Glucuronidation |
11 |
2.86e-05 |
8.76e-04 |
0.79700 |
0.524000 |
0.600000 |
2.60e-03 |
0.000564 |
Interferon alpha/beta signaling |
42 |
2.73e-14 |
3.43e-11 |
0.70400 |
0.649000 |
-0.273000 |
3.43e-13 |
0.002180 |
Classical antibody-mediated complement activation |
10 |
6.74e-04 |
1.19e-02 |
0.69800 |
0.684000 |
-0.139000 |
1.82e-04 |
0.446000 |
Initial triggering of complement |
19 |
1.21e-06 |
9.52e-05 |
0.69100 |
0.614000 |
-0.318000 |
3.63e-06 |
0.016600 |
Phosphorylation of CD3 and TCR zeta chains |
10 |
1.65e-03 |
2.20e-02 |
0.65400 |
0.637000 |
-0.144000 |
4.82e-04 |
0.430000 |
LGI-ADAM interactions |
11 |
9.86e-04 |
1.64e-02 |
0.64800 |
-0.593000 |
-0.261000 |
6.54e-04 |
0.134000 |
Negative regulation of TCF-dependent signaling by WNT ligand antagonists |
10 |
2.05e-03 |
2.58e-02 |
0.64200 |
-0.633000 |
0.110000 |
5.29e-04 |
0.549000 |
Creation of C4 and C2 activators |
12 |
1.55e-03 |
2.14e-02 |
0.59900 |
0.585000 |
-0.132000 |
4.53e-04 |
0.430000 |
Signaling by Activin |
10 |
5.06e-03 |
4.41e-02 |
0.59300 |
-0.527000 |
0.273000 |
3.92e-03 |
0.135000 |
Removal of the Flap Intermediate |
11 |
3.12e-03 |
3.29e-02 |
0.59100 |
0.439000 |
-0.396000 |
1.18e-02 |
0.022900 |
PI-3K cascade:FGFR2 |
14 |
8.00e-04 |
1.38e-02 |
0.58200 |
-0.511000 |
0.279000 |
9.27e-04 |
0.070700 |
PI-3K cascade:FGFR4 |
11 |
3.92e-03 |
3.90e-02 |
0.57900 |
-0.511000 |
0.274000 |
3.37e-03 |
0.116000 |
Cholesterol biosynthesis |
20 |
4.46e-05 |
1.27e-03 |
0.57900 |
-0.539000 |
-0.211000 |
3.05e-05 |
0.102000 |
Removal of the Flap Intermediate from the C-strand |
12 |
2.80e-03 |
3.08e-02 |
0.57100 |
0.481000 |
-0.309000 |
3.95e-03 |
0.064200 |
HSF1-dependent transactivation |
26 |
3.16e-06 |
1.50e-04 |
0.57000 |
-0.560000 |
-0.109000 |
7.74e-07 |
0.336000 |
Processive synthesis on the lagging strand |
12 |
3.09e-03 |
3.29e-02 |
0.56600 |
0.476000 |
-0.307000 |
4.30e-03 |
0.065800 |
Peptide chain elongation |
37 |
2.92e-08 |
5.24e-06 |
0.56000 |
0.558000 |
0.046200 |
4.32e-09 |
0.627000 |
STING mediated induction of host immune responses |
11 |
6.76e-03 |
5.30e-02 |
0.55000 |
0.433000 |
-0.339000 |
1.28e-02 |
0.051800 |
IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation |
11 |
7.15e-03 |
5.51e-02 |
0.54700 |
-0.342000 |
0.427000 |
4.97e-02 |
0.014200 |
TRAF6-mediated induction of TAK1 complex within TLR4 complex |
11 |
7.15e-03 |
5.51e-02 |
0.54700 |
-0.342000 |
0.427000 |
4.97e-02 |
0.014200 |
DNA strand elongation |
26 |
8.88e-06 |
3.01e-04 |
0.54600 |
0.527000 |
-0.144000 |
3.30e-06 |
0.205000 |
JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 |
16 |
1.02e-03 |
1.64e-02 |
0.53600 |
-0.402000 |
0.354000 |
5.39e-03 |
0.014200 |
Response of EIF2AK4 (GCN2) to amino acid deficiency |
45 |
4.65e-09 |
1.17e-06 |
0.53400 |
0.523000 |
0.110000 |
1.33e-09 |
0.202000 |
FRS-mediated FGFR2 signaling |
15 |
1.64e-03 |
2.20e-02 |
0.53400 |
-0.443000 |
0.297000 |
2.96e-03 |
0.046500 |
Selenocysteine synthesis |
40 |
4.00e-08 |
6.27e-06 |
0.53300 |
0.533000 |
0.024000 |
5.48e-09 |
0.793000 |
CREB1 phosphorylation through the activation of Adenylate Cyclase |
11 |
9.19e-03 |
6.50e-02 |
0.53300 |
-0.322000 |
0.424000 |
6.43e-02 |
0.014800 |
Termination of translesion DNA synthesis |
23 |
7.15e-05 |
1.91e-03 |
0.52600 |
0.456000 |
-0.262000 |
1.55e-04 |
0.029400 |
Regulation of IFNA signaling |
12 |
7.56e-03 |
5.65e-02 |
0.52100 |
0.485000 |
-0.190000 |
3.64e-03 |
0.254000 |
Viral mRNA Translation |
37 |
3.07e-07 |
3.21e-05 |
0.52100 |
0.517000 |
0.057500 |
5.20e-08 |
0.545000 |
Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex |
11 |
1.17e-02 |
7.44e-02 |
0.52000 |
0.451000 |
0.259000 |
9.68e-03 |
0.137000 |
FRS-mediated FGFR4 signaling |
12 |
7.84e-03 |
5.76e-02 |
0.51900 |
-0.426000 |
0.296000 |
1.07e-02 |
0.075500 |
Mitotic Telophase/Cytokinesis |
10 |
1.97e-02 |
1.04e-01 |
0.51200 |
0.292000 |
0.421000 |
1.09e-01 |
0.021300 |
Telomere C-strand synthesis initiation |
10 |
1.98e-02 |
1.04e-01 |
0.51100 |
0.462000 |
-0.219000 |
1.14e-02 |
0.231000 |
FCGR activation |
16 |
2.05e-03 |
2.58e-02 |
0.50800 |
0.508000 |
-0.021000 |
4.40e-04 |
0.885000 |
Activation of AMPK downstream of NMDARs |
10 |
2.29e-02 |
1.14e-01 |
0.50200 |
-0.432000 |
-0.256000 |
1.80e-02 |
0.161000 |
Attenuation phase |
17 |
1.84e-03 |
2.39e-02 |
0.49700 |
-0.497000 |
0.021000 |
3.92e-04 |
0.881000 |
Polymerase switching on the C-strand of the telomere |
21 |
5.24e-04 |
9.82e-03 |
0.49000 |
0.394000 |
-0.290000 |
1.76e-03 |
0.021400 |
Cleavage of the damaged pyrimidine |
13 |
9.91e-03 |
6.69e-02 |
0.48600 |
0.431000 |
-0.226000 |
7.19e-03 |
0.159000 |
Depyrimidination |
13 |
9.91e-03 |
6.69e-02 |
0.48600 |
0.431000 |
-0.226000 |
7.19e-03 |
0.159000 |
Recognition and association of DNA glycosylase with site containing an affected pyrimidine |
13 |
9.91e-03 |
6.69e-02 |
0.48600 |
0.431000 |
-0.226000 |
7.19e-03 |
0.159000 |
Lagging Strand Synthesis |
17 |
2.54e-03 |
2.90e-02 |
0.48400 |
0.403000 |
-0.268000 |
4.02e-03 |
0.056100 |
Processive synthesis on the C-strand of the telomere |
14 |
7.55e-03 |
5.65e-02 |
0.48200 |
0.450000 |
-0.173000 |
3.54e-03 |
0.263000 |
ATF6 (ATF6-alpha) activates chaperones |
10 |
3.06e-02 |
1.36e-01 |
0.48200 |
-0.208000 |
0.434000 |
2.54e-01 |
0.017400 |
GRB2 events in EGFR signaling |
10 |
3.22e-02 |
1.40e-01 |
0.47800 |
-0.211000 |
0.430000 |
2.49e-01 |
0.018700 |
Eukaryotic Translation Elongation |
40 |
1.13e-06 |
9.49e-05 |
0.47800 |
0.477000 |
0.040300 |
1.84e-07 |
0.659000 |
Signaling by BMP |
20 |
1.05e-03 |
1.64e-02 |
0.47800 |
-0.346000 |
0.330000 |
7.44e-03 |
0.010600 |
Antimicrobial peptides |
11 |
2.38e-02 |
1.17e-01 |
0.47600 |
0.453000 |
-0.144000 |
9.22e-03 |
0.408000 |
Activation of the pre-replicative complex |
26 |
1.66e-04 |
3.86e-03 |
0.47300 |
0.473000 |
-0.013500 |
3.04e-05 |
0.906000 |
Eukaryotic Translation Termination |
40 |
1.82e-06 |
1.21e-04 |
0.47000 |
0.463000 |
0.078600 |
3.97e-07 |
0.390000 |
Negative regulation of FGFR2 signaling |
21 |
1.12e-03 |
1.69e-02 |
0.46400 |
-0.388000 |
0.256000 |
2.10e-03 |
0.042700 |
EGFR downregulation |
24 |
4.72e-04 |
9.13e-03 |
0.46100 |
-0.362000 |
0.285000 |
2.12e-03 |
0.015700 |
Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) |
12 |
2.20e-02 |
1.11e-01 |
0.46000 |
0.395000 |
-0.237000 |
1.80e-02 |
0.155000 |
Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) |
12 |
2.41e-02 |
1.18e-01 |
0.45500 |
0.405000 |
-0.207000 |
1.51e-02 |
0.215000 |
Prolactin receptor signaling |
11 |
3.33e-02 |
1.42e-01 |
0.45400 |
-0.360000 |
0.276000 |
3.88e-02 |
0.112000 |
Generation of second messenger molecules |
20 |
2.35e-03 |
2.79e-02 |
0.45000 |
0.449000 |
0.018400 |
5.08e-04 |
0.887000 |
Leading Strand Synthesis |
13 |
2.04e-02 |
1.05e-01 |
0.44700 |
0.367000 |
-0.254000 |
2.19e-02 |
0.113000 |
Polymerase switching |
13 |
2.04e-02 |
1.05e-01 |
0.44700 |
0.367000 |
-0.254000 |
2.19e-02 |
0.113000 |
RHO GTPases Activate NADPH Oxidases |
18 |
4.62e-03 |
4.39e-02 |
0.44600 |
0.291000 |
-0.338000 |
3.27e-02 |
0.013000 |
G1/S-Specific Transcription |
24 |
7.97e-04 |
1.38e-02 |
0.44600 |
0.444000 |
-0.032300 |
1.65e-04 |
0.784000 |
Signaling by FGFR4 in disease |
10 |
5.13e-02 |
1.82e-01 |
0.44500 |
-0.155000 |
0.417000 |
3.95e-01 |
0.022500 |
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) |
41 |
5.61e-06 |
2.01e-04 |
0.44400 |
0.428000 |
0.118000 |
2.11e-06 |
0.191000 |
Negative regulation of FGFR4 signaling |
18 |
5.00e-03 |
4.41e-02 |
0.44300 |
-0.367000 |
0.248000 |
7.08e-03 |
0.068400 |
Base-Excision Repair, AP Site Formation |
15 |
1.24e-02 |
7.65e-02 |
0.44100 |
0.381000 |
-0.223000 |
1.07e-02 |
0.135000 |
Downregulation of SMAD2/3:SMAD4 transcriptional activity |
17 |
7.48e-03 |
5.65e-02 |
0.43800 |
-0.368000 |
0.237000 |
8.60e-03 |
0.090300 |
G0 and Early G1 |
24 |
1.01e-03 |
1.64e-02 |
0.43800 |
0.435000 |
-0.051000 |
2.26e-04 |
0.665000 |
SHC-mediated cascade:FGFR2 |
14 |
1.87e-02 |
9.97e-02 |
0.43500 |
-0.307000 |
0.308000 |
4.68e-02 |
0.045700 |
Establishment of Sister Chromatid Cohesion |
10 |
5.88e-02 |
2.02e-01 |
0.43500 |
0.350000 |
0.259000 |
5.54e-02 |
0.157000 |
Formation of a pool of free 40S subunits |
46 |
2.31e-06 |
1.38e-04 |
0.43400 |
0.433000 |
0.033900 |
3.77e-07 |
0.691000 |
Telomere C-strand (Lagging Strand) Synthesis |
27 |
5.17e-04 |
9.82e-03 |
0.43200 |
0.369000 |
-0.226000 |
9.18e-04 |
0.042400 |
Competing endogenous RNAs (ceRNAs) regulate PTEN translation |
10 |
6.35e-02 |
2.14e-01 |
0.42800 |
-0.287000 |
0.318000 |
1.16e-01 |
0.081800 |
Downstream signaling of activated FGFR2 |
20 |
4.06e-03 |
3.95e-02 |
0.42800 |
-0.299000 |
0.307000 |
2.07e-02 |
0.017500 |
Nephrin family interactions |
19 |
5.56e-03 |
4.57e-02 |
0.42800 |
0.290000 |
0.314000 |
2.87e-02 |
0.017800 |
MET activates RAP1 and RAC1 |
11 |
4.92e-02 |
1.78e-01 |
0.42700 |
-0.118000 |
0.411000 |
4.98e-01 |
0.018400 |
PI-3K cascade:FGFR3 |
12 |
3.83e-02 |
1.50e-01 |
0.42600 |
-0.391000 |
0.169000 |
1.92e-02 |
0.310000 |
Transcription of E2F targets under negative control by DREAM complex |
17 |
1.17e-02 |
7.44e-02 |
0.41800 |
0.405000 |
-0.103000 |
3.85e-03 |
0.462000 |
InlB-mediated entry of Listeria monocytogenes into host cell |
11 |
5.60e-02 |
1.94e-01 |
0.41800 |
-0.325000 |
0.262000 |
6.20e-02 |
0.132000 |
GRB2 events in ERBB2 signaling |
14 |
2.71e-02 |
1.29e-01 |
0.41400 |
-0.168000 |
0.379000 |
2.75e-01 |
0.014200 |
GTP hydrolysis and joining of the 60S ribosomal subunit |
52 |
1.83e-06 |
1.21e-04 |
0.41200 |
0.407000 |
0.066300 |
3.87e-07 |
0.409000 |
activated TAK1 mediates p38 MAPK activation |
17 |
1.31e-02 |
7.84e-02 |
0.41200 |
-0.394000 |
0.122000 |
4.93e-03 |
0.385000 |
Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell |
49 |
4.27e-06 |
1.63e-04 |
0.41100 |
0.407000 |
-0.054400 |
8.33e-07 |
0.510000 |
Listeria monocytogenes entry into host cells |
15 |
2.24e-02 |
1.13e-01 |
0.41100 |
-0.342000 |
0.227000 |
2.18e-02 |
0.128000 |
L13a-mediated translational silencing of Ceruloplasmin expression |
50 |
3.86e-06 |
1.63e-04 |
0.40800 |
0.405000 |
0.056200 |
7.55e-07 |
0.492000 |
Regulation of necroptotic cell death |
12 |
5.14e-02 |
1.82e-01 |
0.40700 |
0.319000 |
0.252000 |
5.56e-02 |
0.131000 |
SHC1 events in ERBB4 signaling |
12 |
5.11e-02 |
1.82e-01 |
0.40600 |
-0.080000 |
0.399000 |
6.32e-01 |
0.016800 |
CD28 dependent Vav1 pathway |
12 |
5.23e-02 |
1.84e-01 |
0.40500 |
0.367000 |
0.172000 |
2.77e-02 |
0.303000 |
SHC1 events in EGFR signaling |
11 |
6.66e-02 |
2.22e-01 |
0.40500 |
-0.115000 |
0.388000 |
5.08e-01 |
0.025700 |
Gap-filling DNA repair synthesis and ligation in GG-NER |
19 |
9.32e-03 |
6.50e-02 |
0.40500 |
0.389000 |
-0.114000 |
3.35e-03 |
0.391000 |
Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 |
14 |
3.25e-02 |
1.41e-01 |
0.40400 |
0.401000 |
-0.047400 |
9.35e-03 |
0.759000 |
Mismatch Repair |
13 |
4.14e-02 |
1.59e-01 |
0.40400 |
0.346000 |
-0.209000 |
3.09e-02 |
0.192000 |
Activation of PPARGC1A (PGC-1alpha) by phosphorylation |
10 |
8.72e-02 |
2.63e-01 |
0.40400 |
-0.312000 |
-0.257000 |
8.79e-02 |
0.160000 |
Downstream signaling of activated FGFR4 |
17 |
1.56e-02 |
8.67e-02 |
0.40400 |
-0.261000 |
0.308000 |
6.27e-02 |
0.027900 |
Selenoamino acid metabolism |
52 |
3.22e-06 |
1.50e-04 |
0.40300 |
0.403000 |
0.012100 |
4.97e-07 |
0.880000 |
Glutamate and glutamine metabolism |
12 |
5.39e-02 |
1.89e-01 |
0.40300 |
0.063100 |
-0.398000 |
7.05e-01 |
0.017000 |
HDMs demethylate histones |
19 |
1.03e-02 |
6.86e-02 |
0.40100 |
-0.361000 |
0.174000 |
6.45e-03 |
0.189000 |
MET activates RAS signaling |
10 |
9.12e-02 |
2.72e-01 |
0.40000 |
0.014200 |
0.400000 |
9.38e-01 |
0.028700 |
Regulation of PTEN mRNA translation |
11 |
7.16e-02 |
2.31e-01 |
0.40000 |
-0.191000 |
0.351000 |
2.72e-01 |
0.043900 |
SHC-mediated cascade:FGFR4 |
11 |
7.17e-02 |
2.31e-01 |
0.39900 |
-0.251000 |
0.311000 |
1.50e-01 |
0.074200 |
IRE1alpha activates chaperones |
44 |
3.48e-05 |
1.04e-03 |
0.39500 |
-0.286000 |
-0.273000 |
1.02e-03 |
0.001770 |
Constitutive Signaling by EGFRvIII |
15 |
3.06e-02 |
1.36e-01 |
0.39400 |
-0.172000 |
0.354000 |
2.50e-01 |
0.017600 |
Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants |
15 |
3.06e-02 |
1.36e-01 |
0.39400 |
-0.172000 |
0.354000 |
2.50e-01 |
0.017600 |
Signaling by EGFRvIII in Cancer |
15 |
3.06e-02 |
1.36e-01 |
0.39400 |
-0.172000 |
0.354000 |
2.50e-01 |
0.017600 |
Signaling by Ligand-Responsive EGFR Variants in Cancer |
15 |
3.06e-02 |
1.36e-01 |
0.39400 |
-0.172000 |
0.354000 |
2.50e-01 |
0.017600 |
PCNA-Dependent Long Patch Base Excision Repair |
17 |
1.94e-02 |
1.03e-01 |
0.39300 |
0.373000 |
-0.124000 |
7.77e-03 |
0.376000 |
SRP-dependent cotranslational protein targeting to membrane |
55 |
3.08e-06 |
1.50e-04 |
0.39300 |
0.393000 |
0.017300 |
4.81e-07 |
0.825000 |
XBP1(S) activates chaperone genes |
42 |
6.37e-05 |
1.78e-03 |
0.39300 |
-0.257000 |
-0.297000 |
3.95e-03 |
0.000888 |
Activation of ATR in response to replication stress |
28 |
1.66e-03 |
2.20e-02 |
0.39100 |
0.390000 |
0.024900 |
3.56e-04 |
0.819000 |
Cytosolic sulfonation of small molecules |
13 |
5.11e-02 |
1.82e-01 |
0.39000 |
0.325000 |
-0.216000 |
4.25e-02 |
0.177000 |
PKA activation |
17 |
2.07e-02 |
1.07e-01 |
0.39000 |
-0.344000 |
0.184000 |
1.42e-02 |
0.189000 |
Prolonged ERK activation events |
13 |
5.17e-02 |
1.83e-01 |
0.39000 |
-0.265000 |
0.285000 |
9.79e-02 |
0.074900 |
Signaling by EGFR in Cancer |
18 |
1.70e-02 |
9.19e-02 |
0.38800 |
-0.182000 |
0.343000 |
1.81e-01 |
0.011800 |
PKA-mediated phosphorylation of CREB |
19 |
1.36e-02 |
7.86e-02 |
0.38800 |
-0.301000 |
0.245000 |
2.32e-02 |
0.064200 |
Cyclin A/B1/B2 associated events during G2/M transition |
20 |
1.22e-02 |
7.58e-02 |
0.38400 |
0.326000 |
0.202000 |
1.16e-02 |
0.117000 |
Signaling by NODAL |
12 |
7.23e-02 |
2.32e-01 |
0.38300 |
-0.326000 |
-0.200000 |
5.05e-02 |
0.230000 |
Formation of the ternary complex, and subsequently, the 43S complex |
26 |
3.38e-03 |
3.50e-02 |
0.38300 |
0.355000 |
0.143000 |
1.74e-03 |
0.208000 |
RIPK1-mediated regulated necrosis |
14 |
4.76e-02 |
1.76e-01 |
0.38100 |
0.330000 |
0.190000 |
3.24e-02 |
0.217000 |
Regulated Necrosis |
14 |
4.76e-02 |
1.76e-01 |
0.38100 |
0.330000 |
0.190000 |
3.24e-02 |
0.217000 |
Polo-like kinase mediated events |
13 |
5.95e-02 |
2.03e-01 |
0.38100 |
0.380000 |
0.019400 |
1.76e-02 |
0.904000 |
Signaling by WNT in cancer |
25 |
4.74e-03 |
4.41e-02 |
0.37800 |
-0.370000 |
0.076000 |
1.36e-03 |
0.511000 |
Diseases associated with glycosylation precursor biosynthesis |
16 |
3.28e-02 |
1.42e-01 |
0.37800 |
-0.034700 |
-0.376000 |
8.10e-01 |
0.009200 |
FRS-mediated FGFR3 signaling |
13 |
6.19e-02 |
2.09e-01 |
0.37800 |
-0.321000 |
0.198000 |
4.49e-02 |
0.216000 |
Cap-dependent Translation Initiation |
58 |
4.42e-06 |
1.63e-04 |
0.37700 |
0.377000 |
0.009470 |
6.89e-07 |
0.901000 |
Eukaryotic Translation Initiation |
58 |
4.42e-06 |
1.63e-04 |
0.37700 |
0.377000 |
0.009470 |
6.89e-07 |
0.901000 |
PI3K events in ERBB2 signaling |
14 |
5.07e-02 |
1.82e-01 |
0.37700 |
-0.200000 |
0.319000 |
1.95e-01 |
0.038700 |
DAP12 signaling |
25 |
5.05e-03 |
4.41e-02 |
0.37600 |
0.339000 |
0.162000 |
3.32e-03 |
0.161000 |
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) |
59 |
4.07e-06 |
1.63e-04 |
0.37600 |
0.352000 |
0.130000 |
2.90e-06 |
0.084900 |
Nonsense-Mediated Decay (NMD) |
59 |
4.07e-06 |
1.63e-04 |
0.37600 |
0.352000 |
0.130000 |
2.90e-06 |
0.084900 |
Inhibition of DNA recombination at telomere |
13 |
6.73e-02 |
2.23e-01 |
0.37200 |
0.344000 |
-0.141000 |
3.17e-02 |
0.378000 |
Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template |
28 |
3.02e-03 |
3.27e-02 |
0.37200 |
0.343000 |
-0.143000 |
1.68e-03 |
0.189000 |
Metabolism of folate and pterines |
14 |
5.62e-02 |
1.94e-01 |
0.37100 |
-0.130000 |
-0.347000 |
3.99e-01 |
0.024600 |
Interferon gamma signaling |
61 |
3.65e-06 |
1.63e-04 |
0.37100 |
0.352000 |
-0.117000 |
2.07e-06 |
0.116000 |
Regulation of Complement cascade |
31 |
1.72e-03 |
2.25e-02 |
0.37000 |
0.369000 |
-0.032900 |
3.79e-04 |
0.752000 |
PKA activation in glucagon signalling |
16 |
3.73e-02 |
1.49e-01 |
0.37000 |
-0.364000 |
0.067100 |
1.17e-02 |
0.642000 |
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S |
30 |
2.19e-03 |
2.64e-02 |
0.37000 |
0.338000 |
0.151000 |
1.38e-03 |
0.153000 |
Adherens junctions interactions |
13 |
6.95e-02 |
2.28e-01 |
0.37000 |
-0.251000 |
0.271000 |
1.17e-01 |
0.090800 |
Negative regulation of MET activity |
17 |
3.11e-02 |
1.37e-01 |
0.36900 |
-0.244000 |
0.277000 |
8.23e-02 |
0.048100 |
Diseases of carbohydrate metabolism |
22 |
1.20e-02 |
7.50e-02 |
0.36700 |
-0.261000 |
-0.258000 |
3.39e-02 |
0.036600 |
CASP8 activity is inhibited |
10 |
1.34e-01 |
3.46e-01 |
0.36700 |
0.309000 |
0.198000 |
9.10e-02 |
0.278000 |
Dimerization of procaspase-8 |
10 |
1.34e-01 |
3.46e-01 |
0.36700 |
0.309000 |
0.198000 |
9.10e-02 |
0.278000 |
Regulation by c-FLIP |
10 |
1.34e-01 |
3.46e-01 |
0.36700 |
0.309000 |
0.198000 |
9.10e-02 |
0.278000 |
Activation of RAC1 |
12 |
8.93e-02 |
2.68e-01 |
0.36700 |
-0.004030 |
0.366000 |
9.81e-01 |
0.028000 |
Frs2-mediated activation |
11 |
1.10e-01 |
3.01e-01 |
0.36500 |
-0.242000 |
0.274000 |
1.64e-01 |
0.116000 |
TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest |
13 |
7.62e-02 |
2.40e-01 |
0.36300 |
0.311000 |
-0.188000 |
5.24e-02 |
0.240000 |
Ribosomal scanning and start codon recognition |
30 |
2.78e-03 |
3.08e-02 |
0.36200 |
0.327000 |
0.156000 |
1.95e-03 |
0.138000 |
Orc1 removal from chromatin |
54 |
2.56e-05 |
8.03e-04 |
0.36200 |
0.362000 |
-0.014200 |
4.33e-06 |
0.857000 |
Signaling by Hippo |
18 |
2.95e-02 |
1.36e-01 |
0.36100 |
-0.309000 |
0.187000 |
2.34e-02 |
0.169000 |
Signaling by FGFR4 |
27 |
5.22e-03 |
4.43e-02 |
0.36000 |
-0.210000 |
0.293000 |
5.87e-02 |
0.008540 |
Telomere Extension By Telomerase |
18 |
3.08e-02 |
1.36e-01 |
0.36000 |
0.285000 |
0.219000 |
3.61e-02 |
0.108000 |
DNA Replication Pre-Initiation |
66 |
3.01e-06 |
1.50e-04 |
0.35900 |
0.352000 |
-0.068900 |
7.53e-07 |
0.334000 |
Translesion synthesis by POLK |
12 |
9.87e-02 |
2.85e-01 |
0.35900 |
0.342000 |
-0.107000 |
4.01e-02 |
0.521000 |
Gluconeogenesis |
23 |
1.20e-02 |
7.50e-02 |
0.35900 |
-0.198000 |
-0.299000 |
9.98e-02 |
0.013100 |
DAP12 interactions |
28 |
4.93e-03 |
4.41e-02 |
0.35600 |
0.297000 |
0.196000 |
6.47e-03 |
0.072400 |
Regulation of pyruvate dehydrogenase (PDH) complex |
12 |
1.05e-01 |
2.94e-01 |
0.35400 |
-0.315000 |
-0.162000 |
5.89e-02 |
0.330000 |
Synthesis of PA |
23 |
1.34e-02 |
7.84e-02 |
0.35400 |
-0.203000 |
-0.290000 |
9.21e-02 |
0.016000 |
Signaling by FGFR3 in disease |
16 |
4.93e-02 |
1.78e-01 |
0.35400 |
-0.220000 |
0.277000 |
1.27e-01 |
0.055100 |
Signaling by FGFR3 point mutants in cancer |
16 |
4.93e-02 |
1.78e-01 |
0.35400 |
-0.220000 |
0.277000 |
1.27e-01 |
0.055100 |
Base Excision Repair |
37 |
1.02e-03 |
1.64e-02 |
0.35300 |
0.330000 |
-0.124000 |
5.16e-04 |
0.192000 |
TRAF3-dependent IRF activation pathway |
13 |
8.92e-02 |
2.68e-01 |
0.35200 |
0.323000 |
-0.140000 |
4.39e-02 |
0.381000 |
Spry regulation of FGF signaling |
12 |
1.08e-01 |
2.98e-01 |
0.35100 |
-0.250000 |
0.247000 |
1.34e-01 |
0.139000 |
G1/S Transition |
106 |
3.69e-09 |
1.16e-06 |
0.35100 |
0.351000 |
0.003440 |
4.61e-10 |
0.951000 |
Negative regulation of FGFR3 signaling |
19 |
3.02e-02 |
1.36e-01 |
0.35000 |
-0.298000 |
0.184000 |
2.44e-02 |
0.166000 |
TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) |
10 |
1.59e-01 |
3.84e-01 |
0.35000 |
-0.143000 |
-0.320000 |
4.34e-01 |
0.080000 |
Translation initiation complex formation |
29 |
5.02e-03 |
4.41e-02 |
0.35000 |
0.315000 |
0.151000 |
3.32e-03 |
0.159000 |
SCF(Skp2)-mediated degradation of p27/p21 |
46 |
2.25e-04 |
4.97e-03 |
0.34900 |
0.347000 |
-0.037800 |
4.63e-05 |
0.658000 |
Synthesis of IP2, IP, and Ins in the cytosol |
13 |
9.33e-02 |
2.75e-01 |
0.34900 |
-0.340000 |
-0.078900 |
3.38e-02 |
0.622000 |
PI-3K cascade:FGFR1 |
12 |
1.13e-01 |
3.08e-01 |
0.34800 |
-0.321000 |
0.134000 |
5.42e-02 |
0.423000 |
CD209 (DC-SIGN) signaling |
19 |
3.21e-02 |
1.40e-01 |
0.34800 |
0.037300 |
0.346000 |
7.79e-01 |
0.009100 |
Selective autophagy |
46 |
2.50e-04 |
5.41e-03 |
0.34800 |
-0.255000 |
-0.236000 |
2.79e-03 |
0.005580 |
Physiological factors |
11 |
1.37e-01 |
3.51e-01 |
0.34700 |
-0.325000 |
0.123000 |
6.24e-02 |
0.478000 |
Translesion synthesis by POLI |
12 |
1.16e-01 |
3.14e-01 |
0.34600 |
0.320000 |
-0.132000 |
5.51e-02 |
0.430000 |
Synthesis of active ubiquitin: roles of E1 and E2 enzymes |
19 |
3.47e-02 |
1.46e-01 |
0.34300 |
-0.194000 |
0.283000 |
1.44e-01 |
0.032500 |
Translesion synthesis by REV1 |
11 |
1.44e-01 |
3.62e-01 |
0.34300 |
0.316000 |
-0.133000 |
7.00e-02 |
0.444000 |
Citric acid cycle (TCA cycle) |
18 |
4.21e-02 |
1.61e-01 |
0.34300 |
-0.138000 |
0.313000 |
3.09e-01 |
0.021400 |
NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 |
11 |
1.45e-01 |
3.62e-01 |
0.34200 |
0.340000 |
-0.037800 |
5.07e-02 |
0.828000 |
ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression |
14 |
8.58e-02 |
2.61e-01 |
0.34200 |
0.095900 |
-0.328000 |
5.35e-01 |
0.033500 |
Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation |
26 |
1.06e-02 |
7.01e-02 |
0.34200 |
0.335000 |
0.067500 |
3.10e-03 |
0.551000 |
Pre-NOTCH Processing in Golgi |
14 |
8.69e-02 |
2.63e-01 |
0.34100 |
-0.085900 |
-0.330000 |
5.78e-01 |
0.032300 |
Sulfur amino acid metabolism |
18 |
4.37e-02 |
1.66e-01 |
0.34100 |
-0.237000 |
-0.245000 |
8.17e-02 |
0.071700 |
MECP2 regulates neuronal receptors and channels |
12 |
1.24e-01 |
3.29e-01 |
0.34100 |
0.289000 |
0.181000 |
8.32e-02 |
0.278000 |
Regulation of expression of SLITs and ROBOs |
94 |
1.01e-07 |
1.16e-05 |
0.33900 |
0.333000 |
0.067200 |
2.62e-08 |
0.261000 |
PECAM1 interactions |
11 |
1.52e-01 |
3.75e-01 |
0.33800 |
0.331000 |
-0.065500 |
5.72e-02 |
0.707000 |
Condensation of Prophase Chromosomes |
10 |
1.82e-01 |
4.21e-01 |
0.33700 |
0.337000 |
-0.002220 |
6.47e-02 |
0.990000 |
Activation of gene expression by SREBF (SREBP) |
39 |
1.35e-03 |
1.94e-02 |
0.33700 |
-0.315000 |
-0.121000 |
6.81e-04 |
0.193000 |
Uptake and function of anthrax toxins |
11 |
1.55e-01 |
3.78e-01 |
0.33600 |
-0.334000 |
-0.039600 |
5.51e-02 |
0.820000 |
Caspase activation via Death Receptors in the presence of ligand |
15 |
7.94e-02 |
2.46e-01 |
0.33600 |
0.146000 |
0.302000 |
3.27e-01 |
0.042600 |
TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest |
17 |
5.66e-02 |
1.95e-01 |
0.33600 |
0.178000 |
-0.285000 |
2.05e-01 |
0.042200 |
Mitotic G1 phase and G1/S transition |
121 |
1.67e-09 |
7.01e-07 |
0.33500 |
0.335000 |
-0.000496 |
2.05e-10 |
0.992000 |
Complement cascade |
35 |
2.80e-03 |
3.08e-02 |
0.33500 |
0.327000 |
-0.074700 |
8.34e-04 |
0.445000 |
Assembly of the pre-replicative complex |
52 |
1.63e-04 |
3.86e-03 |
0.33500 |
0.329000 |
-0.062800 |
4.13e-05 |
0.434000 |
Miscellaneous transport and binding events |
18 |
4.87e-02 |
1.78e-01 |
0.33500 |
-0.331000 |
0.052300 |
1.52e-02 |
0.701000 |
Deadenylation of mRNA |
20 |
3.53e-02 |
1.46e-01 |
0.33400 |
0.128000 |
0.309000 |
3.23e-01 |
0.016800 |
EGR2 and SOX10-mediated initiation of Schwann cell myelination |
21 |
3.05e-02 |
1.36e-01 |
0.33300 |
-0.331000 |
0.037900 |
8.69e-03 |
0.764000 |
Energy dependent regulation of mTOR by LKB1-AMPK |
25 |
1.58e-02 |
8.67e-02 |
0.33300 |
-0.331000 |
0.032200 |
4.15e-03 |
0.780000 |
ERBB2 Regulates Cell Motility |
12 |
1.38e-01 |
3.53e-01 |
0.33200 |
-0.205000 |
0.261000 |
2.20e-01 |
0.118000 |
Diseases associated with N-glycosylation of proteins |
16 |
7.58e-02 |
2.40e-01 |
0.32800 |
-0.323000 |
-0.055700 |
2.52e-02 |
0.700000 |
Estrogen-dependent nuclear events downstream of ESR-membrane signaling |
21 |
3.41e-02 |
1.44e-01 |
0.32800 |
-0.109000 |
0.309000 |
3.88e-01 |
0.014300 |
Misspliced GSK3beta mutants stabilize beta-catenin |
14 |
1.07e-01 |
2.95e-01 |
0.32600 |
-0.294000 |
0.141000 |
5.66e-02 |
0.361000 |
S33 mutants of beta-catenin aren't phosphorylated |
14 |
1.07e-01 |
2.95e-01 |
0.32600 |
-0.294000 |
0.141000 |
5.66e-02 |
0.361000 |
S37 mutants of beta-catenin aren't phosphorylated |
14 |
1.07e-01 |
2.95e-01 |
0.32600 |
-0.294000 |
0.141000 |
5.66e-02 |
0.361000 |
S45 mutants of beta-catenin aren't phosphorylated |
14 |
1.07e-01 |
2.95e-01 |
0.32600 |
-0.294000 |
0.141000 |
5.66e-02 |
0.361000 |
T41 mutants of beta-catenin aren't phosphorylated |
14 |
1.07e-01 |
2.95e-01 |
0.32600 |
-0.294000 |
0.141000 |
5.66e-02 |
0.361000 |
phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex |
14 |
1.07e-01 |
2.95e-01 |
0.32600 |
-0.294000 |
0.141000 |
5.66e-02 |
0.361000 |
Ion homeostasis |
42 |
1.23e-03 |
1.81e-02 |
0.32600 |
-0.304000 |
0.119000 |
6.62e-04 |
0.181000 |
TRAF6 mediated IRF7 activation |
15 |
9.18e-02 |
2.72e-01 |
0.32600 |
0.322000 |
0.048300 |
3.06e-02 |
0.746000 |
Signaling by FGFR2 |
49 |
4.61e-04 |
9.13e-03 |
0.32400 |
-0.147000 |
0.288000 |
7.45e-02 |
0.000489 |
Signaling by FGFR2 in disease |
27 |
1.45e-02 |
8.27e-02 |
0.32300 |
-0.244000 |
0.212000 |
2.82e-02 |
0.056600 |
ERBB2 Activates PTK6 Signaling |
10 |
2.08e-01 |
4.55e-01 |
0.32300 |
-0.160000 |
0.281000 |
3.82e-01 |
0.124000 |
Pyruvate metabolism |
23 |
2.81e-02 |
1.32e-01 |
0.32200 |
-0.293000 |
-0.133000 |
1.49e-02 |
0.269000 |
Resolution of Abasic Sites (AP sites) |
31 |
8.35e-03 |
6.06e-02 |
0.32100 |
0.290000 |
-0.137000 |
5.20e-03 |
0.186000 |
Resolution of AP sites via the multiple-nucleotide patch replacement pathway |
19 |
5.42e-02 |
1.89e-01 |
0.32000 |
0.308000 |
-0.087300 |
2.03e-02 |
0.510000 |
Antigen processing-Cross presentation |
75 |
1.19e-05 |
3.94e-04 |
0.31800 |
0.312000 |
-0.064600 |
3.15e-06 |
0.334000 |
Regulation of FZD by ubiquitination |
10 |
2.22e-01 |
4.71e-01 |
0.31700 |
-0.312000 |
0.057000 |
8.79e-02 |
0.755000 |
Recognition of DNA damage by PCNA-containing replication complex |
21 |
4.27e-02 |
1.63e-01 |
0.31700 |
0.301000 |
-0.096700 |
1.68e-02 |
0.443000 |
Signaling by ERBB2 KD Mutants |
22 |
3.70e-02 |
1.48e-01 |
0.31600 |
-0.126000 |
0.290000 |
3.05e-01 |
0.018700 |
Degradation of cysteine and homocysteine |
10 |
2.29e-01 |
4.77e-01 |
0.31400 |
-0.180000 |
-0.257000 |
3.24e-01 |
0.159000 |
Acyl chain remodelling of PS |
13 |
1.48e-01 |
3.66e-01 |
0.31300 |
-0.093100 |
-0.299000 |
5.61e-01 |
0.061900 |
Extension of Telomeres |
41 |
2.45e-03 |
2.88e-02 |
0.31300 |
0.310000 |
-0.042600 |
5.94e-04 |
0.637000 |
Signaling by ERBB2 in Cancer |
23 |
3.62e-02 |
1.47e-01 |
0.31000 |
-0.112000 |
0.289000 |
3.54e-01 |
0.016300 |
Calnexin/calreticulin cycle |
16 |
9.98e-02 |
2.85e-01 |
0.31000 |
-0.310000 |
-0.010700 |
3.19e-02 |
0.941000 |
FGFR2 mutant receptor activation |
17 |
8.68e-02 |
2.63e-01 |
0.31000 |
-0.296000 |
0.091100 |
3.47e-02 |
0.515000 |
Signaling by FGFR1 |
35 |
6.57e-03 |
5.19e-02 |
0.31000 |
-0.128000 |
0.282000 |
1.91e-01 |
0.003910 |
Cross-presentation of soluble exogenous antigens (endosomes) |
41 |
2.81e-03 |
3.08e-02 |
0.30900 |
0.289000 |
-0.109000 |
1.36e-03 |
0.226000 |
Sialic acid metabolism |
23 |
3.75e-02 |
1.49e-01 |
0.30900 |
-0.167000 |
-0.260000 |
1.66e-01 |
0.030900 |
Negative regulation of NOTCH4 signaling |
42 |
2.51e-03 |
2.89e-02 |
0.30900 |
0.298000 |
-0.081000 |
8.45e-04 |
0.364000 |
Glycogen synthesis |
10 |
2.40e-01 |
4.89e-01 |
0.30900 |
-0.289000 |
0.107000 |
1.13e-01 |
0.557000 |
Uptake and actions of bacterial toxins |
24 |
3.29e-02 |
1.42e-01 |
0.30900 |
-0.233000 |
-0.203000 |
4.87e-02 |
0.085700 |
Translation of Replicase and Assembly of the Replication Transcription Complex |
11 |
2.10e-01 |
4.55e-01 |
0.30800 |
-0.244000 |
-0.188000 |
1.61e-01 |
0.280000 |
PINK1-PRKN Mediated Mitophagy |
13 |
1.58e-01 |
3.82e-01 |
0.30800 |
-0.071000 |
-0.300000 |
6.58e-01 |
0.061300 |
Nucleotide-like (purinergic) receptors |
12 |
1.84e-01 |
4.21e-01 |
0.30700 |
0.245000 |
0.185000 |
1.41e-01 |
0.268000 |
Downstream signaling of activated FGFR3 |
18 |
7.91e-02 |
2.46e-01 |
0.30600 |
-0.195000 |
0.237000 |
1.53e-01 |
0.082200 |
DNA Damage Bypass |
34 |
8.41e-03 |
6.07e-02 |
0.30600 |
0.296000 |
-0.079900 |
2.85e-03 |
0.420000 |
FRS-mediated FGFR1 signaling |
13 |
1.61e-01 |
3.87e-01 |
0.30600 |
-0.257000 |
0.165000 |
1.08e-01 |
0.302000 |
EPHA-mediated growth cone collapse |
13 |
1.62e-01 |
3.88e-01 |
0.30600 |
0.289000 |
-0.099900 |
7.15e-02 |
0.533000 |
HSF1 activation |
19 |
7.11e-02 |
2.31e-01 |
0.30500 |
-0.273000 |
-0.135000 |
3.91e-02 |
0.307000 |
Regulation of activated PAK-2p34 by proteasome mediated degradation |
38 |
5.19e-03 |
4.43e-02 |
0.30400 |
0.280000 |
-0.118000 |
2.82e-03 |
0.208000 |
Synthesis of DNA |
97 |
1.67e-06 |
1.21e-04 |
0.30300 |
0.299000 |
-0.052700 |
3.82e-07 |
0.370000 |
Signaling by ERBB2 TMD/JMD mutants |
19 |
7.29e-02 |
2.34e-01 |
0.30300 |
-0.133000 |
0.273000 |
3.17e-01 |
0.039800 |
Telomere Maintenance |
50 |
1.04e-03 |
1.64e-02 |
0.30300 |
0.296000 |
-0.063600 |
2.93e-04 |
0.437000 |
Biosynthesis of specialized proresolving mediators (SPMs) |
12 |
1.93e-01 |
4.33e-01 |
0.30200 |
0.280000 |
-0.113000 |
9.26e-02 |
0.497000 |
TGF-beta receptor signaling activates SMADs |
22 |
4.89e-02 |
1.78e-01 |
0.30200 |
-0.279000 |
0.117000 |
2.36e-02 |
0.342000 |
Ubiquitin Mediated Degradation of Phosphorylated Cdc25A |
39 |
4.85e-03 |
4.41e-02 |
0.30200 |
0.292000 |
-0.076500 |
1.60e-03 |
0.409000 |
p53-Independent DNA Damage Response |
39 |
4.85e-03 |
4.41e-02 |
0.30200 |
0.292000 |
-0.076500 |
1.60e-03 |
0.409000 |
p53-Independent G1/S DNA damage checkpoint |
39 |
4.85e-03 |
4.41e-02 |
0.30200 |
0.292000 |
-0.076500 |
1.60e-03 |
0.409000 |
Role of phospholipids in phagocytosis |
27 |
2.52e-02 |
1.22e-01 |
0.30200 |
0.261000 |
-0.152000 |
1.91e-02 |
0.172000 |
Negative regulation of FGFR1 signaling |
19 |
7.52e-02 |
2.39e-01 |
0.30100 |
-0.255000 |
0.161000 |
5.48e-02 |
0.224000 |
DNA Replication |
104 |
8.19e-07 |
7.35e-05 |
0.30100 |
0.296000 |
-0.055700 |
1.98e-07 |
0.327000 |
Cyclin E associated events during G1/S transition |
67 |
1.19e-04 |
2.94e-03 |
0.30100 |
0.300000 |
0.024600 |
2.26e-05 |
0.729000 |
Signaling by FGFR3 |
28 |
2.31e-02 |
1.14e-01 |
0.30000 |
-0.170000 |
0.247000 |
1.21e-01 |
0.023700 |
ER-Phagosome pathway |
61 |
2.80e-04 |
5.86e-03 |
0.30000 |
0.297000 |
-0.041700 |
6.21e-05 |
0.574000 |
Cyclin A:Cdk2-associated events at S phase entry |
69 |
1.06e-04 |
2.67e-03 |
0.29800 |
0.298000 |
-0.001840 |
1.89e-05 |
0.979000 |
G2/M Checkpoints |
107 |
7.83e-07 |
7.35e-05 |
0.29700 |
0.297000 |
-0.016600 |
1.20e-07 |
0.767000 |
Regulation of MECP2 expression and activity |
26 |
3.35e-02 |
1.42e-01 |
0.29500 |
-0.261000 |
0.138000 |
2.14e-02 |
0.223000 |
Interferon Signaling |
130 |
4.94e-08 |
6.89e-06 |
0.29500 |
0.286000 |
-0.073100 |
1.94e-08 |
0.151000 |
GPVI-mediated activation cascade |
27 |
3.00e-02 |
1.36e-01 |
0.29500 |
0.294000 |
-0.019700 |
8.23e-03 |
0.859000 |
Blood group systems biosynthesis |
10 |
2.74e-01 |
5.29e-01 |
0.29400 |
-0.224000 |
-0.191000 |
2.20e-01 |
0.296000 |
Signaling by ERBB2 ECD mutants |
15 |
1.43e-01 |
3.61e-01 |
0.29400 |
-0.116000 |
0.270000 |
4.37e-01 |
0.070000 |
AMER1 mutants destabilize the destruction complex |
13 |
1.85e-01 |
4.21e-01 |
0.29400 |
-0.265000 |
0.127000 |
9.81e-02 |
0.428000 |
APC truncation mutants have impaired AXIN binding |
13 |
1.85e-01 |
4.21e-01 |
0.29400 |
-0.265000 |
0.127000 |
9.81e-02 |
0.428000 |
AXIN missense mutants destabilize the destruction complex |
13 |
1.85e-01 |
4.21e-01 |
0.29400 |
-0.265000 |
0.127000 |
9.81e-02 |
0.428000 |
AXIN mutants destabilize the destruction complex, activating WNT signaling |
13 |
1.85e-01 |
4.21e-01 |
0.29400 |
-0.265000 |
0.127000 |
9.81e-02 |
0.428000 |
Truncations of AMER1 destabilize the destruction complex |
13 |
1.85e-01 |
4.21e-01 |
0.29400 |
-0.265000 |
0.127000 |
9.81e-02 |
0.428000 |
truncated APC mutants destabilize the destruction complex |
13 |
1.85e-01 |
4.21e-01 |
0.29400 |
-0.265000 |
0.127000 |
9.81e-02 |
0.428000 |
Interleukin-2 signaling |
10 |
2.78e-01 |
5.36e-01 |
0.29200 |
-0.008920 |
-0.292000 |
9.61e-01 |
0.110000 |
ER Quality Control Compartment (ERQC) |
13 |
1.91e-01 |
4.32e-01 |
0.29100 |
-0.286000 |
-0.055100 |
7.41e-02 |
0.731000 |
Ca-dependent events |
33 |
1.59e-02 |
8.67e-02 |
0.28900 |
-0.250000 |
0.146000 |
1.31e-02 |
0.146000 |
Other interleukin signaling |
17 |
1.19e-01 |
3.20e-01 |
0.28900 |
0.223000 |
-0.183000 |
1.11e-01 |
0.191000 |
Transcriptional regulation of granulopoiesis |
26 |
3.89e-02 |
1.51e-01 |
0.28900 |
0.253000 |
-0.138000 |
2.54e-02 |
0.223000 |
Ubiquitin-dependent degradation of Cyclin D |
40 |
6.98e-03 |
5.44e-02 |
0.28800 |
0.278000 |
-0.076000 |
2.38e-03 |
0.406000 |
S Phase |
135 |
6.13e-08 |
7.70e-06 |
0.28800 |
0.288000 |
0.005320 |
8.28e-09 |
0.915000 |
NCAM1 interactions |
27 |
3.65e-02 |
1.47e-01 |
0.28700 |
-0.219000 |
-0.185000 |
4.92e-02 |
0.096200 |
Regulation of cholesterol biosynthesis by SREBP (SREBF) |
50 |
2.19e-03 |
2.64e-02 |
0.28600 |
-0.279000 |
-0.065500 |
6.52e-04 |
0.424000 |
RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known |
35 |
1.39e-02 |
7.99e-02 |
0.28600 |
-0.258000 |
-0.123000 |
8.21e-03 |
0.209000 |
Metabolism of polyamines |
49 |
2.49e-03 |
2.89e-02 |
0.28600 |
0.278000 |
-0.065800 |
7.57e-04 |
0.426000 |
Nucleobase biosynthesis |
13 |
2.06e-01 |
4.53e-01 |
0.28500 |
0.037100 |
-0.282000 |
8.17e-01 |
0.078000 |
TP53 Regulates Transcription of Death Receptors and Ligands |
11 |
2.62e-01 |
5.15e-01 |
0.28500 |
-0.050700 |
0.280000 |
7.71e-01 |
0.108000 |
ROS and RNS production in phagocytes |
26 |
4.36e-02 |
1.66e-01 |
0.28300 |
0.199000 |
-0.202000 |
7.96e-02 |
0.074600 |
Disassembly of the destruction complex and recruitment of AXIN to the membrane |
26 |
4.39e-02 |
1.66e-01 |
0.28300 |
-0.281000 |
0.036400 |
1.32e-02 |
0.748000 |
Regulation of TNFR1 signaling |
25 |
4.95e-02 |
1.79e-01 |
0.28300 |
0.271000 |
-0.081800 |
1.90e-02 |
0.479000 |
Interleukin-12 signaling |
30 |
2.81e-02 |
1.32e-01 |
0.28200 |
0.274000 |
0.066500 |
9.35e-03 |
0.529000 |
ATF4 activates genes in response to endoplasmic reticulum stress |
22 |
7.33e-02 |
2.34e-01 |
0.28200 |
0.265000 |
0.097300 |
3.18e-02 |
0.430000 |
Peroxisomal lipid metabolism |
23 |
6.50e-02 |
2.18e-01 |
0.28100 |
0.164000 |
-0.229000 |
1.74e-01 |
0.057500 |
Prostacyclin signalling through prostacyclin receptor |
11 |
2.72e-01 |
5.28e-01 |
0.28100 |
0.153000 |
-0.235000 |
3.79e-01 |
0.177000 |
Regulation of TP53 Activity through Association with Co-factors |
12 |
2.45e-01 |
4.96e-01 |
0.28000 |
-0.260000 |
-0.103000 |
1.19e-01 |
0.536000 |
CDT1 association with the CDC6:ORC:origin complex |
44 |
5.82e-03 |
4.73e-02 |
0.28000 |
0.269000 |
-0.076200 |
2.03e-03 |
0.382000 |
Transcriptional regulation of pluripotent stem cells |
14 |
1.96e-01 |
4.40e-01 |
0.27900 |
-0.278000 |
-0.006900 |
7.13e-02 |
0.964000 |
CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling |
23 |
7.01e-02 |
2.30e-01 |
0.27800 |
-0.075800 |
0.267000 |
5.29e-01 |
0.026600 |
Signaling by FGFR3 fusions in cancer |
10 |
3.15e-01 |
5.64e-01 |
0.27800 |
-0.071800 |
0.268000 |
6.94e-01 |
0.142000 |
Smooth Muscle Contraction |
34 |
2.01e-02 |
1.05e-01 |
0.27700 |
0.275000 |
0.037500 |
5.58e-03 |
0.706000 |
EPHB-mediated forward signaling |
30 |
3.22e-02 |
1.40e-01 |
0.27700 |
0.230000 |
0.155000 |
2.96e-02 |
0.143000 |
The role of GTSE1 in G2/M progression after G2 checkpoint |
46 |
5.20e-03 |
4.43e-02 |
0.27600 |
0.236000 |
-0.144000 |
5.65e-03 |
0.092000 |
Glyoxylate metabolism and glycine degradation |
21 |
9.14e-02 |
2.72e-01 |
0.27600 |
-0.172000 |
-0.216000 |
1.73e-01 |
0.086400 |
CaM pathway |
31 |
2.90e-02 |
1.34e-01 |
0.27600 |
-0.256000 |
0.104000 |
1.38e-02 |
0.315000 |
Calmodulin induced events |
31 |
2.90e-02 |
1.34e-01 |
0.27600 |
-0.256000 |
0.104000 |
1.38e-02 |
0.315000 |
Vif-mediated degradation of APOBEC3G |
39 |
1.17e-02 |
7.44e-02 |
0.27600 |
0.263000 |
-0.084500 |
4.56e-03 |
0.361000 |
NOTCH2 Activation and Transmission of Signal to the Nucleus |
13 |
2.27e-01 |
4.75e-01 |
0.27600 |
0.251000 |
-0.114000 |
1.17e-01 |
0.476000 |
PLC beta mediated events |
47 |
4.80e-03 |
4.41e-02 |
0.27500 |
-0.235000 |
0.143000 |
5.30e-03 |
0.089600 |
Cell recruitment (pro-inflammatory response) |
18 |
1.29e-01 |
3.39e-01 |
0.27500 |
0.169000 |
-0.217000 |
2.14e-01 |
0.111000 |
Purinergic signaling in leishmaniasis infection |
18 |
1.29e-01 |
3.39e-01 |
0.27500 |
0.169000 |
-0.217000 |
2.14e-01 |
0.111000 |
CLEC7A (Dectin-1) induces NFAT activation |
10 |
3.21e-01 |
5.66e-01 |
0.27500 |
0.002460 |
0.275000 |
9.89e-01 |
0.132000 |
Meiotic synapsis |
24 |
6.65e-02 |
2.22e-01 |
0.27500 |
0.273000 |
-0.026900 |
2.05e-02 |
0.820000 |
Zinc transporters |
10 |
3.23e-01 |
5.68e-01 |
0.27400 |
0.243000 |
-0.128000 |
1.84e-01 |
0.482000 |
Synthesis of Leukotrienes (LT) and Eoxins (EX) |
14 |
2.07e-01 |
4.53e-01 |
0.27400 |
0.270000 |
0.051100 |
8.09e-02 |
0.741000 |
PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases |
11 |
2.91e-01 |
5.43e-01 |
0.27400 |
0.155000 |
0.226000 |
3.74e-01 |
0.194000 |
Metabolism of Angiotensinogen to Angiotensins |
12 |
2.59e-01 |
5.11e-01 |
0.27400 |
-0.208000 |
0.178000 |
2.12e-01 |
0.286000 |
Inflammasomes |
18 |
1.33e-01 |
3.46e-01 |
0.27400 |
0.274000 |
0.010300 |
4.46e-02 |
0.939000 |
Fanconi Anemia Pathway |
22 |
8.46e-02 |
2.59e-01 |
0.27400 |
0.107000 |
-0.252000 |
3.84e-01 |
0.041000 |
Signaling by EGFR |
42 |
9.01e-03 |
6.46e-02 |
0.27400 |
-0.170000 |
0.215000 |
5.70e-02 |
0.016200 |
Adenylate cyclase inhibitory pathway |
14 |
2.09e-01 |
4.55e-01 |
0.27300 |
-0.179000 |
0.206000 |
2.46e-01 |
0.182000 |
Synthesis of substrates in N-glycan biosythesis |
48 |
4.88e-03 |
4.41e-02 |
0.27300 |
-0.134000 |
-0.237000 |
1.08e-01 |
0.004480 |
Vpu mediated degradation of CD4 |
40 |
1.18e-02 |
7.44e-02 |
0.27200 |
0.258000 |
-0.087900 |
4.81e-03 |
0.337000 |
Heme biosynthesis |
11 |
2.95e-01 |
5.47e-01 |
0.27200 |
-0.260000 |
-0.082200 |
1.36e-01 |
0.637000 |
Protein ubiquitination |
41 |
1.07e-02 |
7.04e-02 |
0.27200 |
-0.098400 |
0.253000 |
2.76e-01 |
0.005010 |
Chemokine receptors bind chemokines |
28 |
4.64e-02 |
1.74e-01 |
0.27100 |
0.179000 |
0.204000 |
1.02e-01 |
0.062200 |
Gastrin-CREB signalling pathway via PKC and MAPK |
16 |
1.72e-01 |
4.08e-01 |
0.27100 |
-0.097300 |
0.253000 |
5.01e-01 |
0.080200 |
Downstream signaling of activated FGFR1 |
21 |
1.00e-01 |
2.85e-01 |
0.27000 |
-0.120000 |
0.242000 |
3.42e-01 |
0.054700 |
Myogenesis |
21 |
1.00e-01 |
2.85e-01 |
0.27000 |
-0.194000 |
0.189000 |
1.25e-01 |
0.135000 |
Incretin synthesis, secretion, and inactivation |
10 |
3.37e-01 |
5.83e-01 |
0.27000 |
0.053800 |
0.264000 |
7.68e-01 |
0.148000 |
Arachidonic acid metabolism |
34 |
2.55e-02 |
1.23e-01 |
0.26900 |
0.269000 |
-0.002820 |
6.76e-03 |
0.977000 |
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein |
60 |
1.60e-03 |
2.18e-02 |
0.26800 |
-0.169000 |
-0.209000 |
2.40e-02 |
0.005210 |
Activation of BAD and translocation to mitochondria |
14 |
2.23e-01 |
4.72e-01 |
0.26800 |
0.232000 |
0.134000 |
1.33e-01 |
0.384000 |
Presynaptic depolarization and calcium channel opening |
11 |
3.07e-01 |
5.57e-01 |
0.26800 |
-0.267000 |
-0.018500 |
1.25e-01 |
0.915000 |
Defective CFTR causes cystic fibrosis |
43 |
1.02e-02 |
6.84e-02 |
0.26700 |
0.258000 |
-0.067100 |
3.39e-03 |
0.447000 |
Signaling by FGFR2 IIIa TM |
12 |
2.79e-01 |
5.36e-01 |
0.26700 |
-0.245000 |
-0.106000 |
1.42e-01 |
0.526000 |
TRP channels |
12 |
2.81e-01 |
5.38e-01 |
0.26600 |
0.239000 |
-0.116000 |
1.52e-01 |
0.487000 |
Signaling by FGFR |
58 |
2.23e-03 |
2.67e-02 |
0.26500 |
-0.081200 |
0.253000 |
2.86e-01 |
0.000884 |
Beta-catenin phosphorylation cascade |
16 |
1.85e-01 |
4.21e-01 |
0.26500 |
-0.223000 |
0.143000 |
1.23e-01 |
0.321000 |
Chromosome Maintenance |
65 |
1.10e-03 |
1.69e-02 |
0.26500 |
0.264000 |
-0.023400 |
2.37e-04 |
0.745000 |
FCGR3A-mediated phagocytosis |
59 |
2.09e-03 |
2.58e-02 |
0.26500 |
0.264000 |
-0.014500 |
4.53e-04 |
0.847000 |
Leishmania phagocytosis |
59 |
2.09e-03 |
2.58e-02 |
0.26500 |
0.264000 |
-0.014500 |
4.53e-04 |
0.847000 |
Parasite infection |
59 |
2.09e-03 |
2.58e-02 |
0.26500 |
0.264000 |
-0.014500 |
4.53e-04 |
0.847000 |
Cellular response to heat stress |
72 |
5.43e-04 |
1.00e-02 |
0.26500 |
-0.262000 |
0.034300 |
1.21e-04 |
0.615000 |
The NLRP3 inflammasome |
13 |
2.57e-01 |
5.08e-01 |
0.26400 |
0.168000 |
-0.203000 |
2.93e-01 |
0.204000 |
Autodegradation of the E3 ubiquitin ligase COP1 |
40 |
1.54e-02 |
8.62e-02 |
0.26400 |
0.244000 |
-0.101000 |
7.63e-03 |
0.271000 |
FBXL7 down-regulates AURKA during mitotic entry and in early mitosis |
43 |
1.15e-02 |
7.44e-02 |
0.26300 |
0.254000 |
-0.071000 |
4.03e-03 |
0.421000 |
Stabilization of p53 |
43 |
1.16e-02 |
7.44e-02 |
0.26300 |
0.234000 |
-0.120000 |
7.95e-03 |
0.173000 |
Synaptic adhesion-like molecules |
17 |
1.73e-01 |
4.09e-01 |
0.26300 |
-0.172000 |
-0.199000 |
2.21e-01 |
0.155000 |
Downregulation of TGF-beta receptor signaling |
19 |
1.41e-01 |
3.58e-01 |
0.26200 |
-0.222000 |
0.139000 |
9.39e-02 |
0.294000 |
Hh mutants that don't undergo autocatalytic processing are degraded by ERAD |
41 |
1.51e-02 |
8.49e-02 |
0.26100 |
0.240000 |
-0.103000 |
7.83e-03 |
0.253000 |
Mitophagy |
19 |
1.44e-01 |
3.62e-01 |
0.26100 |
-0.155000 |
-0.210000 |
2.42e-01 |
0.113000 |
The role of Nef in HIV-1 replication and disease pathogenesis |
25 |
7.77e-02 |
2.43e-01 |
0.26100 |
0.258000 |
-0.042900 |
2.58e-02 |
0.710000 |
MAP kinase activation |
56 |
3.40e-03 |
3.50e-02 |
0.26000 |
-0.202000 |
0.164000 |
8.89e-03 |
0.033900 |
FGFR2 alternative splicing |
18 |
1.61e-01 |
3.86e-01 |
0.26000 |
-0.019300 |
0.260000 |
8.87e-01 |
0.056500 |
Nicotinamide salvaging |
12 |
2.98e-01 |
5.48e-01 |
0.26000 |
0.246000 |
0.082400 |
1.40e-01 |
0.621000 |
SCF-beta-TrCP mediated degradation of Emi1 |
43 |
1.31e-02 |
7.84e-02 |
0.26000 |
0.251000 |
-0.067500 |
4.48e-03 |
0.444000 |
Cyclin D associated events in G1 |
38 |
2.20e-02 |
1.11e-01 |
0.26000 |
0.197000 |
0.169000 |
3.54e-02 |
0.072500 |
G1 Phase |
38 |
2.20e-02 |
1.11e-01 |
0.26000 |
0.197000 |
0.169000 |
3.54e-02 |
0.072500 |
Metalloprotease DUBs |
16 |
2.00e-01 |
4.46e-01 |
0.25900 |
0.148000 |
0.213000 |
3.06e-01 |
0.140000 |
Receptor-type tyrosine-protein phosphatases |
13 |
2.72e-01 |
5.28e-01 |
0.25800 |
-0.136000 |
0.220000 |
3.97e-01 |
0.170000 |
MicroRNA (miRNA) biogenesis |
15 |
2.24e-01 |
4.72e-01 |
0.25800 |
-0.209000 |
-0.152000 |
1.61e-01 |
0.308000 |
Regulation of RUNX3 expression and activity |
42 |
1.51e-02 |
8.49e-02 |
0.25800 |
0.214000 |
-0.144000 |
1.63e-02 |
0.107000 |
Aquaporin-mediated transport |
33 |
3.74e-02 |
1.49e-01 |
0.25800 |
-0.256000 |
-0.031400 |
1.09e-02 |
0.755000 |
Glutathione synthesis and recycling |
10 |
3.69e-01 |
6.15e-01 |
0.25800 |
-0.028400 |
-0.256000 |
8.76e-01 |
0.160000 |
Amino acid transport across the plasma membrane |
22 |
1.15e-01 |
3.13e-01 |
0.25600 |
-0.107000 |
-0.233000 |
3.85e-01 |
0.058800 |
Infection with Mycobacterium tuberculosis |
21 |
1.28e-01 |
3.38e-01 |
0.25600 |
0.147000 |
0.209000 |
2.43e-01 |
0.096800 |
Signaling by TGFB family members |
76 |
6.00e-04 |
1.09e-02 |
0.25600 |
-0.194000 |
0.166000 |
3.46e-03 |
0.012400 |
MAP3K8 (TPL2)-dependent MAPK1/3 activation |
12 |
3.09e-01 |
5.58e-01 |
0.25500 |
-0.123000 |
0.224000 |
4.62e-01 |
0.179000 |
Hh mutants abrogate ligand secretion |
43 |
1.52e-02 |
8.53e-02 |
0.25500 |
0.229000 |
-0.111000 |
9.30e-03 |
0.207000 |
SHC-mediated cascade:FGFR3 |
12 |
3.12e-01 |
5.61e-01 |
0.25400 |
-0.152000 |
0.203000 |
3.61e-01 |
0.222000 |
Regulation of HSF1-mediated heat shock response |
56 |
4.59e-03 |
4.39e-02 |
0.25400 |
-0.218000 |
0.129000 |
4.80e-03 |
0.094400 |
G-protein mediated events |
48 |
9.88e-03 |
6.69e-02 |
0.25400 |
-0.214000 |
0.136000 |
1.05e-02 |
0.102000 |
Erythropoietin activates Phosphoinositide-3-kinase (PI3K) |
10 |
3.82e-01 |
6.29e-01 |
0.25300 |
0.244000 |
0.068700 |
1.82e-01 |
0.707000 |
DAG and IP3 signaling |
37 |
2.85e-02 |
1.34e-01 |
0.25300 |
-0.229000 |
0.107000 |
1.58e-02 |
0.259000 |
IKK complex recruitment mediated by RIP1 |
15 |
2.36e-01 |
4.87e-01 |
0.25300 |
-0.019600 |
0.253000 |
8.96e-01 |
0.090400 |
Other semaphorin interactions |
18 |
1.78e-01 |
4.17e-01 |
0.25300 |
0.147000 |
0.206000 |
2.81e-01 |
0.130000 |
Synthesis of Prostaglandins (PG) and Thromboxanes (TX) |
10 |
3.84e-01 |
6.31e-01 |
0.25200 |
0.168000 |
-0.188000 |
3.58e-01 |
0.303000 |
Olfactory Signaling Pathway |
13 |
2.90e-01 |
5.42e-01 |
0.25200 |
-0.035100 |
0.250000 |
8.27e-01 |
0.119000 |
RET signaling |
33 |
4.47e-02 |
1.69e-01 |
0.25100 |
-0.244000 |
-0.059000 |
1.53e-02 |
0.558000 |
Switching of origins to a post-replicative state |
72 |
1.16e-03 |
1.73e-02 |
0.25100 |
0.250000 |
-0.021300 |
2.48e-04 |
0.755000 |
SUMOylation of DNA methylation proteins |
15 |
2.45e-01 |
4.96e-01 |
0.25000 |
-0.128000 |
-0.215000 |
3.91e-01 |
0.149000 |
Dual Incision in GG-NER |
33 |
4.64e-02 |
1.74e-01 |
0.24900 |
0.166000 |
-0.185000 |
9.83e-02 |
0.065400 |
VLDLR internalisation and degradation |
11 |
3.61e-01 |
6.07e-01 |
0.24800 |
0.178000 |
-0.174000 |
3.07e-01 |
0.319000 |
PERK regulates gene expression |
25 |
9.97e-02 |
2.85e-01 |
0.24800 |
0.190000 |
0.161000 |
1.01e-01 |
0.165000 |
G1/S DNA Damage Checkpoints |
53 |
7.63e-03 |
5.67e-02 |
0.24800 |
0.238000 |
-0.068800 |
2.71e-03 |
0.387000 |
RUNX1 regulates transcription of genes involved in differentiation of HSCs |
56 |
5.88e-03 |
4.73e-02 |
0.24800 |
0.233000 |
-0.083000 |
2.54e-03 |
0.283000 |
Glycogen metabolism |
21 |
1.46e-01 |
3.63e-01 |
0.24700 |
-0.240000 |
-0.058700 |
5.66e-02 |
0.641000 |
Cardiac conduction |
97 |
1.50e-04 |
3.63e-03 |
0.24700 |
-0.243000 |
0.042200 |
3.59e-05 |
0.473000 |
HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) |
77 |
9.71e-04 |
1.64e-02 |
0.24600 |
0.227000 |
-0.094200 |
5.86e-04 |
0.154000 |
Mitochondrial calcium ion transport |
16 |
2.38e-01 |
4.88e-01 |
0.24500 |
-0.185000 |
-0.161000 |
2.01e-01 |
0.266000 |
Insulin processing |
19 |
1.83e-01 |
4.21e-01 |
0.24400 |
-0.219000 |
0.109000 |
9.91e-02 |
0.413000 |
Activation of NMDA receptors and postsynaptic events |
63 |
3.66e-03 |
3.71e-02 |
0.24400 |
-0.149000 |
0.193000 |
4.06e-02 |
0.008130 |
Transport of vitamins, nucleosides, and related molecules |
26 |
9.85e-02 |
2.85e-01 |
0.24400 |
0.193000 |
-0.150000 |
8.93e-02 |
0.187000 |
Role of LAT2/NTAL/LAB on calcium mobilization |
14 |
2.88e-01 |
5.41e-01 |
0.24400 |
0.117000 |
0.214000 |
4.48e-01 |
0.166000 |
Interleukin-17 signaling |
60 |
4.91e-03 |
4.41e-02 |
0.24300 |
-0.197000 |
0.143000 |
8.39e-03 |
0.055600 |
p53-Dependent G1 DNA Damage Response |
51 |
1.11e-02 |
7.21e-02 |
0.24300 |
0.226000 |
-0.089900 |
5.34e-03 |
0.267000 |
p53-Dependent G1/S DNA damage checkpoint |
51 |
1.11e-02 |
7.21e-02 |
0.24300 |
0.226000 |
-0.089900 |
5.34e-03 |
0.267000 |
Synthesis of PIPs at the late endosome membrane |
10 |
4.16e-01 |
6.60e-01 |
0.24200 |
0.002480 |
0.242000 |
9.89e-01 |
0.185000 |
Mitochondrial tRNA aminoacylation |
15 |
2.70e-01 |
5.27e-01 |
0.24200 |
-0.226000 |
-0.085000 |
1.30e-01 |
0.569000 |
Regulation of Apoptosis |
40 |
3.06e-02 |
1.36e-01 |
0.24100 |
0.228000 |
-0.079300 |
1.27e-02 |
0.386000 |
N-glycan trimming in the ER and Calnexin/Calreticulin cycle |
24 |
1.24e-01 |
3.29e-01 |
0.24100 |
-0.234000 |
-0.057900 |
4.72e-02 |
0.624000 |
Erythropoietin activates RAS |
12 |
3.55e-01 |
6.01e-01 |
0.24000 |
0.057300 |
0.233000 |
7.31e-01 |
0.162000 |
RHO GTPases activate PAKs |
21 |
1.63e-01 |
3.91e-01 |
0.24000 |
0.239000 |
-0.022000 |
5.81e-02 |
0.862000 |
Influenza Viral RNA Transcription and Replication |
69 |
2.82e-03 |
3.08e-02 |
0.23900 |
0.235000 |
0.042200 |
7.40e-04 |
0.545000 |
MAPK targets/ Nuclear events mediated by MAP kinases |
30 |
7.71e-02 |
2.42e-01 |
0.23900 |
-0.152000 |
0.184000 |
1.51e-01 |
0.080600 |
Macroautophagy |
91 |
4.72e-04 |
9.13e-03 |
0.23800 |
-0.208000 |
-0.116000 |
6.35e-04 |
0.055400 |
Assembly and cell surface presentation of NMDA receptors |
17 |
2.37e-01 |
4.87e-01 |
0.23800 |
-0.116000 |
0.207000 |
4.07e-01 |
0.139000 |
Regulation of RAS by GAPs |
54 |
1.06e-02 |
7.01e-02 |
0.23800 |
0.236000 |
0.029900 |
2.76e-03 |
0.704000 |
Pyruvate metabolism and Citric Acid (TCA) cycle |
42 |
2.89e-02 |
1.34e-01 |
0.23800 |
-0.231000 |
0.054300 |
9.57e-03 |
0.543000 |
Processing of SMDT1 |
11 |
3.95e-01 |
6.40e-01 |
0.23700 |
-0.123000 |
-0.203000 |
4.82e-01 |
0.243000 |
Free fatty acids regulate insulin secretion |
10 |
4.32e-01 |
6.75e-01 |
0.23700 |
-0.237000 |
-0.001830 |
1.95e-01 |
0.992000 |
RNA Polymerase II Transcription Termination |
49 |
1.69e-02 |
9.12e-02 |
0.23600 |
0.167000 |
0.168000 |
4.35e-02 |
0.042700 |
TCR signaling |
89 |
6.15e-04 |
1.10e-02 |
0.23600 |
0.234000 |
0.032800 |
1.39e-04 |
0.594000 |
Transcriptional Regulation by MECP2 |
43 |
2.93e-02 |
1.35e-01 |
0.23400 |
-0.160000 |
0.171000 |
6.95e-02 |
0.052700 |
Post NMDA receptor activation events |
54 |
1.22e-02 |
7.58e-02 |
0.23300 |
-0.196000 |
0.127000 |
1.30e-02 |
0.106000 |
Adenylate cyclase activating pathway |
10 |
4.43e-01 |
6.83e-01 |
0.23300 |
-0.231000 |
0.031100 |
2.06e-01 |
0.865000 |
Depolymerisation of the Nuclear Lamina |
14 |
3.20e-01 |
5.66e-01 |
0.23300 |
0.171000 |
-0.158000 |
2.67e-01 |
0.306000 |
rRNA processing in the nucleus and cytosol |
118 |
7.45e-05 |
1.95e-03 |
0.23300 |
0.230000 |
-0.036800 |
1.68e-05 |
0.491000 |
E3 ubiquitin ligases ubiquitinate target proteins |
25 |
1.32e-01 |
3.46e-01 |
0.23200 |
-0.041500 |
0.229000 |
7.20e-01 |
0.047900 |
Respiratory electron transport |
69 |
3.95e-03 |
3.90e-02 |
0.23200 |
0.206000 |
0.106000 |
3.08e-03 |
0.127000 |
Interleukin-15 signaling |
13 |
3.52e-01 |
6.01e-01 |
0.23200 |
-0.228000 |
-0.042000 |
1.55e-01 |
0.793000 |
Reproduction |
52 |
1.59e-02 |
8.67e-02 |
0.23100 |
0.213000 |
-0.088300 |
7.86e-03 |
0.271000 |
TAK1 activates NFkB by phosphorylation and activation of IKKs complex |
22 |
1.74e-01 |
4.09e-01 |
0.23000 |
-0.225000 |
0.048600 |
6.77e-02 |
0.693000 |
YAP1- and WWTR1 (TAZ)-stimulated gene expression |
14 |
3.29e-01 |
5.75e-01 |
0.23000 |
-0.198000 |
0.118000 |
2.00e-01 |
0.446000 |
SUMOylation of transcription factors |
14 |
3.30e-01 |
5.75e-01 |
0.23000 |
0.016900 |
-0.229000 |
9.13e-01 |
0.137000 |
Diseases of programmed cell death |
18 |
2.40e-01 |
4.90e-01 |
0.23000 |
0.126000 |
-0.192000 |
3.56e-01 |
0.158000 |
Regulation of ornithine decarboxylase (ODC) |
42 |
3.62e-02 |
1.47e-01 |
0.23000 |
0.216000 |
-0.077000 |
1.53e-02 |
0.388000 |
Striated Muscle Contraction |
29 |
1.01e-01 |
2.87e-01 |
0.23000 |
0.191000 |
-0.128000 |
7.54e-02 |
0.234000 |
Vasopressin regulates renal water homeostasis via Aquaporins |
30 |
9.57e-02 |
2.80e-01 |
0.22900 |
-0.228000 |
0.015600 |
3.07e-02 |
0.883000 |
Autophagy |
102 |
3.70e-04 |
7.62e-03 |
0.22800 |
-0.201000 |
-0.108000 |
4.56e-04 |
0.059900 |
Integration of energy metabolism |
85 |
1.37e-03 |
1.96e-02 |
0.22800 |
-0.208000 |
-0.094600 |
9.45e-04 |
0.132000 |
Glutamate binding, activation of AMPA receptors and synaptic plasticity |
25 |
1.43e-01 |
3.62e-01 |
0.22800 |
-0.160000 |
-0.163000 |
1.68e-01 |
0.159000 |
Trafficking of AMPA receptors |
25 |
1.43e-01 |
3.62e-01 |
0.22800 |
-0.160000 |
-0.163000 |
1.68e-01 |
0.159000 |
Fcgamma receptor (FCGR) dependent phagocytosis |
84 |
1.50e-03 |
2.11e-02 |
0.22800 |
0.215000 |
-0.075700 |
6.75e-04 |
0.231000 |
Regulation of glycolysis by fructose 2,6-bisphosphate metabolism |
11 |
4.25e-01 |
6.68e-01 |
0.22800 |
-0.228000 |
-0.004710 |
1.91e-01 |
0.978000 |
Elevation of cytosolic Ca2+ levels |
10 |
4.60e-01 |
6.92e-01 |
0.22800 |
-0.032600 |
-0.225000 |
8.58e-01 |
0.217000 |
Keratinization |
21 |
1.96e-01 |
4.40e-01 |
0.22800 |
-0.044100 |
-0.223000 |
7.26e-01 |
0.076600 |
rRNA processing |
125 |
6.73e-05 |
1.84e-03 |
0.22700 |
0.225000 |
-0.036000 |
1.51e-05 |
0.488000 |
COPI-independent Golgi-to-ER retrograde traffic |
30 |
9.79e-02 |
2.84e-01 |
0.22700 |
-0.213000 |
0.080900 |
4.40e-02 |
0.444000 |
Phase II - Conjugation of compounds |
64 |
7.32e-03 |
5.60e-02 |
0.22700 |
0.179000 |
0.140000 |
1.35e-02 |
0.052600 |
Nucleotide salvage |
18 |
2.48e-01 |
5.01e-01 |
0.22700 |
0.211000 |
-0.084900 |
1.22e-01 |
0.533000 |
Processing of Capped Intronless Pre-mRNA |
19 |
2.31e-01 |
4.78e-01 |
0.22700 |
0.038300 |
0.224000 |
7.73e-01 |
0.091300 |
Cellular hexose transport |
11 |
4.28e-01 |
6.70e-01 |
0.22700 |
-0.068600 |
-0.216000 |
6.93e-01 |
0.214000 |
Signal regulatory protein family interactions |
13 |
3.67e-01 |
6.13e-01 |
0.22700 |
0.014600 |
0.226000 |
9.27e-01 |
0.158000 |
Signaling by FGFR1 in disease |
30 |
9.88e-02 |
2.85e-01 |
0.22700 |
-0.186000 |
0.130000 |
7.78e-02 |
0.219000 |
NGF-stimulated transcription |
33 |
7.91e-02 |
2.46e-01 |
0.22700 |
-0.225000 |
-0.031400 |
2.57e-02 |
0.755000 |
KSRP (KHSRP) binds and destabilizes mRNA |
15 |
3.15e-01 |
5.64e-01 |
0.22600 |
0.208000 |
-0.088600 |
1.62e-01 |
0.552000 |
ABC transporters in lipid homeostasis |
12 |
3.99e-01 |
6.43e-01 |
0.22600 |
-0.224000 |
-0.033600 |
1.80e-01 |
0.840000 |
APC/C:Cdc20 mediated degradation of mitotic proteins |
61 |
9.61e-03 |
6.63e-02 |
0.22600 |
0.209000 |
-0.084100 |
4.70e-03 |
0.256000 |
Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins |
61 |
9.61e-03 |
6.63e-02 |
0.22600 |
0.209000 |
-0.084100 |
4.70e-03 |
0.256000 |
Degradation of DVL |
44 |
3.53e-02 |
1.46e-01 |
0.22500 |
0.204000 |
-0.096200 |
1.95e-02 |
0.270000 |
TBC/RABGAPs |
35 |
7.12e-02 |
2.31e-01 |
0.22500 |
-0.203000 |
-0.097100 |
3.80e-02 |
0.321000 |
HDR through Homologous Recombination (HRR) |
50 |
2.30e-02 |
1.14e-01 |
0.22500 |
0.210000 |
-0.078700 |
1.01e-02 |
0.336000 |
Repression of WNT target genes |
11 |
4.36e-01 |
6.77e-01 |
0.22400 |
0.033500 |
-0.222000 |
8.47e-01 |
0.202000 |
Peptide hormone metabolism |
50 |
2.33e-02 |
1.15e-01 |
0.22400 |
-0.137000 |
0.177000 |
9.33e-02 |
0.030300 |
Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. |
74 |
4.04e-03 |
3.95e-02 |
0.22400 |
0.201000 |
0.098100 |
2.82e-03 |
0.145000 |
VxPx cargo-targeting to cilium |
17 |
2.80e-01 |
5.36e-01 |
0.22400 |
-0.192000 |
0.115000 |
1.71e-01 |
0.413000 |
WNT ligand biogenesis and trafficking |
11 |
4.39e-01 |
6.78e-01 |
0.22300 |
-0.090300 |
0.204000 |
6.04e-01 |
0.241000 |
RHO GTPases activate CIT |
18 |
2.60e-01 |
5.13e-01 |
0.22300 |
0.166000 |
-0.149000 |
2.23e-01 |
0.273000 |
MyD88 cascade initiated on plasma membrane |
70 |
5.52e-03 |
4.56e-02 |
0.22300 |
-0.200000 |
0.098900 |
3.88e-03 |
0.153000 |
Toll Like Receptor 10 (TLR10) Cascade |
70 |
5.52e-03 |
4.56e-02 |
0.22300 |
-0.200000 |
0.098900 |
3.88e-03 |
0.153000 |
Toll Like Receptor 5 (TLR5) Cascade |
70 |
5.52e-03 |
4.56e-02 |
0.22300 |
-0.200000 |
0.098900 |
3.88e-03 |
0.153000 |
Major pathway of rRNA processing in the nucleolus and cytosol |
111 |
2.72e-04 |
5.80e-03 |
0.22300 |
0.218000 |
-0.045300 |
7.32e-05 |
0.410000 |
Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models |
17 |
2.83e-01 |
5.39e-01 |
0.22300 |
0.107000 |
-0.195000 |
4.46e-01 |
0.163000 |
Neurodegenerative Diseases |
17 |
2.83e-01 |
5.39e-01 |
0.22300 |
0.107000 |
-0.195000 |
4.46e-01 |
0.163000 |
RUNX2 regulates bone development |
27 |
1.36e-01 |
3.51e-01 |
0.22200 |
-0.080400 |
0.207000 |
4.70e-01 |
0.062800 |
APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint |
59 |
1.30e-02 |
7.84e-02 |
0.22200 |
0.209000 |
-0.073800 |
5.48e-03 |
0.327000 |
Purine salvage |
10 |
4.79e-01 |
7.04e-01 |
0.22200 |
0.221000 |
-0.013700 |
2.26e-01 |
0.940000 |
Interleukin-12 family signaling |
36 |
7.17e-02 |
2.31e-01 |
0.22100 |
0.221000 |
0.006180 |
2.17e-02 |
0.949000 |
Early Phase of HIV Life Cycle |
10 |
4.81e-01 |
7.04e-01 |
0.22100 |
0.221000 |
-0.011800 |
2.27e-01 |
0.949000 |
Synthesis of PC |
21 |
2.16e-01 |
4.65e-01 |
0.22100 |
-0.218000 |
0.035400 |
8.39e-02 |
0.779000 |
Constitutive Signaling by AKT1 E17K in Cancer |
24 |
1.74e-01 |
4.09e-01 |
0.22100 |
-0.215000 |
-0.050500 |
6.85e-02 |
0.669000 |
Signaling by ROBO receptors |
132 |
7.70e-05 |
1.97e-03 |
0.22000 |
0.201000 |
0.090600 |
7.22e-05 |
0.073000 |
MTOR signalling |
35 |
7.97e-02 |
2.46e-01 |
0.22000 |
-0.219000 |
0.014000 |
2.48e-02 |
0.886000 |
Apoptotic factor-mediated response |
12 |
4.22e-01 |
6.67e-01 |
0.21900 |
0.091500 |
-0.199000 |
5.83e-01 |
0.233000 |
Detoxification of Reactive Oxygen Species |
26 |
1.56e-01 |
3.79e-01 |
0.21900 |
0.212000 |
0.054800 |
6.19e-02 |
0.629000 |
Regulation of actin dynamics for phagocytic cup formation |
61 |
1.31e-02 |
7.84e-02 |
0.21800 |
0.212000 |
-0.052700 |
4.29e-03 |
0.477000 |
Formation of the cornified envelope |
17 |
2.99e-01 |
5.48e-01 |
0.21800 |
-0.150000 |
-0.159000 |
2.86e-01 |
0.257000 |
Phase 0 - rapid depolarisation |
30 |
1.19e-01 |
3.20e-01 |
0.21800 |
-0.216000 |
-0.031000 |
4.09e-02 |
0.769000 |
Antigen activates B Cell Receptor (BCR) leading to generation of second messengers |
31 |
1.11e-01 |
3.03e-01 |
0.21800 |
0.215000 |
0.033600 |
3.83e-02 |
0.747000 |
mRNA 3'-end processing |
42 |
5.13e-02 |
1.82e-01 |
0.21800 |
0.163000 |
0.145000 |
6.85e-02 |
0.105000 |
Sema4D induced cell migration and growth-cone collapse |
19 |
2.61e-01 |
5.13e-01 |
0.21700 |
0.008810 |
-0.217000 |
9.47e-01 |
0.101000 |
Assembly Of The HIV Virion |
10 |
4.97e-01 |
7.14e-01 |
0.21600 |
-0.168000 |
-0.136000 |
3.58e-01 |
0.457000 |
Activation of Matrix Metalloproteinases |
17 |
3.05e-01 |
5.56e-01 |
0.21600 |
-0.214000 |
-0.028600 |
1.27e-01 |
0.838000 |
Response of Mtb to phagocytosis |
18 |
2.85e-01 |
5.41e-01 |
0.21600 |
0.094000 |
0.194000 |
4.90e-01 |
0.154000 |
COPII-mediated vesicle transport |
52 |
2.78e-02 |
1.32e-01 |
0.21500 |
-0.214000 |
0.017900 |
7.64e-03 |
0.824000 |
Pausing and recovery of Tat-mediated HIV elongation |
20 |
2.52e-01 |
5.03e-01 |
0.21500 |
0.048200 |
-0.209000 |
7.09e-01 |
0.106000 |
Tat-mediated HIV elongation arrest and recovery |
20 |
2.52e-01 |
5.03e-01 |
0.21500 |
0.048200 |
-0.209000 |
7.09e-01 |
0.106000 |
Integrin cell surface interactions |
51 |
3.01e-02 |
1.36e-01 |
0.21400 |
0.159000 |
-0.144000 |
4.97e-02 |
0.076400 |
Interleukin receptor SHC signaling |
20 |
2.53e-01 |
5.04e-01 |
0.21400 |
0.115000 |
-0.181000 |
3.75e-01 |
0.162000 |
BBSome-mediated cargo-targeting to cilium |
17 |
3.12e-01 |
5.60e-01 |
0.21400 |
-0.122000 |
0.176000 |
3.84e-01 |
0.210000 |
Processing of DNA double-strand break ends |
50 |
3.30e-02 |
1.42e-01 |
0.21400 |
0.214000 |
0.002290 |
9.01e-03 |
0.978000 |
Glucose metabolism |
69 |
9.27e-03 |
6.50e-02 |
0.21300 |
-0.191000 |
-0.095100 |
6.12e-03 |
0.172000 |
Cdc20:Phospho-APC/C mediated degradation of Cyclin A |
58 |
1.98e-02 |
1.04e-01 |
0.21300 |
0.199000 |
-0.074400 |
8.73e-03 |
0.328000 |
Constitutive Signaling by NOTCH1 HD Domain Mutants |
10 |
5.09e-01 |
7.19e-01 |
0.21200 |
0.202000 |
-0.066300 |
2.70e-01 |
0.717000 |
Signaling by NOTCH1 HD Domain Mutants in Cancer |
10 |
5.09e-01 |
7.19e-01 |
0.21200 |
0.202000 |
-0.066300 |
2.70e-01 |
0.717000 |
Transferrin endocytosis and recycling |
22 |
2.26e-01 |
4.75e-01 |
0.21200 |
-0.186000 |
0.102000 |
1.31e-01 |
0.408000 |
Defects in vitamin and cofactor metabolism |
14 |
3.90e-01 |
6.38e-01 |
0.21200 |
-0.208000 |
0.039800 |
1.78e-01 |
0.797000 |
mRNA decay by 3' to 5' exoribonuclease |
12 |
4.47e-01 |
6.84e-01 |
0.21200 |
0.211000 |
-0.015300 |
2.06e-01 |
0.927000 |
Interleukin-20 family signaling |
15 |
3.70e-01 |
6.15e-01 |
0.21000 |
-0.000251 |
-0.210000 |
9.99e-01 |
0.158000 |
Autodegradation of Cdh1 by Cdh1:APC/C |
50 |
3.65e-02 |
1.47e-01 |
0.21000 |
0.170000 |
-0.125000 |
3.83e-02 |
0.128000 |
Plasma lipoprotein clearance |
25 |
1.92e-01 |
4.33e-01 |
0.21000 |
0.138000 |
-0.158000 |
2.34e-01 |
0.171000 |
TNFR1-induced proapoptotic signaling |
13 |
4.25e-01 |
6.68e-01 |
0.21000 |
0.201000 |
-0.060300 |
2.10e-01 |
0.707000 |
Degradation of AXIN |
42 |
6.39e-02 |
2.15e-01 |
0.20900 |
0.192000 |
-0.082300 |
3.12e-02 |
0.356000 |
APC/C-mediated degradation of cell cycle proteins |
72 |
9.25e-03 |
6.50e-02 |
0.20900 |
0.201000 |
-0.057100 |
3.26e-03 |
0.402000 |
Regulation of mitotic cell cycle |
72 |
9.25e-03 |
6.50e-02 |
0.20900 |
0.201000 |
-0.057100 |
3.26e-03 |
0.402000 |
RHO GTPases Activate WASPs and WAVEs |
34 |
1.10e-01 |
3.01e-01 |
0.20800 |
0.206000 |
0.031700 |
3.77e-02 |
0.749000 |
G2/M DNA damage checkpoint |
51 |
3.69e-02 |
1.48e-01 |
0.20800 |
0.207000 |
0.019300 |
1.05e-02 |
0.812000 |
Phase 2 - plateau phase |
16 |
3.55e-01 |
6.01e-01 |
0.20800 |
-0.206000 |
-0.026000 |
1.53e-01 |
0.857000 |
CDK-mediated phosphorylation and removal of Cdc6 |
58 |
2.43e-02 |
1.18e-01 |
0.20700 |
0.190000 |
-0.081200 |
1.22e-02 |
0.286000 |
FCERI mediated MAPK activation |
28 |
1.66e-01 |
3.96e-01 |
0.20700 |
0.021200 |
0.206000 |
8.46e-01 |
0.059500 |
RMTs methylate histone arginines |
29 |
1.57e-01 |
3.81e-01 |
0.20700 |
-0.080000 |
-0.191000 |
4.56e-01 |
0.075800 |
Surfactant metabolism |
12 |
4.65e-01 |
6.92e-01 |
0.20700 |
-0.088200 |
-0.187000 |
5.97e-01 |
0.262000 |
E2F mediated regulation of DNA replication |
18 |
3.17e-01 |
5.66e-01 |
0.20700 |
0.189000 |
0.083800 |
1.66e-01 |
0.538000 |
Regulation of TP53 Activity through Acetylation |
27 |
1.78e-01 |
4.17e-01 |
0.20700 |
0.020700 |
-0.206000 |
8.53e-01 |
0.064700 |
HSP90 chaperone cycle for steroid hormone receptors (SHR) |
31 |
1.38e-01 |
3.53e-01 |
0.20600 |
-0.199000 |
0.054300 |
5.51e-02 |
0.601000 |
Influenza Infection |
83 |
5.30e-03 |
4.47e-02 |
0.20600 |
0.188000 |
0.083300 |
3.04e-03 |
0.190000 |
UCH proteinases |
68 |
1.34e-02 |
7.84e-02 |
0.20600 |
0.194000 |
-0.069400 |
5.74e-03 |
0.323000 |
Homology Directed Repair |
81 |
5.98e-03 |
4.79e-02 |
0.20600 |
0.193000 |
-0.072300 |
2.76e-03 |
0.261000 |
RAS processing |
17 |
3.40e-01 |
5.88e-01 |
0.20600 |
0.017100 |
0.205000 |
9.03e-01 |
0.143000 |
TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation |
77 |
7.72e-03 |
5.70e-02 |
0.20600 |
-0.165000 |
0.122000 |
1.23e-02 |
0.063800 |
AUF1 (hnRNP D0) binds and destabilizes mRNA |
42 |
7.08e-02 |
2.31e-01 |
0.20500 |
0.195000 |
-0.065600 |
2.93e-02 |
0.463000 |
DCC mediated attractive signaling |
13 |
4.43e-01 |
6.83e-01 |
0.20500 |
0.171000 |
0.113000 |
2.87e-01 |
0.480000 |
Netrin-1 signaling |
41 |
7.65e-02 |
2.41e-01 |
0.20500 |
-0.109000 |
0.173000 |
2.29e-01 |
0.054900 |
Regulation of APC/C activators between G1/S and early anaphase |
65 |
1.75e-02 |
9.38e-02 |
0.20400 |
0.199000 |
-0.046500 |
5.62e-03 |
0.517000 |
ABC transporter disorders |
52 |
3.91e-02 |
1.52e-01 |
0.20400 |
0.190000 |
-0.073700 |
1.76e-02 |
0.359000 |
Synthesis of PIPs at the early endosome membrane |
15 |
3.93e-01 |
6.40e-01 |
0.20400 |
0.003750 |
0.204000 |
9.80e-01 |
0.172000 |
Insertion of tail-anchored proteins into the endoplasmic reticulum membrane |
15 |
3.94e-01 |
6.40e-01 |
0.20300 |
0.197000 |
-0.050400 |
1.87e-01 |
0.735000 |
Trafficking of GluR2-containing AMPA receptors |
14 |
4.22e-01 |
6.67e-01 |
0.20300 |
0.036700 |
-0.199000 |
8.12e-01 |
0.197000 |
Regulation of TP53 Activity through Methylation |
11 |
5.09e-01 |
7.19e-01 |
0.20300 |
-0.093800 |
-0.180000 |
5.90e-01 |
0.302000 |
Budding and maturation of HIV virion |
19 |
3.11e-01 |
5.60e-01 |
0.20300 |
-0.202000 |
-0.017500 |
1.28e-01 |
0.895000 |
Signaling by NOTCH4 |
65 |
1.91e-02 |
1.01e-01 |
0.20200 |
0.199000 |
-0.033800 |
5.54e-03 |
0.637000 |
tRNA Aminoacylation |
20 |
2.97e-01 |
5.48e-01 |
0.20100 |
-0.196000 |
-0.047400 |
1.30e-01 |
0.714000 |
Aggrephagy |
14 |
4.28e-01 |
6.70e-01 |
0.20100 |
-0.024800 |
-0.200000 |
8.72e-01 |
0.196000 |
Translesion Synthesis by POLH |
11 |
5.14e-01 |
7.21e-01 |
0.20100 |
0.176000 |
-0.096100 |
3.11e-01 |
0.581000 |
Biosynthesis of DHA-derived SPMs |
10 |
5.46e-01 |
7.43e-01 |
0.20100 |
0.179000 |
-0.090300 |
3.26e-01 |
0.621000 |
p130Cas linkage to MAPK signaling for integrins |
12 |
4.84e-01 |
7.07e-01 |
0.20100 |
0.093400 |
-0.178000 |
5.75e-01 |
0.287000 |
GRB2:SOS provides linkage to MAPK signaling for Integrins |
12 |
4.86e-01 |
7.07e-01 |
0.20000 |
0.017900 |
-0.199000 |
9.15e-01 |
0.232000 |
Metal ion SLC transporters |
17 |
3.62e-01 |
6.08e-01 |
0.20000 |
0.163000 |
-0.115000 |
2.44e-01 |
0.412000 |
Asparagine N-linked glycosylation |
218 |
3.05e-06 |
1.50e-04 |
0.19900 |
-0.190000 |
-0.060100 |
1.53e-06 |
0.128000 |
Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha |
49 |
5.56e-02 |
1.93e-01 |
0.19900 |
0.197000 |
-0.025600 |
1.72e-02 |
0.757000 |
FCERI mediated Ca+2 mobilization |
26 |
2.18e-01 |
4.66e-01 |
0.19800 |
0.128000 |
0.151000 |
2.59e-01 |
0.182000 |
Hedgehog ligand biogenesis |
46 |
6.72e-02 |
2.23e-01 |
0.19800 |
0.160000 |
-0.116000 |
6.00e-02 |
0.174000 |
Meiosis |
43 |
8.17e-02 |
2.52e-01 |
0.19700 |
0.194000 |
-0.037800 |
2.81e-02 |
0.668000 |
Regulation of KIT signaling |
16 |
3.94e-01 |
6.40e-01 |
0.19700 |
0.174000 |
0.093700 |
2.30e-01 |
0.517000 |
Mitochondrial Fatty Acid Beta-Oxidation |
27 |
2.10e-01 |
4.55e-01 |
0.19700 |
0.194000 |
-0.030700 |
8.09e-02 |
0.782000 |
Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects |
16 |
3.97e-01 |
6.42e-01 |
0.19600 |
0.189000 |
0.054200 |
1.91e-01 |
0.707000 |
Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) |
16 |
3.97e-01 |
6.42e-01 |
0.19600 |
0.189000 |
0.054200 |
1.91e-01 |
0.707000 |
CS/DS degradation |
10 |
5.61e-01 |
7.54e-01 |
0.19600 |
-0.008150 |
0.196000 |
9.64e-01 |
0.283000 |
RUNX2 regulates osteoblast differentiation |
22 |
2.83e-01 |
5.39e-01 |
0.19600 |
-0.013300 |
0.195000 |
9.14e-01 |
0.113000 |
Sealing of the nuclear envelope (NE) by ESCRT-III |
22 |
2.86e-01 |
5.41e-01 |
0.19500 |
-0.178000 |
-0.080300 |
1.49e-01 |
0.514000 |
Cell surface interactions at the vascular wall |
96 |
4.45e-03 |
4.30e-02 |
0.19500 |
0.194000 |
0.013300 |
1.03e-03 |
0.823000 |
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 |
59 |
3.58e-02 |
1.47e-01 |
0.19400 |
0.163000 |
-0.106000 |
3.08e-02 |
0.159000 |
Circadian Clock |
58 |
3.86e-02 |
1.51e-01 |
0.19400 |
-0.144000 |
0.129000 |
5.80e-02 |
0.088600 |
Triglyceride metabolism |
22 |
2.95e-01 |
5.47e-01 |
0.19300 |
0.063900 |
0.182000 |
6.04e-01 |
0.140000 |
Retrograde transport at the Trans-Golgi-Network |
41 |
1.03e-01 |
2.90e-01 |
0.19300 |
-0.030600 |
0.190000 |
7.35e-01 |
0.035200 |
MyD88 dependent cascade initiated on endosome |
78 |
1.34e-02 |
7.84e-02 |
0.19200 |
-0.150000 |
0.120000 |
2.18e-02 |
0.067500 |
Toll Like Receptor 7/8 (TLR7/8) Cascade |
78 |
1.34e-02 |
7.84e-02 |
0.19200 |
-0.150000 |
0.120000 |
2.18e-02 |
0.067500 |
Hyaluronan uptake and degradation |
10 |
5.78e-01 |
7.57e-01 |
0.19100 |
0.151000 |
-0.117000 |
4.07e-01 |
0.523000 |
NRAGE signals death through JNK |
54 |
5.34e-02 |
1.87e-01 |
0.19100 |
-0.132000 |
-0.138000 |
9.34e-02 |
0.080400 |
Basigin interactions |
20 |
3.36e-01 |
5.83e-01 |
0.19100 |
0.158000 |
-0.107000 |
2.22e-01 |
0.409000 |
Metabolism of amino acids and derivatives |
218 |
8.53e-06 |
2.98e-04 |
0.19000 |
0.137000 |
-0.132000 |
5.03e-04 |
0.000826 |
Cytochrome P450 - arranged by substrate type |
29 |
2.10e-01 |
4.55e-01 |
0.19000 |
0.088800 |
0.168000 |
4.08e-01 |
0.118000 |
SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription |
24 |
2.75e-01 |
5.31e-01 |
0.19000 |
0.156000 |
0.109000 |
1.87e-01 |
0.358000 |
Chondroitin sulfate biosynthesis |
15 |
4.46e-01 |
6.84e-01 |
0.19000 |
0.169000 |
0.086600 |
2.58e-01 |
0.561000 |
Signaling by NTRK2 (TRKB) |
21 |
3.23e-01 |
5.68e-01 |
0.18900 |
-0.102000 |
0.160000 |
4.18e-01 |
0.206000 |
FGFR1 mutant receptor activation |
23 |
2.92e-01 |
5.44e-01 |
0.18900 |
-0.187000 |
0.029700 |
1.21e-01 |
0.805000 |
Formation of Fibrin Clot (Clotting Cascade) |
15 |
4.51e-01 |
6.87e-01 |
0.18900 |
0.167000 |
0.087700 |
2.63e-01 |
0.556000 |
HIV elongation arrest and recovery |
21 |
3.30e-01 |
5.75e-01 |
0.18800 |
0.088000 |
-0.166000 |
4.85e-01 |
0.189000 |
Pausing and recovery of HIV elongation |
21 |
3.30e-01 |
5.75e-01 |
0.18800 |
0.088000 |
-0.166000 |
4.85e-01 |
0.189000 |
Synthesis of bile acids and bile salts |
21 |
3.31e-01 |
5.76e-01 |
0.18800 |
-0.177000 |
-0.063800 |
1.62e-01 |
0.613000 |
Formation of the beta-catenin:TCF transactivating complex |
28 |
2.31e-01 |
4.78e-01 |
0.18700 |
-0.128000 |
-0.137000 |
2.42e-01 |
0.210000 |
Late endosomal microautophagy |
22 |
3.16e-01 |
5.64e-01 |
0.18700 |
-0.178000 |
-0.058700 |
1.49e-01 |
0.634000 |
SHC-mediated cascade:FGFR1 |
12 |
5.32e-01 |
7.37e-01 |
0.18700 |
-0.082800 |
0.168000 |
6.19e-01 |
0.314000 |
PI3K Cascade |
30 |
2.08e-01 |
4.55e-01 |
0.18700 |
-0.185000 |
0.025900 |
7.92e-02 |
0.806000 |
Signaling by FGFR in disease |
45 |
9.56e-02 |
2.80e-01 |
0.18700 |
-0.164000 |
0.088900 |
5.70e-02 |
0.303000 |
TNFR1-induced NFkappaB signaling pathway |
24 |
2.87e-01 |
5.41e-01 |
0.18600 |
0.186000 |
0.015700 |
1.15e-01 |
0.894000 |
Deposition of new CENPA-containing nucleosomes at the centromere |
17 |
4.14e-01 |
6.58e-01 |
0.18600 |
0.158000 |
0.098500 |
2.59e-01 |
0.482000 |
Nucleosome assembly |
17 |
4.14e-01 |
6.58e-01 |
0.18600 |
0.158000 |
0.098500 |
2.59e-01 |
0.482000 |
WNT5A-dependent internalization of FZD2, FZD5 and ROR2 |
13 |
5.10e-01 |
7.19e-01 |
0.18600 |
-0.171000 |
-0.074300 |
2.87e-01 |
0.643000 |
APC/C:Cdc20 mediated degradation of Securin |
54 |
6.11e-02 |
2.07e-01 |
0.18600 |
0.159000 |
-0.096800 |
4.36e-02 |
0.219000 |
TICAM1, RIP1-mediated IKK complex recruitment |
12 |
5.37e-01 |
7.38e-01 |
0.18600 |
-0.015800 |
0.185000 |
9.25e-01 |
0.267000 |
TP53 Regulates Transcription of Cell Cycle Genes |
45 |
9.79e-02 |
2.84e-01 |
0.18600 |
0.174000 |
-0.065100 |
4.36e-02 |
0.450000 |
Reduction of cytosolic Ca++ levels |
10 |
5.96e-01 |
7.71e-01 |
0.18600 |
-0.143000 |
0.118000 |
4.33e-01 |
0.519000 |
Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer |
35 |
1.65e-01 |
3.94e-01 |
0.18500 |
-0.066900 |
0.173000 |
4.94e-01 |
0.077000 |
Kinesins |
34 |
1.74e-01 |
4.09e-01 |
0.18500 |
0.128000 |
-0.134000 |
1.95e-01 |
0.178000 |
TNFR2 non-canonical NF-kB pathway |
64 |
3.77e-02 |
1.49e-01 |
0.18500 |
0.183000 |
-0.030200 |
1.16e-02 |
0.677000 |
Processing of Intronless Pre-mRNAs |
12 |
5.39e-01 |
7.39e-01 |
0.18500 |
-0.051000 |
0.178000 |
7.60e-01 |
0.286000 |
ER to Golgi Anterograde Transport |
109 |
3.88e-03 |
3.90e-02 |
0.18500 |
-0.185000 |
-0.001640 |
8.62e-04 |
0.976000 |
Toll Like Receptor 9 (TLR9) Cascade |
81 |
1.60e-02 |
8.71e-02 |
0.18500 |
-0.144000 |
0.116000 |
2.55e-02 |
0.071000 |
RAF activation |
31 |
2.05e-01 |
4.53e-01 |
0.18500 |
-0.182000 |
0.034200 |
8.02e-02 |
0.742000 |
Synthesis of PIPs at the Golgi membrane |
14 |
4.90e-01 |
7.07e-01 |
0.18400 |
-0.063900 |
0.173000 |
6.79e-01 |
0.262000 |
Sema4D in semaphorin signaling |
22 |
3.27e-01 |
5.74e-01 |
0.18400 |
0.082000 |
-0.165000 |
5.06e-01 |
0.181000 |
PIWI-interacting RNA (piRNA) biogenesis |
11 |
5.74e-01 |
7.57e-01 |
0.18400 |
-0.027300 |
-0.182000 |
8.75e-01 |
0.297000 |
RORA activates gene expression |
17 |
4.24e-01 |
6.68e-01 |
0.18300 |
-0.183000 |
0.006360 |
1.91e-01 |
0.964000 |
Purine catabolism |
16 |
4.47e-01 |
6.84e-01 |
0.18300 |
0.183000 |
0.011900 |
2.05e-01 |
0.934000 |
Gap-filling DNA repair synthesis and ligation in TC-NER |
49 |
8.53e-02 |
2.60e-01 |
0.18300 |
0.183000 |
0.006180 |
2.66e-02 |
0.940000 |
Ras activation upon Ca2+ influx through NMDA receptor |
15 |
4.70e-01 |
6.97e-01 |
0.18300 |
-0.031100 |
0.181000 |
8.35e-01 |
0.226000 |
Negative regulators of DDX58/IFIH1 signaling |
24 |
3.00e-01 |
5.50e-01 |
0.18300 |
0.160000 |
-0.088700 |
1.75e-01 |
0.452000 |
WNT5A-dependent internalization of FZD4 |
14 |
4.96e-01 |
7.14e-01 |
0.18300 |
-0.038100 |
-0.179000 |
8.05e-01 |
0.247000 |
Glucagon-type ligand receptors |
13 |
5.24e-01 |
7.32e-01 |
0.18200 |
0.032400 |
-0.179000 |
8.40e-01 |
0.264000 |
FOXO-mediated transcription of cell cycle genes |
16 |
4.51e-01 |
6.87e-01 |
0.18200 |
-0.156000 |
0.094400 |
2.81e-01 |
0.514000 |
Nicotinate metabolism |
21 |
3.54e-01 |
6.01e-01 |
0.18200 |
0.181000 |
0.018000 |
1.51e-01 |
0.886000 |
Carnitine metabolism |
11 |
5.81e-01 |
7.59e-01 |
0.18200 |
-0.103000 |
-0.150000 |
5.54e-01 |
0.390000 |
Platelet sensitization by LDL |
15 |
4.78e-01 |
7.04e-01 |
0.18200 |
-0.115000 |
-0.140000 |
4.41e-01 |
0.346000 |
Apoptotic cleavage of cellular proteins |
31 |
2.19e-01 |
4.66e-01 |
0.18100 |
-0.115000 |
0.140000 |
2.68e-01 |
0.179000 |
SHC1 events in ERBB2 signaling |
20 |
3.78e-01 |
6.25e-01 |
0.18000 |
-0.098000 |
0.151000 |
4.48e-01 |
0.242000 |
CD28 co-stimulation |
32 |
2.12e-01 |
4.59e-01 |
0.18000 |
0.153000 |
0.094500 |
1.34e-01 |
0.355000 |
Tight junction interactions |
10 |
6.18e-01 |
7.85e-01 |
0.18000 |
-0.116000 |
-0.137000 |
5.24e-01 |
0.454000 |
Glutamate Neurotransmitter Release Cycle |
16 |
4.62e-01 |
6.92e-01 |
0.17900 |
0.016700 |
-0.179000 |
9.08e-01 |
0.216000 |
Signaling by cytosolic FGFR1 fusion mutants |
18 |
4.20e-01 |
6.65e-01 |
0.17900 |
-0.170000 |
0.058300 |
2.13e-01 |
0.669000 |
Antigen Presentation: Folding, assembly and peptide loading of class I MHC |
15 |
4.86e-01 |
7.07e-01 |
0.17900 |
-0.036700 |
0.175000 |
8.06e-01 |
0.240000 |
Complex I biogenesis |
39 |
1.55e-01 |
3.78e-01 |
0.17900 |
0.159000 |
0.082100 |
8.59e-02 |
0.375000 |
Downregulation of ERBB2 signaling |
20 |
3.86e-01 |
6.34e-01 |
0.17800 |
-0.151000 |
0.093500 |
2.41e-01 |
0.469000 |
Signaling by Non-Receptor Tyrosine Kinases |
43 |
1.31e-01 |
3.43e-01 |
0.17800 |
-0.031400 |
0.175000 |
7.22e-01 |
0.047300 |
Signaling by PTK6 |
43 |
1.31e-01 |
3.43e-01 |
0.17800 |
-0.031400 |
0.175000 |
7.22e-01 |
0.047300 |
Glucagon signaling in metabolic regulation |
24 |
3.22e-01 |
5.67e-01 |
0.17800 |
-0.176000 |
0.025500 |
1.36e-01 |
0.829000 |
Assembly of active LPL and LIPC lipase complexes |
11 |
5.94e-01 |
7.70e-01 |
0.17800 |
-0.171000 |
0.049200 |
3.27e-01 |
0.777000 |
tRNA modification in the nucleus and cytosol |
31 |
2.31e-01 |
4.79e-01 |
0.17800 |
0.087000 |
-0.155000 |
4.02e-01 |
0.136000 |
Regulation of beta-cell development |
20 |
3.92e-01 |
6.39e-01 |
0.17700 |
-0.143000 |
0.103000 |
2.68e-01 |
0.424000 |
TP53 Regulates Transcription of Cell Death Genes |
34 |
2.06e-01 |
4.53e-01 |
0.17600 |
0.068900 |
0.162000 |
4.87e-01 |
0.101000 |
Acyl chain remodelling of PG |
10 |
6.28e-01 |
7.92e-01 |
0.17600 |
-0.038600 |
-0.172000 |
8.33e-01 |
0.346000 |
Acyl chain remodelling of PC |
17 |
4.55e-01 |
6.89e-01 |
0.17600 |
0.069700 |
-0.161000 |
6.19e-01 |
0.250000 |
Endosomal Sorting Complex Required For Transport (ESCRT) |
22 |
3.67e-01 |
6.13e-01 |
0.17400 |
-0.171000 |
-0.034500 |
1.65e-01 |
0.780000 |
Interleukin-6 family signaling |
17 |
4.61e-01 |
6.92e-01 |
0.17400 |
0.058800 |
-0.164000 |
6.75e-01 |
0.241000 |
HDACs deacetylate histones |
26 |
3.06e-01 |
5.57e-01 |
0.17400 |
-0.025000 |
-0.173000 |
8.25e-01 |
0.128000 |
Pentose phosphate pathway |
13 |
5.54e-01 |
7.48e-01 |
0.17400 |
0.173000 |
0.016200 |
2.79e-01 |
0.919000 |
Activation of SMO |
13 |
5.55e-01 |
7.49e-01 |
0.17400 |
-0.091200 |
-0.148000 |
5.69e-01 |
0.355000 |
G beta:gamma signalling through BTK |
10 |
6.35e-01 |
7.95e-01 |
0.17400 |
0.122000 |
-0.124000 |
5.05e-01 |
0.496000 |
Post-chaperonin tubulin folding pathway |
17 |
4.64e-01 |
6.92e-01 |
0.17400 |
-0.082300 |
-0.153000 |
5.57e-01 |
0.275000 |
Peroxisomal protein import |
47 |
1.20e-01 |
3.22e-01 |
0.17400 |
0.134000 |
-0.110000 |
1.12e-01 |
0.192000 |
IRS-mediated signalling |
34 |
2.18e-01 |
4.66e-01 |
0.17300 |
-0.156000 |
0.074200 |
1.15e-01 |
0.454000 |
Purine ribonucleoside monophosphate biosynthesis |
11 |
6.13e-01 |
7.83e-01 |
0.17200 |
0.065600 |
-0.159000 |
7.06e-01 |
0.360000 |
MyD88-independent TLR4 cascade |
83 |
2.56e-02 |
1.23e-01 |
0.17200 |
-0.135000 |
0.107000 |
3.42e-02 |
0.092800 |
TRIF(TICAM1)-mediated TLR4 signaling |
83 |
2.56e-02 |
1.23e-01 |
0.17200 |
-0.135000 |
0.107000 |
3.42e-02 |
0.092800 |
TNFs bind their physiological receptors |
10 |
6.44e-01 |
8.00e-01 |
0.17100 |
0.170000 |
0.026000 |
3.53e-01 |
0.887000 |
Signaling by NTRKs |
118 |
5.85e-03 |
4.73e-02 |
0.17100 |
-0.170000 |
0.020400 |
1.46e-03 |
0.703000 |
Signaling by NOTCH2 |
21 |
4.00e-01 |
6.44e-01 |
0.17100 |
0.157000 |
0.067700 |
2.14e-01 |
0.591000 |
Ub-specific processing proteases |
151 |
1.51e-03 |
2.11e-02 |
0.17100 |
0.157000 |
0.067700 |
9.32e-04 |
0.152000 |
Cell-cell junction organization |
25 |
3.37e-01 |
5.83e-01 |
0.17000 |
-0.147000 |
0.086400 |
2.04e-01 |
0.455000 |
NOD1/2 Signaling Pathway |
27 |
3.10e-01 |
5.60e-01 |
0.17000 |
-0.042800 |
0.165000 |
7.00e-01 |
0.139000 |
Transport to the Golgi and subsequent modification |
132 |
3.47e-03 |
3.55e-02 |
0.17000 |
-0.170000 |
0.004180 |
7.68e-04 |
0.934000 |
Metabolism of steroids |
102 |
1.26e-02 |
7.71e-02 |
0.17000 |
-0.159000 |
-0.060900 |
5.72e-03 |
0.289000 |
Signaling by the B Cell Receptor (BCR) |
97 |
1.59e-02 |
8.67e-02 |
0.17000 |
0.163000 |
0.045100 |
5.50e-03 |
0.443000 |
RAF-independent MAPK1/3 activation |
21 |
4.05e-01 |
6.51e-01 |
0.16900 |
-0.169000 |
0.007540 |
1.79e-01 |
0.952000 |
NOTCH3 Activation and Transmission of Signal to the Nucleus |
18 |
4.62e-01 |
6.92e-01 |
0.16900 |
0.156000 |
-0.064300 |
2.51e-01 |
0.637000 |
Voltage gated Potassium channels |
24 |
3.58e-01 |
6.04e-01 |
0.16900 |
-0.139000 |
0.096300 |
2.40e-01 |
0.414000 |
Formation of tubulin folding intermediates by CCT/TriC |
16 |
5.05e-01 |
7.19e-01 |
0.16900 |
-0.168000 |
0.020300 |
2.46e-01 |
0.888000 |
Glycolysis |
54 |
1.01e-01 |
2.87e-01 |
0.16900 |
-0.163000 |
-0.044100 |
3.87e-02 |
0.576000 |
NIK-->noncanonical NF-kB signaling |
45 |
1.48e-01 |
3.66e-01 |
0.16900 |
0.166000 |
-0.026200 |
5.35e-02 |
0.761000 |
Host Interactions of HIV factors |
100 |
1.46e-02 |
8.29e-02 |
0.16900 |
0.167000 |
-0.025600 |
4.07e-03 |
0.658000 |
Biological oxidations |
126 |
5.09e-03 |
4.41e-02 |
0.16800 |
0.130000 |
0.106000 |
1.17e-02 |
0.039800 |
Activated NOTCH1 Transmits Signal to the Nucleus |
22 |
3.94e-01 |
6.40e-01 |
0.16800 |
0.055200 |
-0.159000 |
6.54e-01 |
0.197000 |
G beta:gamma signalling through PI3Kgamma |
16 |
5.08e-01 |
7.19e-01 |
0.16800 |
0.103000 |
-0.132000 |
4.75e-01 |
0.359000 |
Cell Cycle Checkpoints |
206 |
1.95e-04 |
4.36e-03 |
0.16800 |
0.167000 |
0.014000 |
3.79e-05 |
0.730000 |
NOTCH1 Intracellular Domain Regulates Transcription |
40 |
1.85e-01 |
4.21e-01 |
0.16800 |
-0.131000 |
0.105000 |
1.52e-01 |
0.252000 |
Transport of inorganic cations/anions and amino acids/oligopeptides |
69 |
5.61e-02 |
1.94e-01 |
0.16700 |
-0.136000 |
-0.097100 |
5.03e-02 |
0.164000 |
Platelet Aggregation (Plug Formation) |
25 |
3.50e-01 |
5.99e-01 |
0.16700 |
0.059600 |
-0.156000 |
6.06e-01 |
0.176000 |
Integrin signaling |
24 |
3.66e-01 |
6.13e-01 |
0.16700 |
0.023300 |
-0.166000 |
8.43e-01 |
0.161000 |
Nuclear Events (kinase and transcription factor activation) |
55 |
1.01e-01 |
2.87e-01 |
0.16700 |
-0.167000 |
0.002630 |
3.24e-02 |
0.973000 |
Extra-nuclear estrogen signaling |
61 |
7.92e-02 |
2.46e-01 |
0.16700 |
0.010300 |
0.167000 |
8.89e-01 |
0.024600 |
G alpha (12/13) signalling events |
65 |
6.77e-02 |
2.24e-01 |
0.16700 |
-0.098200 |
-0.135000 |
1.72e-01 |
0.060400 |
Transport of Mature mRNA derived from an Intron-Containing Transcript |
55 |
1.03e-01 |
2.91e-01 |
0.16600 |
0.142000 |
0.087400 |
6.95e-02 |
0.263000 |
MyD88:MAL(TIRAP) cascade initiated on plasma membrane |
81 |
3.54e-02 |
1.46e-01 |
0.16600 |
-0.131000 |
0.102000 |
4.18e-02 |
0.112000 |
Toll Like Receptor 2 (TLR2) Cascade |
81 |
3.54e-02 |
1.46e-01 |
0.16600 |
-0.131000 |
0.102000 |
4.18e-02 |
0.112000 |
Toll Like Receptor TLR1:TLR2 Cascade |
81 |
3.54e-02 |
1.46e-01 |
0.16600 |
-0.131000 |
0.102000 |
4.18e-02 |
0.112000 |
Toll Like Receptor TLR6:TLR2 Cascade |
81 |
3.54e-02 |
1.46e-01 |
0.16600 |
-0.131000 |
0.102000 |
4.18e-02 |
0.112000 |
Tie2 Signaling |
15 |
5.37e-01 |
7.38e-01 |
0.16600 |
-0.068500 |
0.151000 |
6.46e-01 |
0.310000 |
Presynaptic phase of homologous DNA pairing and strand exchange |
32 |
2.68e-01 |
5.24e-01 |
0.16600 |
0.166000 |
-0.001040 |
1.05e-01 |
0.992000 |
Transcriptional regulation by RUNX3 |
80 |
3.80e-02 |
1.50e-01 |
0.16500 |
0.132000 |
-0.099700 |
4.15e-02 |
0.124000 |
FOXO-mediated transcription of cell death genes |
13 |
5.87e-01 |
7.65e-01 |
0.16500 |
-0.165000 |
-0.013000 |
3.03e-01 |
0.935000 |
Cargo recognition for clathrin-mediated endocytosis |
74 |
4.92e-02 |
1.78e-01 |
0.16500 |
-0.151000 |
0.067400 |
2.52e-02 |
0.317000 |
Caspase activation via extrinsic apoptotic signalling pathway |
22 |
4.08e-01 |
6.51e-01 |
0.16500 |
0.033300 |
0.162000 |
7.87e-01 |
0.189000 |
Ion transport by P-type ATPases |
35 |
2.42e-01 |
4.92e-01 |
0.16500 |
-0.147000 |
0.073900 |
1.32e-01 |
0.450000 |
LDL clearance |
16 |
5.22e-01 |
7.31e-01 |
0.16500 |
0.057500 |
-0.154000 |
6.91e-01 |
0.286000 |
Transcriptional Regulation by E2F6 |
30 |
2.98e-01 |
5.48e-01 |
0.16400 |
0.163000 |
0.022700 |
1.23e-01 |
0.830000 |
Cell death signalling via NRAGE, NRIF and NADE |
63 |
7.97e-02 |
2.46e-01 |
0.16400 |
-0.085500 |
-0.140000 |
2.41e-01 |
0.054700 |
MAP2K and MAPK activation |
31 |
2.86e-01 |
5.41e-01 |
0.16400 |
0.163000 |
-0.018200 |
1.16e-01 |
0.861000 |
Intra-Golgi traffic |
34 |
2.54e-01 |
5.04e-01 |
0.16400 |
-0.084100 |
0.141000 |
3.96e-01 |
0.156000 |
Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase |
18 |
4.85e-01 |
7.07e-01 |
0.16400 |
-0.115000 |
-0.117000 |
3.97e-01 |
0.392000 |
Apoptotic execution phase |
38 |
2.16e-01 |
4.65e-01 |
0.16400 |
-0.099700 |
0.130000 |
2.88e-01 |
0.165000 |
Retrograde neurotrophin signalling |
13 |
5.93e-01 |
7.70e-01 |
0.16400 |
-0.155000 |
-0.053900 |
3.34e-01 |
0.736000 |
GLI3 is processed to GLI3R by the proteasome |
46 |
1.58e-01 |
3.82e-01 |
0.16400 |
0.164000 |
-0.000326 |
5.48e-02 |
0.997000 |
Degradation of GLI1 by the proteasome |
47 |
1.52e-01 |
3.74e-01 |
0.16400 |
0.163000 |
-0.012000 |
5.29e-02 |
0.887000 |
IRS-related events triggered by IGF1R |
37 |
2.27e-01 |
4.75e-01 |
0.16300 |
-0.133000 |
0.094600 |
1.61e-01 |
0.320000 |
Deactivation of the beta-catenin transactivating complex |
30 |
3.02e-01 |
5.54e-01 |
0.16300 |
-0.153000 |
-0.057300 |
1.47e-01 |
0.587000 |
RNA Polymerase I Promoter Clearance |
38 |
2.22e-01 |
4.71e-01 |
0.16300 |
-0.040000 |
-0.158000 |
6.70e-01 |
0.092400 |
Carboxyterminal post-translational modifications of tubulin |
25 |
3.71e-01 |
6.16e-01 |
0.16300 |
0.024900 |
-0.161000 |
8.29e-01 |
0.164000 |
Potential therapeutics for SARS |
32 |
2.82e-01 |
5.39e-01 |
0.16300 |
0.141000 |
0.081700 |
1.68e-01 |
0.424000 |
Abortive elongation of HIV-1 transcript in the absence of Tat |
16 |
5.31e-01 |
7.37e-01 |
0.16300 |
-0.069600 |
-0.147000 |
6.30e-01 |
0.309000 |
CRMPs in Sema3A signaling |
14 |
5.75e-01 |
7.57e-01 |
0.16300 |
0.155000 |
0.050000 |
3.17e-01 |
0.746000 |
Degradation of GLI2 by the proteasome |
46 |
1.65e-01 |
3.93e-01 |
0.16200 |
0.161000 |
-0.020200 |
5.96e-02 |
0.812000 |
Dual incision in TC-NER |
50 |
1.41e-01 |
3.58e-01 |
0.16200 |
0.156000 |
-0.041600 |
5.60e-02 |
0.612000 |
Binding and Uptake of Ligands by Scavenger Receptors |
31 |
2.97e-01 |
5.48e-01 |
0.16200 |
0.029500 |
-0.159000 |
7.76e-01 |
0.126000 |
Signalling to ERKs |
31 |
2.98e-01 |
5.48e-01 |
0.16100 |
-0.114000 |
0.114000 |
2.72e-01 |
0.271000 |
Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells |
12 |
6.26e-01 |
7.91e-01 |
0.16100 |
-0.023400 |
0.160000 |
8.89e-01 |
0.338000 |
Thrombin signalling through proteinase activated receptors (PARs) |
22 |
4.25e-01 |
6.68e-01 |
0.16100 |
0.000653 |
-0.161000 |
9.96e-01 |
0.191000 |
RNA Polymerase I Transcription |
39 |
2.21e-01 |
4.71e-01 |
0.16100 |
-0.022500 |
-0.159000 |
8.08e-01 |
0.085200 |
Regulation of insulin secretion |
58 |
1.07e-01 |
2.95e-01 |
0.16100 |
-0.156000 |
-0.040100 |
4.05e-02 |
0.598000 |
Toll Like Receptor 3 (TLR3) Cascade |
79 |
4.81e-02 |
1.78e-01 |
0.16000 |
-0.130000 |
0.094300 |
4.64e-02 |
0.148000 |
RNA Polymerase I Transcription Initiation |
35 |
2.62e-01 |
5.15e-01 |
0.16000 |
-0.055000 |
-0.150000 |
5.74e-01 |
0.124000 |
Negative regulation of NMDA receptor-mediated neuronal transmission |
15 |
5.64e-01 |
7.56e-01 |
0.16000 |
-0.159000 |
0.014800 |
2.87e-01 |
0.921000 |
Thromboxane signalling through TP receptor |
15 |
5.64e-01 |
7.56e-01 |
0.16000 |
0.006750 |
-0.159000 |
9.64e-01 |
0.285000 |
Downstream TCR signaling |
69 |
7.33e-02 |
2.34e-01 |
0.15900 |
0.159000 |
-0.002740 |
2.23e-02 |
0.969000 |
AKT phosphorylates targets in the cytosol |
13 |
6.10e-01 |
7.82e-01 |
0.15900 |
-0.101000 |
-0.124000 |
5.30e-01 |
0.440000 |
Opioid Signalling |
71 |
6.80e-02 |
2.24e-01 |
0.15900 |
-0.141000 |
0.074100 |
4.03e-02 |
0.281000 |
Synthesis of very long-chain fatty acyl-CoAs |
14 |
5.88e-01 |
7.65e-01 |
0.15900 |
-0.097900 |
0.125000 |
5.26e-01 |
0.417000 |
Class I peroxisomal membrane protein import |
15 |
5.68e-01 |
7.56e-01 |
0.15900 |
0.091700 |
0.130000 |
5.39e-01 |
0.385000 |
Lysosome Vesicle Biogenesis |
28 |
3.51e-01 |
6.00e-01 |
0.15800 |
0.016200 |
-0.157000 |
8.82e-01 |
0.150000 |
Mitochondrial biogenesis |
67 |
8.30e-02 |
2.55e-01 |
0.15800 |
-0.147000 |
-0.057600 |
3.77e-02 |
0.416000 |
Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA |
15 |
5.71e-01 |
7.57e-01 |
0.15800 |
-0.018400 |
0.157000 |
9.02e-01 |
0.293000 |
Dectin-1 mediated noncanonical NF-kB signaling |
46 |
1.81e-01 |
4.21e-01 |
0.15800 |
0.154000 |
-0.032500 |
7.05e-02 |
0.703000 |
Peptide ligand-binding receptors |
66 |
8.72e-02 |
2.63e-01 |
0.15800 |
0.087700 |
0.131000 |
2.18e-01 |
0.066300 |
Unfolded Protein Response (UPR) |
75 |
6.49e-02 |
2.18e-01 |
0.15700 |
-0.125000 |
-0.094400 |
6.17e-02 |
0.158000 |
Costimulation by the CD28 family |
53 |
1.45e-01 |
3.63e-01 |
0.15600 |
0.156000 |
-0.000283 |
4.96e-02 |
0.997000 |
Fatty acid metabolism |
119 |
1.35e-02 |
7.84e-02 |
0.15600 |
0.135000 |
-0.077300 |
1.09e-02 |
0.146000 |
DNA Damage/Telomere Stress Induced Senescence |
23 |
4.33e-01 |
6.75e-01 |
0.15600 |
0.156000 |
-0.005660 |
1.96e-01 |
0.963000 |
Signaling by ERBB2 |
38 |
2.52e-01 |
5.03e-01 |
0.15600 |
-0.110000 |
0.111000 |
2.43e-01 |
0.239000 |
Golgi Associated Vesicle Biogenesis |
46 |
1.91e-01 |
4.31e-01 |
0.15500 |
-0.139000 |
0.068100 |
1.02e-01 |
0.425000 |
Insulin receptor signalling cascade |
39 |
2.45e-01 |
4.96e-01 |
0.15500 |
-0.124000 |
0.092700 |
1.80e-01 |
0.317000 |
Downstream signaling events of B Cell Receptor (BCR) |
67 |
9.14e-02 |
2.72e-01 |
0.15500 |
0.144000 |
0.057600 |
4.22e-02 |
0.415000 |
Signaling by TGF-beta Receptor Complex |
57 |
1.31e-01 |
3.43e-01 |
0.15500 |
-0.129000 |
0.085000 |
9.24e-02 |
0.267000 |
Constitutive Signaling by Overexpressed ERBB2 |
10 |
6.99e-01 |
8.49e-01 |
0.15400 |
-0.065900 |
0.140000 |
7.18e-01 |
0.445000 |
Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters |
18 |
5.28e-01 |
7.35e-01 |
0.15400 |
0.138000 |
-0.068800 |
3.13e-01 |
0.614000 |
NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux |
28 |
3.75e-01 |
6.20e-01 |
0.15300 |
-0.142000 |
-0.056500 |
1.92e-01 |
0.605000 |
SUMOylation of DNA replication proteins |
34 |
3.05e-01 |
5.56e-01 |
0.15300 |
0.152000 |
-0.017700 |
1.26e-01 |
0.858000 |
RNA Polymerase III Transcription Termination |
18 |
5.33e-01 |
7.37e-01 |
0.15300 |
0.152000 |
-0.011600 |
2.63e-01 |
0.932000 |
FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes |
21 |
4.80e-01 |
7.04e-01 |
0.15300 |
-0.139000 |
0.062400 |
2.69e-01 |
0.621000 |
Oxidative Stress Induced Senescence |
55 |
1.47e-01 |
3.65e-01 |
0.15300 |
-0.151000 |
-0.022300 |
5.28e-02 |
0.775000 |
Glycerophospholipid biosynthesis |
87 |
4.93e-02 |
1.78e-01 |
0.15300 |
-0.101000 |
-0.114000 |
1.04e-01 |
0.065800 |
Transport of bile salts and organic acids, metal ions and amine compounds |
44 |
2.18e-01 |
4.66e-01 |
0.15200 |
0.152000 |
-0.007190 |
8.11e-02 |
0.934000 |
Cytosolic sensors of pathogen-associated DNA |
47 |
1.97e-01 |
4.41e-01 |
0.15200 |
0.123000 |
-0.088700 |
1.44e-01 |
0.293000 |
Antiviral mechanism by IFN-stimulated genes |
57 |
1.41e-01 |
3.58e-01 |
0.15200 |
0.151000 |
-0.013900 |
4.89e-02 |
0.856000 |
Ion channel transport |
100 |
3.32e-02 |
1.42e-01 |
0.15100 |
-0.134000 |
0.070500 |
2.11e-02 |
0.224000 |
SARS-CoV-1 Infection |
36 |
2.93e-01 |
5.44e-01 |
0.15100 |
-0.150000 |
-0.017200 |
1.19e-01 |
0.858000 |
Meiotic recombination |
21 |
4.87e-01 |
7.07e-01 |
0.15100 |
0.122000 |
-0.088900 |
3.33e-01 |
0.481000 |
Syndecan interactions |
17 |
5.60e-01 |
7.54e-01 |
0.15100 |
-0.014600 |
-0.150000 |
9.17e-01 |
0.284000 |
Cargo concentration in the ER |
20 |
5.06e-01 |
7.19e-01 |
0.15100 |
-0.148000 |
-0.029000 |
2.52e-01 |
0.823000 |
Negative regulation of MAPK pathway |
37 |
2.87e-01 |
5.41e-01 |
0.15000 |
-0.147000 |
0.029800 |
1.21e-01 |
0.754000 |
Stimuli-sensing channels |
51 |
1.79e-01 |
4.19e-01 |
0.15000 |
-0.124000 |
0.084600 |
1.26e-01 |
0.296000 |
SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion |
13 |
6.45e-01 |
8.00e-01 |
0.15000 |
0.071000 |
-0.132000 |
6.57e-01 |
0.410000 |
DARPP-32 events |
21 |
4.94e-01 |
7.11e-01 |
0.15000 |
-0.132000 |
0.070100 |
2.94e-01 |
0.578000 |
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks |
34 |
3.21e-01 |
5.66e-01 |
0.15000 |
-0.007380 |
-0.149000 |
9.41e-01 |
0.132000 |
Notch-HLH transcription pathway |
24 |
4.50e-01 |
6.87e-01 |
0.14900 |
-0.087000 |
-0.121000 |
4.61e-01 |
0.304000 |
Neutrophil degranulation |
336 |
1.85e-05 |
5.96e-04 |
0.14900 |
0.139000 |
-0.054100 |
1.38e-05 |
0.090800 |
TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain |
11 |
6.93e-01 |
8.45e-01 |
0.14900 |
-0.041700 |
0.143000 |
8.11e-01 |
0.412000 |
RHO GTPases activate IQGAPs |
10 |
7.18e-01 |
8.61e-01 |
0.14900 |
0.039900 |
0.143000 |
8.27e-01 |
0.432000 |
Nucleobase catabolism |
28 |
3.95e-01 |
6.40e-01 |
0.14900 |
0.142000 |
0.044800 |
1.94e-01 |
0.682000 |
Defective B3GALT6 causes EDSP2 and SEMDJL1 |
15 |
6.08e-01 |
7.81e-01 |
0.14900 |
0.049600 |
0.140000 |
7.40e-01 |
0.347000 |
HS-GAG degradation |
17 |
5.68e-01 |
7.56e-01 |
0.14900 |
0.042400 |
-0.143000 |
7.62e-01 |
0.309000 |
HDR through Single Strand Annealing (SSA) |
31 |
3.58e-01 |
6.04e-01 |
0.14900 |
0.107000 |
-0.103000 |
3.02e-01 |
0.321000 |
mRNA Splicing - Major Pathway |
133 |
1.31e-02 |
7.84e-02 |
0.14800 |
0.137000 |
0.056700 |
6.45e-03 |
0.260000 |
Triglyceride catabolism |
14 |
6.30e-01 |
7.93e-01 |
0.14800 |
0.008780 |
0.148000 |
9.55e-01 |
0.337000 |
Metabolism of porphyrins |
19 |
5.36e-01 |
7.38e-01 |
0.14800 |
-0.070000 |
-0.131000 |
5.98e-01 |
0.325000 |
DNA Double-Strand Break Repair |
104 |
3.45e-02 |
1.45e-01 |
0.14700 |
0.127000 |
-0.074400 |
2.52e-02 |
0.191000 |
IL-6-type cytokine receptor ligand interactions |
11 |
6.99e-01 |
8.49e-01 |
0.14700 |
0.071900 |
-0.129000 |
6.80e-01 |
0.460000 |
Signaling by NTRK1 (TRKA) |
103 |
3.62e-02 |
1.47e-01 |
0.14700 |
-0.146000 |
0.017600 |
1.05e-02 |
0.758000 |
Translocation of SLC2A4 (GLUT4) to the plasma membrane |
50 |
1.98e-01 |
4.42e-01 |
0.14700 |
-0.134000 |
0.060700 |
1.01e-01 |
0.458000 |
Response of EIF2AK1 (HRI) to heme deficiency |
12 |
6.79e-01 |
8.33e-01 |
0.14700 |
0.074300 |
0.127000 |
6.56e-01 |
0.448000 |
Acyl chain remodelling of PE |
15 |
6.17e-01 |
7.85e-01 |
0.14600 |
0.021800 |
-0.145000 |
8.84e-01 |
0.332000 |
Branched-chain amino acid catabolism |
19 |
5.44e-01 |
7.41e-01 |
0.14600 |
-0.143000 |
-0.029300 |
2.79e-01 |
0.825000 |
Resolution of D-Loop Structures |
27 |
4.23e-01 |
6.67e-01 |
0.14600 |
0.111000 |
-0.095100 |
3.21e-01 |
0.392000 |
Innate Immune System |
699 |
8.48e-10 |
5.33e-07 |
0.14500 |
0.144000 |
-0.023200 |
1.79e-10 |
0.303000 |
BMAL1:CLOCK,NPAS2 activates circadian gene expression |
22 |
5.00e-01 |
7.15e-01 |
0.14500 |
-0.120000 |
-0.082600 |
3.32e-01 |
0.503000 |
Homologous DNA Pairing and Strand Exchange |
35 |
3.31e-01 |
5.76e-01 |
0.14500 |
0.137000 |
-0.047800 |
1.61e-01 |
0.625000 |
RUNX3 regulates NOTCH signaling |
13 |
6.63e-01 |
8.18e-01 |
0.14500 |
-0.022900 |
0.143000 |
8.86e-01 |
0.371000 |
TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain |
18 |
5.67e-01 |
7.56e-01 |
0.14500 |
0.015400 |
0.144000 |
9.10e-01 |
0.290000 |
DNA Repair |
221 |
1.06e-03 |
1.64e-02 |
0.14500 |
0.137000 |
-0.047600 |
4.75e-04 |
0.225000 |
FCGR3A-mediated IL10 synthesis |
40 |
2.87e-01 |
5.41e-01 |
0.14500 |
0.076800 |
0.122000 |
4.01e-01 |
0.181000 |
Transport of Mature Transcript to Cytoplasm |
62 |
1.46e-01 |
3.63e-01 |
0.14400 |
0.127000 |
0.068000 |
8.31e-02 |
0.355000 |
G beta:gamma signalling through PLC beta |
12 |
6.88e-01 |
8.41e-01 |
0.14400 |
-0.008090 |
-0.144000 |
9.61e-01 |
0.387000 |
TP53 Regulates Transcription of DNA Repair Genes |
48 |
2.25e-01 |
4.74e-01 |
0.14400 |
0.123000 |
-0.074500 |
1.40e-01 |
0.372000 |
Signaling by high-kinase activity BRAF mutants |
29 |
4.06e-01 |
6.51e-01 |
0.14400 |
0.140000 |
-0.035600 |
1.94e-01 |
0.740000 |
Cargo trafficking to the periciliary membrane |
38 |
3.07e-01 |
5.57e-01 |
0.14400 |
-0.099200 |
0.104000 |
2.90e-01 |
0.266000 |
Synthesis of pyrophosphates in the cytosol |
10 |
7.33e-01 |
8.71e-01 |
0.14400 |
-0.140000 |
-0.034900 |
4.45e-01 |
0.849000 |
Deadenylation-dependent mRNA decay |
45 |
2.51e-01 |
5.03e-01 |
0.14300 |
0.094800 |
0.108000 |
2.72e-01 |
0.212000 |
Activation of NF-kappaB in B cells |
55 |
1.85e-01 |
4.21e-01 |
0.14300 |
0.143000 |
0.002570 |
6.60e-02 |
0.974000 |
mTORC1-mediated signalling |
20 |
5.40e-01 |
7.39e-01 |
0.14300 |
0.010300 |
0.143000 |
9.37e-01 |
0.268000 |
Regulation of IFNG signaling |
12 |
6.92e-01 |
8.45e-01 |
0.14300 |
0.138000 |
-0.036700 |
4.07e-01 |
0.826000 |
C-type lectin receptors (CLRs) |
101 |
4.68e-02 |
1.74e-01 |
0.14300 |
0.099200 |
0.103000 |
8.55e-02 |
0.074600 |
Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding |
26 |
4.52e-01 |
6.88e-01 |
0.14300 |
-0.106000 |
0.095900 |
3.52e-01 |
0.398000 |
FOXO-mediated transcription |
52 |
2.06e-01 |
4.53e-01 |
0.14300 |
-0.089400 |
0.111000 |
2.65e-01 |
0.166000 |
Iron uptake and transport |
41 |
2.87e-01 |
5.41e-01 |
0.14300 |
-0.100000 |
0.101000 |
2.67e-01 |
0.262000 |
Resolution of D-loop Structures through Holliday Junction Intermediates |
26 |
4.55e-01 |
6.89e-01 |
0.14200 |
0.088900 |
-0.111000 |
4.33e-01 |
0.328000 |
RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function |
33 |
3.73e-01 |
6.18e-01 |
0.14100 |
-0.120000 |
-0.074700 |
2.33e-01 |
0.458000 |
rRNA modification in the nucleus and cytosol |
46 |
2.52e-01 |
5.04e-01 |
0.14100 |
0.091200 |
-0.108000 |
2.85e-01 |
0.205000 |
IGF1R signaling cascade |
38 |
3.21e-01 |
5.66e-01 |
0.14100 |
-0.108000 |
0.091400 |
2.51e-01 |
0.330000 |
Synthesis of IP3 and IP4 in the cytosol |
20 |
5.53e-01 |
7.48e-01 |
0.14100 |
-0.033500 |
-0.137000 |
7.96e-01 |
0.290000 |
Endogenous sterols |
17 |
6.11e-01 |
7.82e-01 |
0.13900 |
0.011900 |
0.139000 |
9.32e-01 |
0.323000 |
NS1 Mediated Effects on Host Pathways |
28 |
4.45e-01 |
6.84e-01 |
0.13900 |
-0.033000 |
0.135000 |
7.62e-01 |
0.217000 |
GABA receptor activation |
33 |
3.88e-01 |
6.34e-01 |
0.13800 |
-0.091700 |
0.104000 |
3.62e-01 |
0.303000 |
Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors |
25 |
4.89e-01 |
7.07e-01 |
0.13800 |
0.110000 |
-0.083400 |
3.41e-01 |
0.471000 |
Resolution of Sister Chromatid Cohesion |
85 |
9.17e-02 |
2.72e-01 |
0.13800 |
0.104000 |
0.090100 |
9.82e-02 |
0.152000 |
ADP signalling through P2Y purinoceptor 1 |
17 |
6.18e-01 |
7.85e-01 |
0.13700 |
-0.047700 |
-0.129000 |
7.34e-01 |
0.357000 |
Aberrant regulation of mitotic exit in cancer due to RB1 defects |
18 |
6.01e-01 |
7.75e-01 |
0.13700 |
-0.137000 |
-0.014600 |
3.16e-01 |
0.914000 |
HS-GAG biosynthesis |
21 |
5.53e-01 |
7.48e-01 |
0.13700 |
-0.083000 |
0.109000 |
5.10e-01 |
0.386000 |
NCAM signaling for neurite out-growth |
47 |
2.67e-01 |
5.22e-01 |
0.13700 |
-0.137000 |
-0.012800 |
1.06e-01 |
0.879000 |
Transport of Ribonucleoproteins into the Host Nucleus |
23 |
5.23e-01 |
7.31e-01 |
0.13700 |
-0.078600 |
0.112000 |
5.14e-01 |
0.351000 |
Inactivation, recovery and regulation of the phototransduction cascade |
17 |
6.21e-01 |
7.87e-01 |
0.13700 |
-0.121000 |
-0.063200 |
3.87e-01 |
0.652000 |
The phototransduction cascade |
17 |
6.21e-01 |
7.87e-01 |
0.13700 |
-0.121000 |
-0.063200 |
3.87e-01 |
0.652000 |
Positive epigenetic regulation of rRNA expression |
36 |
3.66e-01 |
6.12e-01 |
0.13700 |
0.023600 |
-0.135000 |
8.06e-01 |
0.163000 |
Regulation of PTEN stability and activity |
53 |
2.29e-01 |
4.77e-01 |
0.13600 |
0.132000 |
-0.033300 |
9.63e-02 |
0.675000 |
Phase I - Functionalization of compounds |
58 |
2.01e-01 |
4.47e-01 |
0.13600 |
0.075600 |
0.113000 |
3.20e-01 |
0.136000 |
Regulation of mRNA stability by proteins that bind AU-rich elements |
72 |
1.37e-01 |
3.51e-01 |
0.13600 |
0.133000 |
-0.026500 |
5.06e-02 |
0.698000 |
DNA Double Strand Break Response |
35 |
3.82e-01 |
6.29e-01 |
0.13600 |
0.018000 |
-0.134000 |
8.54e-01 |
0.169000 |
Deubiquitination |
216 |
3.05e-03 |
3.28e-02 |
0.13500 |
0.121000 |
0.060800 |
2.35e-03 |
0.125000 |
Cell Cycle |
500 |
2.08e-06 |
1.30e-04 |
0.13500 |
0.134000 |
0.017900 |
3.94e-07 |
0.497000 |
Processing of Capped Intron-Containing Pre-mRNA |
180 |
7.94e-03 |
5.80e-02 |
0.13500 |
0.117000 |
0.067900 |
7.15e-03 |
0.117000 |
Diseases associated with O-glycosylation of proteins |
43 |
3.11e-01 |
5.60e-01 |
0.13500 |
0.065000 |
-0.118000 |
4.61e-01 |
0.181000 |
TRAF6 mediated NF-kB activation |
20 |
5.81e-01 |
7.59e-01 |
0.13500 |
0.042700 |
-0.128000 |
7.41e-01 |
0.323000 |
Signaling by Insulin receptor |
55 |
2.27e-01 |
4.75e-01 |
0.13400 |
-0.100000 |
0.089700 |
2.00e-01 |
0.250000 |
Metabolism of non-coding RNA |
39 |
3.49e-01 |
5.99e-01 |
0.13400 |
-0.008520 |
0.134000 |
9.27e-01 |
0.148000 |
snRNP Assembly |
39 |
3.49e-01 |
5.99e-01 |
0.13400 |
-0.008520 |
0.134000 |
9.27e-01 |
0.148000 |
Effects of PIP2 hydrolysis |
22 |
5.54e-01 |
7.48e-01 |
0.13400 |
-0.045300 |
-0.126000 |
7.13e-01 |
0.306000 |
Dopamine Neurotransmitter Release Cycle |
14 |
6.87e-01 |
8.40e-01 |
0.13400 |
0.056500 |
0.122000 |
7.15e-01 |
0.431000 |
Cellular response to hypoxia |
56 |
2.24e-01 |
4.72e-01 |
0.13400 |
0.130000 |
0.032800 |
9.32e-02 |
0.671000 |
mRNA Splicing |
141 |
2.37e-02 |
1.17e-01 |
0.13400 |
0.123000 |
0.053900 |
1.22e-02 |
0.271000 |
Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) |
39 |
3.53e-01 |
6.01e-01 |
0.13400 |
-0.103000 |
0.084800 |
2.65e-01 |
0.360000 |
Metabolism of RNA |
494 |
3.18e-06 |
1.50e-04 |
0.13400 |
0.131000 |
0.025900 |
7.90e-07 |
0.329000 |
Neurotransmitter receptors and postsynaptic signal transmission |
121 |
4.04e-02 |
1.56e-01 |
0.13400 |
-0.101000 |
0.087300 |
5.54e-02 |
0.098200 |
Response to elevated platelet cytosolic Ca2+ |
100 |
7.09e-02 |
2.31e-01 |
0.13300 |
0.131000 |
-0.024200 |
2.37e-02 |
0.676000 |
Signaling by NTRK3 (TRKC) |
17 |
6.39e-01 |
7.98e-01 |
0.13300 |
-0.067300 |
0.114000 |
6.31e-01 |
0.415000 |
Transcription-Coupled Nucleotide Excision Repair (TC-NER) |
61 |
2.06e-01 |
4.53e-01 |
0.13200 |
0.131000 |
-0.013200 |
7.72e-02 |
0.859000 |
Oncogene Induced Senescence |
27 |
4.97e-01 |
7.14e-01 |
0.13200 |
0.075600 |
0.108000 |
4.97e-01 |
0.333000 |
Cell Cycle, Mitotic |
405 |
4.17e-05 |
1.22e-03 |
0.13100 |
0.130000 |
0.013500 |
7.89e-06 |
0.643000 |
Interleukin-2 family signaling |
33 |
4.31e-01 |
6.74e-01 |
0.13100 |
0.031400 |
-0.127000 |
7.55e-01 |
0.208000 |
Chondroitin sulfate/dermatan sulfate metabolism |
40 |
3.64e-01 |
6.11e-01 |
0.13000 |
0.108000 |
0.072400 |
2.37e-01 |
0.429000 |
PKMTs methylate histone lysines |
35 |
4.14e-01 |
6.58e-01 |
0.13000 |
-0.085000 |
-0.098300 |
3.84e-01 |
0.315000 |
p75 NTR receptor-mediated signalling |
75 |
1.53e-01 |
3.75e-01 |
0.13000 |
-0.057500 |
-0.116000 |
3.90e-01 |
0.082000 |
GAB1 signalosome |
14 |
7.05e-01 |
8.53e-01 |
0.12900 |
-0.108000 |
0.070000 |
4.83e-01 |
0.651000 |
Ca2+ pathway |
48 |
3.05e-01 |
5.56e-01 |
0.12900 |
-0.127000 |
0.018000 |
1.27e-01 |
0.829000 |
RNA Polymerase III Chain Elongation |
13 |
7.26e-01 |
8.67e-01 |
0.12800 |
0.107000 |
-0.069800 |
5.03e-01 |
0.663000 |
Protein localization |
122 |
5.19e-02 |
1.83e-01 |
0.12800 |
0.108000 |
-0.068800 |
4.06e-02 |
0.191000 |
COPI-mediated anterograde transport |
70 |
1.83e-01 |
4.21e-01 |
0.12800 |
-0.125000 |
-0.023500 |
6.99e-02 |
0.734000 |
Interleukin-10 signaling |
25 |
5.43e-01 |
7.41e-01 |
0.12800 |
0.106000 |
-0.071300 |
3.60e-01 |
0.537000 |
Transcriptional activation of mitochondrial biogenesis |
49 |
3.05e-01 |
5.56e-01 |
0.12700 |
-0.120000 |
-0.044200 |
1.48e-01 |
0.593000 |
Regulation of RUNX2 expression and activity |
57 |
2.52e-01 |
5.03e-01 |
0.12700 |
0.105000 |
0.072000 |
1.70e-01 |
0.348000 |
Activation of BH3-only proteins |
27 |
5.21e-01 |
7.30e-01 |
0.12700 |
0.085000 |
0.094500 |
4.45e-01 |
0.396000 |
Export of Viral Ribonucleoproteins from Nucleus |
24 |
5.66e-01 |
7.56e-01 |
0.12600 |
-0.074000 |
0.102000 |
5.30e-01 |
0.389000 |
Neuronal System |
246 |
3.30e-03 |
3.46e-02 |
0.12600 |
-0.122000 |
0.031900 |
1.08e-03 |
0.392000 |
PCP/CE pathway |
75 |
1.71e-01 |
4.06e-01 |
0.12600 |
0.055200 |
-0.113000 |
4.09e-01 |
0.091500 |
Defective EXT1 causes exostoses 1, TRPS2 and CHDS |
12 |
7.53e-01 |
8.85e-01 |
0.12600 |
-0.123000 |
-0.025500 |
4.61e-01 |
0.878000 |
Defective EXT2 causes exostoses 2 |
12 |
7.53e-01 |
8.85e-01 |
0.12600 |
-0.123000 |
-0.025500 |
4.61e-01 |
0.878000 |
Trafficking and processing of endosomal TLR |
11 |
7.73e-01 |
8.91e-01 |
0.12500 |
0.124000 |
0.018400 |
4.77e-01 |
0.916000 |
Interleukin-6 signaling |
10 |
7.92e-01 |
9.04e-01 |
0.12500 |
-0.037900 |
-0.119000 |
8.36e-01 |
0.515000 |
TNF signaling |
33 |
4.64e-01 |
6.92e-01 |
0.12500 |
0.122000 |
0.026300 |
2.26e-01 |
0.794000 |
Glucagon-like Peptide-1 (GLP1) regulates insulin secretion |
29 |
5.09e-01 |
7.19e-01 |
0.12500 |
-0.123000 |
0.019400 |
2.51e-01 |
0.857000 |
Semaphorin interactions |
59 |
2.55e-01 |
5.05e-01 |
0.12500 |
0.125000 |
-0.001790 |
9.81e-02 |
0.981000 |
O-linked glycosylation of mucins |
31 |
4.87e-01 |
7.07e-01 |
0.12500 |
0.022400 |
-0.123000 |
8.29e-01 |
0.238000 |
Chromatin modifying enzymes |
169 |
2.18e-02 |
1.11e-01 |
0.12400 |
-0.094200 |
-0.080400 |
3.52e-02 |
0.072300 |
Chromatin organization |
169 |
2.18e-02 |
1.11e-01 |
0.12400 |
-0.094200 |
-0.080400 |
3.52e-02 |
0.072300 |
Keratan sulfate biosynthesis |
20 |
6.34e-01 |
7.95e-01 |
0.12300 |
-0.090400 |
-0.084100 |
4.84e-01 |
0.515000 |
Transmission across Chemical Synapses |
160 |
2.78e-02 |
1.32e-01 |
0.12300 |
-0.116000 |
0.039400 |
1.13e-02 |
0.391000 |
Transcriptional Regulation by VENTX |
33 |
4.77e-01 |
7.04e-01 |
0.12300 |
-0.102000 |
-0.067400 |
3.09e-01 |
0.503000 |
MAPK6/MAPK4 signaling |
71 |
2.04e-01 |
4.53e-01 |
0.12200 |
0.105000 |
-0.063400 |
1.28e-01 |
0.356000 |
Metabolism of nitric oxide: NOS3 activation and regulation |
14 |
7.31e-01 |
8.70e-01 |
0.12200 |
0.109000 |
-0.054200 |
4.79e-01 |
0.726000 |
Inhibition of replication initiation of damaged DNA by RB1/E2F1 |
12 |
7.66e-01 |
8.88e-01 |
0.12200 |
0.120000 |
0.020600 |
4.71e-01 |
0.902000 |
Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) |
23 |
6.01e-01 |
7.75e-01 |
0.12200 |
0.109000 |
-0.053500 |
3.65e-01 |
0.657000 |
Platelet degranulation |
96 |
1.22e-01 |
3.24e-01 |
0.12100 |
0.121000 |
0.002990 |
4.01e-02 |
0.960000 |
RNA Polymerase I Promoter Escape |
21 |
6.33e-01 |
7.94e-01 |
0.12100 |
-0.108000 |
-0.053400 |
3.91e-01 |
0.672000 |
PRC2 methylates histones and DNA |
12 |
7.70e-01 |
8.91e-01 |
0.12000 |
-0.033500 |
0.116000 |
8.41e-01 |
0.488000 |
Gap junction trafficking and regulation |
16 |
7.09e-01 |
8.55e-01 |
0.12000 |
-0.120000 |
-0.005180 |
4.07e-01 |
0.971000 |
Fc epsilon receptor (FCERI) signaling |
112 |
9.45e-02 |
2.78e-01 |
0.11900 |
0.090200 |
0.078000 |
1.00e-01 |
0.155000 |
FCERI mediated NF-kB activation |
65 |
2.53e-01 |
5.04e-01 |
0.11900 |
0.112000 |
0.040800 |
1.19e-01 |
0.570000 |
Association of TriC/CCT with target proteins during biosynthesis |
30 |
5.29e-01 |
7.35e-01 |
0.11900 |
-0.072500 |
0.094400 |
4.92e-01 |
0.371000 |
Gene Silencing by RNA |
47 |
3.73e-01 |
6.18e-01 |
0.11900 |
-0.118000 |
-0.009680 |
1.61e-01 |
0.909000 |
cGMP effects |
13 |
7.60e-01 |
8.87e-01 |
0.11900 |
0.117000 |
-0.016900 |
4.64e-01 |
0.916000 |
Amyloid fiber formation |
32 |
5.10e-01 |
7.19e-01 |
0.11900 |
0.065900 |
-0.098500 |
5.19e-01 |
0.335000 |
Pre-NOTCH Expression and Processing |
43 |
4.07e-01 |
6.51e-01 |
0.11800 |
-0.051400 |
-0.107000 |
5.60e-01 |
0.227000 |
Unblocking of NMDA receptors, glutamate binding and activation |
15 |
7.30e-01 |
8.69e-01 |
0.11800 |
-0.085700 |
0.081600 |
5.66e-01 |
0.584000 |
Oncogenic MAPK signaling |
67 |
2.48e-01 |
5.00e-01 |
0.11800 |
-0.116000 |
0.022400 |
1.01e-01 |
0.752000 |
Keratan sulfate/keratin metabolism |
24 |
6.08e-01 |
7.81e-01 |
0.11800 |
-0.082400 |
-0.084300 |
4.85e-01 |
0.475000 |
Interactions of Vpr with host cellular proteins |
26 |
5.85e-01 |
7.64e-01 |
0.11700 |
-0.062500 |
0.099200 |
5.82e-01 |
0.381000 |
Signaling by Retinoic Acid |
31 |
5.30e-01 |
7.35e-01 |
0.11700 |
0.003910 |
-0.117000 |
9.70e-01 |
0.260000 |
Formation of HIV-1 elongation complex containing HIV-1 Tat |
30 |
5.41e-01 |
7.39e-01 |
0.11700 |
-0.009740 |
-0.117000 |
9.26e-01 |
0.269000 |
HIV Transcription Elongation |
30 |
5.41e-01 |
7.39e-01 |
0.11700 |
-0.009740 |
-0.117000 |
9.26e-01 |
0.269000 |
Tat-mediated elongation of the HIV-1 transcript |
30 |
5.41e-01 |
7.39e-01 |
0.11700 |
-0.009740 |
-0.117000 |
9.26e-01 |
0.269000 |
Class A/1 (Rhodopsin-like receptors) |
114 |
9.93e-02 |
2.85e-01 |
0.11700 |
0.094400 |
0.068900 |
8.22e-02 |
0.205000 |
Long-term potentiation |
18 |
6.92e-01 |
8.45e-01 |
0.11700 |
-0.035400 |
0.111000 |
7.95e-01 |
0.414000 |
Regulation of PTEN gene transcription |
54 |
3.36e-01 |
5.83e-01 |
0.11600 |
-0.088400 |
-0.075800 |
2.62e-01 |
0.336000 |
Glycogen breakdown (glycogenolysis) |
14 |
7.54e-01 |
8.85e-01 |
0.11600 |
-0.113000 |
-0.025000 |
4.62e-01 |
0.871000 |
Plasma lipoprotein remodeling |
14 |
7.54e-01 |
8.85e-01 |
0.11600 |
-0.004390 |
-0.116000 |
9.77e-01 |
0.453000 |
Glycosphingolipid metabolism |
31 |
5.36e-01 |
7.38e-01 |
0.11600 |
-0.003960 |
-0.116000 |
9.70e-01 |
0.265000 |
Diseases of metabolism |
164 |
3.89e-02 |
1.51e-01 |
0.11600 |
-0.073900 |
-0.089100 |
1.03e-01 |
0.049600 |
Potassium Channels |
57 |
3.20e-01 |
5.66e-01 |
0.11600 |
-0.103000 |
0.053500 |
1.81e-01 |
0.485000 |
Regulation of signaling by CBL |
18 |
6.98e-01 |
8.48e-01 |
0.11600 |
0.058300 |
0.099900 |
6.69e-01 |
0.463000 |
Asymmetric localization of PCP proteins |
52 |
3.54e-01 |
6.01e-01 |
0.11600 |
0.061900 |
-0.097600 |
4.41e-01 |
0.224000 |
ADP signalling through P2Y purinoceptor 12 |
14 |
7.56e-01 |
8.85e-01 |
0.11600 |
0.059000 |
0.099300 |
7.02e-01 |
0.520000 |
Hyaluronan metabolism |
13 |
7.71e-01 |
8.91e-01 |
0.11600 |
0.040900 |
-0.108000 |
7.98e-01 |
0.500000 |
Transcriptional regulation by RUNX2 |
98 |
1.46e-01 |
3.63e-01 |
0.11500 |
0.059300 |
0.098500 |
3.12e-01 |
0.092600 |
Translation of structural proteins |
21 |
6.62e-01 |
8.17e-01 |
0.11500 |
-0.114000 |
0.003600 |
3.64e-01 |
0.977000 |
ERKs are inactivated |
13 |
7.75e-01 |
8.93e-01 |
0.11400 |
0.070800 |
-0.089900 |
6.58e-01 |
0.575000 |
Nucleotide Excision Repair |
86 |
1.89e-01 |
4.28e-01 |
0.11400 |
0.114000 |
-0.009970 |
6.89e-02 |
0.873000 |
Bile acid and bile salt metabolism |
23 |
6.40e-01 |
7.98e-01 |
0.11400 |
-0.107000 |
-0.040200 |
3.76e-01 |
0.739000 |
Separation of Sister Chromatids |
136 |
7.40e-02 |
2.35e-01 |
0.11400 |
0.113000 |
0.013400 |
2.34e-02 |
0.789000 |
Regulation of TP53 Degradation |
29 |
5.74e-01 |
7.57e-01 |
0.11300 |
-0.055600 |
-0.098600 |
6.04e-01 |
0.359000 |
NR1H2 and NR1H3-mediated signaling |
35 |
5.12e-01 |
7.21e-01 |
0.11300 |
-0.063100 |
-0.093900 |
5.18e-01 |
0.337000 |
EPH-Ephrin signaling |
78 |
2.26e-01 |
4.75e-01 |
0.11300 |
0.113000 |
-0.010800 |
8.60e-02 |
0.869000 |
Global Genome Nucleotide Excision Repair (GG-NER) |
68 |
2.75e-01 |
5.31e-01 |
0.11300 |
0.104000 |
-0.042800 |
1.38e-01 |
0.542000 |
Interaction between L1 and Ankyrins |
23 |
6.46e-01 |
8.00e-01 |
0.11300 |
-0.111000 |
-0.018500 |
3.57e-01 |
0.878000 |
Defective B4GALT7 causes EDS, progeroid type |
15 |
7.57e-01 |
8.85e-01 |
0.11100 |
0.075000 |
0.082300 |
6.15e-01 |
0.581000 |
Non-integrin membrane-ECM interactions |
37 |
5.06e-01 |
7.19e-01 |
0.11100 |
-0.024000 |
-0.108000 |
8.01e-01 |
0.254000 |
N-glycan antennae elongation in the medial/trans-Golgi |
19 |
7.05e-01 |
8.53e-01 |
0.11100 |
-0.037000 |
-0.105000 |
7.80e-01 |
0.430000 |
Sphingolipid de novo biosynthesis |
31 |
5.66e-01 |
7.56e-01 |
0.11100 |
-0.091600 |
0.062000 |
3.78e-01 |
0.551000 |
RNA polymerase II transcribes snRNA genes |
59 |
3.42e-01 |
5.90e-01 |
0.11000 |
-0.052500 |
0.096900 |
4.86e-01 |
0.198000 |
Vpr-mediated nuclear import of PICs |
24 |
6.46e-01 |
8.00e-01 |
0.11000 |
-0.075000 |
0.080600 |
5.25e-01 |
0.494000 |
mRNA decay by 5' to 3' exoribonuclease |
13 |
7.91e-01 |
9.04e-01 |
0.11000 |
-0.063700 |
-0.089300 |
6.91e-01 |
0.577000 |
Defective B3GAT3 causes JDSSDHD |
15 |
7.65e-01 |
8.88e-01 |
0.10900 |
0.058500 |
0.092200 |
6.95e-01 |
0.536000 |
Platelet homeostasis |
65 |
3.18e-01 |
5.66e-01 |
0.10900 |
-0.013400 |
-0.108000 |
8.52e-01 |
0.133000 |
Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways |
44 |
4.60e-01 |
6.92e-01 |
0.10900 |
0.069100 |
0.084000 |
4.28e-01 |
0.336000 |
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
13 |
7.96e-01 |
9.05e-01 |
0.10800 |
0.010600 |
-0.108000 |
9.47e-01 |
0.501000 |
Activation of GABAB receptors |
30 |
5.91e-01 |
7.68e-01 |
0.10800 |
-0.074600 |
0.078200 |
4.80e-01 |
0.459000 |
GABA B receptor activation |
30 |
5.91e-01 |
7.68e-01 |
0.10800 |
-0.074600 |
0.078200 |
4.80e-01 |
0.459000 |
G beta:gamma signalling through CDC42 |
12 |
8.12e-01 |
9.18e-01 |
0.10800 |
0.069300 |
0.082400 |
6.78e-01 |
0.621000 |
Metabolism of nucleotides |
78 |
2.73e-01 |
5.29e-01 |
0.10600 |
0.085000 |
-0.062600 |
1.95e-01 |
0.340000 |
Ovarian tumor domain proteases |
28 |
6.28e-01 |
7.92e-01 |
0.10500 |
0.048100 |
0.093800 |
6.60e-01 |
0.391000 |
Adaptive Immune System |
546 |
1.75e-04 |
4.00e-03 |
0.10500 |
0.095200 |
0.045000 |
1.69e-04 |
0.075000 |
N-Glycan antennae elongation |
12 |
8.19e-01 |
9.24e-01 |
0.10500 |
0.007390 |
-0.105000 |
9.65e-01 |
0.529000 |
Membrane Trafficking |
491 |
4.63e-04 |
9.13e-03 |
0.10400 |
-0.102000 |
0.020800 |
1.24e-04 |
0.435000 |
p75NTR signals via NF-kB |
10 |
8.51e-01 |
9.39e-01 |
0.10400 |
-0.102000 |
-0.017100 |
5.75e-01 |
0.925000 |
Visual phototransduction |
50 |
4.47e-01 |
6.84e-01 |
0.10400 |
-0.072100 |
-0.074800 |
3.78e-01 |
0.361000 |
NOTCH4 Intracellular Domain Regulates Transcription |
17 |
7.60e-01 |
8.87e-01 |
0.10400 |
-0.003670 |
0.104000 |
9.79e-01 |
0.459000 |
RHO GTPases Activate Formins |
96 |
2.15e-01 |
4.65e-01 |
0.10400 |
0.045200 |
0.093400 |
4.45e-01 |
0.115000 |
Nuclear Pore Complex (NPC) Disassembly |
27 |
6.48e-01 |
8.01e-01 |
0.10400 |
-0.005810 |
0.103000 |
9.58e-01 |
0.353000 |
Diseases of glycosylation |
107 |
1.82e-01 |
4.21e-01 |
0.10300 |
-0.019500 |
-0.102000 |
7.28e-01 |
0.069900 |
MET promotes cell motility |
28 |
6.40e-01 |
7.98e-01 |
0.10300 |
-0.033700 |
0.097600 |
7.58e-01 |
0.372000 |
Platelet calcium homeostasis |
20 |
7.27e-01 |
8.67e-01 |
0.10300 |
-0.088100 |
-0.053800 |
4.96e-01 |
0.677000 |
Cell-Cell communication |
77 |
2.95e-01 |
5.47e-01 |
0.10300 |
0.025500 |
0.100000 |
6.99e-01 |
0.130000 |
SUMOylation of transcription cofactors |
36 |
5.65e-01 |
7.56e-01 |
0.10300 |
-0.091200 |
-0.048000 |
3.44e-01 |
0.619000 |
Formation of the Early Elongation Complex |
25 |
6.73e-01 |
8.28e-01 |
0.10300 |
-0.070400 |
-0.075200 |
5.43e-01 |
0.516000 |
Formation of the HIV-1 Early Elongation Complex |
25 |
6.73e-01 |
8.28e-01 |
0.10300 |
-0.070400 |
-0.075200 |
5.43e-01 |
0.516000 |
Regulation of TP53 Activity |
135 |
1.24e-01 |
3.29e-01 |
0.10200 |
-0.034400 |
-0.096300 |
4.92e-01 |
0.054000 |
Inositol phosphate metabolism |
41 |
5.35e-01 |
7.38e-01 |
0.10100 |
-0.082200 |
-0.058900 |
3.63e-01 |
0.515000 |
Amine ligand-binding receptors |
11 |
8.45e-01 |
9.39e-01 |
0.10100 |
-0.085900 |
0.053400 |
6.22e-01 |
0.759000 |
RHO GTPases activate PKNs |
31 |
6.23e-01 |
7.88e-01 |
0.10100 |
0.085400 |
0.054100 |
4.11e-01 |
0.603000 |
RHO GTPase Effectors |
205 |
4.57e-02 |
1.72e-01 |
0.10100 |
0.101000 |
-0.002660 |
1.30e-02 |
0.948000 |
Regulation of TP53 Expression and Degradation |
30 |
6.35e-01 |
7.95e-01 |
0.10100 |
-0.069900 |
-0.072400 |
5.08e-01 |
0.493000 |
Metabolism of carbohydrates |
215 |
4.09e-02 |
1.57e-01 |
0.10100 |
-0.065400 |
-0.076400 |
9.99e-02 |
0.054400 |
Signaling by KIT in disease |
20 |
7.39e-01 |
8.74e-01 |
0.10100 |
0.060100 |
0.080600 |
6.42e-01 |
0.533000 |
Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants |
20 |
7.39e-01 |
8.74e-01 |
0.10100 |
0.060100 |
0.080600 |
6.42e-01 |
0.533000 |
Degradation of beta-catenin by the destruction complex |
69 |
3.57e-01 |
6.03e-01 |
0.10000 |
0.098300 |
-0.018700 |
1.59e-01 |
0.788000 |
Metabolic disorders of biological oxidation enzymes |
18 |
7.63e-01 |
8.88e-01 |
0.10000 |
-0.043600 |
0.090000 |
7.49e-01 |
0.509000 |
Immune System |
1422 |
7.88e-09 |
1.65e-06 |
0.09970 |
0.099600 |
-0.003410 |
1.03e-09 |
0.835000 |
HIV Transcription Initiation |
37 |
5.78e-01 |
7.57e-01 |
0.09950 |
-0.083600 |
0.054000 |
3.80e-01 |
0.570000 |
RNA Polymerase II HIV Promoter Escape |
37 |
5.78e-01 |
7.57e-01 |
0.09950 |
-0.083600 |
0.054000 |
3.80e-01 |
0.570000 |
RNA Polymerase II Promoter Escape |
37 |
5.78e-01 |
7.57e-01 |
0.09950 |
-0.083600 |
0.054000 |
3.80e-01 |
0.570000 |
RNA Polymerase II Transcription Initiation |
37 |
5.78e-01 |
7.57e-01 |
0.09950 |
-0.083600 |
0.054000 |
3.80e-01 |
0.570000 |
RNA Polymerase II Transcription Initiation And Promoter Clearance |
37 |
5.78e-01 |
7.57e-01 |
0.09950 |
-0.083600 |
0.054000 |
3.80e-01 |
0.570000 |
RNA Polymerase II Transcription Pre-Initiation And Promoter Opening |
37 |
5.78e-01 |
7.57e-01 |
0.09950 |
-0.083600 |
0.054000 |
3.80e-01 |
0.570000 |
Signaling by PDGFR in disease |
19 |
7.55e-01 |
8.85e-01 |
0.09940 |
-0.090600 |
0.041000 |
4.94e-01 |
0.757000 |
Mitochondrial protein import |
49 |
4.86e-01 |
7.07e-01 |
0.09930 |
0.051400 |
-0.084900 |
5.34e-01 |
0.304000 |
Collagen degradation |
25 |
6.93e-01 |
8.45e-01 |
0.09900 |
-0.095000 |
-0.027700 |
4.11e-01 |
0.811000 |
ESR-mediated signaling |
133 |
1.44e-01 |
3.62e-01 |
0.09900 |
-0.044800 |
0.088300 |
3.73e-01 |
0.079600 |
Signaling by ERBB4 |
40 |
5.59e-01 |
7.54e-01 |
0.09850 |
-0.072300 |
0.066900 |
4.29e-01 |
0.464000 |
ABC-family proteins mediated transport |
73 |
3.49e-01 |
5.99e-01 |
0.09830 |
0.049900 |
-0.084700 |
4.62e-01 |
0.211000 |
Platelet activation, signaling and aggregation |
197 |
6.06e-02 |
2.06e-01 |
0.09820 |
0.095700 |
-0.022100 |
2.11e-02 |
0.595000 |
ZBP1(DAI) mediated induction of type I IFNs |
18 |
7.72e-01 |
8.91e-01 |
0.09810 |
0.001230 |
-0.098100 |
9.93e-01 |
0.471000 |
G2/M Transition |
151 |
1.17e-01 |
3.15e-01 |
0.09800 |
0.097900 |
0.005030 |
3.84e-02 |
0.915000 |
Intrinsic Pathway for Apoptosis |
42 |
5.49e-01 |
7.45e-01 |
0.09770 |
0.097600 |
0.003990 |
2.74e-01 |
0.964000 |
Leishmania infection |
157 |
1.10e-01 |
3.01e-01 |
0.09750 |
0.093700 |
-0.026900 |
4.34e-02 |
0.563000 |
TCF dependent signaling in response to WNT |
133 |
1.56e-01 |
3.79e-01 |
0.09710 |
-0.097100 |
0.002830 |
5.38e-02 |
0.955000 |
A tetrasaccharide linker sequence is required for GAG synthesis |
19 |
7.67e-01 |
8.89e-01 |
0.09670 |
0.068800 |
0.067900 |
6.04e-01 |
0.608000 |
Mitotic G2-G2/M phases |
153 |
1.21e-01 |
3.24e-01 |
0.09660 |
0.096200 |
0.007830 |
4.05e-02 |
0.868000 |
Chaperone Mediated Autophagy |
13 |
8.35e-01 |
9.31e-01 |
0.09650 |
-0.074600 |
-0.061200 |
6.41e-01 |
0.703000 |
NOTCH3 Intracellular Domain Regulates Transcription |
21 |
7.47e-01 |
8.82e-01 |
0.09620 |
-0.025200 |
0.092900 |
8.42e-01 |
0.461000 |
Class B/2 (Secretin family receptors) |
38 |
5.94e-01 |
7.70e-01 |
0.09570 |
-0.093500 |
0.020400 |
3.19e-01 |
0.828000 |
Elastic fibre formation |
35 |
6.20e-01 |
7.87e-01 |
0.09570 |
-0.061300 |
-0.073400 |
5.30e-01 |
0.453000 |
EML4 and NUDC in mitotic spindle formation |
77 |
3.51e-01 |
6.00e-01 |
0.09560 |
0.023500 |
0.092600 |
7.21e-01 |
0.160000 |
Rab regulation of trafficking |
104 |
2.45e-01 |
4.96e-01 |
0.09550 |
-0.090100 |
-0.031500 |
1.13e-01 |
0.579000 |
Negative regulation of the PI3K/AKT network |
87 |
3.08e-01 |
5.57e-01 |
0.09540 |
-0.006560 |
0.095200 |
9.16e-01 |
0.126000 |
Signaling by PDGFRA extracellular domain mutants |
12 |
8.51e-01 |
9.39e-01 |
0.09470 |
0.017200 |
0.093100 |
9.18e-01 |
0.577000 |
Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants |
12 |
8.51e-01 |
9.39e-01 |
0.09470 |
0.017200 |
0.093100 |
9.18e-01 |
0.577000 |
Regulation of lipid metabolism by PPARalpha |
102 |
2.57e-01 |
5.08e-01 |
0.09470 |
-0.002390 |
0.094600 |
9.67e-01 |
0.099300 |
Vesicle-mediated transport |
521 |
1.24e-03 |
1.81e-02 |
0.09460 |
-0.094100 |
0.009770 |
2.74e-04 |
0.706000 |
Activation of HOX genes during differentiation |
42 |
5.70e-01 |
7.57e-01 |
0.09450 |
-0.060100 |
0.072900 |
5.01e-01 |
0.414000 |
Activation of anterior HOX genes in hindbrain development during early embryogenesis |
42 |
5.70e-01 |
7.57e-01 |
0.09450 |
-0.060100 |
0.072900 |
5.01e-01 |
0.414000 |
Signaling by MET |
58 |
4.63e-01 |
6.92e-01 |
0.09420 |
-0.069300 |
0.063800 |
3.62e-01 |
0.401000 |
Senescence-Associated Secretory Phenotype (SASP) |
39 |
6.02e-01 |
7.75e-01 |
0.09320 |
0.027600 |
-0.089000 |
7.66e-01 |
0.337000 |
Assembly of collagen fibrils and other multimeric structures |
44 |
5.66e-01 |
7.56e-01 |
0.09310 |
-0.004990 |
-0.093000 |
9.54e-01 |
0.286000 |
PPARA activates gene expression |
100 |
2.77e-01 |
5.33e-01 |
0.09290 |
-0.011900 |
0.092200 |
8.37e-01 |
0.112000 |
Gap junction trafficking |
14 |
8.36e-01 |
9.31e-01 |
0.09260 |
-0.092400 |
0.005370 |
5.50e-01 |
0.972000 |
Formation of HIV elongation complex in the absence of HIV Tat |
31 |
6.74e-01 |
8.28e-01 |
0.09230 |
0.019100 |
-0.090300 |
8.54e-01 |
0.385000 |
Negative epigenetic regulation of rRNA expression |
36 |
6.33e-01 |
7.94e-01 |
0.09220 |
0.090900 |
0.015500 |
3.46e-01 |
0.872000 |
SLC-mediated transmembrane transport |
148 |
1.55e-01 |
3.78e-01 |
0.09220 |
0.010200 |
-0.091600 |
8.31e-01 |
0.055100 |
ERK/MAPK targets |
22 |
7.56e-01 |
8.85e-01 |
0.09220 |
-0.071800 |
0.057800 |
5.60e-01 |
0.639000 |
TP53 Regulates Metabolic Genes |
71 |
4.08e-01 |
6.51e-01 |
0.09200 |
-0.077200 |
0.050000 |
2.61e-01 |
0.467000 |
SUMOylation of chromatin organization proteins |
44 |
5.73e-01 |
7.57e-01 |
0.09190 |
-0.084900 |
0.035200 |
3.30e-01 |
0.686000 |
NEP/NS2 Interacts with the Cellular Export Machinery |
23 |
7.51e-01 |
8.85e-01 |
0.09120 |
-0.035600 |
0.083900 |
7.68e-01 |
0.486000 |
SLC transporter disorders |
59 |
4.83e-01 |
7.07e-01 |
0.09100 |
-0.075300 |
-0.051100 |
3.18e-01 |
0.497000 |
RNA Polymerase III Transcription Initiation From Type 1 Promoter |
20 |
7.82e-01 |
8.97e-01 |
0.09060 |
0.075800 |
-0.049800 |
5.58e-01 |
0.700000 |
VEGFR2 mediated vascular permeability |
27 |
7.18e-01 |
8.61e-01 |
0.09060 |
-0.068000 |
0.059800 |
5.41e-01 |
0.591000 |
Post-translational modification: synthesis of GPI-anchored proteins |
54 |
5.26e-01 |
7.33e-01 |
0.08920 |
-0.069900 |
0.055500 |
3.75e-01 |
0.481000 |
Hedgehog 'on' state |
68 |
4.46e-01 |
6.84e-01 |
0.08920 |
0.078500 |
-0.042300 |
2.63e-01 |
0.547000 |
HCMV Late Events |
41 |
6.16e-01 |
7.85e-01 |
0.08910 |
-0.084300 |
-0.028600 |
3.51e-01 |
0.751000 |
Signaling by Erythropoietin |
23 |
7.62e-01 |
8.87e-01 |
0.08900 |
0.031600 |
0.083200 |
7.93e-01 |
0.490000 |
Inwardly rectifying K+ channels |
21 |
7.80e-01 |
8.97e-01 |
0.08890 |
-0.035300 |
-0.081600 |
7.79e-01 |
0.518000 |
O-linked glycosylation |
67 |
4.54e-01 |
6.89e-01 |
0.08890 |
-0.009280 |
-0.088400 |
8.96e-01 |
0.212000 |
Interleukin-7 signaling |
16 |
8.28e-01 |
9.29e-01 |
0.08870 |
0.041000 |
-0.078700 |
7.77e-01 |
0.586000 |
Downstream signal transduction |
28 |
7.21e-01 |
8.64e-01 |
0.08840 |
-0.039200 |
0.079200 |
7.20e-01 |
0.469000 |
trans-Golgi Network Vesicle Budding |
59 |
5.03e-01 |
7.19e-01 |
0.08830 |
-0.088200 |
0.004160 |
2.42e-01 |
0.956000 |
HCMV Infection |
64 |
4.78e-01 |
7.04e-01 |
0.08800 |
-0.087800 |
0.004760 |
2.25e-01 |
0.948000 |
Caspase-mediated cleavage of cytoskeletal proteins |
11 |
8.81e-01 |
9.53e-01 |
0.08760 |
-0.070300 |
-0.052300 |
6.87e-01 |
0.764000 |
Plasma lipoprotein assembly, remodeling, and clearance |
45 |
5.97e-01 |
7.72e-01 |
0.08750 |
0.040800 |
-0.077400 |
6.36e-01 |
0.370000 |
Protein-protein interactions at synapses |
60 |
5.05e-01 |
7.19e-01 |
0.08740 |
-0.084800 |
-0.021100 |
2.57e-01 |
0.778000 |
Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal |
73 |
4.37e-01 |
6.77e-01 |
0.08730 |
0.048400 |
0.072700 |
4.75e-01 |
0.284000 |
Amplification of signal from the kinetochores |
73 |
4.37e-01 |
6.77e-01 |
0.08730 |
0.048400 |
0.072700 |
4.75e-01 |
0.284000 |
COPI-dependent Golgi-to-ER retrograde traffic |
67 |
4.68e-01 |
6.94e-01 |
0.08720 |
0.002920 |
-0.087200 |
9.67e-01 |
0.218000 |
TP53 Regulates Transcription of Genes Involved in Cytochrome C Release |
14 |
8.53e-01 |
9.39e-01 |
0.08710 |
-0.076500 |
-0.041600 |
6.20e-01 |
0.788000 |
Nonhomologous End-Joining (NHEJ) |
28 |
7.30e-01 |
8.69e-01 |
0.08670 |
0.084800 |
-0.017800 |
4.38e-01 |
0.871000 |
Gamma carboxylation, hypusine formation and arylsulfatase activation |
26 |
7.48e-01 |
8.83e-01 |
0.08640 |
-0.033000 |
-0.079800 |
7.71e-01 |
0.481000 |
Mitochondrial translation |
70 |
4.64e-01 |
6.92e-01 |
0.08590 |
-0.069500 |
-0.050500 |
3.15e-01 |
0.466000 |
The citric acid (TCA) cycle and respiratory electron transport |
114 |
2.89e-01 |
5.41e-01 |
0.08570 |
0.046300 |
0.072100 |
3.94e-01 |
0.185000 |
Degradation of the extracellular matrix |
71 |
4.64e-01 |
6.92e-01 |
0.08520 |
-0.042200 |
-0.074000 |
5.39e-01 |
0.281000 |
Chaperonin-mediated protein folding |
68 |
4.80e-01 |
7.04e-01 |
0.08500 |
-0.068200 |
0.050700 |
3.32e-01 |
0.470000 |
Constitutive Signaling by Aberrant PI3K in Cancer |
56 |
5.48e-01 |
7.44e-01 |
0.08500 |
0.041500 |
0.074100 |
5.91e-01 |
0.338000 |
RNA Polymerase I Transcription Termination |
21 |
7.97e-01 |
9.06e-01 |
0.08490 |
-0.058000 |
-0.062100 |
6.46e-01 |
0.623000 |
ISG15 antiviral mechanism |
51 |
5.78e-01 |
7.57e-01 |
0.08490 |
0.071000 |
0.046600 |
3.81e-01 |
0.566000 |
tRNA processing |
84 |
4.06e-01 |
6.51e-01 |
0.08480 |
0.060500 |
-0.059300 |
3.38e-01 |
0.348000 |
Toll Like Receptor 4 (TLR4) Cascade |
107 |
3.21e-01 |
5.66e-01 |
0.08440 |
-0.062000 |
0.057400 |
2.69e-01 |
0.306000 |
Diseases associated with the TLR signaling cascade |
20 |
8.08e-01 |
9.16e-01 |
0.08430 |
-0.084100 |
-0.005270 |
5.15e-01 |
0.967000 |
Diseases of Immune System |
20 |
8.08e-01 |
9.16e-01 |
0.08430 |
-0.084100 |
-0.005270 |
5.15e-01 |
0.967000 |
HCMV Early Events |
46 |
6.16e-01 |
7.85e-01 |
0.08390 |
-0.067600 |
0.049800 |
4.28e-01 |
0.560000 |
Programmed Cell Death |
140 |
2.38e-01 |
4.88e-01 |
0.08320 |
0.070100 |
0.044800 |
1.53e-01 |
0.361000 |
MHC class II antigen presentation |
88 |
4.03e-01 |
6.48e-01 |
0.08320 |
0.047800 |
-0.068100 |
4.39e-01 |
0.270000 |
Signaling by PDGF |
47 |
6.16e-01 |
7.85e-01 |
0.08300 |
-0.081200 |
0.017200 |
3.36e-01 |
0.838000 |
Hemostasis |
427 |
1.43e-02 |
8.18e-02 |
0.08300 |
0.082900 |
-0.002520 |
3.57e-03 |
0.929000 |
Antigen processing: Ubiquitination & Proteasome degradation |
244 |
8.49e-02 |
2.59e-01 |
0.08290 |
-0.018400 |
0.080900 |
6.22e-01 |
0.030400 |
DDX58/IFIH1-mediated induction of interferon-alpha/beta |
48 |
6.10e-01 |
7.82e-01 |
0.08290 |
0.063100 |
-0.053800 |
4.50e-01 |
0.519000 |
G-protein beta:gamma signalling |
23 |
7.90e-01 |
9.04e-01 |
0.08280 |
0.067100 |
-0.048500 |
5.78e-01 |
0.688000 |
Mitotic Prometaphase |
154 |
2.11e-01 |
4.58e-01 |
0.08260 |
0.068100 |
0.046800 |
1.46e-01 |
0.318000 |
RNA Polymerase III Abortive And Retractive Initiation |
33 |
7.15e-01 |
8.60e-01 |
0.08240 |
0.081900 |
0.009780 |
4.16e-01 |
0.923000 |
RNA Polymerase III Transcription |
33 |
7.15e-01 |
8.60e-01 |
0.08240 |
0.081900 |
0.009780 |
4.16e-01 |
0.923000 |
Signal transduction by L1 |
19 |
8.25e-01 |
9.26e-01 |
0.08240 |
0.071200 |
0.041400 |
5.91e-01 |
0.755000 |
Transcriptional regulation of white adipocyte differentiation |
69 |
4.99e-01 |
7.14e-01 |
0.08220 |
-0.019400 |
0.079900 |
7.80e-01 |
0.252000 |
Signaling by WNT |
204 |
1.33e-01 |
3.46e-01 |
0.08190 |
-0.081600 |
0.006480 |
4.53e-02 |
0.874000 |
Regulation of PLK1 Activity at G2/M Transition |
72 |
4.88e-01 |
7.07e-01 |
0.08170 |
-0.033300 |
0.074600 |
6.26e-01 |
0.275000 |
Apoptosis |
137 |
2.64e-01 |
5.16e-01 |
0.08110 |
0.065800 |
0.047400 |
1.85e-01 |
0.339000 |
Nuclear signaling by ERBB4 |
25 |
7.83e-01 |
8.98e-01 |
0.08090 |
-0.080500 |
-0.008550 |
4.86e-01 |
0.941000 |
G alpha (s) signalling events |
78 |
4.67e-01 |
6.94e-01 |
0.08090 |
-0.051800 |
0.062100 |
4.30e-01 |
0.344000 |
Estrogen-dependent gene expression |
76 |
4.77e-01 |
7.04e-01 |
0.08080 |
-0.075300 |
0.029200 |
2.57e-01 |
0.660000 |
Organelle biogenesis and maintenance |
220 |
1.21e-01 |
3.24e-01 |
0.08080 |
-0.080700 |
0.002190 |
3.99e-02 |
0.956000 |
Neurexins and neuroligins |
37 |
7.01e-01 |
8.50e-01 |
0.08020 |
-0.035000 |
-0.072200 |
7.13e-01 |
0.448000 |
Regulation of localization of FOXO transcription factors |
12 |
8.91e-01 |
9.56e-01 |
0.08020 |
-0.057500 |
0.055900 |
7.30e-01 |
0.738000 |
Intra-Golgi and retrograde Golgi-to-ER traffic |
153 |
2.36e-01 |
4.86e-01 |
0.07980 |
-0.042800 |
0.067400 |
3.63e-01 |
0.152000 |
Insulin receptor recycling |
17 |
8.50e-01 |
9.39e-01 |
0.07970 |
-0.033000 |
0.072600 |
8.14e-01 |
0.604000 |
Disorders of transmembrane transporters |
111 |
3.54e-01 |
6.01e-01 |
0.07930 |
0.049400 |
-0.062000 |
3.69e-01 |
0.260000 |
Regulation of TP53 Activity through Phosphorylation |
76 |
4.92e-01 |
7.10e-01 |
0.07910 |
0.003990 |
-0.079000 |
9.52e-01 |
0.234000 |
Phospholipid metabolism |
162 |
2.29e-01 |
4.77e-01 |
0.07850 |
-0.047200 |
-0.062800 |
3.01e-01 |
0.169000 |
Laminin interactions |
22 |
8.19e-01 |
9.24e-01 |
0.07790 |
-0.016900 |
-0.076000 |
8.91e-01 |
0.537000 |
Nuclear Receptor transcription pathway |
43 |
6.78e-01 |
8.32e-01 |
0.07780 |
-0.077600 |
0.004590 |
3.79e-01 |
0.958000 |
Interleukin-35 Signalling |
10 |
9.13e-01 |
9.66e-01 |
0.07780 |
0.047800 |
-0.061400 |
7.94e-01 |
0.737000 |
Post-translational protein phosphorylation |
67 |
5.47e-01 |
7.43e-01 |
0.07770 |
-0.069600 |
0.034400 |
3.25e-01 |
0.627000 |
Translation |
178 |
2.05e-01 |
4.53e-01 |
0.07770 |
0.074800 |
-0.020900 |
8.63e-02 |
0.632000 |
Infectious disease |
501 |
1.34e-02 |
7.84e-02 |
0.07750 |
0.076600 |
0.011600 |
3.67e-03 |
0.659000 |
ADORA2B mediated anti-inflammatory cytokines production |
55 |
6.10e-01 |
7.82e-01 |
0.07750 |
-0.052000 |
0.057400 |
5.06e-01 |
0.462000 |
Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA |
15 |
8.75e-01 |
9.50e-01 |
0.07710 |
-0.031800 |
0.070200 |
8.31e-01 |
0.638000 |
Phosphorylation of the APC/C |
17 |
8.63e-01 |
9.43e-01 |
0.07630 |
-0.031600 |
-0.069400 |
8.22e-01 |
0.620000 |
Clathrin-mediated endocytosis |
110 |
3.88e-01 |
6.34e-01 |
0.07610 |
-0.070300 |
0.029100 |
2.04e-01 |
0.599000 |
Amino acids regulate mTORC1 |
42 |
6.97e-01 |
8.48e-01 |
0.07580 |
-0.055400 |
0.051800 |
5.35e-01 |
0.562000 |
Golgi Cisternae Pericentriolar Stack Reorganization |
12 |
9.02e-01 |
9.59e-01 |
0.07570 |
0.017500 |
-0.073600 |
9.16e-01 |
0.659000 |
APC/C:Cdc20 mediated degradation of Cyclin B |
18 |
8.57e-01 |
9.39e-01 |
0.07560 |
0.014600 |
-0.074200 |
9.15e-01 |
0.586000 |
SUMOylation of RNA binding proteins |
36 |
7.35e-01 |
8.72e-01 |
0.07550 |
-0.073000 |
0.019500 |
4.49e-01 |
0.840000 |
Cytokine Signaling in Immune system |
605 |
7.55e-03 |
5.65e-02 |
0.07540 |
0.074600 |
0.010600 |
1.96e-03 |
0.659000 |
Cell junction organization |
46 |
6.83e-01 |
8.36e-01 |
0.07460 |
-0.068600 |
-0.029300 |
4.21e-01 |
0.731000 |
RNA Polymerase II Pre-transcription Events |
62 |
6.00e-01 |
7.75e-01 |
0.07420 |
-0.068300 |
0.029200 |
3.53e-01 |
0.692000 |
Class I MHC mediated antigen processing & presentation |
291 |
9.63e-02 |
2.81e-01 |
0.07420 |
0.019900 |
0.071500 |
5.62e-01 |
0.037000 |
Presynaptic function of Kainate receptors |
13 |
8.99e-01 |
9.58e-01 |
0.07390 |
0.010800 |
-0.073100 |
9.46e-01 |
0.648000 |
Muscle contraction |
154 |
2.89e-01 |
5.41e-01 |
0.07380 |
-0.072800 |
0.012100 |
1.20e-01 |
0.797000 |
CLEC7A (Dectin-1) signaling |
80 |
5.29e-01 |
7.35e-01 |
0.07310 |
0.059800 |
0.042100 |
3.56e-01 |
0.516000 |
Golgi-to-ER retrograde transport |
97 |
4.63e-01 |
6.92e-01 |
0.07310 |
-0.064100 |
-0.035200 |
2.76e-01 |
0.550000 |
Signaling by VEGF |
95 |
4.71e-01 |
6.97e-01 |
0.07300 |
0.071700 |
-0.013600 |
2.28e-01 |
0.820000 |
Mitotic Metaphase and Anaphase |
185 |
2.38e-01 |
4.88e-01 |
0.07250 |
0.072500 |
0.001970 |
9.03e-02 |
0.963000 |
Cellular Senescence |
108 |
4.36e-01 |
6.77e-01 |
0.07200 |
-0.066100 |
-0.028500 |
2.36e-01 |
0.609000 |
Scavenging by Class A Receptors |
13 |
9.05e-01 |
9.60e-01 |
0.07180 |
0.039900 |
0.059700 |
8.03e-01 |
0.709000 |
Signaling by Rho GTPases |
319 |
9.32e-02 |
2.75e-01 |
0.07130 |
0.066300 |
-0.026400 |
4.31e-02 |
0.421000 |
Interactions of Rev with host cellular proteins |
26 |
8.21e-01 |
9.24e-01 |
0.07130 |
0.003180 |
0.071200 |
9.78e-01 |
0.530000 |
Transport of small molecules |
456 |
3.58e-02 |
1.47e-01 |
0.07120 |
-0.059600 |
-0.039000 |
3.07e-02 |
0.157000 |
Metabolism of water-soluble vitamins and cofactors |
89 |
5.14e-01 |
7.21e-01 |
0.07100 |
-0.044500 |
-0.055300 |
4.69e-01 |
0.368000 |
Beta-catenin independent WNT signaling |
116 |
4.19e-01 |
6.65e-01 |
0.07100 |
0.020100 |
-0.068100 |
7.10e-01 |
0.206000 |
mRNA Capping |
21 |
8.58e-01 |
9.39e-01 |
0.06980 |
-0.067500 |
0.018000 |
5.93e-01 |
0.887000 |
Late Phase of HIV Life Cycle |
99 |
4.89e-01 |
7.07e-01 |
0.06970 |
-0.068100 |
0.014600 |
2.42e-01 |
0.802000 |
Metabolism of steroid hormones |
18 |
8.78e-01 |
9.52e-01 |
0.06960 |
0.045400 |
0.052800 |
7.39e-01 |
0.698000 |
Signaling by NOTCH1 |
61 |
6.44e-01 |
8.00e-01 |
0.06960 |
-0.065100 |
0.024600 |
3.80e-01 |
0.740000 |
G alpha (q) signalling events |
118 |
4.33e-01 |
6.75e-01 |
0.06920 |
0.021100 |
0.065900 |
6.93e-01 |
0.217000 |
Signaling by Interleukins |
325 |
1.04e-01 |
2.91e-01 |
0.06920 |
0.068200 |
0.011900 |
3.59e-02 |
0.715000 |
Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) |
22 |
8.54e-01 |
9.39e-01 |
0.06910 |
-0.059600 |
0.035000 |
6.29e-01 |
0.776000 |
Regulation of Glucokinase by Glucokinase Regulatory Protein |
22 |
8.54e-01 |
9.39e-01 |
0.06910 |
-0.059600 |
0.035000 |
6.29e-01 |
0.776000 |
VEGFA-VEGFR2 Pathway |
89 |
5.38e-01 |
7.39e-01 |
0.06840 |
0.066600 |
-0.015300 |
2.78e-01 |
0.803000 |
Transcriptional regulation by small RNAs |
33 |
7.97e-01 |
9.05e-01 |
0.06790 |
-0.067400 |
0.008110 |
5.03e-01 |
0.936000 |
Mitotic Anaphase |
184 |
2.89e-01 |
5.41e-01 |
0.06760 |
0.067600 |
-0.000155 |
1.15e-01 |
0.997000 |
Ephrin signaling |
19 |
8.80e-01 |
9.53e-01 |
0.06700 |
0.043500 |
0.051000 |
7.43e-01 |
0.700000 |
VEGFR2 mediated cell proliferation |
19 |
8.81e-01 |
9.53e-01 |
0.06690 |
0.057800 |
0.033700 |
6.63e-01 |
0.800000 |
CD28 dependent PI3K/Akt signaling |
21 |
8.72e-01 |
9.50e-01 |
0.06600 |
0.050900 |
0.042000 |
6.87e-01 |
0.739000 |
Toll-like Receptor Cascades |
122 |
4.56e-01 |
6.89e-01 |
0.06580 |
-0.041500 |
0.051100 |
4.29e-01 |
0.331000 |
Growth hormone receptor signaling |
17 |
8.99e-01 |
9.58e-01 |
0.06480 |
-0.064100 |
0.009290 |
6.47e-01 |
0.947000 |
GPCR ligand binding |
155 |
3.84e-01 |
6.31e-01 |
0.06470 |
0.042800 |
0.048500 |
3.59e-01 |
0.299000 |
Formation of TC-NER Pre-Incision Complex |
38 |
7.89e-01 |
9.04e-01 |
0.06460 |
0.028000 |
0.058200 |
7.65e-01 |
0.535000 |
M Phase |
285 |
1.76e-01 |
4.14e-01 |
0.06450 |
0.063800 |
0.009880 |
6.54e-02 |
0.775000 |
Metabolism of vitamins and cofactors |
134 |
4.38e-01 |
6.78e-01 |
0.06450 |
-0.041500 |
-0.049300 |
4.08e-01 |
0.325000 |
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) |
73 |
6.37e-01 |
7.96e-01 |
0.06430 |
-0.058600 |
0.026500 |
3.87e-01 |
0.696000 |
Signaling by Receptor Tyrosine Kinases |
396 |
9.71e-02 |
2.83e-01 |
0.06370 |
-0.056000 |
0.030300 |
5.78e-02 |
0.304000 |
Nuclear Envelope (NE) Reassembly |
58 |
7.13e-01 |
8.60e-01 |
0.06250 |
-0.057200 |
-0.025200 |
4.52e-01 |
0.740000 |
Metabolism of fat-soluble vitamins |
27 |
8.54e-01 |
9.39e-01 |
0.06250 |
-0.011000 |
-0.061500 |
9.21e-01 |
0.580000 |
Defective B3GALTL causes Peters-plus syndrome (PpS) |
31 |
8.35e-01 |
9.31e-01 |
0.06220 |
0.019600 |
-0.059100 |
8.51e-01 |
0.569000 |
O-glycosylation of TSR domain-containing proteins |
32 |
8.32e-01 |
9.31e-01 |
0.06200 |
0.013000 |
-0.060600 |
8.99e-01 |
0.553000 |
p38MAPK events |
12 |
9.33e-01 |
9.82e-01 |
0.06200 |
0.039700 |
-0.047500 |
8.12e-01 |
0.776000 |
Axon guidance |
394 |
1.12e-01 |
3.06e-01 |
0.06190 |
0.049100 |
0.037800 |
9.72e-02 |
0.202000 |
Interleukin-37 signaling |
18 |
9.02e-01 |
9.59e-01 |
0.06190 |
0.032000 |
-0.052900 |
8.14e-01 |
0.698000 |
PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling |
81 |
6.31e-01 |
7.93e-01 |
0.06180 |
-0.015800 |
0.059700 |
8.06e-01 |
0.354000 |
Signaling by Hedgehog |
111 |
5.33e-01 |
7.37e-01 |
0.06180 |
-0.061100 |
-0.009020 |
2.67e-01 |
0.870000 |
Rev-mediated nuclear export of HIV RNA |
25 |
8.67e-01 |
9.47e-01 |
0.06170 |
0.005150 |
0.061500 |
9.64e-01 |
0.595000 |
Neurotransmitter release cycle |
29 |
8.48e-01 |
9.39e-01 |
0.06160 |
-0.057800 |
0.021400 |
5.90e-01 |
0.842000 |
Diseases of signal transduction by growth factor receptors and second messengers |
307 |
1.90e-01 |
4.31e-01 |
0.06080 |
-0.059500 |
0.012600 |
7.49e-02 |
0.706000 |
RIP-mediated NFkB activation via ZBP1 |
15 |
9.21e-01 |
9.72e-01 |
0.06060 |
-0.024600 |
-0.055400 |
8.69e-01 |
0.711000 |
Extracellular matrix organization |
212 |
3.20e-01 |
5.66e-01 |
0.06040 |
-0.012600 |
-0.059100 |
7.54e-01 |
0.140000 |
Retinoid metabolism and transport |
25 |
8.73e-01 |
9.50e-01 |
0.06020 |
0.029300 |
-0.052600 |
8.00e-01 |
0.649000 |
Transcriptional regulation by RUNX1 |
146 |
4.57e-01 |
6.91e-01 |
0.06010 |
0.041300 |
-0.043600 |
3.90e-01 |
0.364000 |
SUMO E3 ligases SUMOylate target proteins |
131 |
4.98e-01 |
7.14e-01 |
0.05990 |
0.059800 |
0.003840 |
2.39e-01 |
0.940000 |
Signaling by NOTCH3 |
38 |
8.16e-01 |
9.22e-01 |
0.05990 |
0.055800 |
0.021700 |
5.52e-01 |
0.817000 |
Fatty acyl-CoA biosynthesis |
22 |
8.90e-01 |
9.56e-01 |
0.05940 |
0.019800 |
-0.056000 |
8.72e-01 |
0.649000 |
Mitochondrial translation elongation |
64 |
7.15e-01 |
8.60e-01 |
0.05930 |
-0.030200 |
-0.051100 |
6.77e-01 |
0.480000 |
Intraflagellar transport |
35 |
8.32e-01 |
9.31e-01 |
0.05920 |
-0.030300 |
0.050900 |
7.57e-01 |
0.603000 |
Intracellular signaling by second messengers |
254 |
2.72e-01 |
5.28e-01 |
0.05910 |
-0.053300 |
0.025500 |
1.46e-01 |
0.486000 |
Interleukin-3, Interleukin-5 and GM-CSF signaling |
37 |
8.28e-01 |
9.29e-01 |
0.05850 |
-0.024100 |
-0.053300 |
8.00e-01 |
0.575000 |
Signaling by BRAF and RAF fusions |
53 |
7.65e-01 |
8.88e-01 |
0.05810 |
-0.058100 |
0.002860 |
4.65e-01 |
0.971000 |
Cilium Assembly |
153 |
4.66e-01 |
6.93e-01 |
0.05800 |
-0.050500 |
0.028500 |
2.82e-01 |
0.544000 |
Anti-inflammatory response favouring Leishmania parasite infection |
88 |
6.47e-01 |
8.00e-01 |
0.05770 |
0.055200 |
0.017100 |
3.72e-01 |
0.782000 |
Leishmania parasite growth and survival |
88 |
6.47e-01 |
8.00e-01 |
0.05770 |
0.055200 |
0.017100 |
3.72e-01 |
0.782000 |
Signaling by NOTCH |
146 |
4.86e-01 |
7.07e-01 |
0.05770 |
0.044400 |
-0.036900 |
3.56e-01 |
0.443000 |
Recycling pathway of L1 |
27 |
8.74e-01 |
9.50e-01 |
0.05760 |
-0.024300 |
0.052200 |
8.27e-01 |
0.639000 |
tRNA processing in the nucleus |
47 |
7.95e-01 |
9.05e-01 |
0.05730 |
0.035700 |
0.044800 |
6.73e-01 |
0.595000 |
SUMOylation |
137 |
5.17e-01 |
7.25e-01 |
0.05700 |
0.056500 |
-0.007850 |
2.55e-01 |
0.874000 |
RAB geranylgeranylation |
46 |
8.02e-01 |
9.10e-01 |
0.05670 |
0.037300 |
0.042700 |
6.62e-01 |
0.617000 |
Transport of the SLBP independent Mature mRNA |
24 |
8.91e-01 |
9.56e-01 |
0.05670 |
-0.027000 |
0.049800 |
8.19e-01 |
0.673000 |
Mitochondrial translation termination |
64 |
7.37e-01 |
8.73e-01 |
0.05660 |
-0.043200 |
-0.036500 |
5.50e-01 |
0.614000 |
Protein folding |
74 |
7.02e-01 |
8.50e-01 |
0.05660 |
-0.053500 |
0.018600 |
4.27e-01 |
0.783000 |
HIV Infection |
176 |
4.35e-01 |
6.77e-01 |
0.05660 |
0.056500 |
0.002020 |
1.97e-01 |
0.963000 |
Mitotic Spindle Checkpoint |
88 |
6.62e-01 |
8.17e-01 |
0.05610 |
0.016500 |
0.053600 |
7.89e-01 |
0.385000 |
Transport of the SLBP Dependant Mature mRNA |
25 |
8.90e-01 |
9.56e-01 |
0.05570 |
0.001050 |
0.055700 |
9.93e-01 |
0.630000 |
Sphingolipid metabolism |
62 |
7.56e-01 |
8.85e-01 |
0.05500 |
-0.047900 |
-0.027000 |
5.15e-01 |
0.713000 |
EPH-ephrin mediated repulsion of cells |
40 |
8.35e-01 |
9.31e-01 |
0.05490 |
0.018600 |
-0.051700 |
8.39e-01 |
0.572000 |
Molecules associated with elastic fibres |
27 |
8.86e-01 |
9.55e-01 |
0.05480 |
-0.022800 |
-0.049900 |
8.38e-01 |
0.654000 |
Rho GTPase cycle |
123 |
5.87e-01 |
7.65e-01 |
0.05400 |
0.016800 |
-0.051400 |
7.49e-01 |
0.326000 |
G-protein activation |
15 |
9.37e-01 |
9.83e-01 |
0.05390 |
-0.053900 |
0.002670 |
7.18e-01 |
0.986000 |
HIV Life Cycle |
108 |
6.29e-01 |
7.92e-01 |
0.05380 |
-0.050700 |
0.017900 |
3.64e-01 |
0.749000 |
NoRC negatively regulates rRNA expression |
33 |
8.69e-01 |
9.48e-01 |
0.05330 |
0.053300 |
0.001060 |
5.96e-01 |
0.992000 |
Heparan sulfate/heparin (HS-GAG) metabolism |
37 |
8.55e-01 |
9.39e-01 |
0.05310 |
-0.005110 |
0.052900 |
9.57e-01 |
0.578000 |
Metabolism of cofactors |
19 |
9.24e-01 |
9.75e-01 |
0.05270 |
-0.051300 |
0.012000 |
6.99e-01 |
0.928000 |
Nuclear import of Rev protein |
24 |
9.05e-01 |
9.61e-01 |
0.05250 |
-0.030800 |
0.042500 |
7.94e-01 |
0.718000 |
HATs acetylate histones |
64 |
7.72e-01 |
8.91e-01 |
0.05210 |
-0.046900 |
-0.022500 |
5.17e-01 |
0.755000 |
Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon |
12 |
9.53e-01 |
9.87e-01 |
0.05190 |
0.018800 |
0.048300 |
9.10e-01 |
0.772000 |
Signaling by RAF1 mutants |
34 |
8.73e-01 |
9.50e-01 |
0.05180 |
0.050700 |
0.010800 |
6.09e-01 |
0.913000 |
Metabolism |
1438 |
6.17e-03 |
4.90e-02 |
0.05180 |
0.021100 |
-0.047300 |
1.94e-01 |
0.003600 |
Interleukin-4 and Interleukin-13 signaling |
82 |
7.22e-01 |
8.64e-01 |
0.05170 |
0.028300 |
0.043300 |
6.58e-01 |
0.499000 |
PI3K/AKT Signaling in Cancer |
81 |
7.25e-01 |
8.66e-01 |
0.05160 |
-0.025700 |
0.044800 |
6.90e-01 |
0.487000 |
RAB GEFs exchange GTP for GDP on RABs |
78 |
7.35e-01 |
8.72e-01 |
0.05140 |
-0.045800 |
0.023200 |
4.85e-01 |
0.723000 |
Nervous system development |
412 |
2.17e-01 |
4.66e-01 |
0.05070 |
0.032900 |
0.038500 |
2.56e-01 |
0.183000 |
RNA Polymerase III Transcription Initiation |
28 |
9.00e-01 |
9.58e-01 |
0.05020 |
0.048400 |
-0.013400 |
6.58e-01 |
0.902000 |
Mitotic Prophase |
66 |
7.81e-01 |
8.97e-01 |
0.05020 |
-0.012000 |
0.048700 |
8.66e-01 |
0.494000 |
RNA Polymerase III Transcription Initiation From Type 3 Promoter |
23 |
9.19e-01 |
9.71e-01 |
0.04970 |
0.048000 |
0.012900 |
6.90e-01 |
0.915000 |
Factors involved in megakaryocyte development and platelet production |
96 |
7.06e-01 |
8.53e-01 |
0.04940 |
0.037800 |
0.031900 |
5.23e-01 |
0.590000 |
Mitochondrial translation initiation |
64 |
7.93e-01 |
9.05e-01 |
0.04930 |
-0.036100 |
-0.033600 |
6.18e-01 |
0.643000 |
Sema3A PAK dependent Axon repulsion |
15 |
9.47e-01 |
9.86e-01 |
0.04920 |
0.049200 |
0.002020 |
7.42e-01 |
0.989000 |
Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants |
47 |
8.47e-01 |
9.39e-01 |
0.04870 |
-0.047400 |
0.011100 |
5.75e-01 |
0.895000 |
Constitutive Signaling by NOTCH1 PEST Domain Mutants |
47 |
8.47e-01 |
9.39e-01 |
0.04870 |
-0.047400 |
0.011100 |
5.75e-01 |
0.895000 |
Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer |
47 |
8.47e-01 |
9.39e-01 |
0.04870 |
-0.047400 |
0.011100 |
5.75e-01 |
0.895000 |
Signaling by NOTCH1 PEST Domain Mutants in Cancer |
47 |
8.47e-01 |
9.39e-01 |
0.04870 |
-0.047400 |
0.011100 |
5.75e-01 |
0.895000 |
Signaling by NOTCH1 in Cancer |
47 |
8.47e-01 |
9.39e-01 |
0.04870 |
-0.047400 |
0.011100 |
5.75e-01 |
0.895000 |
RHO GTPases Activate ROCKs |
18 |
9.38e-01 |
9.83e-01 |
0.04860 |
0.046800 |
0.013200 |
7.31e-01 |
0.923000 |
Initiation of Nuclear Envelope (NE) Reformation |
18 |
9.39e-01 |
9.83e-01 |
0.04850 |
0.047700 |
0.008480 |
7.26e-01 |
0.950000 |
RNA Polymerase II Transcription |
895 |
6.06e-02 |
2.06e-01 |
0.04760 |
0.004220 |
0.047400 |
8.34e-01 |
0.018300 |
SUMOylation of DNA damage response and repair proteins |
56 |
8.30e-01 |
9.30e-01 |
0.04720 |
0.047200 |
0.001560 |
5.42e-01 |
0.984000 |
Regulation of RUNX1 Expression and Activity |
16 |
9.48e-01 |
9.86e-01 |
0.04710 |
-0.028600 |
0.037400 |
8.43e-01 |
0.795000 |
Interleukin-1 signaling |
79 |
7.76e-01 |
8.94e-01 |
0.04640 |
0.042100 |
0.019500 |
5.18e-01 |
0.765000 |
Signaling by SCF-KIT |
42 |
8.80e-01 |
9.53e-01 |
0.04520 |
0.040400 |
0.020300 |
6.51e-01 |
0.820000 |
Collagen formation |
69 |
8.11e-01 |
9.17e-01 |
0.04510 |
0.014200 |
-0.042900 |
8.39e-01 |
0.539000 |
Nuclear Envelope Breakdown |
41 |
8.83e-01 |
9.54e-01 |
0.04510 |
0.017900 |
0.041400 |
8.43e-01 |
0.647000 |
Paradoxical activation of RAF signaling by kinase inactive BRAF |
37 |
8.98e-01 |
9.58e-01 |
0.04420 |
0.023500 |
-0.037400 |
8.05e-01 |
0.694000 |
Signaling by RAS mutants |
37 |
8.98e-01 |
9.58e-01 |
0.04420 |
0.023500 |
-0.037400 |
8.05e-01 |
0.694000 |
Signaling by moderate kinase activity BRAF mutants |
37 |
8.98e-01 |
9.58e-01 |
0.04420 |
0.023500 |
-0.037400 |
8.05e-01 |
0.694000 |
Signaling downstream of RAS mutants |
37 |
8.98e-01 |
9.58e-01 |
0.04420 |
0.023500 |
-0.037400 |
8.05e-01 |
0.694000 |
RA biosynthesis pathway |
13 |
9.63e-01 |
9.88e-01 |
0.04410 |
0.026800 |
0.035100 |
8.67e-01 |
0.827000 |
mRNA Splicing - Minor Pathway |
37 |
9.00e-01 |
9.58e-01 |
0.04370 |
0.007840 |
-0.043000 |
9.34e-01 |
0.651000 |
Formation of RNA Pol II elongation complex |
42 |
8.87e-01 |
9.55e-01 |
0.04370 |
-0.041800 |
-0.012500 |
6.39e-01 |
0.889000 |
RNA Polymerase II Transcription Elongation |
42 |
8.87e-01 |
9.55e-01 |
0.04370 |
-0.041800 |
-0.012500 |
6.39e-01 |
0.889000 |
NRIF signals cell death from the nucleus |
10 |
9.73e-01 |
9.88e-01 |
0.04300 |
-0.037600 |
-0.020900 |
8.37e-01 |
0.909000 |
Transport of Mature mRNA Derived from an Intronless Transcript |
30 |
9.21e-01 |
9.72e-01 |
0.04280 |
-0.040700 |
0.013500 |
7.00e-01 |
0.898000 |
SUMOylation of intracellular receptors |
25 |
9.34e-01 |
9.82e-01 |
0.04280 |
0.039100 |
-0.017400 |
7.35e-01 |
0.880000 |
Signaling by GPCR |
407 |
3.42e-01 |
5.90e-01 |
0.04260 |
-0.038000 |
0.019300 |
1.92e-01 |
0.507000 |
Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation |
10 |
9.74e-01 |
9.88e-01 |
0.04220 |
-0.033300 |
-0.025900 |
8.55e-01 |
0.887000 |
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding |
22 |
9.44e-01 |
9.85e-01 |
0.04180 |
-0.041100 |
-0.007340 |
7.39e-01 |
0.953000 |
RNA Pol II CTD phosphorylation and interaction with CE |
20 |
9.51e-01 |
9.86e-01 |
0.04110 |
-0.040300 |
0.008210 |
7.55e-01 |
0.949000 |
RNA Pol II CTD phosphorylation and interaction with CE during HIV infection |
20 |
9.51e-01 |
9.86e-01 |
0.04110 |
-0.040300 |
0.008210 |
7.55e-01 |
0.949000 |
RNA Polymerase III Transcription Initiation From Type 2 Promoter |
19 |
9.53e-01 |
9.87e-01 |
0.04110 |
0.033700 |
-0.023400 |
7.99e-01 |
0.860000 |
Transcription of the HIV genome |
53 |
8.77e-01 |
9.52e-01 |
0.04070 |
-0.040600 |
0.003300 |
6.10e-01 |
0.967000 |
Signal amplification |
24 |
9.43e-01 |
9.85e-01 |
0.04040 |
-0.039600 |
-0.007730 |
7.37e-01 |
0.948000 |
Signal Transduction |
1627 |
3.38e-02 |
1.44e-01 |
0.04010 |
-0.038500 |
0.011300 |
1.26e-02 |
0.465000 |
Viral Messenger RNA Synthesis |
29 |
9.33e-01 |
9.82e-01 |
0.04010 |
-0.032100 |
0.024100 |
7.65e-01 |
0.823000 |
Death Receptor Signalling |
112 |
7.66e-01 |
8.88e-01 |
0.04000 |
0.013600 |
-0.037600 |
8.04e-01 |
0.492000 |
Transcriptional Regulation by TP53 |
297 |
5.09e-01 |
7.19e-01 |
0.03940 |
0.035800 |
-0.016400 |
2.91e-01 |
0.628000 |
Cellular responses to stress |
364 |
4.52e-01 |
6.87e-01 |
0.03880 |
0.025200 |
0.029500 |
4.12e-01 |
0.337000 |
Epigenetic regulation of gene expression |
70 |
8.58e-01 |
9.39e-01 |
0.03840 |
0.003250 |
-0.038200 |
9.63e-01 |
0.581000 |
Gene expression (Transcription) |
993 |
1.37e-01 |
3.51e-01 |
0.03820 |
0.002390 |
0.038100 |
9.01e-01 |
0.046500 |
Activation of G protein gated Potassium channels |
16 |
9.66e-01 |
9.88e-01 |
0.03780 |
0.017000 |
-0.033800 |
9.06e-01 |
0.815000 |
G protein gated Potassium channels |
16 |
9.66e-01 |
9.88e-01 |
0.03780 |
0.017000 |
-0.033800 |
9.06e-01 |
0.815000 |
Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits |
16 |
9.66e-01 |
9.88e-01 |
0.03780 |
0.017000 |
-0.033800 |
9.06e-01 |
0.815000 |
Synthesis of PIPs at the plasma membrane |
51 |
8.97e-01 |
9.58e-01 |
0.03780 |
-0.017800 |
0.033300 |
8.26e-01 |
0.681000 |
Adrenaline,noradrenaline inhibits insulin secretion |
18 |
9.63e-01 |
9.88e-01 |
0.03730 |
-0.007710 |
-0.036500 |
9.55e-01 |
0.789000 |
Cellular responses to external stimuli |
369 |
4.78e-01 |
7.04e-01 |
0.03720 |
0.029300 |
0.022900 |
3.38e-01 |
0.453000 |
Formation of Incision Complex in GG-NER |
32 |
9.37e-01 |
9.83e-01 |
0.03700 |
0.002410 |
-0.036900 |
9.81e-01 |
0.718000 |
PTEN Regulation |
118 |
7.95e-01 |
9.05e-01 |
0.03620 |
-0.005430 |
-0.035700 |
9.19e-01 |
0.504000 |
L1CAM interactions |
85 |
8.49e-01 |
9.39e-01 |
0.03590 |
-0.025200 |
0.025500 |
6.88e-01 |
0.685000 |
SUMOylation of SUMOylation proteins |
23 |
9.57e-01 |
9.88e-01 |
0.03580 |
-0.026900 |
0.023600 |
8.24e-01 |
0.844000 |
Interleukin-1 family signaling |
104 |
8.22e-01 |
9.25e-01 |
0.03560 |
0.028400 |
0.021400 |
6.17e-01 |
0.706000 |
Diseases associated with glycosaminoglycan metabolism |
33 |
9.42e-01 |
9.84e-01 |
0.03480 |
0.007020 |
0.034100 |
9.44e-01 |
0.735000 |
Interconversion of nucleotide di- and triphosphates |
22 |
9.61e-01 |
9.88e-01 |
0.03460 |
-0.016400 |
0.030400 |
8.94e-01 |
0.805000 |
G alpha (z) signalling events |
35 |
9.41e-01 |
9.84e-01 |
0.03410 |
-0.034000 |
-0.001250 |
7.28e-01 |
0.990000 |
MET activates PTK2 signaling |
17 |
9.71e-01 |
9.88e-01 |
0.03380 |
-0.033800 |
-0.000508 |
8.10e-01 |
0.997000 |
APC-Cdc20 mediated degradation of Nek2A |
20 |
9.67e-01 |
9.88e-01 |
0.03340 |
0.020400 |
-0.026500 |
8.75e-01 |
0.838000 |
Inactivation of APC/C via direct inhibition of the APC/C complex |
19 |
9.70e-01 |
9.88e-01 |
0.03260 |
-0.019900 |
-0.025800 |
8.81e-01 |
0.846000 |
Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components |
19 |
9.70e-01 |
9.88e-01 |
0.03260 |
-0.019900 |
-0.025800 |
8.81e-01 |
0.846000 |
Post-translational protein modification |
1006 |
2.35e-01 |
4.86e-01 |
0.03240 |
-0.028200 |
0.015900 |
1.38e-01 |
0.405000 |
Anchoring of the basal body to the plasma membrane |
81 |
8.86e-01 |
9.55e-01 |
0.03170 |
-0.029900 |
0.010500 |
6.42e-01 |
0.870000 |
Nitric oxide stimulates guanylate cyclase |
19 |
9.74e-01 |
9.88e-01 |
0.03040 |
0.023400 |
0.019400 |
8.60e-01 |
0.883000 |
Activation of kainate receptors upon glutamate binding |
21 |
9.71e-01 |
9.88e-01 |
0.03040 |
-0.007040 |
-0.029500 |
9.55e-01 |
0.815000 |
Generic Transcription Pathway |
798 |
3.63e-01 |
6.09e-01 |
0.03020 |
0.003710 |
0.029900 |
8.61e-01 |
0.157000 |
G alpha (i) signalling events |
190 |
7.91e-01 |
9.04e-01 |
0.02890 |
-0.020700 |
0.020100 |
6.24e-01 |
0.634000 |
Metabolism of lipids |
525 |
5.61e-01 |
7.54e-01 |
0.02780 |
-0.008760 |
-0.026300 |
7.34e-01 |
0.307000 |
Aberrant regulation of mitotic cell cycle due to RB1 defects |
33 |
9.63e-01 |
9.88e-01 |
0.02780 |
0.027500 |
-0.003890 |
7.85e-01 |
0.969000 |
Diseases of mitotic cell cycle |
33 |
9.63e-01 |
9.88e-01 |
0.02780 |
0.027500 |
-0.003890 |
7.85e-01 |
0.969000 |
DNA Damage Recognition in GG-NER |
27 |
9.70e-01 |
9.88e-01 |
0.02760 |
0.001780 |
-0.027600 |
9.87e-01 |
0.804000 |
Developmental Biology |
613 |
5.20e-01 |
7.29e-01 |
0.02740 |
0.001420 |
0.027400 |
9.53e-01 |
0.253000 |
Vitamin B5 (pantothenate) metabolism |
13 |
9.87e-01 |
9.97e-01 |
0.02640 |
0.017000 |
-0.020200 |
9.16e-01 |
0.900000 |
Transport of Mature mRNAs Derived from Intronless Transcripts |
31 |
9.69e-01 |
9.88e-01 |
0.02620 |
-0.017600 |
0.019400 |
8.66e-01 |
0.852000 |
Collagen chain trimerization |
33 |
9.70e-01 |
9.88e-01 |
0.02500 |
-0.023800 |
-0.007690 |
8.13e-01 |
0.939000 |
PIP3 activates AKT signaling |
218 |
8.20e-01 |
9.24e-01 |
0.02480 |
-0.020200 |
0.014500 |
6.09e-01 |
0.714000 |
GPCR downstream signalling |
377 |
7.22e-01 |
8.64e-01 |
0.02440 |
-0.020100 |
0.013700 |
5.06e-01 |
0.650000 |
B-WICH complex positively regulates rRNA expression |
24 |
9.81e-01 |
9.94e-01 |
0.02310 |
0.022600 |
-0.005010 |
8.48e-01 |
0.966000 |
Metabolism of proteins |
1380 |
3.81e-01 |
6.28e-01 |
0.02300 |
-0.021900 |
0.006880 |
1.85e-01 |
0.678000 |
Cell-extracellular matrix interactions |
14 |
9.89e-01 |
9.97e-01 |
0.02290 |
0.022000 |
-0.006440 |
8.87e-01 |
0.967000 |
Centrosome maturation |
70 |
9.47e-01 |
9.86e-01 |
0.02280 |
-0.000492 |
-0.022800 |
9.94e-01 |
0.742000 |
Recruitment of mitotic centrosome proteins and complexes |
70 |
9.47e-01 |
9.86e-01 |
0.02280 |
-0.000492 |
-0.022800 |
9.94e-01 |
0.742000 |
Recruitment of NuMA to mitotic centrosomes |
69 |
9.49e-01 |
9.86e-01 |
0.02260 |
-0.016200 |
-0.015800 |
8.16e-01 |
0.821000 |
SUMOylation of ubiquitinylation proteins |
28 |
9.80e-01 |
9.94e-01 |
0.02190 |
-0.000877 |
0.021900 |
9.94e-01 |
0.841000 |
eNOS activation |
10 |
9.93e-01 |
9.98e-01 |
0.02170 |
-0.021300 |
0.004250 |
9.07e-01 |
0.981000 |
Glycosaminoglycan metabolism |
89 |
9.41e-01 |
9.84e-01 |
0.02140 |
0.020300 |
-0.006850 |
7.41e-01 |
0.911000 |
FLT3 Signaling |
226 |
8.61e-01 |
9.42e-01 |
0.02120 |
-0.018700 |
0.009930 |
6.30e-01 |
0.798000 |
SARS-CoV Infections |
67 |
9.58e-01 |
9.88e-01 |
0.02060 |
-0.011500 |
0.017100 |
8.71e-01 |
0.809000 |
Loss of Nlp from mitotic centrosomes |
60 |
9.64e-01 |
9.88e-01 |
0.02020 |
-0.019100 |
0.006610 |
7.99e-01 |
0.930000 |
Loss of proteins required for interphase microtubule organization from the centrosome |
60 |
9.64e-01 |
9.88e-01 |
0.02020 |
-0.019100 |
0.006610 |
7.99e-01 |
0.930000 |
Neddylation |
181 |
9.12e-01 |
9.66e-01 |
0.01860 |
0.002440 |
0.018400 |
9.55e-01 |
0.670000 |
Signaling by Nuclear Receptors |
185 |
9.13e-01 |
9.66e-01 |
0.01830 |
-0.015700 |
0.009300 |
7.14e-01 |
0.828000 |
Hedgehog 'off' state |
84 |
9.60e-01 |
9.88e-01 |
0.01800 |
-0.016700 |
0.006700 |
7.92e-01 |
0.916000 |
Rap1 signalling |
15 |
9.93e-01 |
9.98e-01 |
0.01770 |
0.005570 |
0.016800 |
9.70e-01 |
0.910000 |
Prefoldin mediated transfer of substrate to CCT/TriC |
20 |
9.91e-01 |
9.97e-01 |
0.01770 |
-0.017700 |
0.000436 |
8.91e-01 |
0.997000 |
Synthesis of glycosylphosphatidylinositol (GPI) |
14 |
9.94e-01 |
9.98e-01 |
0.01730 |
-0.015900 |
0.006930 |
9.18e-01 |
0.964000 |
PI Metabolism |
75 |
9.72e-01 |
9.88e-01 |
0.01600 |
0.015900 |
-0.002080 |
8.13e-01 |
0.975000 |
Pre-NOTCH Transcription and Translation |
30 |
9.89e-01 |
9.97e-01 |
0.01540 |
0.003200 |
-0.015000 |
9.76e-01 |
0.887000 |
ECM proteoglycans |
41 |
9.86e-01 |
9.97e-01 |
0.01490 |
0.002760 |
-0.014700 |
9.76e-01 |
0.871000 |
Disease |
1014 |
7.43e-01 |
8.77e-01 |
0.01460 |
-0.004100 |
-0.014100 |
8.29e-01 |
0.459000 |
MAPK family signaling cascades |
250 |
9.38e-01 |
9.83e-01 |
0.01320 |
-0.013100 |
-0.001950 |
7.23e-01 |
0.958000 |
CTLA4 inhibitory signaling |
21 |
9.95e-01 |
9.98e-01 |
0.01300 |
0.000517 |
0.013000 |
9.97e-01 |
0.918000 |
Collagen biosynthesis and modifying enzymes |
51 |
9.89e-01 |
9.97e-01 |
0.01230 |
0.012000 |
-0.002680 |
8.82e-01 |
0.974000 |
Postmitotic nuclear pore complex (NPC) reformation |
20 |
9.96e-01 |
9.98e-01 |
0.01210 |
0.004150 |
0.011300 |
9.74e-01 |
0.930000 |
AURKA Activation by TPX2 |
62 |
9.90e-01 |
9.97e-01 |
0.01020 |
0.005490 |
-0.008610 |
9.40e-01 |
0.907000 |
Signalling to RAS |
18 |
9.98e-01 |
9.99e-01 |
0.00865 |
0.008550 |
0.001350 |
9.50e-01 |
0.992000 |
Glutathione conjugation |
27 |
9.98e-01 |
9.99e-01 |
0.00659 |
0.000814 |
0.006540 |
9.94e-01 |
0.953000 |
RAF/MAP kinase cascade |
212 |
9.87e-01 |
9.97e-01 |
0.00646 |
-0.001680 |
0.006240 |
9.67e-01 |
0.876000 |
MAPK1/MAPK3 signaling |
217 |
9.99e-01 |
9.99e-01 |
0.00205 |
0.001580 |
-0.001310 |
9.68e-01 |
0.974000 |