01 |
0.10600 |
-0.065100 |
-0.083400 |
4.26e-01 |
0.308000 |
AKT phosphorylates targets in the cytosol |
12 |
8.17e-01 |
8.95e-01 |
0.10600 |
-0.103000 |
0.024500 |
5.38e-01 |
0.883000 |
Sema3A PAK dependent Axon repulsion |
12 |
8.22e-01 |
8.95e-01 |
0.10500 |
0.078400 |
0.070200 |
6.38e-01 |
0.674000 |
Anti-inflammatory response favouring Leishmania parasite infection |
94 |
2.12e-01 |
4.25e-01 |
0.10500 |
0.105000 |
-0.007080 |
7.92e-02 |
0.906000 |
Leishmania parasite growth and survival |
94 |
2.12e-01 |
4.25e-01 |
0.10500 |
0.105000 |
-0.007080 |
7.92e-02 |
0.906000 |
Oncogenic MAPK signaling |
55 |
4.05e-01 |
6.04e-01 |
0.10500 |
-0.024200 |
-0.102000 |
7.57e-01 |
0.189000 |
Signaling by high-kinase activity BRAF mutants |
22 |
6.91e-01 |
8.22e-01 |
0.10500 |
0.085100 |
-0.061900 |
4.90e-01 |
0.616000 |
Adenylate cyclase inhibitory pathway |
12 |
8.22e-01 |
8.95e-01 |
0.10500 |
0.035300 |
0.098900 |
8.33e-01 |
0.553000 |
Organelle biogenesis and maintenance |
199 |
4.15e-02 |
1.73e-01 |
0.10500 |
-0.089200 |
-0.055200 |
3.08e-02 |
0.182000 |
Diseases of metabolism |
162 |
7.27e-02 |
2.40e-01 |
0.10500 |
0.105000 |
0.002540 |
2.21e-02 |
0.956000 |
Cyclin D associated events in G1 |
31 |
6.07e-01 |
7.61e-01 |
0.10500 |
-0.084700 |
-0.061200 |
4.15e-01 |
0.556000 |
G1 Phase |
31 |
6.07e-01 |
7.61e-01 |
0.10500 |
-0.084700 |
-0.061200 |
4.15e-01 |
0.556000 |
Platelet Aggregation (Plug Formation) |
28 |
6.40e-01 |
7.81e-01 |
0.10400 |
0.049800 |
0.091200 |
6.49e-01 |
0.404000 |
Signaling by Activin |
10 |
8.50e-01 |
9.03e-01 |
0.10400 |
-0.057600 |
0.086100 |
7.53e-01 |
0.637000 |
Signaling by PDGFR in disease |
17 |
7.58e-01 |
8.58e-01 |
0.10400 |
-0.067000 |
0.079000 |
6.33e-01 |
0.573000 |
APC/C-mediated degradation of cell cycle proteins |
63 |
3.65e-01 |
5.72e-01 |
0.10300 |
0.008480 |
-0.103000 |
9.07e-01 |
0.158000 |
Regulation of mitotic cell cycle |
63 |
3.65e-01 |
5.72e-01 |
0.10300 |
0.008480 |
-0.103000 |
9.07e-01 |
0.158000 |
SLC-mediated transmembrane transport |
156 |
8.31e-02 |
2.61e-01 |
0.10300 |
-0.073600 |
0.072200 |
1.14e-01 |
0.121000 |
HCMV Infection |
58 |
4.05e-01 |
6.04e-01 |
0.10300 |
-0.080800 |
-0.063800 |
2.88e-01 |
0.402000 |
HCMV Late Events |
36 |
5.68e-01 |
7.33e-01 |
0.10300 |
-0.099700 |
-0.025400 |
3.01e-01 |
0.792000 |
Cell-Cell communication |
76 |
3.02e-01 |
5.09e-01 |
0.10300 |
0.002160 |
-0.103000 |
9.74e-01 |
0.122000 |
Signaling by VEGF |
88 |
2.56e-01 |
4.69e-01 |
0.10300 |
-0.070400 |
-0.074800 |
2.55e-01 |
0.226000 |
Sialic acid metabolism |
23 |
7.00e-01 |
8.29e-01 |
0.10200 |
0.044000 |
0.092500 |
7.15e-01 |
0.443000 |
Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding |
23 |
6.97e-01 |
8.28e-01 |
0.10200 |
0.097400 |
-0.030300 |
4.19e-01 |
0.801000 |
Potential therapeutics for SARS |
26 |
6.70e-01 |
8.09e-01 |
0.10200 |
-0.023500 |
-0.099000 |
8.36e-01 |
0.382000 |
STING mediated induction of host immune responses |
10 |
8.59e-01 |
9.07e-01 |
0.10100 |
0.094700 |
0.035800 |
6.04e-01 |
0.845000 |
Defects in vitamin and cofactor metabolism |
14 |
8.08e-01 |
8.93e-01 |
0.10100 |
-0.025400 |
-0.098000 |
8.69e-01 |
0.526000 |
Diseases of glycosylation |
103 |
2.08e-01 |
4.25e-01 |
0.10100 |
0.101000 |
-0.010500 |
7.85e-02 |
0.855000 |
The NLRP3 inflammasome |
11 |
8.44e-01 |
9.01e-01 |
0.10100 |
0.054200 |
-0.085100 |
7.56e-01 |
0.625000 |
Peroxisomal lipid metabolism |
22 |
7.13e-01 |
8.38e-01 |
0.10100 |
0.033500 |
-0.095100 |
7.86e-01 |
0.440000 |
Signaling by PDGFRA extracellular domain mutants |
10 |
8.59e-01 |
9.07e-01 |
0.10100 |
-0.101000 |
0.005260 |
5.82e-01 |
0.977000 |
Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants |
10 |
8.59e-01 |
9.07e-01 |
0.10100 |
-0.101000 |
0.005260 |
5.82e-01 |
0.977000 |
Complex I biogenesis |
35 |
5.92e-01 |
7.50e-01 |
0.10000 |
0.099600 |
0.011100 |
3.08e-01 |
0.909000 |
TCR signaling |
79 |
3.13e-01 |
5.19e-01 |
0.10000 |
-0.050500 |
-0.086400 |
4.39e-01 |
0.185000 |
RNA Polymerase III Transcription Initiation From Type 1 Promoter |
17 |
7.73e-01 |
8.66e-01 |
0.09980 |
0.068700 |
-0.072400 |
6.24e-01 |
0.606000 |
Metabolism of porphyrins |
20 |
7.47e-01 |
8.49e-01 |
0.09940 |
0.066300 |
0.074000 |
6.08e-01 |
0.567000 |
Autophagy |
90 |
2.69e-01 |
4.82e-01 |
0.09930 |
-0.025800 |
-0.095900 |
6.72e-01 |
0.117000 |
Intracellular signaling by second messengers |
224 |
3.90e-02 |
1.67e-01 |
0.09910 |
-0.098700 |
0.009310 |
1.13e-02 |
0.811000 |
Signaling by TGFB family members |
68 |
3.75e-01 |
5.74e-01 |
0.09900 |
-0.090000 |
-0.041300 |
2.00e-01 |
0.557000 |
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding |
20 |
7.47e-01 |
8.49e-01 |
0.09880 |
-0.098300 |
-0.010800 |
4.47e-01 |
0.934000 |
Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways |
41 |
5.47e-01 |
7.16e-01 |
0.09860 |
-0.073600 |
0.065500 |
4.15e-01 |
0.468000 |
Netrin-1 signaling |
40 |
5.58e-01 |
7.28e-01 |
0.09820 |
-0.083700 |
0.051300 |
3.60e-01 |
0.575000 |
VEGFA-VEGFR2 Pathway |
83 |
3.10e-01 |
5.17e-01 |
0.09810 |
-0.079100 |
-0.058000 |
2.14e-01 |
0.362000 |
HS-GAG biosynthesis |
18 |
7.72e-01 |
8.66e-01 |
0.09760 |
0.031600 |
-0.092300 |
8.17e-01 |
0.498000 |
Acyl chain remodelling of PG |
13 |
8.34e-01 |
8.98e-01 |
0.09730 |
0.055200 |
0.080100 |
7.30e-01 |
0.617000 |
RA biosynthesis pathway |
12 |
8.45e-01 |
9.01e-01 |
0.09720 |
0.021600 |
0.094700 |
8.97e-01 |
0.570000 |
E3 ubiquitin ligases ubiquitinate target proteins |
22 |
7.30e-01 |
8.45e-01 |
0.09710 |
-0.083900 |
0.048800 |
4.96e-01 |
0.692000 |
G alpha (12/13) signalling events |
61 |
4.27e-01 |
6.21e-01 |
0.09700 |
0.094500 |
0.021700 |
2.02e-01 |
0.769000 |
Post-translational modification: synthesis of GPI-anchored proteins |
50 |
5.03e-01 |
6.83e-01 |
0.09660 |
0.047200 |
0.084300 |
5.64e-01 |
0.303000 |
Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon |
12 |
8.44e-01 |
9.01e-01 |
0.09640 |
-0.048400 |
0.083300 |
7.71e-01 |
0.617000 |
G alpha (s) signalling events |
78 |
3.46e-01 |
5.55e-01 |
0.09620 |
0.054900 |
0.079000 |
4.03e-01 |
0.228000 |
Signaling by Hedgehog |
91 |
2.89e-01 |
4.97e-01 |
0.09620 |
0.091800 |
0.028600 |
1.31e-01 |
0.638000 |
Amino acids regulate mTORC1 |
33 |
6.35e-01 |
7.78e-01 |
0.09560 |
0.026400 |
-0.091900 |
7.93e-01 |
0.361000 |
TAK1 activates NFkB by phosphorylation and activation of IKKs complex |
20 |
7.63e-01 |
8.61e-01 |
0.09550 |
-0.091100 |
-0.028800 |
4.81e-01 |
0.824000 |
Downstream TCR signaling |
62 |
4.36e-01 |
6.27e-01 |
0.09540 |
-0.057200 |
-0.076400 |
4.37e-01 |
0.299000 |
Defective B3GAT3 causes JDSSDHD |
14 |
8.29e-01 |
8.96e-01 |
0.09480 |
-0.093600 |
-0.014900 |
5.44e-01 |
0.923000 |
Intrinsic Pathway for Apoptosis |
41 |
5.73e-01 |
7.38e-01 |
0.09470 |
0.067500 |
-0.066300 |
4.55e-01 |
0.463000 |
Opioid Signalling |
67 |
4.09e-01 |
6.05e-01 |
0.09450 |
-0.006350 |
0.094300 |
9.29e-01 |
0.183000 |
Transport of bile salts and organic acids, metal ions and amine compounds |
52 |
4.97e-01 |
6.79e-01 |
0.09430 |
-0.049600 |
0.080200 |
5.37e-01 |
0.318000 |
Uptake and function of anthrax toxins |
11 |
8.65e-01 |
9.12e-01 |
0.09420 |
-0.012500 |
-0.093300 |
9.43e-01 |
0.592000 |
Defective B3GALT6 causes EDSP2 and SEMDJL1 |
13 |
8.42e-01 |
9.01e-01 |
0.09410 |
-0.092500 |
-0.017200 |
5.64e-01 |
0.915000 |
O-glycosylation of TSR domain-containing proteins |
30 |
6.77e-01 |
8.14e-01 |
0.09400 |
0.073200 |
0.058900 |
4.88e-01 |
0.577000 |
Frs2-mediated activation |
10 |
8.74e-01 |
9.16e-01 |
0.09390 |
-0.059900 |
0.072400 |
7.43e-01 |
0.692000 |
RNA Polymerase I Promoter Escape |
16 |
8.12e-01 |
8.95e-01 |
0.09380 |
-0.047200 |
-0.081000 |
7.44e-01 |
0.575000 |
Signaling by SCF-KIT |
34 |
6.41e-01 |
7.81e-01 |
0.09350 |
-0.006350 |
0.093300 |
9.49e-01 |
0.347000 |
RHO GTPases activate PKNs |
27 |
7.04e-01 |
8.30e-01 |
0.09320 |
-0.093100 |
0.004130 |
4.03e-01 |
0.970000 |
MET promotes cell motility |
26 |
7.18e-01 |
8.39e-01 |
0.09300 |
0.055200 |
0.074900 |
6.26e-01 |
0.509000 |
MAP2K and MAPK activation |
24 |
7.30e-01 |
8.45e-01 |
0.09300 |
0.077000 |
-0.052200 |
5.14e-01 |
0.658000 |
Rab regulation of trafficking |
90 |
3.18e-01 |
5.25e-01 |
0.09300 |
-0.086000 |
-0.035300 |
1.59e-01 |
0.564000 |
Defective B3GALTL causes Peters-plus syndrome (PpS) |
29 |
6.92e-01 |
8.22e-01 |
0.09290 |
0.069000 |
0.062200 |
5.21e-01 |
0.562000 |
Apoptosis |
126 |
2.00e-01 |
4.17e-01 |
0.09280 |
0.001310 |
-0.092800 |
9.80e-01 |
0.073000 |
Interleukin-37 signaling |
15 |
8.26e-01 |
8.95e-01 |
0.09180 |
-0.042900 |
0.081100 |
7.74e-01 |
0.587000 |
Signaling by BRAF and RAF fusions |
43 |
5.81e-01 |
7.47e-01 |
0.09130 |
0.056500 |
-0.071700 |
5.22e-01 |
0.416000 |
Neurexins and neuroligins |
37 |
6.30e-01 |
7.76e-01 |
0.09100 |
-0.036000 |
0.083500 |
7.05e-01 |
0.380000 |
Negative regulation of FGFR1 signaling |
16 |
8.23e-01 |
8.95e-01 |
0.09090 |
-0.075300 |
-0.050900 |
6.02e-01 |
0.725000 |
IKK complex recruitment mediated by RIP1 |
15 |
8.32e-01 |
8.97e-01 |
0.09000 |
-0.077900 |
0.045100 |
6.01e-01 |
0.763000 |
NCAM signaling for neurite out-growth |
44 |
5.84e-01 |
7.48e-01 |
0.08990 |
-0.039700 |
0.080700 |
6.49e-01 |
0.355000 |
PI Metabolism |
68 |
4.38e-01 |
6.28e-01 |
0.08980 |
-0.083700 |
0.032600 |
2.34e-01 |
0.643000 |
Negative regulation of FGFR3 signaling |
16 |
8.28e-01 |
8.96e-01 |
0.08930 |
-0.042700 |
-0.078500 |
7.68e-01 |
0.587000 |
MyD88:MAL(TIRAP) cascade initiated on plasma membrane |
71 |
4.30e-01 |
6.21e-01 |
0.08870 |
-0.071200 |
0.052800 |
3.00e-01 |
0.442000 |
Toll Like Receptor 2 (TLR2) Cascade |
71 |
4.30e-01 |
6.21e-01 |
0.08870 |
-0.071200 |
0.052800 |
3.00e-01 |
0.442000 |
Toll Like Receptor TLR1:TLR2 Cascade |
71 |
4.30e-01 |
6.21e-01 |
0.08870 |
-0.071200 |
0.052800 |
3.00e-01 |
0.442000 |
Toll Like Receptor TLR6:TLR2 Cascade |
71 |
4.30e-01 |
6.21e-01 |
0.08870 |
-0.071200 |
0.052800 |
3.00e-01 |
0.442000 |
Prefoldin mediated transfer of substrate to CCT/TriC |
19 |
8.02e-01 |
8.90e-01 |
0.08840 |
-0.082200 |
-0.032500 |
5.35e-01 |
0.806000 |
Metabolism of amino acids and derivatives |
196 |
1.03e-01 |
2.93e-01 |
0.08840 |
0.086200 |
-0.019800 |
3.84e-02 |
0.634000 |
Assembly and cell surface presentation of NMDA receptors |
17 |
8.18e-01 |
8.95e-01 |
0.08830 |
0.056200 |
-0.068100 |
6.88e-01 |
0.627000 |
Stimuli-sensing channels |
55 |
5.25e-01 |
6.97e-01 |
0.08820 |
0.030300 |
-0.082900 |
6.98e-01 |
0.288000 |
Phospholipid metabolism |
151 |
1.74e-01 |
3.85e-01 |
0.08810 |
-0.086300 |
0.018000 |
6.82e-02 |
0.704000 |
Potassium Channels |
50 |
5.60e-01 |
7.29e-01 |
0.08800 |
0.087000 |
-0.013100 |
2.88e-01 |
0.873000 |
Glycerophospholipid biosynthesis |
83 |
3.87e-01 |
5.87e-01 |
0.08760 |
-0.087400 |
0.005740 |
1.70e-01 |
0.928000 |
PIP3 activates AKT signaling |
191 |
1.19e-01 |
3.14e-01 |
0.08740 |
-0.083400 |
-0.026300 |
4.79e-02 |
0.532000 |
ERK/MAPK targets |
20 |
7.95e-01 |
8.84e-01 |
0.08740 |
-0.085700 |
0.017200 |
5.07e-01 |
0.894000 |
Metalloprotease DUBs |
15 |
8.42e-01 |
9.01e-01 |
0.08710 |
0.080700 |
-0.032700 |
5.89e-01 |
0.826000 |
Keratinization |
26 |
7.47e-01 |
8.49e-01 |
0.08710 |
-0.038300 |
-0.078200 |
7.35e-01 |
0.491000 |
Cargo recognition for clathrin-mediated endocytosis |
64 |
4.91e-01 |
6.76e-01 |
0.08670 |
-0.023800 |
-0.083400 |
7.43e-01 |
0.250000 |
Interleukin-1 family signaling |
94 |
3.48e-01 |
5.57e-01 |
0.08660 |
0.083400 |
-0.023000 |
1.63e-01 |
0.700000 |
ADORA2B mediated anti-inflammatory cytokines production |
63 |
5.01e-01 |
6.83e-01 |
0.08640 |
0.071300 |
0.048700 |
3.28e-01 |
0.504000 |
SARS-CoV-1 Infection |
29 |
7.30e-01 |
8.45e-01 |
0.08560 |
0.082300 |
0.023400 |
4.43e-01 |
0.827000 |
Signaling by NODAL |
15 |
8.48e-01 |
9.02e-01 |
0.08550 |
-0.021200 |
0.082800 |
8.87e-01 |
0.579000 |
Cell-cell junction organization |
27 |
7.42e-01 |
8.47e-01 |
0.08550 |
0.046500 |
-0.071700 |
6.76e-01 |
0.519000 |
Vitamin B5 (pantothenate) metabolism |
12 |
8.79e-01 |
9.19e-01 |
0.08540 |
-0.073400 |
-0.043700 |
6.60e-01 |
0.793000 |
RAB GEFs exchange GTP for GDP on RABs |
63 |
5.14e-01 |
6.90e-01 |
0.08430 |
-0.083700 |
-0.009620 |
2.51e-01 |
0.895000 |
Cytokine Signaling in Immune system |
554 |
3.94e-03 |
3.82e-02 |
0.08390 |
0.083200 |
0.010800 |
9.46e-04 |
0.669000 |
Signaling by RAF1 mutants |
26 |
7.62e-01 |
8.61e-01 |
0.08330 |
0.081800 |
-0.016000 |
4.71e-01 |
0.888000 |
PTEN Regulation |
99 |
3.66e-01 |
5.72e-01 |
0.08330 |
-0.058500 |
-0.059300 |
3.16e-01 |
0.309000 |
NR1H2 and NR1H3-mediated signaling |
35 |
6.99e-01 |
8.29e-01 |
0.08330 |
0.072000 |
0.041800 |
4.61e-01 |
0.669000 |
Dectin-2 family |
10 |
9.00e-01 |
9.35e-01 |
0.08320 |
0.071200 |
-0.043000 |
6.97e-01 |
0.814000 |
Tight junction interactions |
12 |
8.85e-01 |
9.23e-01 |
0.08270 |
0.076600 |
0.031300 |
6.46e-01 |
0.851000 |
Defective EXT1 causes exostoses 1, TRPS2 and CHDS |
10 |
9.03e-01 |
9.35e-01 |
0.08250 |
-0.082400 |
0.000625 |
6.52e-01 |
0.997000 |
Defective EXT2 causes exostoses 2 |
10 |
9.03e-01 |
9.35e-01 |
0.08250 |
-0.082400 |
0.000625 |
6.52e-01 |
0.997000 |
Free fatty acids regulate insulin secretion |
11 |
8.96e-01 |
9.32e-01 |
0.08210 |
-0.068800 |
-0.044700 |
6.93e-01 |
0.797000 |
Programmed Cell Death |
129 |
2.77e-01 |
4.89e-01 |
0.08180 |
0.011500 |
-0.081000 |
8.23e-01 |
0.113000 |
Infection with Mycobacterium tuberculosis |
20 |
8.17e-01 |
8.95e-01 |
0.08150 |
-0.068900 |
0.043700 |
5.94e-01 |
0.735000 |
Signaling by Rho GTPases |
288 |
6.25e-02 |
2.21e-01 |
0.08150 |
-0.077800 |
-0.024300 |
2.40e-02 |
0.481000 |
Ephrin signaling |
17 |
8.45e-01 |
9.01e-01 |
0.08100 |
-0.021700 |
0.078100 |
8.77e-01 |
0.578000 |
Metabolism of steroids |
97 |
3.94e-01 |
5.96e-01 |
0.08060 |
-0.079400 |
-0.013600 |
1.78e-01 |
0.817000 |
TP53 Regulates Metabolic Genes |
58 |
5.68e-01 |
7.33e-01 |
0.08050 |
-0.077500 |
0.021900 |
3.08e-01 |
0.774000 |
C-type lectin receptors (CLRs) |
89 |
4.29e-01 |
6.21e-01 |
0.08040 |
-0.036900 |
-0.071400 |
5.48e-01 |
0.245000 |
Adrenaline,noradrenaline inhibits insulin secretion |
19 |
8.35e-01 |
8.98e-01 |
0.08010 |
0.047400 |
0.064500 |
7.21e-01 |
0.626000 |
Signaling by NTRK1 (TRKA) |
94 |
4.06e-01 |
6.04e-01 |
0.07990 |
-0.076200 |
0.024200 |
2.03e-01 |
0.686000 |
Resolution of Abasic Sites (AP sites) |
29 |
7.57e-01 |
8.58e-01 |
0.07970 |
-0.074900 |
0.027100 |
4.85e-01 |
0.801000 |
Formation of TC-NER Pre-Incision Complex |
31 |
7.56e-01 |
8.57e-01 |
0.07810 |
-0.027300 |
-0.073200 |
7.93e-01 |
0.481000 |
DAP12 signaling |
20 |
8.32e-01 |
8.97e-01 |
0.07800 |
0.025800 |
-0.073600 |
8.42e-01 |
0.569000 |
Regulation of KIT signaling |
10 |
9.14e-01 |
9.39e-01 |
0.07790 |
0.050800 |
0.059100 |
7.81e-01 |
0.746000 |
Interleukin-1 signaling |
70 |
5.33e-01 |
7.06e-01 |
0.07720 |
0.070300 |
-0.031800 |
3.10e-01 |
0.646000 |
Cellular responses to external stimuli |
318 |
6.65e-02 |
2.27e-01 |
0.07700 |
-0.067200 |
-0.037500 |
4.08e-02 |
0.253000 |
Keratan sulfate/keratin metabolism |
21 |
8.34e-01 |
8.98e-01 |
0.07640 |
0.041100 |
0.064400 |
7.44e-01 |
0.610000 |
Interleukin-15 signaling |
11 |
9.08e-01 |
9.35e-01 |
0.07590 |
-0.035900 |
0.066900 |
8.37e-01 |
0.701000 |
Metabolism of RNA |
424 |
3.08e-02 |
1.43e-01 |
0.07580 |
-0.070300 |
-0.028500 |
1.40e-02 |
0.320000 |
Post-chaperonin tubulin folding pathway |
16 |
8.72e-01 |
9.16e-01 |
0.07520 |
0.073300 |
-0.016900 |
6.12e-01 |
0.907000 |
NCAM1 interactions |
27 |
7.95e-01 |
8.84e-01 |
0.07510 |
-0.015400 |
0.073500 |
8.90e-01 |
0.509000 |
Sphingolipid de novo biosynthesis |
27 |
8.00e-01 |
8.88e-01 |
0.07400 |
0.069300 |
-0.025900 |
5.33e-01 |
0.816000 |
Non-integrin membrane-ECM interactions |
35 |
7.49e-01 |
8.51e-01 |
0.07370 |
-0.050600 |
0.053600 |
6.05e-01 |
0.583000 |
Elastic fibre formation |
31 |
7.83e-01 |
8.73e-01 |
0.07320 |
0.043100 |
0.059200 |
6.78e-01 |
0.569000 |
UCH proteinases |
59 |
6.20e-01 |
7.68e-01 |
0.07310 |
-0.052800 |
0.050600 |
4.83e-01 |
0.502000 |
PI3K/AKT Signaling in Cancer |
74 |
5.55e-01 |
7.26e-01 |
0.07310 |
-0.072900 |
-0.005490 |
2.79e-01 |
0.935000 |
Cyclin A:Cdk2-associated events at S phase entry |
56 |
6.41e-01 |
7.81e-01 |
0.07300 |
0.001480 |
-0.073000 |
9.85e-01 |
0.346000 |
Transcriptional Regulation by VENTX |
32 |
7.78e-01 |
8.70e-01 |
0.07290 |
-0.062600 |
-0.037300 |
5.40e-01 |
0.715000 |
Long-term potentiation |
17 |
8.73e-01 |
9.16e-01 |
0.07280 |
0.021500 |
-0.069500 |
8.78e-01 |
0.620000 |
Amyloid fiber formation |
29 |
8.06e-01 |
8.93e-01 |
0.07090 |
0.053800 |
0.046300 |
6.17e-01 |
0.666000 |
Regulation of RUNX1 Expression and Activity |
14 |
9.01e-01 |
9.35e-01 |
0.07000 |
-0.057900 |
0.039200 |
7.07e-01 |
0.800000 |
Hemostasis |
396 |
6.06e-02 |
2.17e-01 |
0.06960 |
0.064200 |
-0.027000 |
2.99e-02 |
0.361000 |
Sealing of the nuclear envelope (NE) by ESCRT-III |
19 |
8.70e-01 |
9.16e-01 |
0.06950 |
0.038700 |
-0.057700 |
7.71e-01 |
0.663000 |
RNA Polymerase III Transcription Initiation From Type 2 Promoter |
16 |
8.89e-01 |
9.25e-01 |
0.06940 |
0.038500 |
-0.057800 |
7.90e-01 |
0.689000 |
Activation of BH3-only proteins |
26 |
8.30e-01 |
8.96e-01 |
0.06920 |
-0.001460 |
-0.069200 |
9.90e-01 |
0.542000 |
Cellular responses to stress |
314 |
1.20e-01 |
3.16e-01 |
0.06840 |
-0.062900 |
-0.026900 |
5.70e-02 |
0.416000 |
HDACs deacetylate histones |
22 |
8.59e-01 |
9.07e-01 |
0.06770 |
-0.064900 |
0.019100 |
5.98e-01 |
0.877000 |
Adaptive Immune System |
499 |
3.95e-02 |
1.69e-01 |
0.06680 |
0.029600 |
-0.059900 |
2.63e-01 |
0.023500 |
tRNA processing |
75 |
6.12e-01 |
7.64e-01 |
0.06680 |
-0.051700 |
-0.042200 |
4.39e-01 |
0.528000 |
Paradoxical activation of RAF signaling by kinase inactive BRAF |
29 |
8.25e-01 |
8.95e-01 |
0.06620 |
0.029400 |
-0.059300 |
7.84e-01 |
0.580000 |
Signaling by RAS mutants |
29 |
8.25e-01 |
8.95e-01 |
0.06620 |
0.029400 |
-0.059300 |
7.84e-01 |
0.580000 |
Signaling by moderate kinase activity BRAF mutants |
29 |
8.25e-01 |
8.95e-01 |
0.06620 |
0.029400 |
-0.059300 |
7.84e-01 |
0.580000 |
Signaling downstream of RAS mutants |
29 |
8.25e-01 |
8.95e-01 |
0.06620 |
0.029400 |
-0.059300 |
7.84e-01 |
0.580000 |
Regulation of mRNA stability by proteins that bind AU-rich elements |
59 |
6.85e-01 |
8.19e-01 |
0.06610 |
-0.036100 |
-0.055300 |
6.32e-01 |
0.463000 |
Platelet sensitization by LDL |
14 |
9.13e-01 |
9.39e-01 |
0.06580 |
0.008320 |
-0.065300 |
9.57e-01 |
0.672000 |
Neuronal System |
225 |
2.38e-01 |
4.52e-01 |
0.06560 |
-0.061000 |
0.024200 |
1.17e-01 |
0.534000 |
NOTCH3 Intracellular Domain Regulates Transcription |
21 |
8.75e-01 |
9.16e-01 |
0.06480 |
0.037500 |
-0.052800 |
7.66e-01 |
0.675000 |
Antigen processing: Ubiquitination & Proteasome degradation |
212 |
2.75e-01 |
4.87e-01 |
0.06480 |
-0.052700 |
-0.037700 |
1.88e-01 |
0.346000 |
Diseases of signal transduction by growth factor receptors and second messengers |
269 |
2.00e-01 |
4.17e-01 |
0.06400 |
-0.063500 |
-0.008400 |
7.49e-02 |
0.814000 |
Clathrin-mediated endocytosis |
95 |
5.60e-01 |
7.29e-01 |
0.06380 |
0.015600 |
-0.061900 |
7.94e-01 |
0.298000 |
p75 NTR receptor-mediated signalling |
73 |
6.46e-01 |
7.86e-01 |
0.06380 |
0.058400 |
0.025700 |
3.89e-01 |
0.704000 |
tRNA modification in the nucleus and cytosol |
28 |
8.48e-01 |
9.02e-01 |
0.06290 |
0.062300 |
0.008470 |
5.68e-01 |
0.938000 |
Respiratory electron transport |
57 |
7.17e-01 |
8.39e-01 |
0.06260 |
0.062500 |
-0.001360 |
4.15e-01 |
0.986000 |
Cell death signalling via NRAGE, NRIF and NADE |
59 |
7.13e-01 |
8.38e-01 |
0.06240 |
0.028600 |
0.055500 |
7.05e-01 |
0.462000 |
Vesicle-mediated transport |
455 |
8.17e-02 |
2.59e-01 |
0.06190 |
-0.001800 |
-0.061900 |
9.48e-01 |
0.025200 |
Unblocking of NMDA receptors, glutamate binding and activation |
14 |
9.23e-01 |
9.44e-01 |
0.06170 |
0.016900 |
-0.059300 |
9.13e-01 |
0.701000 |
Cell junction organization |
49 |
7.63e-01 |
8.61e-01 |
0.06110 |
-0.021400 |
-0.057200 |
7.95e-01 |
0.489000 |
Cyclin E associated events during G1/S transition |
54 |
7.38e-01 |
8.46e-01 |
0.06100 |
0.030500 |
-0.052900 |
6.99e-01 |
0.502000 |
Membrane Trafficking |
429 |
1.02e-01 |
2.93e-01 |
0.06100 |
-0.016800 |
-0.058600 |
5.54e-01 |
0.039400 |
cGMP effects |
13 |
9.32e-01 |
9.50e-01 |
0.06080 |
0.038500 |
0.047000 |
8.10e-01 |
0.769000 |
Association of TriC/CCT with target proteins during biosynthesis |
29 |
8.53e-01 |
9.06e-01 |
0.06070 |
0.011700 |
0.059600 |
9.13e-01 |
0.579000 |
Nicotinate metabolism |
18 |
9.07e-01 |
9.35e-01 |
0.06060 |
-0.036900 |
-0.048000 |
7.86e-01 |
0.724000 |
Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. |
62 |
7.15e-01 |
8.38e-01 |
0.06050 |
0.057800 |
0.017800 |
4.32e-01 |
0.808000 |
Cilium Assembly |
139 |
4.75e-01 |
6.59e-01 |
0.06040 |
-0.015800 |
-0.058300 |
7.49e-01 |
0.237000 |
Fc epsilon receptor (FCERI) signaling |
95 |
5.96e-01 |
7.53e-01 |
0.06020 |
-0.055700 |
0.022800 |
3.49e-01 |
0.702000 |
Transport to the Golgi and subsequent modification |
120 |
5.43e-01 |
7.14e-01 |
0.05860 |
0.058500 |
0.003600 |
2.70e-01 |
0.946000 |
Integrin signaling |
20 |
9.05e-01 |
9.35e-01 |
0.05790 |
0.010700 |
0.056900 |
9.34e-01 |
0.660000 |
ER to Golgi Anterograde Transport |
100 |
6.06e-01 |
7.61e-01 |
0.05770 |
0.047400 |
-0.032900 |
4.14e-01 |
0.570000 |
Assembly of collagen fibrils and other multimeric structures |
36 |
8.36e-01 |
8.98e-01 |
0.05730 |
0.053100 |
-0.021800 |
5.82e-01 |
0.821000 |
Negative regulation of the PI3K/AKT network |
80 |
6.78e-01 |
8.14e-01 |
0.05730 |
-0.056400 |
-0.010300 |
3.84e-01 |
0.874000 |
Inflammasomes |
16 |
9.25e-01 |
9.44e-01 |
0.05730 |
0.003600 |
0.057200 |
9.80e-01 |
0.692000 |
Infectious disease |
451 |
1.17e-01 |
3.12e-01 |
0.05730 |
0.012500 |
-0.055900 |
6.54e-01 |
0.044100 |
Unfolded Protein Response (UPR) |
65 |
7.29e-01 |
8.45e-01 |
0.05710 |
0.000148 |
0.057100 |
9.98e-01 |
0.427000 |
Peroxisomal protein import |
45 |
8.03e-01 |
8.90e-01 |
0.05680 |
0.031500 |
-0.047300 |
7.15e-01 |
0.584000 |
Disorders of transmembrane transporters |
109 |
5.93e-01 |
7.50e-01 |
0.05680 |
-0.056700 |
0.002880 |
3.08e-01 |
0.959000 |
Peptide hormone metabolism |
46 |
8.08e-01 |
8.93e-01 |
0.05590 |
0.054900 |
0.010300 |
5.20e-01 |
0.904000 |
Insulin receptor recycling |
12 |
9.45e-01 |
9.59e-01 |
0.05580 |
0.050200 |
-0.024400 |
7.63e-01 |
0.884000 |
Signaling by Receptor Tyrosine Kinases |
356 |
2.19e-01 |
4.32e-01 |
0.05460 |
-0.025400 |
-0.048300 |
4.14e-01 |
0.120000 |
Neurotransmitter receptors and postsynaptic signal transmission |
114 |
6.14e-01 |
7.64e-01 |
0.05370 |
-0.053600 |
-0.004090 |
3.24e-01 |
0.940000 |
Transcriptional regulation of granulopoiesis |
29 |
8.84e-01 |
9.23e-01 |
0.05360 |
0.015900 |
0.051200 |
8.82e-01 |
0.634000 |
PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling |
76 |
7.23e-01 |
8.42e-01 |
0.05360 |
-0.053200 |
-0.006170 |
4.23e-01 |
0.926000 |
Ion channel transport |
97 |
6.59e-01 |
7.98e-01 |
0.05340 |
0.038600 |
-0.036800 |
5.12e-01 |
0.532000 |
COPII-mediated vesicle transport |
47 |
8.23e-01 |
8.95e-01 |
0.05310 |
0.044700 |
0.028600 |
5.96e-01 |
0.735000 |
NRAGE signals death through JNK |
51 |
8.10e-01 |
8.95e-01 |
0.05290 |
0.038100 |
0.036700 |
6.38e-01 |
0.650000 |
RAS processing |
11 |
9.56e-01 |
9.67e-01 |
0.05240 |
0.031400 |
0.042000 |
8.57e-01 |
0.810000 |
Platelet calcium homeostasis |
20 |
9.23e-01 |
9.44e-01 |
0.05190 |
-0.045500 |
-0.024900 |
7.25e-01 |
0.847000 |
Ion transport by P-type ATPases |
34 |
8.74e-01 |
9.16e-01 |
0.05170 |
0.041800 |
0.030400 |
6.73e-01 |
0.759000 |
COPI-mediated anterograde transport |
64 |
7.74e-01 |
8.66e-01 |
0.05150 |
0.046600 |
-0.022100 |
5.20e-01 |
0.761000 |
Diseases associated with O-glycosylation of proteins |
45 |
8.37e-01 |
8.98e-01 |
0.05110 |
0.040300 |
-0.031400 |
6.41e-01 |
0.716000 |
Interconversion of nucleotide di- and triphosphates |
22 |
9.19e-01 |
9.43e-01 |
0.05090 |
0.014500 |
0.048800 |
9.07e-01 |
0.692000 |
Metabolism of lipids |
484 |
1.73e-01 |
3.84e-01 |
0.05060 |
-0.043900 |
-0.025200 |
1.02e-01 |
0.349000 |
Mitochondrial Fatty Acid Beta-Oxidation |
25 |
9.08e-01 |
9.35e-01 |
0.05040 |
0.031300 |
-0.039500 |
7.87e-01 |
0.732000 |
Protein-protein interactions at synapses |
53 |
8.18e-01 |
8.95e-01 |
0.05020 |
0.049800 |
-0.006850 |
5.31e-01 |
0.931000 |
Signaling by NTRKs |
107 |
6.69e-01 |
8.09e-01 |
0.04990 |
-0.030500 |
0.039500 |
5.86e-01 |
0.482000 |
Signaling by GPCR |
420 |
2.34e-01 |
4.50e-01 |
0.04930 |
0.042400 |
0.025200 |
1.40e-01 |
0.381000 |
RNA Polymerase III Transcription Initiation |
23 |
9.20e-01 |
9.43e-01 |
0.04920 |
0.005370 |
-0.048900 |
9.64e-01 |
0.685000 |
Negative regulation of FGFR4 signaling |
16 |
9.45e-01 |
9.59e-01 |
0.04890 |
-0.036500 |
-0.032400 |
8.00e-01 |
0.822000 |
G alpha (i) signalling events |
199 |
5.05e-01 |
6.84e-01 |
0.04820 |
0.048000 |
-0.004230 |
2.45e-01 |
0.919000 |
Diseases associated with glycosaminoglycan metabolism |
30 |
9.05e-01 |
9.35e-01 |
0.04750 |
-0.025300 |
-0.040300 |
8.11e-01 |
0.703000 |
SARS-CoV Infections |
55 |
8.30e-01 |
8.96e-01 |
0.04740 |
0.032400 |
-0.034600 |
6.78e-01 |
0.658000 |
Class I MHC mediated antigen processing & presentation |
252 |
4.69e-01 |
6.56e-01 |
0.04510 |
0.009890 |
-0.044000 |
7.88e-01 |
0.232000 |
O-linked glycosylation of mucins |
34 |
9.02e-01 |
9.35e-01 |
0.04500 |
0.044500 |
0.007020 |
6.54e-01 |
0.944000 |
Axon guidance |
360 |
3.49e-01 |
5.57e-01 |
0.04500 |
0.044500 |
0.007150 |
1.51e-01 |
0.817000 |
Toll Like Receptor 4 (TLR4) Cascade |
97 |
7.46e-01 |
8.49e-01 |
0.04480 |
-0.025100 |
0.037100 |
6.71e-01 |
0.528000 |
O-linked glycosylation |
68 |
8.21e-01 |
8.95e-01 |
0.04440 |
0.041000 |
0.017200 |
5.60e-01 |
0.807000 |
GPVI-mediated activation cascade |
25 |
9.34e-01 |
9.50e-01 |
0.04230 |
0.028700 |
-0.031200 |
8.04e-01 |
0.787000 |
IRE1alpha activates chaperones |
39 |
9.08e-01 |
9.35e-01 |
0.04070 |
0.040700 |
0.000184 |
6.60e-01 |
0.998000 |
RNA Polymerase III Transcription Initiation From Type 3 Promoter |
19 |
9.55e-01 |
9.67e-01 |
0.04020 |
0.015400 |
0.037200 |
9.08e-01 |
0.779000 |
MECP2 regulates neuronal receptors and channels |
11 |
9.73e-01 |
9.84e-01 |
0.04020 |
-0.034500 |
0.020500 |
8.43e-01 |
0.906000 |
Death Receptor Signalling |
108 |
7.73e-01 |
8.66e-01 |
0.04010 |
-0.000654 |
-0.040100 |
9.91e-01 |
0.473000 |
MAPK family signaling cascades |
213 |
6.06e-01 |
7.61e-01 |
0.03980 |
-0.037500 |
0.013300 |
3.47e-01 |
0.740000 |
Visual phototransduction |
55 |
8.78e-01 |
9.19e-01 |
0.03950 |
-0.022100 |
0.032700 |
7.77e-01 |
0.675000 |
G alpha (q) signalling events |
119 |
7.61e-01 |
8.61e-01 |
0.03940 |
0.039000 |
0.005340 |
4.63e-01 |
0.920000 |
Transcriptional regulation by RUNX3 |
74 |
8.46e-01 |
9.01e-01 |
0.03930 |
-0.022900 |
-0.031900 |
7.33e-01 |
0.636000 |
Signal Transduction |
1520 |
6.21e-02 |
2.21e-01 |
0.03770 |
-0.037600 |
-0.001000 |
1.84e-02 |
0.950000 |
L1CAM interactions |
78 |
8.55e-01 |
9.07e-01 |
0.03690 |
0.014500 |
0.033900 |
8.25e-01 |
0.605000 |
ECM proteoglycans |
42 |
9.19e-01 |
9.43e-01 |
0.03650 |
0.022100 |
-0.029000 |
8.04e-01 |
0.745000 |
Beta-catenin independent WNT signaling |
104 |
8.19e-01 |
8.95e-01 |
0.03620 |
0.030600 |
0.019300 |
5.91e-01 |
0.734000 |
Metabolism of fat-soluble vitamins |
25 |
9.53e-01 |
9.66e-01 |
0.03610 |
0.021500 |
0.029000 |
8.53e-01 |
0.802000 |
Retinoid metabolism and transport |
24 |
9.55e-01 |
9.67e-01 |
0.03570 |
0.034900 |
-0.007610 |
7.68e-01 |
0.949000 |
XBP1(S) activates chaperone genes |
38 |
9.30e-01 |
9.50e-01 |
0.03550 |
0.035100 |
-0.005850 |
7.09e-01 |
0.950000 |
Rho GTPase cycle |
111 |
8.13e-01 |
8.95e-01 |
0.03550 |
0.005510 |
0.035100 |
9.20e-01 |
0.524000 |
FCERI mediated NF-kB activation |
53 |
9.05e-01 |
9.35e-01 |
0.03520 |
0.028500 |
-0.020600 |
7.20e-01 |
0.796000 |
Aggrephagy |
15 |
9.77e-01 |
9.86e-01 |
0.03230 |
0.015300 |
-0.028400 |
9.18e-01 |
0.849000 |
Toll-like Receptor Cascades |
108 |
8.54e-01 |
9.06e-01 |
0.03160 |
0.026700 |
0.016800 |
6.32e-01 |
0.764000 |
Transcriptional regulation by RUNX1 |
132 |
8.56e-01 |
9.07e-01 |
0.02840 |
-0.024300 |
-0.014700 |
6.31e-01 |
0.771000 |
Base-Excision Repair, AP Site Formation |
16 |
9.81e-01 |
9.88e-01 |
0.02840 |
0.026800 |
0.009370 |
8.53e-01 |
0.948000 |
Degradation of beta-catenin by the destruction complex |
59 |
9.33e-01 |
9.50e-01 |
0.02800 |
-0.006690 |
0.027200 |
9.29e-01 |
0.718000 |
Post-translational protein modification |
894 |
3.98e-01 |
6.00e-01 |
0.02750 |
-0.024900 |
-0.011700 |
2.17e-01 |
0.562000 |
Nervous system development |
380 |
6.77e-01 |
8.14e-01 |
0.02670 |
0.026200 |
0.005250 |
3.85e-01 |
0.862000 |
GPCR downstream signalling |
388 |
7.20e-01 |
8.40e-01 |
0.02430 |
0.024000 |
0.003530 |
4.21e-01 |
0.906000 |
Neddylation |
159 |
8.75e-01 |
9.16e-01 |
0.02400 |
-0.013400 |
-0.020000 |
7.72e-01 |
0.665000 |
Metabolism of water-soluble vitamins and cofactors |
83 |
9.33e-01 |
9.50e-01 |
0.02380 |
-0.023300 |
-0.004940 |
7.15e-01 |
0.938000 |
Transport of small molecules |
449 |
7.00e-01 |
8.29e-01 |
0.02350 |
0.023200 |
0.003760 |
4.04e-01 |
0.892000 |
Metabolism of proteins |
1221 |
4.47e-01 |
6.36e-01 |
0.02220 |
0.021600 |
-0.005150 |
2.19e-01 |
0.769000 |
FLT3 Signaling |
192 |
8.82e-01 |
9.21e-01 |
0.02120 |
-0.018800 |
-0.009900 |
6.55e-01 |
0.814000 |
RNA Polymerase III Abortive And Retractive Initiation |
27 |
9.82e-01 |
9.88e-01 |
0.02120 |
0.018500 |
-0.010400 |
8.68e-01 |
0.926000 |
RNA Polymerase III Transcription |
27 |
9.82e-01 |
9.88e-01 |
0.02120 |
0.018500 |
-0.010400 |
8.68e-01 |
0.926000 |
Metabolism of vitamins and cofactors |
124 |
9.23e-01 |
9.44e-01 |
0.02080 |
0.001320 |
-0.020800 |
9.80e-01 |
0.691000 |
Metabolism of carbohydrates |
196 |
8.86e-01 |
9.23e-01 |
0.02040 |
-0.005480 |
0.019600 |
8.95e-01 |
0.637000 |
Molecules associated with elastic fibres |
26 |
9.87e-01 |
9.91e-01 |
0.01860 |
0.018600 |
-0.001140 |
8.70e-01 |
0.992000 |
Disease |
947 |
7.23e-01 |
8.42e-01 |
0.01580 |
0.000463 |
-0.015800 |
9.81e-01 |
0.421000 |
Influenza Viral RNA Transcription and Replication |
55 |
9.80e-01 |
9.88e-01 |
0.01570 |
0.000260 |
-0.015700 |
9.97e-01 |
0.841000 |
RAF/MAP kinase cascade |
179 |
9.41e-01 |
9.56e-01 |
0.01530 |
-0.005500 |
-0.014300 |
9.00e-01 |
0.743000 |
MAPK6/MAPK4 signaling |
61 |
9.83e-01 |
9.89e-01 |
0.01380 |
-0.009490 |
-0.010000 |
8.98e-01 |
0.893000 |
Negative regulation of FGFR2 signaling |
18 |
9.95e-01 |
9.99e-01 |
0.01300 |
-0.011400 |
-0.006280 |
9.33e-01 |
0.963000 |
Developmental Biology |
590 |
8.87e-01 |
9.23e-01 |
0.01210 |
-0.009710 |
-0.007200 |
6.91e-01 |
0.768000 |
Metabolism |
1314 |
8.71e-01 |
9.16e-01 |
0.00898 |
-0.007010 |
-0.005610 |
6.80e-01 |
0.741000 |
COPI-independent Golgi-to-ER retrograde traffic |
26 |
9.97e-01 |
9.99e-01 |
0.00885 |
-0.001930 |
-0.008640 |
9.86e-01 |
0.939000 |
MAPK1/MAPK3 signaling |
184 |
9.91e-01 |
9.95e-01 |
0.00580 |
-0.004960 |
-0.003010 |
9.08e-01 |
0.944000 |
Constitutive Signaling by Aberrant PI3K in Cancer |
52 |
9.99e-01 |
1.00e+00 |
0.00351 |
-0.001140 |
0.003320 |
9.89e-01 |
0.967000 |
Cytosolic sensors of pathogen-associated DNA |
44 |
1.00e+00 |
1.00e+00 |
0.00199 |
0.001630 |
-0.001150 |
9.85e-01 |
0.990000 |
Fatty acid metabolism |
113 |
9.99e-01 |
1.00e+00 |
0.00188 |
0.001710 |
-0.000784 |
9.75e-01 |
0.989000 |