Class C/3 (Metabotropic glutamate/pheromone receptors)
|
39
|
1.33e-10
|
4.66e-09
|
0.68900
|
-5.26e-01
|
-0.445000
|
1.29e-08
|
1.49e-06
|
Eicosanoids
|
12
|
8.41e-05
|
7.70e-04
|
0.66900
|
6.50e-01
|
-0.159000
|
9.59e-05
|
3.40e-01
|
Scavenging of heme from plasma
|
12
|
2.05e-03
|
1.33e-02
|
0.63700
|
-5.53e-01
|
-0.316000
|
9.15e-04
|
5.82e-02
|
Prednisone ADME
|
10
|
6.78e-03
|
3.57e-02
|
0.63000
|
-3.33e-01
|
-0.534000
|
6.84e-02
|
3.43e-03
|
Glucuronidation
|
25
|
8.10e-06
|
9.14e-05
|
0.61700
|
-4.85e-01
|
-0.381000
|
2.72e-05
|
9.62e-04
|
SARS-CoV-1 modulates host translation machinery
|
34
|
1.07e-07
|
2.22e-06
|
0.60900
|
5.29e-01
|
0.301000
|
9.22e-08
|
2.35e-03
|
Sensory perception of sweet, bitter, and umami (glutamate) taste
|
41
|
1.59e-07
|
3.03e-06
|
0.55500
|
-4.48e-01
|
-0.329000
|
7.04e-07
|
2.71e-04
|
Peptide chain elongation
|
84
|
1.58e-14
|
1.16e-12
|
0.54800
|
4.68e-01
|
0.285000
|
1.16e-13
|
6.49e-06
|
Eukaryotic Translation Elongation
|
88
|
7.71e-15
|
6.62e-13
|
0.54100
|
4.64e-01
|
0.278000
|
5.12e-14
|
6.66e-06
|
TICAM1-dependent activation of IRF3/IRF7
|
12
|
1.42e-02
|
6.18e-02
|
0.53800
|
3.68e-01
|
0.393000
|
2.74e-02
|
1.84e-02
|
Aspirin ADME
|
44
|
1.76e-07
|
3.28e-06
|
0.53800
|
-3.72e-01
|
-0.388000
|
1.92e-05
|
8.43e-06
|
Eukaryotic Translation Termination
|
87
|
5.27e-14
|
3.54e-12
|
0.52600
|
4.56e-01
|
0.262000
|
1.83e-13
|
2.34e-05
|
Selenocysteine synthesis
|
87
|
5.84e-14
|
3.61e-12
|
0.52500
|
4.55e-01
|
0.262000
|
2.01e-13
|
2.42e-05
|
Viral mRNA Translation
|
84
|
3.14e-13
|
1.67e-11
|
0.52200
|
4.45e-01
|
0.272000
|
1.74e-12
|
1.61e-05
|
PINK1-PRKN Mediated Mitophagy
|
21
|
1.06e-03
|
7.80e-03
|
0.51600
|
3.48e-01
|
0.382000
|
5.81e-03
|
2.46e-03
|
Pexophagy
|
11
|
2.64e-02
|
1.00e-01
|
0.51600
|
4.20e-01
|
0.299000
|
1.59e-02
|
8.60e-02
|
TICAM1,TRAF6-dependent induction of TAK1 complex
|
10
|
3.87e-02
|
1.34e-01
|
0.51500
|
3.48e-01
|
0.380000
|
5.70e-02
|
3.72e-02
|
SCF(Skp2)-mediated degradation of p27/p21
|
58
|
9.06e-09
|
2.50e-07
|
0.51100
|
3.55e-01
|
0.368000
|
2.91e-06
|
1.25e-06
|
Response of EIF2AK4 (GCN2) to amino acid deficiency
|
95
|
5.58e-14
|
3.60e-12
|
0.50400
|
4.35e-01
|
0.254000
|
2.25e-13
|
1.89e-05
|
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC)
|
89
|
6.26e-13
|
2.85e-11
|
0.50100
|
4.26e-01
|
0.263000
|
3.56e-12
|
1.75e-05
|
Digestion
|
18
|
3.38e-03
|
2.03e-02
|
0.49800
|
-2.41e-01
|
-0.435000
|
7.67e-02
|
1.39e-03
|
cGMP effects
|
15
|
6.92e-03
|
3.58e-02
|
0.49700
|
-1.75e-01
|
-0.465000
|
2.41e-01
|
1.83e-03
|
Apoptotic cleavage of cell adhesion proteins
|
11
|
2.62e-02
|
1.00e-01
|
0.49300
|
-4.67e-01
|
-0.160000
|
7.37e-03
|
3.58e-01
|
Autodegradation of Cdh1 by Cdh1:APC/C
|
62
|
1.34e-08
|
3.45e-07
|
0.48900
|
3.21e-01
|
0.368000
|
1.23e-05
|
5.20e-07
|
Formation of a pool of free 40S subunits
|
94
|
3.80e-13
|
1.84e-11
|
0.48800
|
4.28e-01
|
0.234000
|
6.78e-13
|
8.80e-05
|
Golgi Cisternae Pericentriolar Stack Reorganization
|
14
|
1.72e-02
|
7.26e-02
|
0.48500
|
2.94e-01
|
0.385000
|
5.69e-02
|
1.26e-02
|
Expression and translocation of olfactory receptors
|
356
|
1.04e-44
|
1.61e-41
|
0.48300
|
-3.01e-01
|
-0.377000
|
1.26e-22
|
1.49e-34
|
Sensory perception of taste
|
47
|
1.51e-06
|
2.20e-05
|
0.48300
|
-3.56e-01
|
-0.326000
|
2.34e-05
|
1.12e-04
|
Competing endogenous RNAs (ceRNAs) regulate PTEN translation
|
16
|
1.23e-03
|
8.68e-03
|
0.48200
|
-4.56e-01
|
0.157000
|
1.58e-03
|
2.76e-01
|
TICAM1, RIP1-mediated IKK complex recruitment
|
18
|
5.99e-03
|
3.27e-02
|
0.48200
|
3.35e-01
|
0.347000
|
1.38e-02
|
1.09e-02
|
Mitophagy
|
27
|
4.87e-04
|
3.84e-03
|
0.48000
|
3.12e-01
|
0.364000
|
4.95e-03
|
1.05e-03
|
Activation of the TFAP2 (AP-2) family of transcription factors
|
11
|
4.53e-02
|
1.50e-01
|
0.47900
|
3.51e-01
|
0.326000
|
4.37e-02
|
6.08e-02
|
Senescence-Associated Secretory Phenotype (SASP)
|
53
|
2.63e-07
|
4.72e-06
|
0.47800
|
2.65e-01
|
0.398000
|
8.29e-04
|
5.31e-07
|
APC/C:Cdc20 mediated degradation of Cyclin B
|
24
|
1.14e-03
|
8.25e-03
|
0.47800
|
2.86e-01
|
0.383000
|
1.54e-02
|
1.17e-03
|
Olfactory Signaling Pathway
|
363
|
3.44e-44
|
1.77e-41
|
0.47500
|
-2.93e-01
|
-0.374000
|
7.56e-22
|
1.25e-34
|
SARS-CoV-2 modulates host translation machinery
|
46
|
2.34e-06
|
3.12e-05
|
0.47400
|
4.00e-01
|
0.253000
|
2.62e-06
|
2.95e-03
|
GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2
|
50
|
1.25e-06
|
1.86e-05
|
0.47100
|
3.21e-01
|
0.345000
|
8.54e-05
|
2.40e-05
|
The role of GTSE1 in G2/M progression after G2 checkpoint
|
58
|
1.45e-07
|
2.81e-06
|
0.47100
|
3.56e-01
|
0.308000
|
2.66e-06
|
5.07e-05
|
SUMOylation of immune response proteins
|
10
|
6.51e-02
|
1.95e-01
|
0.47000
|
2.86e-01
|
0.373000
|
1.17e-01
|
4.10e-02
|
GTP hydrolysis and joining of the 60S ribosomal subunit
|
104
|
2.76e-13
|
1.52e-11
|
0.46700
|
4.10e-01
|
0.223000
|
4.97e-13
|
8.24e-05
|
Hh mutants are degraded by ERAD
|
54
|
5.85e-07
|
9.32e-06
|
0.46600
|
3.49e-01
|
0.309000
|
9.11e-06
|
8.65e-05
|
AUF1 (hnRNP D0) binds and destabilizes mRNA
|
53
|
7.67e-07
|
1.17e-05
|
0.46600
|
3.53e-01
|
0.304000
|
8.89e-06
|
1.28e-04
|
Mitochondrial iron-sulfur cluster biogenesis
|
12
|
4.18e-02
|
1.42e-01
|
0.46400
|
3.05e-01
|
0.350000
|
6.75e-02
|
3.56e-02
|
Ubiquitin-dependent degradation of Cyclin D
|
50
|
1.92e-06
|
2.72e-05
|
0.46200
|
3.63e-01
|
0.287000
|
9.15e-06
|
4.47e-04
|
SRP-dependent cotranslational protein targeting to membrane
|
105
|
6.66e-13
|
2.94e-11
|
0.46200
|
3.90e-01
|
0.247000
|
5.11e-12
|
1.17e-05
|
Vpu mediated degradation of CD4
|
50
|
2.21e-06
|
3.02e-05
|
0.46100
|
3.44e-01
|
0.307000
|
2.56e-05
|
1.70e-04
|
Activation of RAC1
|
11
|
4.50e-02
|
1.50e-01
|
0.46100
|
-4.25e-01
|
-0.178000
|
1.46e-02
|
3.06e-01
|
Autodegradation of the E3 ubiquitin ligase COP1
|
50
|
1.99e-06
|
2.78e-05
|
0.46100
|
3.67e-01
|
0.279000
|
6.93e-06
|
6.54e-04
|
Aberrant regulation of mitotic cell cycle due to RB1 defects
|
36
|
3.19e-05
|
3.18e-04
|
0.46000
|
1.52e-01
|
0.435000
|
1.14e-01
|
6.38e-06
|
Formation of the ternary complex, and subsequently, the 43S complex
|
46
|
3.43e-06
|
4.31e-05
|
0.45800
|
4.14e-01
|
0.195000
|
1.14e-06
|
2.21e-02
|
L13a-mediated translational silencing of Ceruloplasmin expression
|
103
|
1.06e-12
|
4.42e-11
|
0.45800
|
4.02e-01
|
0.220000
|
1.74e-12
|
1.17e-04
|
Ubiquitin Mediated Degradation of Phosphorylated Cdc25A
|
50
|
2.70e-06
|
3.51e-05
|
0.45800
|
3.41e-01
|
0.305000
|
2.93e-05
|
1.93e-04
|
p53-Independent DNA Damage Response
|
50
|
2.70e-06
|
3.51e-05
|
0.45800
|
3.41e-01
|
0.305000
|
2.93e-05
|
1.93e-04
|
p53-Independent G1/S DNA damage checkpoint
|
50
|
2.70e-06
|
3.51e-05
|
0.45800
|
3.41e-01
|
0.305000
|
2.93e-05
|
1.93e-04
|
Selenoamino acid metabolism
|
103
|
1.26e-12
|
5.13e-11
|
0.45800
|
3.98e-01
|
0.226000
|
2.92e-12
|
7.18e-05
|
Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects
|
17
|
6.84e-03
|
3.57e-02
|
0.45600
|
1.13e-01
|
0.442000
|
4.20e-01
|
1.60e-03
|
Defective binding of RB1 mutants to E2F1,(E2F2, E2F3)
|
17
|
6.84e-03
|
3.57e-02
|
0.45600
|
1.13e-01
|
0.442000
|
4.20e-01
|
1.60e-03
|
Cap-dependent Translation Initiation
|
111
|
1.64e-13
|
9.39e-12
|
0.45600
|
3.99e-01
|
0.221000
|
3.54e-13
|
5.74e-05
|
Eukaryotic Translation Initiation
|
111
|
1.64e-13
|
9.39e-12
|
0.45600
|
3.99e-01
|
0.221000
|
3.54e-13
|
5.74e-05
|
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1
|
72
|
1.27e-08
|
3.40e-07
|
0.45500
|
3.25e-01
|
0.318000
|
1.88e-06
|
2.97e-06
|
APC/C:Cdc20 mediated degradation of Securin
|
66
|
5.89e-08
|
1.28e-06
|
0.45400
|
3.33e-01
|
0.309000
|
2.84e-06
|
1.42e-05
|
Regulation of RUNX3 expression and activity
|
53
|
2.02e-06
|
2.79e-05
|
0.45000
|
3.24e-01
|
0.312000
|
4.51e-05
|
8.31e-05
|
SCF-beta-TrCP mediated degradation of Emi1
|
53
|
2.23e-06
|
3.02e-05
|
0.44800
|
3.32e-01
|
0.301000
|
2.93e-05
|
1.49e-04
|
Regulation of activated PAK-2p34 by proteasome mediated degradation
|
48
|
7.21e-06
|
8.38e-05
|
0.44800
|
3.47e-01
|
0.283000
|
3.09e-05
|
7.02e-04
|
FBXL7 down-regulates AURKA during mitotic entry and in early mitosis
|
53
|
2.29e-06
|
3.08e-05
|
0.44700
|
3.43e-01
|
0.286000
|
1.55e-05
|
3.10e-04
|
NF-kB is activated and signals survival
|
12
|
5.33e-02
|
1.69e-01
|
0.44600
|
3.39e-01
|
0.290000
|
4.18e-02
|
8.24e-02
|
Diseases of mitotic cell cycle
|
37
|
5.34e-05
|
5.12e-04
|
0.44500
|
1.55e-01
|
0.417000
|
1.02e-01
|
1.16e-05
|
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC)
|
108
|
2.58e-12
|
9.72e-11
|
0.44400
|
3.74e-01
|
0.239000
|
1.78e-11
|
1.72e-05
|
Nonsense-Mediated Decay (NMD)
|
108
|
2.58e-12
|
9.72e-11
|
0.44400
|
3.74e-01
|
0.239000
|
1.78e-11
|
1.72e-05
|
Stabilization of p53
|
55
|
1.67e-06
|
2.40e-05
|
0.44400
|
3.40e-01
|
0.286000
|
1.32e-05
|
2.42e-04
|
RIPK1-mediated regulated necrosis
|
27
|
1.37e-03
|
9.48e-03
|
0.44300
|
3.63e-01
|
0.254000
|
1.09e-03
|
2.24e-02
|
Regulation of necroptotic cell death
|
27
|
1.37e-03
|
9.48e-03
|
0.44300
|
3.63e-01
|
0.254000
|
1.09e-03
|
2.24e-02
|
MET activates RAS signaling
|
11
|
1.73e-02
|
7.28e-02
|
0.44300
|
-3.88e-01
|
0.214000
|
2.59e-02
|
2.20e-01
|
Major pathway of rRNA processing in the nucleolus and cytosol
|
171
|
7.00e-19
|
9.84e-17
|
0.44300
|
3.70e-01
|
0.243000
|
6.15e-17
|
4.13e-08
|
Negative regulation of NOTCH4 signaling
|
52
|
4.11e-06
|
5.08e-05
|
0.44200
|
3.15e-01
|
0.310000
|
8.64e-05
|
1.08e-04
|
Phosphorylation of the APC/C
|
20
|
6.56e-03
|
3.50e-02
|
0.44100
|
1.98e-01
|
0.394000
|
1.24e-01
|
2.30e-03
|
Aberrant regulation of mitotic exit in cancer due to RB1 defects
|
20
|
5.73e-03
|
3.15e-02
|
0.44000
|
1.65e-01
|
0.408000
|
2.02e-01
|
1.57e-03
|
p53-Dependent G1 DNA Damage Response
|
64
|
2.84e-07
|
4.88e-06
|
0.43900
|
3.09e-01
|
0.312000
|
1.94e-05
|
1.53e-05
|
p53-Dependent G1/S DNA damage checkpoint
|
64
|
2.84e-07
|
4.88e-06
|
0.43900
|
3.09e-01
|
0.312000
|
1.94e-05
|
1.53e-05
|
CDK-mediated phosphorylation and removal of Cdc6
|
71
|
5.79e-08
|
1.28e-06
|
0.43800
|
2.88e-01
|
0.330000
|
2.66e-05
|
1.54e-06
|
Cross-presentation of soluble exogenous antigens (endosomes)
|
46
|
1.90e-05
|
1.96e-04
|
0.43500
|
3.61e-01
|
0.243000
|
2.24e-05
|
4.40e-03
|
rRNA processing in the nucleus and cytosol
|
180
|
5.58e-19
|
8.63e-17
|
0.43400
|
3.55e-01
|
0.250000
|
1.96e-16
|
6.69e-09
|
Hh mutants abrogate ligand secretion
|
57
|
1.94e-06
|
2.72e-05
|
0.43400
|
3.23e-01
|
0.291000
|
2.49e-05
|
1.46e-04
|
Digestion and absorption
|
23
|
4.06e-03
|
2.37e-02
|
0.43400
|
-2.15e-01
|
-0.377000
|
7.42e-02
|
1.76e-03
|
Fatty acids
|
15
|
7.35e-03
|
3.74e-02
|
0.43300
|
4.19e-01
|
-0.107000
|
4.94e-03
|
4.73e-01
|
Defective CFTR causes cystic fibrosis
|
59
|
1.43e-06
|
2.11e-05
|
0.42900
|
3.45e-01
|
0.255000
|
4.47e-06
|
6.92e-04
|
Cdc20:Phospho-APC/C mediated degradation of Cyclin A
|
71
|
1.19e-07
|
2.42e-06
|
0.42900
|
3.05e-01
|
0.301000
|
8.48e-06
|
1.15e-05
|
Vif-mediated degradation of APOBEC3G
|
50
|
1.41e-05
|
1.48e-04
|
0.42600
|
3.30e-01
|
0.270000
|
5.47e-05
|
9.38e-04
|
G1/S DNA Damage Checkpoints
|
66
|
4.32e-07
|
7.02e-06
|
0.42600
|
2.92e-01
|
0.311000
|
4.10e-05
|
1.26e-05
|
Unwinding of DNA
|
12
|
6.71e-02
|
1.98e-01
|
0.42600
|
2.53e-01
|
0.343000
|
1.30e-01
|
3.95e-02
|
Influenza Viral RNA Transcription and Replication
|
129
|
3.33e-13
|
1.72e-11
|
0.42500
|
3.37e-01
|
0.260000
|
3.69e-11
|
3.50e-07
|
Processing and activation of SUMO
|
10
|
9.27e-02
|
2.45e-01
|
0.42100
|
1.50e-01
|
0.393000
|
4.12e-01
|
3.13e-02
|
TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway
|
16
|
3.14e-02
|
1.15e-01
|
0.42000
|
2.86e-01
|
0.308000
|
4.78e-02
|
3.28e-02
|
APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint
|
72
|
1.79e-07
|
3.30e-06
|
0.42000
|
3.02e-01
|
0.293000
|
9.61e-06
|
1.72e-05
|
Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins
|
75
|
1.00e-07
|
2.09e-06
|
0.42000
|
2.95e-01
|
0.298000
|
1.01e-05
|
7.76e-06
|
APC/C:Cdc20 mediated degradation of mitotic proteins
|
74
|
1.33e-07
|
2.65e-06
|
0.41900
|
2.95e-01
|
0.297000
|
1.16e-05
|
9.75e-06
|
Dectin-1 mediated noncanonical NF-kB signaling
|
60
|
2.79e-06
|
3.53e-05
|
0.41800
|
3.06e-01
|
0.284000
|
4.17e-05
|
1.38e-04
|
Regulation of APC/C activators between G1/S and early anaphase
|
79
|
4.88e-08
|
1.12e-06
|
0.41700
|
2.71e-01
|
0.317000
|
3.18e-05
|
1.07e-06
|
Interaction With Cumulus Cells And The Zona Pellucida
|
11
|
4.64e-02
|
1.53e-01
|
0.41700
|
1.50e-02
|
-0.417000
|
9.31e-01
|
1.67e-02
|
NRIF signals cell death from the nucleus
|
16
|
3.30e-02
|
1.20e-01
|
0.41700
|
3.18e-01
|
0.269000
|
2.74e-02
|
6.28e-02
|
rRNA processing
|
186
|
6.40e-18
|
7.61e-16
|
0.41500
|
3.36e-01
|
0.244000
|
2.63e-15
|
8.62e-09
|
Regulation of expression of SLITs and ROBOs
|
159
|
2.22e-15
|
2.01e-13
|
0.41400
|
3.36e-01
|
0.243000
|
2.70e-13
|
1.16e-07
|
Early Phase of HIV Life Cycle
|
14
|
4.20e-02
|
1.42e-01
|
0.41400
|
1.64e-01
|
0.380000
|
2.89e-01
|
1.37e-02
|
Degradation of DVL
|
55
|
9.93e-06
|
1.08e-04
|
0.41400
|
3.03e-01
|
0.282000
|
1.01e-04
|
2.95e-04
|
Respiratory electron transport
|
90
|
3.66e-09
|
1.11e-07
|
0.41400
|
2.14e-01
|
0.354000
|
4.41e-04
|
6.34e-09
|
Negative regulation of activity of TFAP2 (AP-2) family transcription factors
|
10
|
1.23e-01
|
2.99e-01
|
0.41400
|
3.04e-01
|
0.281000
|
9.64e-02
|
1.24e-01
|
Ribosomal scanning and start codon recognition
|
53
|
7.66e-06
|
8.71e-05
|
0.41300
|
3.73e-01
|
0.178000
|
2.60e-06
|
2.51e-02
|
Activation of the phototransduction cascade
|
11
|
1.00e-01
|
2.60e-01
|
0.41300
|
-2.75e-01
|
-0.308000
|
1.14e-01
|
7.69e-02
|
NIK–>noncanonical NF-kB signaling
|
57
|
7.20e-06
|
8.38e-05
|
0.41200
|
3.01e-01
|
0.281000
|
8.22e-05
|
2.39e-04
|
GLI3 is processed to GLI3R by the proteasome
|
58
|
6.55e-06
|
7.79e-05
|
0.41000
|
3.10e-01
|
0.269000
|
4.51e-05
|
4.02e-04
|
APC/C-mediated degradation of cell cycle proteins
|
86
|
2.36e-08
|
5.69e-07
|
0.40900
|
2.69e-01
|
0.307000
|
1.58e-05
|
8.26e-07
|
Regulation of mitotic cell cycle
|
86
|
2.36e-08
|
5.69e-07
|
0.40900
|
2.69e-01
|
0.307000
|
1.58e-05
|
8.26e-07
|
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S
|
54
|
9.21e-06
|
1.02e-04
|
0.40600
|
3.67e-01
|
0.173000
|
3.02e-06
|
2.78e-02
|
Purine ribonucleoside monophosphate biosynthesis
|
11
|
6.57e-02
|
1.96e-01
|
0.40600
|
4.34e-02
|
0.403000
|
8.03e-01
|
2.05e-02
|
Degradation of GLI2 by the proteasome
|
58
|
8.19e-06
|
9.17e-05
|
0.40600
|
3.12e-01
|
0.259000
|
3.87e-05
|
6.50e-04
|
Regulation of ornithine decarboxylase (ODC)
|
49
|
6.30e-05
|
5.90e-04
|
0.40200
|
2.89e-01
|
0.280000
|
4.70e-04
|
7.06e-04
|
Assembly of the pre-replicative complex
|
82
|
7.51e-08
|
1.61e-06
|
0.40100
|
2.24e-01
|
0.332000
|
4.60e-04
|
1.94e-07
|
Nitric oxide stimulates guanylate cyclase
|
22
|
8.11e-03
|
4.03e-02
|
0.40000
|
-1.26e-01
|
-0.380000
|
3.05e-01
|
2.04e-03
|
Translation initiation complex formation
|
53
|
1.52e-05
|
1.59e-04
|
0.40000
|
3.63e-01
|
0.168000
|
4.70e-06
|
3.46e-02
|
Degradation of GLI1 by the proteasome
|
58
|
1.22e-05
|
1.30e-04
|
0.40000
|
2.91e-01
|
0.274000
|
1.25e-04
|
3.11e-04
|
Defective C1GALT1C1 causes TNPS
|
18
|
2.96e-02
|
1.10e-01
|
0.39900
|
-2.56e-01
|
-0.306000
|
6.05e-02
|
2.44e-02
|
mRNA Splicing - Minor Pathway
|
51
|
3.37e-05
|
3.34e-04
|
0.39800
|
3.47e-01
|
0.195000
|
1.77e-05
|
1.61e-02
|
Assembly of the ORC complex at the origin of replication
|
10
|
5.18e-02
|
1.66e-01
|
0.39700
|
-3.49e-01
|
0.189000
|
5.60e-02
|
3.00e-01
|
Cytosolic iron-sulfur cluster assembly
|
10
|
1.44e-01
|
3.31e-01
|
0.39700
|
2.52e-01
|
0.307000
|
1.68e-01
|
9.30e-02
|
Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase
|
20
|
1.56e-02
|
6.69e-02
|
0.39700
|
1.55e-01
|
0.365000
|
2.29e-01
|
4.72e-03
|
Cyclin E associated events during G1/S transition
|
81
|
1.75e-07
|
3.28e-06
|
0.39600
|
2.54e-01
|
0.303000
|
7.59e-05
|
2.32e-06
|
Response of EIF2AK1 (HRI) to heme deficiency
|
14
|
6.64e-02
|
1.97e-01
|
0.39500
|
3.19e-01
|
0.234000
|
3.88e-02
|
1.30e-01
|
Influenza Infection
|
148
|
5.50e-13
|
2.58e-11
|
0.39500
|
3.01e-01
|
0.255000
|
2.38e-10
|
8.14e-08
|
APC-Cdc20 mediated degradation of Nek2A
|
26
|
6.65e-03
|
3.53e-02
|
0.39400
|
2.30e-01
|
0.320000
|
4.19e-02
|
4.76e-03
|
Josephin domain DUBs
|
11
|
1.18e-01
|
2.93e-01
|
0.39400
|
2.15e-01
|
0.330000
|
2.17e-01
|
5.83e-02
|
Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins.
|
95
|
7.15e-09
|
2.01e-07
|
0.39300
|
1.90e-01
|
0.345000
|
1.38e-03
|
6.27e-09
|
Cyclin A:Cdk2-associated events at S phase entry
|
83
|
1.44e-07
|
2.81e-06
|
0.39300
|
2.52e-01
|
0.303000
|
7.40e-05
|
1.87e-06
|
Suppression of phagosomal maturation
|
13
|
8.79e-02
|
2.36e-01
|
0.39100
|
2.80e-01
|
0.273000
|
8.00e-02
|
8.89e-02
|
Lysosome Vesicle Biogenesis
|
33
|
3.69e-04
|
2.97e-03
|
0.39000
|
1.32e-03
|
0.390000
|
9.90e-01
|
1.06e-04
|
TNFR1-induced proapoptotic signaling
|
13
|
8.81e-02
|
2.36e-01
|
0.38900
|
2.40e-01
|
0.306000
|
1.33e-01
|
5.60e-02
|
ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression
|
16
|
2.13e-02
|
8.52e-02
|
0.38900
|
-5.39e-03
|
0.389000
|
9.70e-01
|
7.06e-03
|
Defective GALNT12 causes CRCS1
|
18
|
3.42e-02
|
1.22e-01
|
0.38900
|
-2.30e-01
|
-0.314000
|
9.17e-02
|
2.11e-02
|
Synthesis of active ubiquitin: roles of E1 and E2 enzymes
|
27
|
6.50e-03
|
3.48e-02
|
0.38700
|
2.24e-01
|
0.316000
|
4.41e-02
|
4.45e-03
|
Switching of origins to a post-replicative state
|
90
|
4.93e-08
|
1.12e-06
|
0.38700
|
2.14e-01
|
0.322000
|
4.37e-04
|
1.24e-07
|
ERKs are inactivated
|
13
|
8.36e-02
|
2.30e-01
|
0.38700
|
1.89e-01
|
0.337000
|
2.37e-01
|
3.52e-02
|
TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest
|
18
|
3.62e-02
|
1.27e-01
|
0.38700
|
2.40e-01
|
0.303000
|
7.83e-02
|
2.58e-02
|
Asymmetric localization of PCP proteins
|
62
|
1.25e-05
|
1.32e-04
|
0.38600
|
2.87e-01
|
0.258000
|
9.34e-05
|
4.37e-04
|
Heme degradation
|
16
|
3.61e-02
|
1.27e-01
|
0.38400
|
-9.74e-02
|
-0.372000
|
5.00e-01
|
1.00e-02
|
Pausing and recovery of Tat-mediated HIV elongation
|
27
|
7.62e-03
|
3.84e-02
|
0.38400
|
2.70e-01
|
0.274000
|
1.53e-02
|
1.37e-02
|
Tat-mediated HIV elongation arrest and recovery
|
27
|
7.62e-03
|
3.84e-02
|
0.38400
|
2.70e-01
|
0.274000
|
1.53e-02
|
1.37e-02
|
Glucocorticoid biosynthesis
|
10
|
1.20e-01
|
2.95e-01
|
0.38300
|
-7.31e-02
|
-0.376000
|
6.89e-01
|
3.95e-02
|
Transcriptional regulation of granulopoiesis
|
31
|
5.94e-04
|
4.61e-03
|
0.38200
|
-3.24e-02
|
0.381000
|
7.55e-01
|
2.40e-04
|
Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha
|
62
|
1.55e-05
|
1.61e-04
|
0.38200
|
2.91e-01
|
0.247000
|
7.37e-05
|
7.64e-04
|
Sensory Perception
|
567
|
2.25e-44
|
1.74e-41
|
0.38200
|
-2.27e-01
|
-0.307000
|
2.22e-20
|
4.38e-36
|
DNA Replication Pre-Initiation
|
97
|
2.78e-08
|
6.51e-07
|
0.38100
|
2.27e-01
|
0.306000
|
1.12e-04
|
1.84e-07
|
p75NTR signals via NF-kB
|
15
|
6.67e-02
|
1.98e-01
|
0.38100
|
3.11e-01
|
0.219000
|
3.68e-02
|
1.41e-01
|
Regulation of Apoptosis
|
51
|
1.17e-04
|
1.04e-03
|
0.38100
|
2.89e-01
|
0.247000
|
3.48e-04
|
2.27e-03
|
tRNA processing in the nucleus
|
55
|
5.57e-05
|
5.29e-04
|
0.38000
|
2.28e-01
|
0.303000
|
3.42e-03
|
9.84e-05
|
mRNA Splicing
|
184
|
8.99e-15
|
7.32e-13
|
0.37900
|
2.92e-01
|
0.242000
|
8.19e-12
|
1.44e-08
|
SUMOylation of transcription factors
|
20
|
1.95e-02
|
7.99e-02
|
0.37900
|
1.15e-01
|
0.361000
|
3.72e-01
|
5.22e-03
|
Translation
|
262
|
1.10e-20
|
2.44e-18
|
0.37800
|
3.00e-01
|
0.231000
|
6.20e-17
|
1.12e-10
|
Class I peroxisomal membrane protein import
|
19
|
3.06e-02
|
1.13e-01
|
0.37800
|
3.34e-01
|
0.178000
|
1.18e-02
|
1.79e-01
|
Defective GALNT3 causes HFTC
|
18
|
4.27e-02
|
1.44e-01
|
0.37800
|
-2.49e-01
|
-0.284000
|
6.69e-02
|
3.69e-02
|
Mitochondrial translation termination
|
87
|
2.95e-07
|
5.01e-06
|
0.37600
|
2.86e-01
|
0.244000
|
3.98e-06
|
8.51e-05
|
Spry regulation of FGF signaling
|
16
|
6.11e-02
|
1.86e-01
|
0.37400
|
2.11e-01
|
0.309000
|
1.45e-01
|
3.22e-02
|
SARS-CoV-1-host interactions
|
90
|
2.14e-07
|
3.90e-06
|
0.37400
|
2.60e-01
|
0.268000
|
1.95e-05
|
1.07e-05
|
Mitochondrial translation
|
93
|
1.27e-07
|
2.56e-06
|
0.37400
|
2.82e-01
|
0.245000
|
2.61e-06
|
4.35e-05
|
Diseases associated with glycosylation precursor biosynthesis
|
15
|
7.20e-02
|
2.08e-01
|
0.37300
|
1.96e-01
|
0.317000
|
1.89e-01
|
3.34e-02
|
NGF-stimulated transcription
|
39
|
1.12e-03
|
8.12e-03
|
0.37100
|
1.88e-01
|
0.320000
|
4.25e-02
|
5.47e-04
|
Mitochondrial translation initiation
|
87
|
4.79e-07
|
7.71e-06
|
0.36900
|
2.84e-01
|
0.236000
|
4.69e-06
|
1.38e-04
|
MyD88 deficiency (TLR2/4)
|
16
|
1.57e-02
|
6.70e-02
|
0.36900
|
-2.00e-01
|
0.310000
|
1.66e-01
|
3.15e-02
|
Cellular response to hypoxia
|
71
|
7.36e-06
|
8.43e-05
|
0.36900
|
2.65e-01
|
0.257000
|
1.13e-04
|
1.78e-04
|
Infection with Mycobacterium tuberculosis
|
25
|
1.55e-02
|
6.67e-02
|
0.36900
|
2.68e-01
|
0.253000
|
2.02e-02
|
2.83e-02
|
TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest
|
14
|
7.42e-02
|
2.12e-01
|
0.36800
|
1.14e-01
|
0.350000
|
4.58e-01
|
2.33e-02
|
Condensation of Prometaphase Chromosomes
|
11
|
1.26e-01
|
3.03e-01
|
0.36700
|
9.72e-02
|
0.354000
|
5.77e-01
|
4.19e-02
|
Aspartate and asparagine metabolism
|
11
|
1.60e-01
|
3.53e-01
|
0.36700
|
-2.91e-01
|
-0.224000
|
9.45e-02
|
1.98e-01
|
Metabolism of polyamines
|
55
|
1.14e-04
|
1.02e-03
|
0.36700
|
2.74e-01
|
0.244000
|
4.30e-04
|
1.73e-03
|
Orc1 removal from chromatin
|
69
|
1.10e-05
|
1.18e-04
|
0.36700
|
2.31e-01
|
0.285000
|
8.83e-04
|
4.27e-05
|
Mitochondrial translation elongation
|
87
|
6.52e-07
|
1.03e-05
|
0.36600
|
2.77e-01
|
0.239000
|
7.85e-06
|
1.18e-04
|
Response of Mtb to phagocytosis
|
22
|
2.80e-02
|
1.05e-01
|
0.36400
|
2.71e-01
|
0.244000
|
2.78e-02
|
4.80e-02
|
Signaling by NOTCH4
|
79
|
2.72e-06
|
3.51e-05
|
0.36400
|
2.72e-01
|
0.242000
|
2.87e-05
|
1.99e-04
|
Processing of Capped Intron-Containing Pre-mRNA
|
232
|
9.08e-17
|
1.00e-14
|
0.36200
|
2.62e-01
|
0.250000
|
5.62e-12
|
5.46e-11
|
Degradation of AXIN
|
53
|
1.98e-04
|
1.68e-03
|
0.36200
|
2.79e-01
|
0.231000
|
4.51e-04
|
3.58e-03
|
HIV elongation arrest and recovery
|
29
|
9.59e-03
|
4.49e-02
|
0.36200
|
2.63e-01
|
0.248000
|
1.40e-02
|
2.07e-02
|
Pausing and recovery of HIV elongation
|
29
|
9.59e-03
|
4.49e-02
|
0.36200
|
2.63e-01
|
0.248000
|
1.40e-02
|
2.07e-02
|
SARS-CoV-1 activates/modulates innate immune responses
|
37
|
1.62e-03
|
1.10e-02
|
0.36200
|
1.38e-01
|
0.334000
|
1.47e-01
|
4.31e-04
|
Polo-like kinase mediated events
|
16
|
4.98e-02
|
1.62e-01
|
0.36200
|
7.57e-02
|
0.354000
|
6.00e-01
|
1.43e-02
|
PERK regulates gene expression
|
32
|
3.39e-03
|
2.03e-02
|
0.36100
|
3.42e-01
|
0.115000
|
8.05e-04
|
2.61e-01
|
Dectin-2 family
|
28
|
1.05e-02
|
4.88e-02
|
0.36100
|
-3.01e-01
|
-0.199000
|
5.84e-03
|
6.87e-02
|
ATF4 activates genes in response to endoplasmic reticulum stress
|
28
|
7.28e-03
|
3.73e-02
|
0.36000
|
3.40e-01
|
0.120000
|
1.87e-03
|
2.71e-01
|
Erythrocytes take up carbon dioxide and release oxygen
|
12
|
1.47e-01
|
3.32e-01
|
0.36000
|
-2.23e-01
|
-0.283000
|
1.82e-01
|
8.97e-02
|
O2/CO2 exchange in erythrocytes
|
12
|
1.47e-01
|
3.32e-01
|
0.36000
|
-2.23e-01
|
-0.283000
|
1.82e-01
|
8.97e-02
|
Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon
|
17
|
3.61e-02
|
1.27e-01
|
0.36000
|
3.59e-02
|
0.358000
|
7.97e-01
|
1.06e-02
|
TNFR2 non-canonical NF-kB pathway
|
94
|
3.45e-07
|
5.73e-06
|
0.36000
|
2.74e-01
|
0.233000
|
4.30e-06
|
9.67e-05
|
RUNX1 regulates transcription of genes involved in differentiation of HSCs
|
68
|
2.02e-05
|
2.07e-04
|
0.35900
|
2.22e-01
|
0.283000
|
1.54e-03
|
5.55e-05
|
CASP8 activity is inhibited
|
11
|
1.47e-01
|
3.32e-01
|
0.35900
|
3.38e-01
|
0.122000
|
5.23e-02
|
4.82e-01
|
Dimerization of procaspase-8
|
11
|
1.47e-01
|
3.32e-01
|
0.35900
|
3.38e-01
|
0.122000
|
5.23e-02
|
4.82e-01
|
Regulation by c-FLIP
|
11
|
1.47e-01
|
3.32e-01
|
0.35900
|
3.38e-01
|
0.122000
|
5.23e-02
|
4.82e-01
|
Activation of NF-kappaB in B cells
|
64
|
4.18e-05
|
4.09e-04
|
0.35900
|
2.70e-01
|
0.236000
|
1.87e-04
|
1.08e-03
|
mRNA Splicing - Major Pathway
|
174
|
1.55e-12
|
6.16e-11
|
0.35800
|
2.73e-01
|
0.230000
|
4.71e-10
|
1.53e-07
|
RHO GTPases activate KTN1
|
11
|
7.71e-02
|
2.16e-01
|
0.35700
|
-1.31e-01
|
0.332000
|
4.51e-01
|
5.62e-02
|
Hedgehog ligand biogenesis
|
63
|
5.42e-05
|
5.17e-04
|
0.35700
|
2.65e-01
|
0.239000
|
2.74e-04
|
1.02e-03
|
Nuclear events mediated by NFE2L2
|
76
|
4.81e-06
|
5.90e-05
|
0.35600
|
1.78e-01
|
0.309000
|
7.38e-03
|
3.19e-06
|
E2F mediated regulation of DNA replication
|
20
|
7.56e-03
|
3.83e-02
|
0.35600
|
-2.32e-01
|
0.269000
|
7.23e-02
|
3.70e-02
|
Regulation of TNFR1 signaling
|
37
|
3.25e-03
|
1.97e-02
|
0.35500
|
2.73e-01
|
0.227000
|
4.05e-03
|
1.68e-02
|
DNA Damage Recognition in GG-NER
|
36
|
4.22e-03
|
2.42e-02
|
0.35300
|
2.44e-01
|
0.254000
|
1.12e-02
|
8.30e-03
|
Defective Intrinsic Pathway for Apoptosis
|
25
|
2.22e-02
|
8.76e-02
|
0.35200
|
2.68e-01
|
0.229000
|
2.04e-02
|
4.75e-02
|
p75NTR recruits signalling complexes
|
12
|
1.61e-01
|
3.54e-01
|
0.35200
|
2.65e-01
|
0.232000
|
1.12e-01
|
1.64e-01
|
Diseases of programmed cell death
|
43
|
1.32e-03
|
9.26e-03
|
0.35100
|
1.96e-01
|
0.292000
|
2.63e-02
|
9.31e-04
|
Inactivation of APC/C via direct inhibition of the APC/C complex
|
21
|
3.58e-02
|
1.26e-01
|
0.34900
|
1.51e-01
|
0.315000
|
2.31e-01
|
1.25e-02
|
Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components
|
21
|
3.58e-02
|
1.26e-01
|
0.34900
|
1.51e-01
|
0.315000
|
2.31e-01
|
1.25e-02
|
DNA Replication
|
125
|
6.69e-09
|
1.91e-07
|
0.34900
|
2.02e-01
|
0.285000
|
9.90e-05
|
3.85e-08
|
Synthesis of DNA
|
118
|
1.93e-08
|
4.90e-07
|
0.34800
|
1.94e-01
|
0.288000
|
2.65e-04
|
6.14e-08
|
Cyclin D associated events in G1
|
46
|
9.54e-04
|
7.13e-03
|
0.34700
|
1.86e-01
|
0.293000
|
2.90e-02
|
5.85e-04
|
G1 Phase
|
46
|
9.54e-04
|
7.13e-03
|
0.34700
|
1.86e-01
|
0.293000
|
2.90e-02
|
5.85e-04
|
Nucleotide biosynthesis
|
14
|
7.65e-02
|
2.15e-01
|
0.34600
|
2.40e-02
|
0.346000
|
8.76e-01
|
2.52e-02
|
Translation of Replicase and Assembly of the Replication Transcription Complex 9694676
|
14
|
7.07e-02
|
2.06e-01
|
0.34600
|
-7.23e-05
|
0.346000
|
1.00e+00
|
2.49e-02
|
G1/S Transition
|
126
|
6.52e-09
|
1.90e-07
|
0.34600
|
1.87e-01
|
0.291000
|
2.95e-04
|
1.63e-08
|
Synthesis of bile acids and bile salts via 27-hydroxycholesterol
|
15
|
1.13e-01
|
2.82e-01
|
0.34500
|
-2.42e-01
|
-0.246000
|
1.05e-01
|
9.87e-02
|
TBC/RABGAPs
|
42
|
6.96e-04
|
5.32e-03
|
0.34500
|
5.99e-02
|
0.340000
|
5.02e-01
|
1.40e-04
|
Thyroxine biosynthesis
|
10
|
2.31e-01
|
4.38e-01
|
0.34400
|
-2.77e-01
|
-0.204000
|
1.29e-01
|
2.64e-01
|
FGFR1c ligand binding and activation
|
11
|
2.06e-01
|
4.02e-01
|
0.34300
|
2.42e-01
|
0.243000
|
1.65e-01
|
1.63e-01
|
Signaling by activated point mutants of FGFR1
|
11
|
2.06e-01
|
4.02e-01
|
0.34300
|
2.42e-01
|
0.243000
|
1.65e-01
|
1.63e-01
|
Regulation of signaling by NODAL
|
10
|
1.03e-01
|
2.65e-01
|
0.34300
|
2.47e-01
|
-0.238000
|
1.76e-01
|
1.93e-01
|
Abortive elongation of HIV-1 transcript in the absence of Tat
|
23
|
3.80e-02
|
1.32e-01
|
0.34100
|
2.47e-01
|
0.235000
|
4.00e-02
|
5.14e-02
|
Regulation of TP53 Activity through Methylation
|
18
|
7.34e-02
|
2.10e-01
|
0.34100
|
2.83e-01
|
0.190000
|
3.75e-02
|
1.64e-01
|
Recycling of bile acids and salts
|
18
|
7.55e-02
|
2.13e-01
|
0.34100
|
-2.05e-01
|
-0.272000
|
1.33e-01
|
4.54e-02
|
Regulation of TLR by endogenous ligand
|
17
|
2.23e-02
|
8.80e-02
|
0.34000
|
-2.56e-01
|
0.224000
|
6.73e-02
|
1.10e-01
|
UCH proteinases
|
81
|
9.44e-06
|
1.03e-04
|
0.34000
|
2.75e-01
|
0.200000
|
1.92e-05
|
1.84e-03
|
POU5F1 (OCT4), SOX2, NANOG repress genes related to differentiation
|
10
|
1.22e-01
|
2.98e-01
|
0.34000
|
-1.26e-01
|
0.316000
|
4.92e-01
|
8.40e-02
|
Methylation
|
14
|
1.01e-01
|
2.63e-01
|
0.33900
|
3.30e-01
|
0.078500
|
3.24e-02
|
6.11e-01
|
Mitotic G1 phase and G1/S transition
|
144
|
9.61e-10
|
3.16e-08
|
0.33800
|
1.71e-01
|
0.291000
|
3.89e-04
|
1.53e-09
|
Adherens junctions interactions
|
26
|
2.67e-02
|
1.01e-01
|
0.33700
|
-2.14e-01
|
-0.260000
|
5.85e-02
|
2.19e-02
|
MET activates PTK2 signaling
|
18
|
8.25e-02
|
2.29e-01
|
0.33600
|
-2.60e-01
|
-0.212000
|
5.59e-02
|
1.20e-01
|
Cellular response to starvation
|
147
|
1.55e-09
|
4.78e-08
|
0.33600
|
2.61e-01
|
0.212000
|
4.86e-08
|
9.36e-06
|
Folding of actin by CCT/TriC
|
10
|
1.96e-01
|
3.94e-01
|
0.33600
|
3.30e-01
|
0.063200
|
7.11e-02
|
7.29e-01
|
Interactions of Rev with host cellular proteins
|
35
|
4.08e-03
|
2.37e-02
|
0.33500
|
8.53e-02
|
0.324000
|
3.82e-01
|
9.17e-04
|
Receptor Mediated Mitophagy
|
10
|
2.07e-01
|
4.03e-01
|
0.33500
|
8.27e-02
|
0.324000
|
6.51e-01
|
7.58e-02
|
Constitutive Signaling by Overexpressed ERBB2
|
10
|
1.71e-01
|
3.69e-01
|
0.33500
|
8.87e-04
|
0.335000
|
9.96e-01
|
6.70e-02
|
Lysine catabolism
|
12
|
1.54e-01
|
3.43e-01
|
0.33400
|
-8.92e-02
|
-0.322000
|
5.93e-01
|
5.34e-02
|
Phospholipase C-mediated cascade: FGFR1
|
16
|
1.11e-01
|
2.79e-01
|
0.33400
|
2.65e-01
|
0.203000
|
6.67e-02
|
1.60e-01
|
IKK complex recruitment mediated by RIP1
|
22
|
3.41e-02
|
1.22e-01
|
0.33400
|
9.78e-02
|
0.319000
|
4.27e-01
|
9.59e-03
|
RNA Polymerase III Transcription Initiation From Type 3 Promoter
|
28
|
2.16e-02
|
8.62e-02
|
0.33300
|
2.07e-01
|
0.261000
|
5.82e-02
|
1.66e-02
|
Nuclear import of Rev protein
|
32
|
7.65e-03
|
3.84e-02
|
0.33300
|
1.01e-01
|
0.317000
|
3.22e-01
|
1.89e-03
|
Regulation of mRNA stability by proteins that bind AU-rich elements
|
87
|
7.31e-06
|
8.43e-05
|
0.33300
|
2.55e-01
|
0.215000
|
4.04e-05
|
5.28e-04
|
Passive transport by Aquaporins
|
13
|
1.45e-01
|
3.31e-01
|
0.33300
|
-1.18e-01
|
-0.311000
|
4.60e-01
|
5.22e-02
|
FGFR1 ligand binding and activation
|
15
|
1.30e-01
|
3.10e-01
|
0.33100
|
2.68e-01
|
0.194000
|
7.21e-02
|
1.94e-01
|
TNF signaling
|
45
|
2.46e-03
|
1.55e-02
|
0.33100
|
2.40e-01
|
0.228000
|
5.38e-03
|
8.26e-03
|
Complex I biogenesis
|
49
|
1.11e-03
|
8.08e-03
|
0.32900
|
1.57e-01
|
0.290000
|
5.78e-02
|
4.47e-04
|
G1/S-Specific Transcription
|
28
|
1.21e-02
|
5.45e-02
|
0.32900
|
5.89e-02
|
0.324000
|
5.90e-01
|
3.00e-03
|
SUMOylation of SUMOylation proteins
|
33
|
8.25e-03
|
4.07e-02
|
0.32900
|
1.16e-01
|
0.308000
|
2.50e-01
|
2.20e-03
|
Regulation of BACH1 activity
|
15
|
1.31e-01
|
3.12e-01
|
0.32900
|
1.80e-01
|
0.275000
|
2.27e-01
|
6.51e-02
|
Regulation of RAS by GAPs
|
65
|
1.89e-04
|
1.61e-03
|
0.32800
|
2.11e-01
|
0.251000
|
3.28e-03
|
4.60e-04
|
Rev-mediated nuclear export of HIV RNA
|
33
|
5.77e-03
|
3.16e-02
|
0.32800
|
5.74e-02
|
0.323000
|
5.68e-01
|
1.34e-03
|
Translesion Synthesis by POLH
|
19
|
7.79e-02
|
2.17e-01
|
0.32700
|
1.75e-01
|
0.276000
|
1.86e-01
|
3.72e-02
|
Regulation of glycolysis by fructose 2,6-bisphosphate metabolism
|
11
|
1.55e-01
|
3.45e-01
|
0.32600
|
-5.87e-03
|
0.326000
|
9.73e-01
|
6.10e-02
|
Cleavage of the damaged pyrimidine
|
16
|
8.71e-02
|
2.36e-01
|
0.32600
|
6.81e-02
|
0.319000
|
6.37e-01
|
2.72e-02
|
Depyrimidination
|
16
|
8.71e-02
|
2.36e-01
|
0.32600
|
6.81e-02
|
0.319000
|
6.37e-01
|
2.72e-02
|
Recognition and association of DNA glycosylase with site containing an affected pyrimidine
|
16
|
8.71e-02
|
2.36e-01
|
0.32600
|
6.81e-02
|
0.319000
|
6.37e-01
|
2.72e-02
|
Metabolism of RNA
|
639
|
7.30e-36
|
2.82e-33
|
0.32500
|
2.42e-01
|
0.217000
|
1.06e-25
|
6.89e-21
|
rRNA modification in the nucleus and cytosol
|
55
|
7.39e-04
|
5.60e-03
|
0.32500
|
1.85e-01
|
0.267000
|
1.77e-02
|
6.17e-04
|
Carnitine metabolism
|
11
|
1.08e-01
|
2.75e-01
|
0.32500
|
-1.91e-01
|
0.263000
|
2.74e-01
|
1.31e-01
|
TRAF3-dependent IRF activation pathway
|
15
|
1.06e-01
|
2.70e-01
|
0.32500
|
7.39e-02
|
0.316000
|
6.20e-01
|
3.41e-02
|
Mitochondrial protein import
|
54
|
7.06e-04
|
5.37e-03
|
0.32400
|
1.52e-01
|
0.286000
|
5.30e-02
|
2.80e-04
|
Formation of apoptosome
|
10
|
1.56e-01
|
3.47e-01
|
0.32300
|
3.10e-01
|
-0.092100
|
8.95e-02
|
6.14e-01
|
Regulation of the apoptosome activity
|
10
|
1.56e-01
|
3.47e-01
|
0.32300
|
3.10e-01
|
-0.092100
|
8.95e-02
|
6.14e-01
|
NEP/NS2 Interacts with the Cellular Export Machinery
|
30
|
1.04e-02
|
4.85e-02
|
0.32300
|
5.72e-02
|
0.318000
|
5.88e-01
|
2.55e-03
|
Signaling by ROBO receptors
|
203
|
5.29e-12
|
1.95e-10
|
0.32300
|
2.57e-01
|
0.195000
|
2.52e-10
|
1.69e-06
|
Androgen biosynthesis
|
11
|
2.02e-01
|
4.01e-01
|
0.32200
|
-8.39e-02
|
-0.311000
|
6.30e-01
|
7.41e-02
|
RNA Polymerase III Transcription Initiation
|
36
|
9.11e-03
|
4.38e-02
|
0.32200
|
1.67e-01
|
0.275000
|
8.25e-02
|
4.33e-03
|
Regulation of innate immune responses to cytosolic DNA
|
14
|
1.66e-01
|
3.61e-01
|
0.32100
|
2.64e-01
|
0.182000
|
8.68e-02
|
2.39e-01
|
Export of Viral Ribonucleoproteins from Nucleus
|
31
|
1.16e-02
|
5.29e-02
|
0.32100
|
8.31e-02
|
0.310000
|
4.23e-01
|
2.85e-03
|
Beta defensins
|
28
|
4.11e-03
|
2.38e-02
|
0.32000
|
2.57e-01
|
-0.190000
|
1.84e-02
|
8.23e-02
|
Metabolism of amine-derived hormones
|
17
|
1.17e-01
|
2.92e-01
|
0.31900
|
-2.58e-01
|
-0.187000
|
6.57e-02
|
1.81e-01
|
Attenuation phase
|
25
|
4.48e-02
|
1.50e-01
|
0.31900
|
2.37e-01
|
0.213000
|
4.02e-02
|
6.55e-02
|
Energy dependent regulation of mTOR by LKB1-AMPK
|
28
|
6.21e-03
|
3.34e-02
|
0.31600
|
-1.11e-01
|
0.296000
|
3.10e-01
|
6.62e-03
|
Translation of Replicase and Assembly of the Replication Transcription Complex 9679504
|
13
|
1.07e-01
|
2.72e-01
|
0.31600
|
-6.44e-02
|
0.309000
|
6.87e-01
|
5.35e-02
|
Apoptotic factor-mediated response
|
17
|
8.82e-02
|
2.36e-01
|
0.31600
|
3.09e-01
|
0.065900
|
2.76e-02
|
6.38e-01
|
TRAF6 mediated NF-kB activation
|
24
|
3.29e-02
|
1.20e-01
|
0.31600
|
6.79e-02
|
0.308000
|
5.65e-01
|
8.96e-03
|
FCERI mediated NF-kB activation
|
74
|
1.30e-04
|
1.14e-03
|
0.31500
|
2.28e-01
|
0.216000
|
6.76e-04
|
1.28e-03
|
TRAF6-mediated induction of TAK1 complex within TLR4 complex
|
15
|
9.66e-02
|
2.52e-01
|
0.31500
|
1.94e-03
|
0.315000
|
9.90e-01
|
3.49e-02
|
ER-Phagosome pathway
|
87
|
2.74e-05
|
2.75e-04
|
0.31400
|
2.04e-01
|
0.239000
|
1.01e-03
|
1.17e-04
|
Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1
|
16
|
1.34e-01
|
3.17e-01
|
0.31400
|
1.53e-01
|
0.274000
|
2.88e-01
|
5.80e-02
|
PCP/CE pathway
|
90
|
2.12e-05
|
2.15e-04
|
0.31300
|
2.13e-01
|
0.229000
|
4.68e-04
|
1.71e-04
|
Bicarbonate transporters
|
10
|
2.94e-01
|
5.14e-01
|
0.31300
|
-1.73e-01
|
-0.260000
|
3.43e-01
|
1.54e-01
|
Purine salvage
|
12
|
1.87e-01
|
3.82e-01
|
0.31300
|
6.79e-02
|
0.305000
|
6.84e-01
|
6.72e-02
|
Free fatty acids regulate insulin secretion
|
10
|
1.72e-01
|
3.69e-01
|
0.31200
|
-2.95e-01
|
0.104000
|
1.07e-01
|
5.68e-01
|
Nuclear Events (kinase and transcription factor activation)
|
60
|
4.66e-04
|
3.69e-03
|
0.31200
|
1.28e-01
|
0.285000
|
8.60e-02
|
1.35e-04
|
XBP1(S) activates chaperone genes
|
47
|
1.81e-03
|
1.19e-02
|
0.31100
|
8.70e-02
|
0.299000
|
3.02e-01
|
3.90e-04
|
Host Interactions of HIV factors
|
122
|
4.29e-07
|
7.02e-06
|
0.31100
|
1.79e-01
|
0.255000
|
6.56e-04
|
1.12e-06
|
Miscellaneous substrates
|
12
|
1.10e-01
|
2.78e-01
|
0.30900
|
2.50e-01
|
-0.182000
|
1.34e-01
|
2.74e-01
|
Negative regulation of FGFR1 signaling
|
32
|
2.38e-02
|
9.29e-02
|
0.30900
|
2.15e-01
|
0.222000
|
3.49e-02
|
2.99e-02
|
KEAP1-NFE2L2 pathway
|
103
|
3.57e-06
|
4.45e-05
|
0.30900
|
1.47e-01
|
0.272000
|
9.94e-03
|
1.89e-06
|
Formation of HIV-1 elongation complex containing HIV-1 Tat
|
38
|
1.21e-02
|
5.45e-02
|
0.30800
|
2.13e-01
|
0.223000
|
2.31e-02
|
1.74e-02
|
HIV Transcription Elongation
|
38
|
1.21e-02
|
5.45e-02
|
0.30800
|
2.13e-01
|
0.223000
|
2.31e-02
|
1.74e-02
|
Tat-mediated elongation of the HIV-1 transcript
|
38
|
1.21e-02
|
5.45e-02
|
0.30800
|
2.13e-01
|
0.223000
|
2.31e-02
|
1.74e-02
|
SUMOylation of ubiquitinylation proteins
|
37
|
6.92e-03
|
3.58e-02
|
0.30700
|
6.69e-02
|
0.300000
|
4.81e-01
|
1.61e-03
|
Keratinization
|
213
|
8.76e-12
|
3.15e-10
|
0.30700
|
-1.49e-01
|
-0.269000
|
1.85e-04
|
1.34e-11
|
FCGR activation
|
12
|
1.21e-01
|
2.97e-01
|
0.30700
|
1.42e-01
|
-0.272000
|
3.96e-01
|
1.03e-01
|
Zinc influx into cells by the SLC39 gene family
|
10
|
3.05e-01
|
5.20e-01
|
0.30700
|
1.59e-01
|
0.262000
|
3.85e-01
|
1.51e-01
|
Selective autophagy
|
59
|
1.15e-03
|
8.25e-03
|
0.30600
|
2.11e-01
|
0.222000
|
4.97e-03
|
3.18e-03
|
NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10
|
12
|
1.75e-01
|
3.73e-01
|
0.30600
|
1.27e-02
|
0.306000
|
9.39e-01
|
6.65e-02
|
The NLRP3 inflammasome
|
16
|
1.29e-01
|
3.09e-01
|
0.30600
|
9.50e-02
|
0.290000
|
5.11e-01
|
4.43e-02
|
Transcriptional regulation of testis differentiation
|
12
|
1.90e-01
|
3.85e-01
|
0.30500
|
3.98e-02
|
0.302000
|
8.11e-01
|
6.96e-02
|
Transport of the SLBP Dependant Mature mRNA
|
34
|
1.41e-02
|
6.18e-02
|
0.30400
|
1.03e-01
|
0.286000
|
2.98e-01
|
3.83e-03
|
Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer’s disease models
|
22
|
8.29e-02
|
2.29e-01
|
0.30400
|
2.22e-01
|
0.208000
|
7.10e-02
|
9.19e-02
|
Neurodegenerative Diseases
|
22
|
8.29e-02
|
2.29e-01
|
0.30400
|
2.22e-01
|
0.208000
|
7.10e-02
|
9.19e-02
|
Gap junction degradation
|
10
|
3.02e-01
|
5.18e-01
|
0.30400
|
-2.72e-01
|
-0.136000
|
1.36e-01
|
4.56e-01
|
Platelet Adhesion to exposed collagen
|
13
|
1.97e-01
|
3.95e-01
|
0.30400
|
-2.86e-01
|
-0.103000
|
7.43e-02
|
5.22e-01
|
STAT5 activation downstream of FLT3 ITD mutants
|
10
|
2.96e-01
|
5.16e-01
|
0.30400
|
1.20e-01
|
0.279000
|
5.11e-01
|
1.27e-01
|
IRE1alpha activates chaperones
|
49
|
2.04e-03
|
1.33e-02
|
0.30300
|
9.06e-02
|
0.289000
|
2.73e-01
|
4.54e-04
|
Metabolism of non-coding RNA
|
50
|
2.23e-03
|
1.43e-02
|
0.30300
|
1.13e-01
|
0.281000
|
1.68e-01
|
5.82e-04
|
snRNP Assembly
|
50
|
2.23e-03
|
1.43e-02
|
0.30300
|
1.13e-01
|
0.281000
|
1.68e-01
|
5.82e-04
|
Positive epigenetic regulation of rRNA expression
|
43
|
6.86e-03
|
3.57e-02
|
0.30300
|
1.54e-01
|
0.260000
|
7.96e-02
|
3.15e-03
|
Base-Excision Repair, AP Site Formation
|
18
|
8.38e-02
|
2.31e-01
|
0.30200
|
2.93e-02
|
0.301000
|
8.30e-01
|
2.73e-02
|
RNA Polymerase II Pre-transcription Events
|
73
|
3.00e-04
|
2.46e-03
|
0.30200
|
2.15e-01
|
0.212000
|
1.52e-03
|
1.72e-03
|
Hedgehog ‘on’ state
|
83
|
1.03e-04
|
9.28e-04
|
0.30100
|
2.10e-01
|
0.216000
|
9.50e-04
|
6.64e-04
|
Chylomicron remodeling
|
10
|
2.06e-01
|
4.02e-01
|
0.30100
|
7.11e-02
|
-0.293000
|
6.97e-01
|
1.09e-01
|
VLDLR internalisation and degradation
|
16
|
1.70e-01
|
3.66e-01
|
0.30100
|
1.99e-01
|
0.226000
|
1.69e-01
|
1.18e-01
|
SUMOylation of DNA replication proteins
|
44
|
4.20e-03
|
2.42e-02
|
0.30000
|
8.85e-02
|
0.287000
|
3.10e-01
|
9.80e-04
|
Synthesis, secretion, and inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP)
|
12
|
2.65e-01
|
4.79e-01
|
0.30000
|
2.31e-01
|
0.192000
|
1.66e-01
|
2.50e-01
|
Paracetamol ADME
|
27
|
3.34e-02
|
1.21e-01
|
0.30000
|
-2.90e-01
|
-0.077200
|
9.20e-03
|
4.87e-01
|
Inflammasomes
|
21
|
9.11e-02
|
2.43e-01
|
0.29900
|
1.48e-01
|
0.260000
|
2.41e-01
|
3.89e-02
|
Regulation of TP53 Activity through Association with Co-factors
|
14
|
1.10e-01
|
2.78e-01
|
0.29900
|
-2.88e-01
|
0.080200
|
6.18e-02
|
6.03e-01
|
Synthesis of PIPs at the late endosome membrane
|
10
|
1.78e-01
|
3.76e-01
|
0.29900
|
-2.26e-01
|
0.196000
|
2.16e-01
|
2.84e-01
|
Transcription of the HIV genome
|
62
|
1.16e-03
|
8.27e-03
|
0.29900
|
2.22e-01
|
0.200000
|
2.51e-03
|
6.46e-03
|
S Phase
|
157
|
2.72e-08
|
6.47e-07
|
0.29900
|
1.65e-01
|
0.249000
|
3.59e-04
|
7.24e-08
|
Assembly Of The HIV Virion
|
16
|
1.47e-01
|
3.33e-01
|
0.29700
|
9.96e-02
|
0.280000
|
4.90e-01
|
5.24e-02
|
PRC2 methylates histones and DNA
|
13
|
1.20e-01
|
2.95e-01
|
0.29700
|
-1.23e-01
|
0.271000
|
4.42e-01
|
9.12e-02
|
Transport of Mature mRNAs Derived from Intronless Transcripts
|
41
|
6.28e-03
|
3.37e-02
|
0.29700
|
7.43e-02
|
0.287000
|
4.11e-01
|
1.46e-03
|
Formation of HIV elongation complex in the absence of HIV Tat
|
40
|
1.39e-02
|
6.13e-02
|
0.29600
|
2.11e-01
|
0.207000
|
2.07e-02
|
2.36e-02
|
HIV Transcription Initiation
|
43
|
9.28e-03
|
4.38e-02
|
0.29600
|
2.43e-01
|
0.168000
|
5.72e-03
|
5.71e-02
|
RNA Polymerase II HIV Promoter Escape
|
43
|
9.28e-03
|
4.38e-02
|
0.29600
|
2.43e-01
|
0.168000
|
5.72e-03
|
5.71e-02
|
RNA Polymerase II Promoter Escape
|
43
|
9.28e-03
|
4.38e-02
|
0.29600
|
2.43e-01
|
0.168000
|
5.72e-03
|
5.71e-02
|
RNA Polymerase II Transcription Initiation
|
43
|
9.28e-03
|
4.38e-02
|
0.29600
|
2.43e-01
|
0.168000
|
5.72e-03
|
5.71e-02
|
RNA Polymerase II Transcription Initiation And Promoter Clearance
|
43
|
9.28e-03
|
4.38e-02
|
0.29600
|
2.43e-01
|
0.168000
|
5.72e-03
|
5.71e-02
|
RNA Polymerase II Transcription Pre-Initiation And Promoter Opening
|
43
|
9.28e-03
|
4.38e-02
|
0.29600
|
2.43e-01
|
0.168000
|
5.72e-03
|
5.71e-02
|
Tie2 Signaling
|
18
|
7.09e-02
|
2.06e-01
|
0.29600
|
-2.92e-01
|
0.043400
|
3.17e-02
|
7.50e-01
|
Regulation of RUNX1 Expression and Activity
|
25
|
2.18e-02
|
8.66e-02
|
0.29500
|
-2.86e-01
|
0.074500
|
1.33e-02
|
5.19e-01
|
IRAK4 deficiency (TLR2/4)
|
17
|
5.84e-02
|
1.80e-01
|
0.29500
|
-1.73e-01
|
0.239000
|
2.17e-01
|
8.77e-02
|
G2/M Checkpoints
|
129
|
8.44e-07
|
1.28e-05
|
0.29500
|
1.62e-01
|
0.246000
|
1.45e-03
|
1.35e-06
|
Degradation of beta-catenin by the destruction complex
|
81
|
1.81e-04
|
1.55e-03
|
0.29500
|
1.93e-01
|
0.223000
|
2.67e-03
|
5.22e-04
|
Negative regulation of FLT3
|
15
|
1.80e-01
|
3.78e-01
|
0.29500
|
2.70e-01
|
0.118000
|
7.03e-02
|
4.28e-01
|
Chemokine receptors bind chemokines
|
56
|
1.26e-04
|
1.11e-03
|
0.29500
|
2.68e-01
|
-0.123000
|
5.24e-04
|
1.12e-01
|
Transcriptional regulation by RUNX3
|
93
|
5.27e-05
|
5.09e-04
|
0.29400
|
2.18e-01
|
0.197000
|
2.69e-04
|
9.95e-04
|
Cytochrome c-mediated apoptotic response
|
12
|
1.57e-01
|
3.48e-01
|
0.29400
|
2.80e-01
|
-0.089600
|
9.34e-02
|
5.91e-01
|
RIP-mediated NFkB activation via ZBP1
|
16
|
1.82e-01
|
3.80e-01
|
0.29300
|
1.71e-01
|
0.238000
|
2.37e-01
|
9.94e-02
|
Membrane binding and targetting of GAG proteins
|
14
|
2.05e-01
|
4.02e-01
|
0.29300
|
1.15e-01
|
0.269000
|
4.57e-01
|
8.10e-02
|
Synthesis And Processing Of GAG, GAGPOL Polyproteins
|
14
|
2.05e-01
|
4.02e-01
|
0.29300
|
1.15e-01
|
0.269000
|
4.57e-01
|
8.10e-02
|
Nucleotide salvage
|
21
|
4.37e-02
|
1.47e-01
|
0.29200
|
-7.02e-02
|
0.284000
|
5.78e-01
|
2.44e-02
|
Viral Messenger RNA Synthesis
|
42
|
1.11e-02
|
5.07e-02
|
0.29200
|
1.56e-01
|
0.247000
|
8.11e-02
|
5.55e-03
|
Interactions of Vpr with host cellular proteins
|
33
|
1.37e-02
|
6.03e-02
|
0.29200
|
2.11e-02
|
0.291000
|
8.33e-01
|
3.79e-03
|
Collagen chain trimerization
|
42
|
6.20e-03
|
3.34e-02
|
0.29200
|
-6.59e-02
|
-0.284000
|
4.60e-01
|
1.43e-03
|
HSF1 activation
|
27
|
6.00e-02
|
1.83e-01
|
0.29200
|
2.15e-01
|
0.197000
|
5.30e-02
|
7.62e-02
|
Nuclear events stimulated by ALK signaling in cancer
|
18
|
8.72e-02
|
2.36e-01
|
0.29200
|
-6.14e-03
|
0.292000
|
9.64e-01
|
3.22e-02
|
Regulation of PTEN stability and activity
|
66
|
1.06e-03
|
7.80e-03
|
0.29100
|
1.97e-01
|
0.215000
|
5.65e-03
|
2.54e-03
|
Synthesis of glycosylphosphatidylinositol (GPI)
|
17
|
8.73e-02
|
2.36e-01
|
0.29100
|
-4.64e-02
|
0.287000
|
7.41e-01
|
4.02e-02
|
RNA polymerase II transcribes snRNA genes
|
77
|
3.40e-04
|
2.76e-03
|
0.29100
|
1.86e-01
|
0.224000
|
4.84e-03
|
6.83e-04
|
Alpha-protein kinase 1 signaling pathway
|
10
|
3.52e-01
|
5.68e-01
|
0.29100
|
1.76e-01
|
0.231000
|
3.34e-01
|
2.06e-01
|
Defective pyroptosis
|
11
|
2.19e-01
|
4.20e-01
|
0.29100
|
-2.29e-02
|
0.290000
|
8.95e-01
|
9.60e-02
|
ABC transporter disorders
|
75
|
3.19e-04
|
2.59e-03
|
0.29100
|
2.53e-01
|
0.143000
|
1.50e-04
|
3.26e-02
|
ABC transporters in lipid homeostasis
|
17
|
1.37e-01
|
3.21e-01
|
0.29000
|
-8.07e-02
|
-0.279000
|
5.65e-01
|
4.65e-02
|
Transport of the SLBP independent Mature mRNA
|
33
|
2.43e-02
|
9.41e-02
|
0.29000
|
1.05e-01
|
0.271000
|
2.97e-01
|
7.14e-03
|
Formation of TC-NER Pre-Incision Complex
|
51
|
5.22e-03
|
2.89e-02
|
0.29000
|
2.22e-01
|
0.186000
|
6.06e-03
|
2.14e-02
|
MET activates RAP1 and RAC1
|
11
|
1.79e-01
|
3.78e-01
|
0.28900
|
-2.59e-01
|
0.129000
|
1.37e-01
|
4.59e-01
|
Downstream TCR signaling
|
92
|
6.07e-05
|
5.73e-04
|
0.28900
|
2.49e-01
|
0.147000
|
3.64e-05
|
1.51e-02
|
Inhibition of replication initiation of damaged DNA by RB1/E2F1
|
11
|
2.21e-01
|
4.23e-01
|
0.28900
|
-2.67e-02
|
0.288000
|
8.78e-01
|
9.86e-02
|
HIV Infection
|
216
|
2.74e-10
|
9.21e-09
|
0.28800
|
1.77e-01
|
0.227000
|
6.83e-06
|
8.11e-09
|
Pyrimidine salvage
|
10
|
2.07e-01
|
4.03e-01
|
0.28800
|
-1.47e-01
|
0.248000
|
4.21e-01
|
1.74e-01
|
Vpr-mediated nuclear import of PICs
|
32
|
1.79e-02
|
7.41e-02
|
0.28800
|
2.45e-02
|
0.287000
|
8.11e-01
|
4.98e-03
|
ATF6 (ATF6-alpha) activates chaperone genes
|
10
|
3.60e-01
|
5.74e-01
|
0.28700
|
1.74e-01
|
0.229000
|
3.42e-01
|
2.10e-01
|
B-WICH complex positively regulates rRNA expression
|
29
|
5.37e-02
|
1.69e-01
|
0.28700
|
2.03e-01
|
0.203000
|
5.83e-02
|
5.84e-02
|
NOTCH3 Activation and Transmission of Signal to the Nucleus
|
25
|
5.19e-02
|
1.66e-01
|
0.28700
|
2.81e-01
|
0.058000
|
1.50e-02
|
6.16e-01
|
Cleavage of the damaged purine
|
11
|
1.76e-01
|
3.73e-01
|
0.28700
|
-1.75e-01
|
0.227000
|
3.15e-01
|
1.92e-01
|
Depurination
|
11
|
1.76e-01
|
3.73e-01
|
0.28700
|
-1.75e-01
|
0.227000
|
3.15e-01
|
1.92e-01
|
Recognition and association of DNA glycosylase with site containing an affected purine
|
11
|
1.76e-01
|
3.73e-01
|
0.28700
|
-1.75e-01
|
0.227000
|
3.15e-01
|
1.92e-01
|
Formation of RNA Pol II elongation complex
|
53
|
4.94e-03
|
2.75e-02
|
0.28600
|
1.96e-01
|
0.209000
|
1.34e-02
|
8.63e-03
|
RNA Polymerase II Transcription Elongation
|
53
|
4.94e-03
|
2.75e-02
|
0.28600
|
1.96e-01
|
0.209000
|
1.34e-02
|
8.63e-03
|
Advanced glycosylation endproduct receptor signaling
|
13
|
2.72e-01
|
4.87e-01
|
0.28600
|
2.06e-01
|
0.199000
|
1.99e-01
|
2.14e-01
|
The citric acid (TCA) cycle and respiratory electron transport
|
143
|
3.17e-07
|
5.32e-06
|
0.28600
|
1.35e-01
|
0.252000
|
5.30e-03
|
1.84e-07
|
Termination of O-glycan biosynthesis
|
25
|
8.07e-02
|
2.24e-01
|
0.28500
|
-2.27e-01
|
-0.173000
|
4.94e-02
|
1.34e-01
|
Ketone body metabolism
|
10
|
3.66e-01
|
5.80e-01
|
0.28500
|
-1.75e-01
|
-0.225000
|
3.38e-01
|
2.17e-01
|
IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation
|
14
|
1.86e-01
|
3.81e-01
|
0.28500
|
4.09e-02
|
0.282000
|
7.91e-01
|
6.76e-02
|
Signal regulatory protein family interactions
|
13
|
1.33e-01
|
3.14e-01
|
0.28500
|
-1.64e-01
|
0.233000
|
3.06e-01
|
1.46e-01
|
Negative regulation of TCF-dependent signaling by WNT ligand antagonists
|
15
|
1.23e-01
|
2.98e-01
|
0.28500
|
-6.00e-02
|
0.278000
|
6.87e-01
|
6.20e-02
|
HIV Life Cycle
|
139
|
6.98e-07
|
1.09e-05
|
0.28500
|
1.47e-01
|
0.244000
|
2.82e-03
|
6.78e-07
|
SARS-CoV-1 Infection
|
134
|
1.56e-06
|
2.26e-05
|
0.28400
|
1.68e-01
|
0.229000
|
7.92e-04
|
4.45e-06
|
Transport of Mature mRNA Derived from an Intronless Transcript
|
40
|
1.10e-02
|
5.07e-02
|
0.28400
|
7.51e-02
|
0.274000
|
4.11e-01
|
2.70e-03
|
N-glycan trimming in the ER and Calnexin/Calreticulin cycle
|
34
|
3.34e-02
|
1.21e-01
|
0.28300
|
1.60e-01
|
0.234000
|
1.06e-01
|
1.83e-02
|
Negative regulation of FGFR3 signaling
|
28
|
6.24e-02
|
1.89e-01
|
0.28300
|
1.68e-01
|
0.228000
|
1.25e-01
|
3.69e-02
|
TP53 Regulates Transcription of DNA Repair Genes
|
57
|
3.83e-03
|
2.27e-02
|
0.28300
|
2.02e-01
|
0.197000
|
8.19e-03
|
9.93e-03
|
RAB geranylgeranylation
|
57
|
2.40e-03
|
1.53e-02
|
0.28200
|
1.07e-01
|
0.261000
|
1.64e-01
|
6.41e-04
|
Killing mechanisms
|
11
|
3.10e-01
|
5.27e-01
|
0.28200
|
9.95e-02
|
0.263000
|
5.68e-01
|
1.30e-01
|
WNT5:FZD7-mediated leishmania damping
|
11
|
3.10e-01
|
5.27e-01
|
0.28200
|
9.95e-02
|
0.263000
|
5.68e-01
|
1.30e-01
|
Antigen processing-Cross presentation
|
100
|
6.60e-05
|
6.11e-04
|
0.28100
|
1.94e-01
|
0.203000
|
7.94e-04
|
4.45e-04
|
Assembly of active LPL and LIPC lipase complexes
|
17
|
7.48e-02
|
2.13e-01
|
0.28100
|
2.02e-01
|
-0.195000
|
1.49e-01
|
1.65e-01
|
Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA
|
17
|
1.84e-01
|
3.80e-01
|
0.28100
|
2.40e-01
|
0.145000
|
8.63e-02
|
3.00e-01
|
Nuclear Pore Complex (NPC) Disassembly
|
34
|
1.95e-02
|
7.99e-02
|
0.28000
|
4.01e-02
|
0.277000
|
6.86e-01
|
5.18e-03
|
Regulation of PTEN mRNA translation
|
25
|
3.50e-02
|
1.24e-01
|
0.27800
|
-2.71e-01
|
0.062400
|
1.90e-02
|
5.89e-01
|
GRB2 events in EGFR signaling
|
13
|
1.97e-01
|
3.95e-01
|
0.27800
|
-2.77e-01
|
0.015100
|
8.33e-02
|
9.25e-01
|
Tryptophan catabolism
|
12
|
2.88e-01
|
5.08e-01
|
0.27700
|
-2.60e-01
|
-0.096000
|
1.18e-01
|
5.65e-01
|
Endosomal/Vacuolar pathway
|
12
|
2.63e-01
|
4.78e-01
|
0.27700
|
2.72e-01
|
0.051200
|
1.02e-01
|
7.59e-01
|
Downstream signaling events of B Cell Receptor (BCR)
|
78
|
6.60e-04
|
5.10e-03
|
0.27700
|
2.08e-01
|
0.183000
|
1.48e-03
|
5.20e-03
|
Cytosolic sulfonation of small molecules
|
21
|
4.51e-02
|
1.50e-01
|
0.27700
|
-1.71e-01
|
0.218000
|
1.75e-01
|
8.43e-02
|
Transport of organic anions
|
10
|
3.88e-01
|
5.98e-01
|
0.27600
|
-2.22e-01
|
-0.164000
|
2.23e-01
|
3.70e-01
|
CLEC7A (Dectin-1) signaling
|
96
|
1.27e-04
|
1.12e-03
|
0.27600
|
1.72e-01
|
0.216000
|
3.57e-03
|
2.61e-04
|
Protein ubiquitination
|
61
|
2.49e-03
|
1.56e-02
|
0.27600
|
1.23e-01
|
0.247000
|
9.71e-02
|
8.51e-04
|
Formation of the Early Elongation Complex
|
32
|
5.10e-02
|
1.65e-01
|
0.27600
|
2.05e-01
|
0.184000
|
4.43e-02
|
7.21e-02
|
Formation of the HIV-1 Early Elongation Complex
|
32
|
5.10e-02
|
1.65e-01
|
0.27600
|
2.05e-01
|
0.184000
|
4.43e-02
|
7.21e-02
|
Late Phase of HIV Life Cycle
|
126
|
6.43e-06
|
7.71e-05
|
0.27500
|
1.48e-01
|
0.232000
|
4.19e-03
|
6.58e-06
|
Transport of Ribonucleoproteins into the Host Nucleus
|
30
|
4.41e-02
|
1.48e-01
|
0.27500
|
8.32e-02
|
0.262000
|
4.30e-01
|
1.29e-02
|
CYP2E1 reactions
|
11
|
3.45e-01
|
5.61e-01
|
0.27500
|
-2.41e-01
|
-0.132000
|
1.66e-01
|
4.48e-01
|
Presynaptic nicotinic acetylcholine receptors
|
12
|
3.30e-01
|
5.45e-01
|
0.27500
|
1.98e-01
|
0.191000
|
2.36e-01
|
2.52e-01
|
Downregulation of ERBB2:ERBB3 signaling
|
13
|
2.99e-01
|
5.16e-01
|
0.27500
|
1.75e-01
|
0.212000
|
2.76e-01
|
1.86e-01
|
Glutamate and glutamine metabolism
|
12
|
2.21e-01
|
4.24e-01
|
0.27400
|
-3.81e-02
|
0.271000
|
8.19e-01
|
1.04e-01
|
Activation of PPARGC1A (PGC-1alpha) by phosphorylation
|
10
|
3.58e-01
|
5.73e-01
|
0.27400
|
8.40e-02
|
0.260000
|
6.46e-01
|
1.54e-01
|
Unfolded Protein Response (UPR)
|
90
|
2.56e-04
|
2.14e-03
|
0.27300
|
1.71e-01
|
0.214000
|
5.14e-03
|
4.54e-04
|
Transcriptional Regulation by E2F6
|
32
|
1.50e-02
|
6.48e-02
|
0.27300
|
-7.08e-02
|
0.264000
|
4.88e-01
|
9.72e-03
|
Postmitotic nuclear pore complex (NPC) reformation
|
26
|
8.66e-02
|
2.36e-01
|
0.27300
|
1.43e-01
|
0.233000
|
2.07e-01
|
3.99e-02
|
WNT5A-dependent internalization of FZD4
|
15
|
2.51e-01
|
4.66e-01
|
0.27300
|
2.20e-01
|
0.161000
|
1.40e-01
|
2.79e-01
|
FGFR2c ligand binding and activation
|
12
|
3.29e-01
|
5.45e-01
|
0.27200
|
1.52e-01
|
0.226000
|
3.61e-01
|
1.76e-01
|
NS1 Mediated Effects on Host Pathways
|
39
|
2.01e-02
|
8.18e-02
|
0.27200
|
8.96e-02
|
0.256000
|
3.33e-01
|
5.57e-03
|
Defective B3GALTL causes PpS
|
36
|
2.43e-02
|
9.41e-02
|
0.27100
|
-6.97e-02
|
-0.262000
|
4.69e-01
|
6.44e-03
|
Signaling by Activin
|
15
|
2.55e-01
|
4.70e-01
|
0.27100
|
2.17e-01
|
0.162000
|
1.45e-01
|
2.76e-01
|
Phospholipase C-mediated cascade; FGFR3
|
12
|
3.38e-01
|
5.53e-01
|
0.27100
|
1.70e-01
|
0.211000
|
3.09e-01
|
2.05e-01
|
Acyl chain remodelling of PI
|
16
|
1.21e-01
|
2.97e-01
|
0.27100
|
8.57e-02
|
-0.257000
|
5.53e-01
|
7.49e-02
|
Xenobiotics
|
24
|
1.11e-01
|
2.79e-01
|
0.27100
|
-1.50e-01
|
-0.225000
|
2.03e-01
|
5.58e-02
|
Negative regulators of DDX58/IFIH1 signaling
|
34
|
2.88e-02
|
1.08e-01
|
0.27100
|
5.97e-02
|
0.264000
|
5.47e-01
|
7.73e-03
|
E3 ubiquitin ligases ubiquitinate target proteins
|
43
|
1.72e-02
|
7.26e-02
|
0.27000
|
1.22e-01
|
0.242000
|
1.67e-01
|
6.12e-03
|
RNA Polymerase III Transcription Initiation From Type 1 Promoter
|
28
|
7.60e-02
|
2.14e-01
|
0.27000
|
1.41e-01
|
0.231000
|
1.98e-01
|
3.47e-02
|
G0 and Early G1
|
27
|
6.55e-02
|
1.96e-01
|
0.27000
|
7.60e-02
|
0.259000
|
4.94e-01
|
1.99e-02
|
Fanconi Anemia Pathway
|
36
|
4.06e-02
|
1.39e-01
|
0.27000
|
1.79e-01
|
0.201000
|
6.28e-02
|
3.65e-02
|
Laminin interactions
|
23
|
1.30e-01
|
3.09e-01
|
0.26900
|
-1.82e-01
|
-0.198000
|
1.30e-01
|
9.95e-02
|
Regulation of NF-kappa B signaling
|
17
|
2.11e-01
|
4.08e-01
|
0.26900
|
2.29e-01
|
0.141000
|
1.01e-01
|
3.14e-01
|
SHC1 events in EGFR signaling
|
14
|
1.65e-01
|
3.60e-01
|
0.26900
|
-2.57e-01
|
0.079200
|
9.61e-02
|
6.08e-01
|
SARS-CoV-2 modulates autophagy
|
11
|
3.03e-01
|
5.18e-01
|
0.26800
|
2.71e-02
|
0.267000
|
8.76e-01
|
1.25e-01
|
Regulation of TP53 Activity through Phosphorylation
|
88
|
4.25e-04
|
3.40e-03
|
0.26800
|
1.74e-01
|
0.204000
|
4.73e-03
|
9.19e-04
|
Interaction between L1 and Ankyrins
|
28
|
3.39e-02
|
1.22e-01
|
0.26800
|
3.74e-02
|
-0.266000
|
7.32e-01
|
1.49e-02
|
SHC1 events in ERBB4 signaling
|
14
|
1.54e-01
|
3.43e-01
|
0.26800
|
-2.41e-01
|
0.117000
|
1.18e-01
|
4.47e-01
|
Transcription of E2F targets under negative control by DREAM complex
|
19
|
1.72e-01
|
3.69e-01
|
0.26800
|
1.23e-01
|
0.238000
|
3.54e-01
|
7.22e-02
|
tRNA processing
|
98
|
1.74e-04
|
1.50e-03
|
0.26800
|
1.61e-01
|
0.214000
|
5.83e-03
|
2.55e-04
|
TNFR1-induced NFkappaB signaling pathway
|
22
|
1.46e-01
|
3.32e-01
|
0.26800
|
1.86e-01
|
0.192000
|
1.30e-01
|
1.19e-01
|
Induction of Cell-Cell Fusion
|
12
|
3.45e-01
|
5.61e-01
|
0.26700
|
-1.59e-01
|
-0.215000
|
3.41e-01
|
1.97e-01
|
TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain
|
13
|
1.97e-01
|
3.95e-01
|
0.26700
|
-6.49e-02
|
0.259000
|
6.86e-01
|
1.05e-01
|
Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex
|
13
|
2.65e-01
|
4.79e-01
|
0.26700
|
5.67e-02
|
0.261000
|
7.23e-01
|
1.03e-01
|
Calnexin/calreticulin cycle
|
25
|
1.13e-01
|
2.82e-01
|
0.26700
|
1.79e-01
|
0.198000
|
1.22e-01
|
8.58e-02
|
Reactions specific to the complex N-glycan synthesis pathway
|
10
|
4.10e-01
|
6.16e-01
|
0.26700
|
-2.24e-01
|
-0.144000
|
2.19e-01
|
4.31e-01
|
Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC)
|
30
|
5.37e-02
|
1.69e-01
|
0.26600
|
8.09e-02
|
0.254000
|
4.43e-01
|
1.61e-02
|
Regulation of Glucokinase by Glucokinase Regulatory Protein
|
30
|
5.37e-02
|
1.69e-01
|
0.26600
|
8.09e-02
|
0.254000
|
4.43e-01
|
1.61e-02
|
FOXO-mediated transcription of cell death genes
|
15
|
2.59e-01
|
4.73e-01
|
0.26600
|
2.30e-01
|
0.133000
|
1.22e-01
|
3.71e-01
|
ER Quality Control Compartment (ERQC)
|
20
|
1.77e-01
|
3.74e-01
|
0.26600
|
2.01e-01
|
0.174000
|
1.19e-01
|
1.78e-01
|
WNT ligand biogenesis and trafficking
|
25
|
1.15e-01
|
2.87e-01
|
0.26600
|
1.77e-01
|
0.198000
|
1.26e-01
|
8.61e-02
|
SUMOylation of RNA binding proteins
|
45
|
9.85e-03
|
4.60e-02
|
0.26600
|
4.62e-02
|
0.262000
|
5.92e-01
|
2.40e-03
|
NoRC negatively regulates rRNA expression
|
43
|
2.08e-02
|
8.38e-02
|
0.26500
|
1.26e-01
|
0.233000
|
1.53e-01
|
8.09e-03
|
Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation
|
10
|
4.15e-01
|
6.20e-01
|
0.26500
|
2.21e-01
|
0.147000
|
2.27e-01
|
4.21e-01
|
Regulated proteolysis of p75NTR
|
11
|
3.59e-01
|
5.73e-01
|
0.26500
|
2.45e-01
|
0.102000
|
1.60e-01
|
5.59e-01
|
KSRP (KHSRP) binds and destabilizes mRNA
|
17
|
1.66e-01
|
3.61e-01
|
0.26500
|
2.63e-01
|
0.027900
|
6.00e-02
|
8.42e-01
|
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol
|
24
|
1.28e-01
|
3.08e-01
|
0.26500
|
-1.94e-01
|
-0.180000
|
1.01e-01
|
1.26e-01
|
Antiviral mechanism by IFN-stimulated genes
|
78
|
1.07e-03
|
7.84e-03
|
0.26500
|
1.42e-01
|
0.223000
|
2.99e-02
|
6.57e-04
|
Drug ADME
|
104
|
1.34e-04
|
1.16e-03
|
0.26400
|
-2.06e-01
|
-0.166000
|
2.89e-04
|
3.41e-03
|
RNA Polymerase III Transcription Initiation From Type 2 Promoter
|
27
|
9.58e-02
|
2.51e-01
|
0.26400
|
1.46e-01
|
0.219000
|
1.88e-01
|
4.85e-02
|
FGFR2 ligand binding and activation
|
19
|
1.87e-01
|
3.82e-01
|
0.26400
|
2.28e-01
|
0.133000
|
8.57e-02
|
3.16e-01
|
Inhibition of DNA recombination at telomere
|
20
|
1.84e-01
|
3.80e-01
|
0.26300
|
1.82e-01
|
0.190000
|
1.60e-01
|
1.41e-01
|
Transport of Mature mRNA derived from an Intron-Containing Transcript
|
67
|
3.29e-03
|
1.99e-02
|
0.26200
|
1.54e-01
|
0.213000
|
2.92e-02
|
2.61e-03
|
Cellular response to chemical stress
|
187
|
7.84e-08
|
1.66e-06
|
0.26200
|
1.26e-01
|
0.230000
|
2.84e-03
|
5.72e-08
|
Activation of AMPK downstream of NMDARs
|
10
|
3.95e-01
|
6.04e-01
|
0.26200
|
8.85e-02
|
0.246000
|
6.28e-01
|
1.77e-01
|
MTOR signalling
|
40
|
8.14e-03
|
4.03e-02
|
0.26200
|
-6.83e-02
|
0.253000
|
4.55e-01
|
5.71e-03
|
Regulation of IFNA/IFNB signaling
|
22
|
1.52e-01
|
3.43e-01
|
0.26100
|
-1.44e-01
|
-0.218000
|
2.41e-01
|
7.67e-02
|
Regulation of RUNX2 expression and activity
|
71
|
2.70e-03
|
1.68e-02
|
0.26100
|
1.84e-01
|
0.185000
|
7.32e-03
|
6.87e-03
|
O-glycosylation of TSR domain-containing proteins
|
37
|
2.73e-02
|
1.03e-01
|
0.26100
|
-5.57e-02
|
-0.255000
|
5.58e-01
|
7.27e-03
|
Bile acid and bile salt metabolism
|
45
|
1.96e-02
|
8.01e-02
|
0.26100
|
-1.22e-01
|
-0.231000
|
1.56e-01
|
7.45e-03
|
Signaling by WNT in cancer
|
32
|
1.55e-02
|
6.67e-02
|
0.26100
|
-1.52e-01
|
0.212000
|
1.37e-01
|
3.80e-02
|
RNA Pol II CTD phosphorylation and interaction with CE
|
26
|
1.04e-01
|
2.65e-01
|
0.26100
|
2.30e-01
|
0.122000
|
4.21e-02
|
2.81e-01
|
RNA Pol II CTD phosphorylation and interaction with CE during HIV infection
|
26
|
1.04e-01
|
2.65e-01
|
0.26100
|
2.30e-01
|
0.122000
|
4.21e-02
|
2.81e-01
|
Regulation of gene expression by Hypoxia-inducible Factor
|
11
|
3.84e-01
|
5.94e-01
|
0.26100
|
1.24e-01
|
0.229000
|
4.77e-01
|
1.88e-01
|
Mitochondrial tRNA aminoacylation
|
18
|
2.03e-01
|
4.01e-01
|
0.26100
|
1.11e-01
|
0.236000
|
4.16e-01
|
8.32e-02
|
Nucleotide-like (purinergic) receptors
|
13
|
3.33e-01
|
5.48e-01
|
0.26100
|
-2.15e-01
|
-0.147000
|
1.80e-01
|
3.58e-01
|
Mismatch Repair
|
15
|
2.87e-01
|
5.07e-01
|
0.26000
|
1.71e-01
|
0.196000
|
2.51e-01
|
1.88e-01
|
mTORC1-mediated signalling
|
23
|
7.17e-02
|
2.07e-01
|
0.26000
|
-4.10e-02
|
0.257000
|
7.34e-01
|
3.28e-02
|
HCMV Late Events
|
54
|
6.71e-03
|
3.55e-02
|
0.26000
|
7.99e-02
|
0.248000
|
3.10e-01
|
1.64e-03
|
RUNX3 regulates p14-ARF
|
10
|
4.18e-01
|
6.24e-01
|
0.26000
|
1.19e-01
|
0.231000
|
5.14e-01
|
2.06e-01
|
HSF1-dependent transactivation
|
35
|
5.31e-02
|
1.68e-01
|
0.26000
|
2.13e-01
|
0.149000
|
2.92e-02
|
1.28e-01
|
Negative epigenetic regulation of rRNA expression
|
45
|
2.09e-02
|
8.38e-02
|
0.26000
|
1.26e-01
|
0.227000
|
1.45e-01
|
8.37e-03
|
ISG15 antiviral mechanism
|
71
|
2.41e-03
|
1.53e-02
|
0.25900
|
1.33e-01
|
0.222000
|
5.21e-02
|
1.19e-03
|
SHC-mediated cascade:FGFR1
|
21
|
1.60e-01
|
3.53e-01
|
0.25900
|
1.14e-01
|
0.233000
|
3.68e-01
|
6.44e-02
|
FGFR3 mutant receptor activation
|
11
|
4.03e-01
|
6.11e-01
|
0.25900
|
1.66e-01
|
0.199000
|
3.41e-01
|
2.52e-01
|
Signaling by activated point mutants of FGFR3
|
11
|
4.03e-01
|
6.11e-01
|
0.25900
|
1.66e-01
|
0.199000
|
3.41e-01
|
2.52e-01
|
Transport of Mature Transcript to Cytoplasm
|
76
|
1.67e-03
|
1.11e-02
|
0.25900
|
1.37e-01
|
0.219000
|
3.82e-02
|
9.43e-04
|
tRNA Aminoacylation
|
24
|
1.04e-01
|
2.66e-01
|
0.25800
|
5.99e-02
|
0.251000
|
6.11e-01
|
3.35e-02
|
Collagen biosynthesis and modifying enzymes
|
65
|
4.00e-03
|
2.35e-02
|
0.25700
|
-1.20e-01
|
-0.228000
|
9.45e-02
|
1.50e-03
|
Purine catabolism
|
17
|
2.36e-01
|
4.46e-01
|
0.25700
|
2.27e-01
|
0.121000
|
1.06e-01
|
3.86e-01
|
Mitotic Metaphase and Anaphase
|
222
|
1.18e-08
|
3.21e-07
|
0.25700
|
1.40e-01
|
0.216000
|
3.31e-04
|
2.96e-08
|
ATF6 (ATF6-alpha) activates chaperones
|
11
|
4.08e-01
|
6.16e-01
|
0.25700
|
1.57e-01
|
0.203000
|
3.67e-01
|
2.43e-01
|
Regulated Necrosis
|
53
|
1.39e-02
|
6.13e-02
|
0.25700
|
1.92e-01
|
0.171000
|
1.57e-02
|
3.16e-02
|
mitochondrial fatty acid beta-oxidation of saturated fatty acids
|
11
|
2.78e-01
|
4.96e-01
|
0.25700
|
-7.03e-02
|
0.247000
|
6.87e-01
|
1.56e-01
|
Processing of Intronless Pre-mRNAs
|
19
|
1.80e-01
|
3.79e-01
|
0.25700
|
7.92e-02
|
0.244000
|
5.50e-01
|
6.55e-02
|
PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases
|
14
|
2.67e-01
|
4.83e-01
|
0.25600
|
-2.51e-01
|
-0.054000
|
1.04e-01
|
7.26e-01
|
Budding and maturation of HIV virion
|
28
|
9.44e-02
|
2.48e-01
|
0.25600
|
1.18e-01
|
0.227000
|
2.79e-01
|
3.76e-02
|
FGFR2 alternative splicing
|
26
|
1.23e-01
|
2.99e-01
|
0.25600
|
2.01e-01
|
0.158000
|
7.67e-02
|
1.62e-01
|
Diseases associated with N-glycosylation of proteins
|
19
|
1.40e-01
|
3.26e-01
|
0.25500
|
-2.90e-03
|
0.255000
|
9.83e-01
|
5.38e-02
|
mRNA decay by 3’ to 5’ exoribonuclease
|
16
|
1.86e-01
|
3.81e-01
|
0.25500
|
2.55e-01
|
-0.011900
|
7.72e-02
|
9.34e-01
|
AKT phosphorylates targets in the cytosol
|
14
|
3.24e-01
|
5.42e-01
|
0.25500
|
1.54e-01
|
0.204000
|
3.19e-01
|
1.87e-01
|
RNA Polymerase III Abortive And Retractive Initiation
|
41
|
3.38e-02
|
1.22e-01
|
0.25500
|
1.26e-01
|
0.222000
|
1.63e-01
|
1.41e-02
|
RNA Polymerase III Transcription
|
41
|
3.38e-02
|
1.22e-01
|
0.25500
|
1.26e-01
|
0.222000
|
1.63e-01
|
1.41e-02
|
Detoxification of Reactive Oxygen Species
|
35
|
5.83e-02
|
1.79e-01
|
0.25500
|
1.39e-01
|
0.213000
|
1.54e-01
|
2.90e-02
|
Separation of Sister Chromatids
|
161
|
2.77e-06
|
3.53e-05
|
0.25400
|
1.53e-01
|
0.203000
|
8.33e-04
|
8.41e-06
|
Mitotic Anaphase
|
221
|
1.98e-08
|
4.95e-07
|
0.25400
|
1.37e-01
|
0.214000
|
4.50e-04
|
4.26e-08
|
Protein localization
|
147
|
8.40e-06
|
9.35e-05
|
0.25400
|
1.49e-01
|
0.205000
|
1.83e-03
|
1.68e-05
|
HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand
|
37
|
4.82e-02
|
1.58e-01
|
0.25400
|
2.21e-01
|
0.124000
|
1.99e-02
|
1.91e-01
|
Cell Cycle Checkpoints
|
248
|
1.53e-09
|
4.78e-08
|
0.25400
|
1.19e-01
|
0.224000
|
1.23e-03
|
1.22e-09
|
TP53 Regulates Transcription of Cell Cycle Genes
|
49
|
1.85e-02
|
7.65e-02
|
0.25300
|
1.25e-01
|
0.220000
|
1.29e-01
|
7.75e-03
|
Highly calcium permeable postsynaptic nicotinic acetylcholine receptors
|
11
|
3.11e-01
|
5.28e-01
|
0.25300
|
2.51e-01
|
-0.029000
|
1.49e-01
|
8.68e-01
|
Cytosolic sensors of pathogen-associated DNA
|
60
|
9.28e-03
|
4.38e-02
|
0.25300
|
1.78e-01
|
0.179000
|
1.68e-02
|
1.65e-02
|
Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha)
|
14
|
3.31e-01
|
5.46e-01
|
0.25200
|
1.45e-01
|
0.206000
|
3.49e-01
|
1.81e-01
|
RNA Polymerase III Chain Elongation
|
18
|
2.47e-01
|
4.61e-01
|
0.25200
|
1.81e-01
|
0.175000
|
1.83e-01
|
1.98e-01
|
Negative regulation of MAPK pathway
|
41
|
2.71e-02
|
1.02e-01
|
0.25200
|
6.97e-02
|
0.242000
|
4.40e-01
|
7.35e-03
|
Plasma lipoprotein remodeling
|
32
|
3.85e-02
|
1.34e-01
|
0.25200
|
9.99e-03
|
-0.251000
|
9.22e-01
|
1.38e-02
|
Transcriptional regulation by small RNAs
|
46
|
2.09e-02
|
8.38e-02
|
0.25200
|
9.50e-02
|
0.233000
|
2.65e-01
|
6.27e-03
|
Translocation of ZAP-70 to Immunological synapse
|
17
|
1.32e-01
|
3.13e-01
|
0.25100
|
2.15e-01
|
-0.129000
|
1.25e-01
|
3.56e-01
|
mRNA Capping
|
28
|
1.10e-01
|
2.78e-01
|
0.25000
|
2.11e-01
|
0.135000
|
5.30e-02
|
2.18e-01
|
RHO GTPases Activate NADPH Oxidases
|
22
|
7.50e-02
|
2.13e-01
|
0.25000
|
-1.20e-01
|
0.219000
|
3.29e-01
|
7.47e-02
|
DNA strand elongation
|
31
|
8.78e-02
|
2.36e-01
|
0.25000
|
1.36e-01
|
0.210000
|
1.89e-01
|
4.31e-02
|
Insertion of tail-anchored proteins into the endoplasmic reticulum membrane
|
18
|
1.30e-01
|
3.09e-01
|
0.25000
|
-8.92e-02
|
0.233000
|
5.13e-01
|
8.63e-02
|
HDACs deacetylate histones
|
29
|
5.93e-02
|
1.81e-01
|
0.25000
|
6.12e-03
|
0.250000
|
9.55e-01
|
1.99e-02
|
Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors
|
34
|
6.58e-02
|
1.96e-01
|
0.24900
|
1.14e-01
|
0.222000
|
2.52e-01
|
2.52e-02
|
SUMOylation of chromatin organization proteins
|
54
|
3.93e-03
|
2.32e-02
|
0.24900
|
-2.80e-02
|
0.247000
|
7.22e-01
|
1.67e-03
|
NOTCH4 Activation and Transmission of Signal to the Nucleus
|
11
|
3.65e-01
|
5.79e-01
|
0.24900
|
2.46e-01
|
0.034500
|
1.57e-01
|
8.43e-01
|
RHO GTPases Activate WASPs and WAVEs
|
34
|
7.66e-02
|
2.15e-01
|
0.24900
|
1.77e-01
|
0.175000
|
7.45e-02
|
7.75e-02
|
Intrinsic Pathway of Fibrin Clot Formation
|
21
|
1.97e-01
|
3.95e-01
|
0.24800
|
-1.34e-01
|
-0.209000
|
2.87e-01
|
9.77e-02
|
IRF3-mediated induction of type I IFN
|
11
|
3.87e-01
|
5.96e-01
|
0.24800
|
2.40e-01
|
0.064000
|
1.69e-01
|
7.13e-01
|
Fertilization
|
26
|
1.22e-01
|
2.97e-01
|
0.24700
|
-9.40e-02
|
-0.228000
|
4.07e-01
|
4.38e-02
|
Metabolism of porphyrins
|
27
|
1.02e-01
|
2.63e-01
|
0.24700
|
-6.85e-02
|
-0.237000
|
5.38e-01
|
3.30e-02
|
TP53 Regulates Metabolic Genes
|
83
|
1.02e-03
|
7.60e-03
|
0.24600
|
7.64e-02
|
0.234000
|
2.29e-01
|
2.23e-04
|
SHC-mediated cascade:FGFR3
|
17
|
2.03e-01
|
4.01e-01
|
0.24600
|
1.09e-02
|
0.246000
|
9.38e-01
|
7.92e-02
|
Acetylcholine binding and downstream events
|
14
|
3.22e-01
|
5.39e-01
|
0.24600
|
2.29e-01
|
0.089700
|
1.38e-01
|
5.61e-01
|
Postsynaptic nicotinic acetylcholine receptors
|
14
|
3.22e-01
|
5.39e-01
|
0.24600
|
2.29e-01
|
0.089700
|
1.38e-01
|
5.61e-01
|
Resolution of Abasic Sites (AP sites)
|
37
|
5.17e-02
|
1.66e-01
|
0.24600
|
9.43e-02
|
0.227000
|
3.21e-01
|
1.69e-02
|
p38MAPK events
|
13
|
2.34e-01
|
4.41e-01
|
0.24600
|
-1.04e-01
|
0.223000
|
5.18e-01
|
1.64e-01
|
MAPK6/MAPK4 signaling
|
89
|
1.42e-03
|
9.71e-03
|
0.24600
|
1.83e-01
|
0.164000
|
2.82e-03
|
7.59e-03
|
mRNA 3’-end processing
|
53
|
2.03e-02
|
8.20e-02
|
0.24500
|
1.62e-01
|
0.184000
|
4.09e-02
|
2.07e-02
|
FGFR2 mutant receptor activation
|
32
|
9.43e-02
|
2.48e-01
|
0.24500
|
1.93e-01
|
0.151000
|
5.91e-02
|
1.40e-01
|
RUNX3 regulates NOTCH signaling
|
13
|
3.33e-01
|
5.48e-01
|
0.24300
|
2.38e-01
|
0.052800
|
1.38e-01
|
7.42e-01
|
RAF-independent MAPK1/3 activation
|
22
|
2.03e-01
|
4.01e-01
|
0.24300
|
1.83e-01
|
0.160000
|
1.38e-01
|
1.93e-01
|
Pyrimidine catabolism
|
12
|
4.10e-01
|
6.16e-01
|
0.24300
|
-2.06e-01
|
-0.128000
|
2.16e-01
|
4.42e-01
|
Epigenetic regulation of gene expression
|
83
|
1.41e-03
|
9.71e-03
|
0.24200
|
8.38e-02
|
0.227000
|
1.87e-01
|
3.38e-04
|
Cell recruitment (pro-inflammatory response)
|
25
|
1.44e-01
|
3.31e-01
|
0.24200
|
9.52e-02
|
0.223000
|
4.10e-01
|
5.37e-02
|
Purinergic signaling in leishmaniasis infection
|
25
|
1.44e-01
|
3.31e-01
|
0.24200
|
9.52e-02
|
0.223000
|
4.10e-01
|
5.37e-02
|
Inactivation of CSF3 (G-CSF) signaling
|
23
|
1.78e-01
|
3.76e-01
|
0.24200
|
2.13e-01
|
0.114000
|
7.68e-02
|
3.43e-01
|
Signalling to RAS
|
20
|
1.19e-01
|
2.95e-01
|
0.24100
|
-9.45e-02
|
0.221000
|
4.65e-01
|
8.67e-02
|
Acetylcholine regulates insulin secretion
|
10
|
3.27e-01
|
5.45e-01
|
0.24000
|
-1.65e-01
|
0.175000
|
3.67e-01
|
3.39e-01
|
Activation of ATR in response to replication stress
|
37
|
4.81e-02
|
1.58e-01
|
0.24000
|
5.41e-02
|
0.234000
|
5.69e-01
|
1.38e-02
|
Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants
|
19
|
2.59e-01
|
4.73e-01
|
0.24000
|
1.91e-01
|
0.145000
|
1.50e-01
|
2.72e-01
|
Signaling by Ligand-Responsive EGFR Variants in Cancer
|
19
|
2.59e-01
|
4.73e-01
|
0.24000
|
1.91e-01
|
0.145000
|
1.50e-01
|
2.72e-01
|
TP53 Regulates Transcription of Cell Death Genes
|
42
|
2.30e-02
|
9.03e-02
|
0.23900
|
3.47e-03
|
0.239000
|
9.69e-01
|
7.27e-03
|
Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters
|
20
|
2.46e-01
|
4.61e-01
|
0.23900
|
1.72e-01
|
0.167000
|
1.84e-01
|
1.97e-01
|
ZBP1(DAI) mediated induction of type I IFNs
|
20
|
2.47e-01
|
4.61e-01
|
0.23900
|
1.63e-01
|
0.175000
|
2.07e-01
|
1.76e-01
|
VEGFR2 mediated vascular permeability
|
26
|
8.84e-02
|
2.36e-01
|
0.23800
|
-2.37e-01
|
0.021700
|
3.62e-02
|
8.48e-01
|
Chaperone Mediated Autophagy
|
19
|
2.02e-01
|
4.00e-01
|
0.23800
|
2.36e-01
|
0.031600
|
7.48e-02
|
8.12e-01
|
Collagen degradation
|
39
|
6.36e-02
|
1.92e-01
|
0.23800
|
-1.35e-01
|
-0.196000
|
1.45e-01
|
3.38e-02
|
MET receptor recycling
|
10
|
3.35e-01
|
5.50e-01
|
0.23800
|
-1.81e-01
|
0.155000
|
3.23e-01
|
3.96e-01
|
Phosphorylation of CD3 and TCR zeta chains
|
20
|
1.38e-01
|
3.22e-01
|
0.23800
|
2.30e-01
|
-0.059800
|
7.46e-02
|
6.43e-01
|
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks
|
41
|
5.90e-02
|
1.81e-01
|
0.23700
|
1.54e-01
|
0.180000
|
8.71e-02
|
4.58e-02
|
Recognition of DNA damage by PCNA-containing replication complex
|
29
|
1.36e-01
|
3.21e-01
|
0.23700
|
1.74e-01
|
0.161000
|
1.05e-01
|
1.34e-01
|
Signal amplification
|
33
|
2.81e-02
|
1.05e-01
|
0.23700
|
-1.79e-01
|
0.155000
|
7.46e-02
|
1.24e-01
|
Processing of DNA double-strand break ends
|
61
|
1.26e-02
|
5.63e-02
|
0.23700
|
1.11e-01
|
0.209000
|
1.32e-01
|
4.80e-03
|
TCR signaling
|
112
|
2.90e-04
|
2.38e-03
|
0.23600
|
2.15e-01
|
0.097000
|
8.41e-05
|
7.59e-02
|
Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA
|
17
|
2.56e-01
|
4.70e-01
|
0.23600
|
2.31e-01
|
0.046100
|
9.87e-02
|
7.42e-01
|
Regulation of PTEN gene transcription
|
59
|
3.82e-03
|
2.27e-02
|
0.23600
|
-4.11e-02
|
0.232000
|
5.85e-01
|
2.05e-03
|
RNA Polymerase II Transcription Termination
|
62
|
1.49e-02
|
6.45e-02
|
0.23600
|
1.57e-01
|
0.176000
|
3.28e-02
|
1.66e-02
|
Pentose phosphate pathway
|
12
|
2.99e-01
|
5.16e-01
|
0.23500
|
-8.37e-02
|
0.220000
|
6.15e-01
|
1.87e-01
|
Cyclin A/B1/B2 associated events during G2/M transition
|
24
|
1.53e-01
|
3.43e-01
|
0.23500
|
5.66e-02
|
0.228000
|
6.31e-01
|
5.27e-02
|
Signaling by NOTCH3
|
48
|
2.49e-02
|
9.54e-02
|
0.23500
|
2.26e-01
|
0.063400
|
6.65e-03
|
4.48e-01
|
Triglyceride catabolism
|
23
|
1.68e-01
|
3.64e-01
|
0.23500
|
-6.04e-02
|
-0.227000
|
6.16e-01
|
5.93e-02
|
Negative regulation of FGFR2 signaling
|
33
|
1.06e-01
|
2.70e-01
|
0.23500
|
1.44e-01
|
0.185000
|
1.51e-01
|
6.54e-02
|
Role of LAT2/NTAL/LAB on calcium mobilization
|
13
|
3.87e-01
|
5.96e-01
|
0.23500
|
-2.17e-01
|
-0.089900
|
1.76e-01
|
5.75e-01
|
Signaling by FGFR2
|
72
|
7.95e-03
|
3.97e-02
|
0.23400
|
1.60e-01
|
0.171000
|
1.89e-02
|
1.19e-02
|
Mitotic G2-G2/M phases
|
177
|
5.95e-06
|
7.19e-05
|
0.23400
|
1.32e-01
|
0.194000
|
2.51e-03
|
8.75e-06
|
Metalloprotease DUBs
|
19
|
2.01e-01
|
4.00e-01
|
0.23300
|
9.03e-03
|
0.233000
|
9.46e-01
|
7.85e-02
|
Base Excision Repair
|
45
|
3.20e-02
|
1.17e-01
|
0.23300
|
5.56e-02
|
0.226000
|
5.19e-01
|
8.72e-03
|
Diseases associated with O-glycosylation of proteins
|
66
|
1.20e-02
|
5.45e-02
|
0.23300
|
-1.37e-01
|
-0.188000
|
5.47e-02
|
8.20e-03
|
Degradation of cysteine and homocysteine
|
14
|
3.48e-01
|
5.64e-01
|
0.23300
|
6.24e-02
|
0.224000
|
6.86e-01
|
1.47e-01
|
Thromboxane signalling through TP receptor
|
24
|
8.60e-02
|
2.36e-01
|
0.23200
|
-1.21e-01
|
0.198000
|
3.05e-01
|
9.27e-02
|
Cellular response to heat stress
|
95
|
1.66e-03
|
1.11e-02
|
0.23200
|
1.27e-01
|
0.194000
|
3.25e-02
|
1.05e-03
|
Chylomicron assembly
|
10
|
5.12e-01
|
7.00e-01
|
0.23200
|
-1.32e-01
|
-0.191000
|
4.70e-01
|
2.96e-01
|
Regulation of HSF1-mediated heat shock response
|
78
|
4.88e-03
|
2.73e-02
|
0.23100
|
1.11e-01
|
0.203000
|
8.96e-02
|
1.95e-03
|
MET promotes cell motility
|
29
|
1.40e-01
|
3.26e-01
|
0.23100
|
-2.00e-01
|
-0.116000
|
6.22e-02
|
2.80e-01
|
SUMOylation of DNA methylation proteins
|
16
|
1.95e-01
|
3.94e-01
|
0.23100
|
-1.36e-01
|
0.186000
|
3.46e-01
|
1.97e-01
|
PCNA-Dependent Long Patch Base Excision Repair
|
21
|
2.50e-01
|
4.66e-01
|
0.23000
|
1.34e-01
|
0.188000
|
2.88e-01
|
1.37e-01
|
Nuclear Envelope Breakdown
|
50
|
2.03e-02
|
8.21e-02
|
0.23000
|
3.37e-02
|
0.227000
|
6.80e-01
|
5.40e-03
|
G2/M Transition
|
175
|
1.08e-05
|
1.17e-04
|
0.22900
|
1.28e-01
|
0.190000
|
3.34e-03
|
1.42e-05
|
Signaling by CSF3 (G-CSF)
|
28
|
1.67e-01
|
3.62e-01
|
0.22800
|
1.57e-01
|
0.166000
|
1.50e-01
|
1.29e-01
|
Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells
|
15
|
3.84e-01
|
5.94e-01
|
0.22800
|
1.67e-01
|
0.155000
|
2.63e-01
|
2.97e-01
|
Disorders of Developmental Biology
|
11
|
3.74e-01
|
5.85e-01
|
0.22800
|
-4.69e-02
|
0.223000
|
7.88e-01
|
2.00e-01
|
Disorders of Nervous System Development
|
11
|
3.74e-01
|
5.85e-01
|
0.22800
|
-4.69e-02
|
0.223000
|
7.88e-01
|
2.00e-01
|
Loss of function of MECP2 in Rett syndrome
|
11
|
3.74e-01
|
5.85e-01
|
0.22800
|
-4.69e-02
|
0.223000
|
7.88e-01
|
2.00e-01
|
Pervasive developmental disorders
|
11
|
3.74e-01
|
5.85e-01
|
0.22800
|
-4.69e-02
|
0.223000
|
7.88e-01
|
2.00e-01
|
HDL remodeling
|
10
|
4.58e-01
|
6.66e-01
|
0.22800
|
-2.34e-02
|
-0.227000
|
8.98e-01
|
2.15e-01
|
Interleukin-10 signaling
|
45
|
4.68e-02
|
1.54e-01
|
0.22700
|
2.08e-01
|
0.090800
|
1.56e-02
|
2.92e-01
|
Processing of Capped Intronless Pre-mRNA
|
28
|
1.50e-01
|
3.39e-01
|
0.22700
|
9.34e-02
|
0.207000
|
3.92e-01
|
5.77e-02
|
TFAP2 (AP-2) family regulates transcription of growth factors and their receptors
|
12
|
3.57e-01
|
5.72e-01
|
0.22700
|
-2.85e-02
|
0.225000
|
8.64e-01
|
1.77e-01
|
SUMOylation of intracellular receptors
|
29
|
5.57e-02
|
1.74e-01
|
0.22700
|
-1.66e-01
|
0.155000
|
1.22e-01
|
1.50e-01
|
POU5F1 (OCT4), SOX2, NANOG activate genes related to proliferation
|
12
|
3.42e-01
|
5.59e-01
|
0.22700
|
-2.20e-01
|
0.052800
|
1.86e-01
|
7.52e-01
|
Cell Cycle, Mitotic
|
476
|
2.59e-14
|
1.82e-12
|
0.22700
|
9.83e-02
|
0.204000
|
2.34e-04
|
1.99e-14
|
MECP2 regulates neuronal receptors and channels
|
17
|
2.12e-01
|
4.09e-01
|
0.22700
|
-2.17e-01
|
0.065400
|
1.21e-01
|
6.40e-01
|
Activation of HOX genes during differentiation
|
61
|
8.99e-03
|
4.36e-02
|
0.22600
|
2.28e-02
|
0.225000
|
7.58e-01
|
2.33e-03
|
Activation of anterior HOX genes in hindbrain development during early embryogenesis
|
61
|
8.99e-03
|
4.36e-02
|
0.22600
|
2.28e-02
|
0.225000
|
7.58e-01
|
2.33e-03
|
Cellular responses to stress
|
682
|
3.08e-19
|
5.29e-17
|
0.22600
|
1.24e-01
|
0.189000
|
3.43e-08
|
2.80e-17
|
Metabolism of steroid hormones
|
33
|
5.51e-02
|
1.72e-01
|
0.22600
|
4.61e-02
|
-0.221000
|
6.47e-01
|
2.78e-02
|
Cholesterol biosynthesis
|
24
|
2.23e-01
|
4.26e-01
|
0.22600
|
1.73e-01
|
0.145000
|
1.43e-01
|
2.18e-01
|
Cellular responses to stimuli
|
696
|
1.62e-19
|
3.14e-17
|
0.22500
|
1.22e-01
|
0.189000
|
3.36e-08
|
1.38e-17
|
Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template
|
38
|
8.73e-02
|
2.36e-01
|
0.22400
|
1.08e-01
|
0.196000
|
2.48e-01
|
3.62e-02
|
DNA Double Strand Break Response
|
42
|
7.39e-02
|
2.11e-01
|
0.22400
|
1.36e-01
|
0.178000
|
1.28e-01
|
4.56e-02
|
Transcriptional Regulation by TP53
|
346
|
1.75e-10
|
6.02e-09
|
0.22400
|
9.32e-02
|
0.204000
|
2.85e-03
|
7.01e-11
|
Keratan sulfate degradation
|
12
|
3.95e-01
|
6.04e-01
|
0.22300
|
-2.23e-01
|
-0.008010
|
1.81e-01
|
9.62e-01
|
Neddylation
|
228
|
7.35e-07
|
1.14e-05
|
0.22300
|
1.20e-01
|
0.188000
|
1.81e-03
|
9.83e-07
|
Regulation of localization of FOXO transcription factors
|
11
|
4.81e-01
|
6.78e-01
|
0.22300
|
-2.08e-01
|
-0.080900
|
2.33e-01
|
6.42e-01
|
Macroautophagy
|
111
|
4.39e-04
|
3.50e-03
|
0.22300
|
5.47e-02
|
0.216000
|
3.19e-01
|
8.48e-05
|
Interleukin-1 signaling
|
109
|
1.39e-03
|
9.63e-03
|
0.22200
|
1.55e-01
|
0.159000
|
5.13e-03
|
4.01e-03
|
Interconversion of nucleotide di- and triphosphates
|
29
|
1.20e-01
|
2.96e-01
|
0.22200
|
2.99e-02
|
0.220000
|
7.80e-01
|
4.04e-02
|
Nucleotide Excision Repair
|
107
|
1.64e-03
|
1.10e-02
|
0.22200
|
1.56e-01
|
0.158000
|
5.27e-03
|
4.85e-03
|
Hedgehog ‘off’ state
|
97
|
2.87e-03
|
1.77e-02
|
0.22100
|
1.76e-01
|
0.134000
|
2.73e-03
|
2.23e-02
|
Signaling by FGFR2 IIIa TM
|
19
|
3.13e-01
|
5.30e-01
|
0.22100
|
1.84e-01
|
0.122000
|
1.64e-01
|
3.57e-01
|
Deposition of new CENPA-containing nucleosomes at the centromere
|
26
|
1.35e-01
|
3.18e-01
|
0.22100
|
-2.47e-04
|
0.221000
|
9.98e-01
|
5.12e-02
|
Nucleosome assembly
|
26
|
1.35e-01
|
3.18e-01
|
0.22100
|
-2.47e-04
|
0.221000
|
9.98e-01
|
5.12e-02
|
DNA Damage Bypass
|
46
|
5.81e-02
|
1.79e-01
|
0.22000
|
1.08e-01
|
0.192000
|
2.07e-01
|
2.40e-02
|
Negative regulation of FGFR4 signaling
|
30
|
1.65e-01
|
3.60e-01
|
0.22000
|
1.31e-01
|
0.177000
|
2.15e-01
|
9.31e-02
|
Transcriptional regulation of pluripotent stem cells
|
30
|
6.04e-02
|
1.84e-01
|
0.22000
|
-1.49e-01
|
0.162000
|
1.58e-01
|
1.25e-01
|
Phase 0 - rapid depolarisation
|
31
|
6.10e-02
|
1.86e-01
|
0.22000
|
1.00e-01
|
-0.195000
|
3.33e-01
|
5.96e-02
|
Signaling by PDGFR in disease
|
20
|
2.08e-01
|
4.04e-01
|
0.22000
|
-2.19e-01
|
0.014400
|
8.98e-02
|
9.11e-01
|
Nuclear Envelope (NE) Reassembly
|
73
|
1.10e-02
|
5.07e-02
|
0.21900
|
1.02e-01
|
0.194000
|
1.32e-01
|
4.11e-03
|
Oncogene Induced Senescence
|
35
|
1.28e-01
|
3.08e-01
|
0.21900
|
1.48e-01
|
0.162000
|
1.31e-01
|
9.72e-02
|
ERK/MAPK targets
|
20
|
2.28e-01
|
4.32e-01
|
0.21900
|
1.09e-02
|
0.219000
|
9.33e-01
|
9.05e-02
|
Initial triggering of complement
|
21
|
1.53e-01
|
3.43e-01
|
0.21900
|
1.01e-01
|
-0.194000
|
4.25e-01
|
1.23e-01
|
Biosynthesis of specialized proresolving mediators (SPMs)
|
19
|
1.72e-01
|
3.69e-01
|
0.21900
|
-1.51e-01
|
0.159000
|
2.56e-01
|
2.32e-01
|
The phototransduction cascade
|
32
|
1.28e-01
|
3.08e-01
|
0.21800
|
-7.51e-02
|
-0.205000
|
4.62e-01
|
4.48e-02
|
Synthesis of PE
|
12
|
4.00e-01
|
6.09e-01
|
0.21800
|
-7.51e-03
|
0.218000
|
9.64e-01
|
1.91e-01
|
M Phase
|
335
|
1.29e-09
|
4.16e-08
|
0.21800
|
9.47e-02
|
0.196000
|
2.85e-03
|
6.14e-10
|
Binding and Uptake of Ligands by Scavenger Receptors
|
41
|
8.69e-02
|
2.36e-01
|
0.21800
|
-1.84e-01
|
-0.117000
|
4.17e-02
|
1.95e-01
|
Synthesis of bile acids and bile salts
|
34
|
1.39e-01
|
3.26e-01
|
0.21700
|
-1.42e-01
|
-0.165000
|
1.51e-01
|
9.68e-02
|
ADP signalling through P2Y purinoceptor 1
|
25
|
1.03e-01
|
2.65e-01
|
0.21700
|
-1.71e-01
|
0.135000
|
1.40e-01
|
2.43e-01
|
Neutrophil degranulation
|
458
|
9.69e-16
|
9.98e-14
|
0.21700
|
-1.42e-02
|
0.217000
|
6.02e-01
|
1.63e-15
|
Collagen formation
|
88
|
5.37e-03
|
2.97e-02
|
0.21700
|
-1.11e-01
|
-0.186000
|
7.15e-02
|
2.51e-03
|
Calcitonin-like ligand receptors
|
10
|
5.32e-01
|
7.13e-01
|
0.21700
|
-2.03e-01
|
-0.077300
|
2.67e-01
|
6.72e-01
|
Na+/Cl- dependent neurotransmitter transporters
|
18
|
2.01e-01
|
4.00e-01
|
0.21600
|
1.82e-01
|
-0.116000
|
1.80e-01
|
3.93e-01
|
Pre-NOTCH Processing in Golgi
|
18
|
2.34e-01
|
4.41e-01
|
0.21600
|
-4.75e-02
|
0.211000
|
7.27e-01
|
1.22e-01
|
Hormone ligand-binding receptors
|
13
|
4.22e-01
|
6.27e-01
|
0.21600
|
-4.80e-02
|
-0.210000
|
7.64e-01
|
1.89e-01
|
Maturation of nucleoprotein 9683610
|
11
|
4.12e-01
|
6.18e-01
|
0.21600
|
4.70e-02
|
-0.211000
|
7.87e-01
|
2.26e-01
|
Transcription-Coupled Nucleotide Excision Repair (TC-NER)
|
76
|
1.33e-02
|
5.90e-02
|
0.21600
|
1.53e-01
|
0.152000
|
2.12e-02
|
2.17e-02
|
Autophagy
|
125
|
2.87e-04
|
2.37e-03
|
0.21500
|
5.21e-02
|
0.209000
|
3.14e-01
|
5.39e-05
|
Protein methylation
|
16
|
3.37e-01
|
5.53e-01
|
0.21500
|
3.46e-02
|
0.212000
|
8.11e-01
|
1.41e-01
|
Homology Directed Repair
|
99
|
2.99e-03
|
1.83e-02
|
0.21500
|
1.06e-01
|
0.187000
|
6.92e-02
|
1.28e-03
|
Resolution of AP sites via the multiple-nucleotide patch replacement pathway
|
24
|
2.42e-01
|
4.54e-01
|
0.21300
|
9.29e-02
|
0.192000
|
4.31e-01
|
1.03e-01
|
Beta-catenin phosphorylation cascade
|
16
|
2.76e-01
|
4.93e-01
|
0.21300
|
-5.91e-02
|
0.205000
|
6.82e-01
|
1.56e-01
|
Endosomal Sorting Complex Required For Transport (ESCRT)
|
31
|
1.61e-01
|
3.54e-01
|
0.21300
|
9.38e-02
|
0.191000
|
3.66e-01
|
6.50e-02
|
Mitotic Prophase
|
78
|
7.09e-03
|
3.64e-02
|
0.21300
|
5.28e-02
|
0.206000
|
4.20e-01
|
1.66e-03
|
trans-Golgi Network Vesicle Budding
|
67
|
4.37e-03
|
2.49e-02
|
0.21300
|
-6.91e-02
|
0.201000
|
3.28e-01
|
4.44e-03
|
Constitutive Signaling by NOTCH1 HD Domain Mutants
|
15
|
4.28e-01
|
6.33e-01
|
0.21200
|
1.79e-01
|
0.115000
|
2.31e-01
|
4.41e-01
|
Signaling by NOTCH1 HD Domain Mutants in Cancer
|
15
|
4.28e-01
|
6.33e-01
|
0.21200
|
1.79e-01
|
0.115000
|
2.31e-01
|
4.41e-01
|
Cell-cell junction organization
|
56
|
4.58e-02
|
1.52e-01
|
0.21200
|
-1.44e-01
|
-0.156000
|
6.25e-02
|
4.33e-02
|
Gap-filling DNA repair synthesis and ligation in GG-NER
|
25
|
2.52e-01
|
4.66e-01
|
0.21200
|
1.53e-01
|
0.148000
|
1.87e-01
|
2.02e-01
|
TNFs bind their physiological receptors
|
25
|
1.88e-01
|
3.82e-01
|
0.21200
|
2.10e-01
|
0.027700
|
6.88e-02
|
8.10e-01
|
Activation of SMO
|
17
|
3.53e-01
|
5.69e-01
|
0.21200
|
6.84e-02
|
0.201000
|
6.25e-01
|
1.52e-01
|
HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA)
|
93
|
4.78e-03
|
2.69e-02
|
0.21200
|
9.96e-02
|
0.187000
|
9.67e-02
|
1.82e-03
|
Global Genome Nucleotide Excision Repair (GG-NER)
|
81
|
1.17e-02
|
5.32e-02
|
0.21200
|
1.37e-01
|
0.161000
|
3.24e-02
|
1.21e-02
|
Signaling by FLT3 fusion proteins
|
19
|
2.02e-01
|
4.00e-01
|
0.21200
|
-1.86e-01
|
0.101000
|
1.60e-01
|
4.45e-01
|
Signaling by FGFR3
|
39
|
9.80e-02
|
2.55e-01
|
0.21200
|
8.02e-02
|
0.196000
|
3.86e-01
|
3.42e-02
|
Telomere C-strand synthesis initiation
|
11
|
4.67e-01
|
6.71e-01
|
0.21200
|
9.64e-03
|
0.211000
|
9.56e-01
|
2.25e-01
|
HCMV Infection
|
79
|
7.34e-03
|
3.74e-02
|
0.21100
|
5.36e-02
|
0.204000
|
4.10e-01
|
1.73e-03
|
Generation of second messenger molecules
|
30
|
7.73e-02
|
2.16e-01
|
0.21100
|
1.31e-01
|
-0.165000
|
2.15e-01
|
1.18e-01
|
Gap-filling DNA repair synthesis and ligation in TC-NER
|
62
|
3.40e-02
|
1.22e-01
|
0.21000
|
1.65e-01
|
0.131000
|
2.45e-02
|
7.53e-02
|
DNA Repair
|
276
|
2.72e-07
|
4.84e-06
|
0.21000
|
1.15e-01
|
0.176000
|
1.04e-03
|
4.66e-07
|
Cellular hexose transport
|
21
|
1.91e-01
|
3.86e-01
|
0.21000
|
1.99e-01
|
-0.066100
|
1.14e-01
|
6.00e-01
|
Diseases associated with the TLR signaling cascade
|
29
|
9.58e-02
|
2.51e-01
|
0.21000
|
-8.28e-02
|
0.193000
|
4.40e-01
|
7.23e-02
|
Diseases of Immune System
|
29
|
9.58e-02
|
2.51e-01
|
0.21000
|
-8.28e-02
|
0.193000
|
4.40e-01
|
7.23e-02
|
RNA Polymerase I Transcription Termination
|
27
|
2.34e-01
|
4.41e-01
|
0.21000
|
1.55e-01
|
0.142000
|
1.64e-01
|
2.02e-01
|
Peroxisomal lipid metabolism
|
28
|
2.16e-01
|
4.15e-01
|
0.20900
|
1.16e-01
|
0.174000
|
2.88e-01
|
1.11e-01
|
RNA Polymerase I Promoter Clearance
|
46
|
7.09e-02
|
2.06e-01
|
0.20900
|
8.35e-02
|
0.192000
|
3.27e-01
|
2.45e-02
|
RHOJ GTPase cycle
|
51
|
3.42e-02
|
1.22e-01
|
0.20900
|
-2.08e-01
|
-0.017900
|
1.01e-02
|
8.25e-01
|
Cell Cycle
|
601
|
2.17e-15
|
2.01e-13
|
0.20800
|
8.16e-02
|
0.192000
|
6.15e-04
|
8.32e-16
|
Initiation of Nuclear Envelope (NE) Reformation
|
18
|
3.87e-01
|
5.96e-01
|
0.20700
|
1.32e-01
|
0.160000
|
3.32e-01
|
2.41e-01
|
Signaling by FGFR1
|
49
|
6.82e-02
|
2.00e-01
|
0.20700
|
9.95e-02
|
0.182000
|
2.28e-01
|
2.78e-02
|
BBSome-mediated cargo-targeting to cilium
|
23
|
2.71e-01
|
4.87e-01
|
0.20700
|
1.91e-01
|
0.080200
|
1.13e-01
|
5.06e-01
|
PI-3K cascade:FGFR1
|
21
|
3.26e-01
|
5.45e-01
|
0.20700
|
1.71e-01
|
0.115000
|
1.74e-01
|
3.60e-01
|
Plasma lipoprotein assembly
|
19
|
3.73e-01
|
5.85e-01
|
0.20600
|
-1.52e-01
|
-0.139000
|
2.50e-01
|
2.96e-01
|
Toll Like Receptor 3 (TLR3) Cascade
|
99
|
4.01e-03
|
2.35e-02
|
0.20600
|
8.17e-02
|
0.189000
|
1.60e-01
|
1.15e-03
|
FRS-mediated FGFR1 signaling
|
23
|
2.88e-01
|
5.08e-01
|
0.20600
|
9.91e-02
|
0.180000
|
4.10e-01
|
1.34e-01
|
PD-1 signaling
|
21
|
1.86e-01
|
3.81e-01
|
0.20600
|
1.76e-01
|
-0.106000
|
1.62e-01
|
4.01e-01
|
NOTCH4 Intracellular Domain Regulates Transcription
|
19
|
3.76e-01
|
5.86e-01
|
0.20500
|
1.41e-01
|
0.149000
|
2.86e-01
|
2.61e-01
|
Inactivation, recovery and regulation of the phototransduction cascade
|
31
|
1.77e-01
|
3.75e-01
|
0.20500
|
-7.79e-02
|
-0.190000
|
4.53e-01
|
6.74e-02
|
Caspase activation via Death Receptors in the presence of ligand
|
16
|
4.37e-01
|
6.44e-01
|
0.20500
|
1.27e-01
|
0.161000
|
3.79e-01
|
2.66e-01
|
JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1
|
15
|
3.21e-01
|
5.39e-01
|
0.20400
|
-1.90e-01
|
0.074200
|
2.03e-01
|
6.19e-01
|
NOTCH3 Intracellular Domain Regulates Transcription
|
24
|
2.74e-01
|
4.92e-01
|
0.20400
|
1.83e-01
|
0.089800
|
1.21e-01
|
4.46e-01
|
Ribavirin ADME
|
11
|
4.71e-01
|
6.72e-01
|
0.20400
|
-2.04e-02
|
0.203000
|
9.07e-01
|
2.44e-01
|
TAK1-dependent IKK and NF-kappa-B activation
|
41
|
1.23e-01
|
2.98e-01
|
0.20300
|
1.22e-01
|
0.163000
|
1.75e-01
|
7.17e-02
|
Triglyceride metabolism
|
36
|
9.80e-02
|
2.55e-01
|
0.20300
|
-4.68e-03
|
-0.203000
|
9.61e-01
|
3.48e-02
|
TP53 Regulates Transcription of Death Receptors and Ligands
|
12
|
5.18e-01
|
7.04e-01
|
0.20300
|
7.75e-02
|
0.188000
|
6.42e-01
|
2.60e-01
|
Metabolism of cofactors
|
19
|
3.82e-01
|
5.93e-01
|
0.20300
|
1.32e-01
|
0.155000
|
3.20e-01
|
2.43e-01
|
RNA Polymerase I Transcription
|
47
|
7.64e-02
|
2.15e-01
|
0.20300
|
7.67e-02
|
0.188000
|
3.63e-01
|
2.58e-02
|
Interleukin-20 family signaling
|
24
|
2.51e-01
|
4.66e-01
|
0.20300
|
-5.25e-02
|
-0.196000
|
6.56e-01
|
9.66e-02
|
Transcriptional regulation by RUNX2
|
116
|
2.79e-03
|
1.73e-02
|
0.20300
|
1.22e-01
|
0.162000
|
2.34e-02
|
2.54e-03
|
Organic anion transporters
|
10
|
4.68e-01
|
6.71e-01
|
0.20200
|
8.72e-02
|
-0.182000
|
6.33e-01
|
3.18e-01
|
Dual incision in TC-NER
|
63
|
4.37e-02
|
1.47e-01
|
0.20100
|
1.57e-01
|
0.125000
|
3.09e-02
|
8.54e-02
|
SUMOylation of DNA damage response and repair proteins
|
71
|
9.29e-03
|
4.38e-02
|
0.20100
|
-1.56e-02
|
0.200000
|
8.20e-01
|
3.49e-03
|
Presynaptic depolarization and calcium channel opening
|
12
|
5.39e-01
|
7.21e-01
|
0.20100
|
-9.78e-02
|
-0.175000
|
5.58e-01
|
2.93e-01
|
TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition)
|
16
|
3.90e-01
|
5.98e-01
|
0.20100
|
3.31e-02
|
0.198000
|
8.19e-01
|
1.71e-01
|
Cargo concentration in the ER
|
32
|
9.38e-02
|
2.47e-01
|
0.20000
|
-8.04e-02
|
0.184000
|
4.31e-01
|
7.21e-02
|
COPII-mediated vesicle transport
|
66
|
1.33e-02
|
5.90e-02
|
0.20000
|
-1.57e-02
|
0.200000
|
8.25e-01
|
5.01e-03
|
CD28 dependent Vav1 pathway
|
11
|
4.69e-01
|
6.71e-01
|
0.20000
|
1.96e-01
|
-0.039900
|
2.60e-01
|
8.19e-01
|
Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta)
|
14
|
5.04e-01
|
6.95e-01
|
0.20000
|
1.32e-01
|
0.150000
|
3.92e-01
|
3.32e-01
|
Mucopolysaccharidoses
|
10
|
5.20e-01
|
7.04e-01
|
0.20000
|
-1.99e-01
|
0.017600
|
2.76e-01
|
9.23e-01
|
Transcriptional Regulation by VENTX
|
41
|
7.53e-02
|
2.13e-01
|
0.20000
|
-1.60e-03
|
0.200000
|
9.86e-01
|
2.70e-02
|
Polymerase switching on the C-strand of the telomere
|
24
|
2.52e-01
|
4.66e-01
|
0.19900
|
3.81e-02
|
0.196000
|
7.47e-01
|
9.72e-02
|
Synthesis of PIPs at the plasma membrane
|
48
|
3.87e-02
|
1.34e-01
|
0.19900
|
-1.95e-01
|
0.038700
|
1.94e-02
|
6.43e-01
|
Cellular Senescence
|
130
|
6.89e-04
|
5.30e-03
|
0.19800
|
4.29e-02
|
0.194000
|
3.99e-01
|
1.36e-04
|
STING mediated induction of host immune responses
|
13
|
5.02e-01
|
6.93e-01
|
0.19800
|
1.86e-01
|
0.069200
|
2.46e-01
|
6.66e-01
|
Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways
|
49
|
7.23e-02
|
2.08e-01
|
0.19800
|
6.12e-02
|
0.188000
|
4.58e-01
|
2.26e-02
|
Synthesis of Prostaglandins (PG) and Thromboxanes (TX)
|
14
|
5.01e-01
|
6.92e-01
|
0.19800
|
1.03e-01
|
0.169000
|
5.03e-01
|
2.74e-01
|
Signaling by BMP
|
27
|
1.93e-01
|
3.90e-01
|
0.19800
|
-4.85e-03
|
-0.198000
|
9.65e-01
|
7.55e-02
|
Defensins
|
36
|
7.04e-02
|
2.05e-01
|
0.19800
|
1.71e-01
|
-0.099000
|
7.57e-02
|
3.04e-01
|
SUMOylation
|
164
|
6.37e-05
|
5.93e-04
|
0.19800
|
1.70e-02
|
0.197000
|
7.07e-01
|
1.35e-05
|
Glycolysis
|
68
|
2.44e-02
|
9.41e-02
|
0.19800
|
5.09e-02
|
0.191000
|
4.68e-01
|
6.48e-03
|
Receptor-type tyrosine-protein phosphatases
|
16
|
4.10e-01
|
6.16e-01
|
0.19800
|
-4.24e-02
|
-0.193000
|
7.69e-01
|
1.82e-01
|
Interleukin-6 signaling
|
11
|
4.83e-01
|
6.78e-01
|
0.19700
|
3.43e-02
|
-0.194000
|
8.44e-01
|
2.65e-01
|
Erythropoietin activates RAS
|
14
|
3.54e-01
|
5.69e-01
|
0.19600
|
-1.22e-01
|
0.154000
|
4.29e-01
|
3.19e-01
|
MAPK targets/ Nuclear events mediated by MAP kinases
|
29
|
1.85e-01
|
3.81e-01
|
0.19600
|
1.84e-02
|
0.195000
|
8.63e-01
|
6.87e-02
|
DCC mediated attractive signaling
|
14
|
5.16e-01
|
7.04e-01
|
0.19600
|
-1.20e-01
|
-0.155000
|
4.38e-01
|
3.15e-01
|
Peroxisomal protein import
|
62
|
5.40e-02
|
1.69e-01
|
0.19600
|
1.52e-01
|
0.123000
|
3.83e-02
|
9.32e-02
|
Ub-specific processing proteases
|
153
|
7.43e-04
|
5.61e-03
|
0.19600
|
1.18e-01
|
0.156000
|
1.15e-02
|
8.72e-04
|
Synthesis of Leukotrienes (LT) and Eoxins (EX)
|
21
|
3.06e-01
|
5.21e-01
|
0.19600
|
1.93e-01
|
0.029100
|
1.25e-01
|
8.18e-01
|
Signaling by NTRK1 (TRKA)
|
114
|
2.27e-03
|
1.45e-02
|
0.19600
|
5.02e-02
|
0.189000
|
3.54e-01
|
4.89e-04
|
Acyl chain remodelling of PG
|
18
|
2.81e-01
|
5.01e-01
|
0.19500
|
8.11e-02
|
-0.178000
|
5.51e-01
|
1.92e-01
|
Cytoprotection by HMOX1
|
58
|
5.33e-02
|
1.69e-01
|
0.19500
|
7.39e-02
|
0.181000
|
3.30e-01
|
1.73e-02
|
G2/M DNA damage checkpoint
|
58
|
4.94e-02
|
1.62e-01
|
0.19500
|
6.16e-02
|
0.185000
|
4.17e-01
|
1.48e-02
|
NOTCH1 Intracellular Domain Regulates Transcription
|
44
|
8.67e-02
|
2.36e-01
|
0.19500
|
3.23e-02
|
0.192000
|
7.11e-01
|
2.73e-02
|
Activation of the pre-replicative complex
|
31
|
1.89e-01
|
3.83e-01
|
0.19500
|
4.60e-02
|
0.189000
|
6.57e-01
|
6.78e-02
|
PTEN Regulation
|
150
|
2.06e-04
|
1.73e-03
|
0.19400
|
2.07e-02
|
0.193000
|
6.61e-01
|
4.32e-05
|
Signaling by NOTCH2
|
32
|
2.09e-01
|
4.05e-01
|
0.19400
|
1.74e-01
|
0.086300
|
8.81e-02
|
3.98e-01
|
HDR through Homologous Recombination (HRR)
|
64
|
5.15e-02
|
1.66e-01
|
0.19400
|
1.22e-01
|
0.151000
|
9.22e-02
|
3.62e-02
|
Formation of Fibrin Clot (Clotting Cascade)
|
37
|
1.82e-01
|
3.80e-01
|
0.19400
|
-1.43e-01
|
-0.131000
|
1.31e-01
|
1.69e-01
|
Diseases of DNA repair
|
49
|
1.02e-01
|
2.63e-01
|
0.19400
|
1.13e-01
|
0.158000
|
1.71e-01
|
5.62e-02
|
Dual Incision in GG-NER
|
39
|
1.66e-01
|
3.61e-01
|
0.19300
|
1.23e-01
|
0.149000
|
1.84e-01
|
1.06e-01
|
Ovarian tumor domain proteases
|
36
|
1.22e-01
|
2.98e-01
|
0.19300
|
4.80e-03
|
0.193000
|
9.60e-01
|
4.46e-02
|
MyD88-independent TLR4 cascade
|
103
|
4.47e-03
|
2.53e-02
|
0.19300
|
4.68e-02
|
0.187000
|
4.11e-01
|
1.01e-03
|
TRIF(TICAM1)-mediated TLR4 signaling
|
103
|
4.47e-03
|
2.53e-02
|
0.19300
|
4.68e-02
|
0.187000
|
4.11e-01
|
1.01e-03
|
Nephrin family interactions
|
21
|
3.81e-01
|
5.92e-01
|
0.19300
|
-1.21e-01
|
-0.151000
|
3.37e-01
|
2.32e-01
|
Leading Strand Synthesis
|
13
|
5.55e-01
|
7.34e-01
|
0.19200
|
1.28e-01
|
0.144000
|
4.25e-01
|
3.70e-01
|
Polymerase switching
|
13
|
5.55e-01
|
7.34e-01
|
0.19200
|
1.28e-01
|
0.144000
|
4.25e-01
|
3.70e-01
|
Biosynthesis of DHA-derived SPMs
|
17
|
3.00e-01
|
5.17e-01
|
0.19200
|
-1.16e-01
|
0.153000
|
4.06e-01
|
2.76e-01
|
Chromosome Maintenance
|
86
|
1.43e-02
|
6.22e-02
|
0.19200
|
6.70e-02
|
0.180000
|
2.83e-01
|
3.95e-03
|
RHO GTPases activate IQGAPs
|
11
|
5.21e-01
|
7.04e-01
|
0.19100
|
-1.90e-01
|
0.014900
|
2.75e-01
|
9.32e-01
|
DNA Damage/Telomere Stress Induced Senescence
|
28
|
2.15e-01
|
4.13e-01
|
0.19000
|
1.62e-02
|
0.190000
|
8.82e-01
|
8.25e-02
|
FGFR3 ligand binding and activation
|
12
|
5.78e-01
|
7.47e-01
|
0.19000
|
9.77e-02
|
0.163000
|
5.58e-01
|
3.28e-01
|
FGFR3c ligand binding and activation
|
12
|
5.78e-01
|
7.47e-01
|
0.19000
|
9.77e-02
|
0.163000
|
5.58e-01
|
3.28e-01
|
Formation of Incision Complex in GG-NER
|
40
|
1.62e-01
|
3.54e-01
|
0.19000
|
9.93e-02
|
0.162000
|
2.77e-01
|
7.60e-02
|
Termination of translesion DNA synthesis
|
31
|
2.52e-01
|
4.66e-01
|
0.19000
|
1.16e-01
|
0.150000
|
2.63e-01
|
1.48e-01
|
SUMO E3 ligases SUMOylate target proteins
|
158
|
1.79e-04
|
1.54e-03
|
0.18900
|
1.10e-02
|
0.189000
|
8.12e-01
|
4.24e-05
|
Synthesis of bile acids and bile salts via 24-hydroxycholesterol
|
14
|
4.09e-01
|
6.16e-01
|
0.18900
|
5.91e-02
|
-0.179000
|
7.02e-01
|
2.46e-01
|
Mitotic Spindle Checkpoint
|
106
|
6.87e-03
|
3.57e-02
|
0.18900
|
7.30e-02
|
0.174000
|
1.94e-01
|
1.96e-03
|
FGFR2b ligand binding and activation
|
10
|
5.19e-01
|
7.04e-01
|
0.18900
|
1.73e-01
|
-0.075800
|
3.44e-01
|
6.78e-01
|
RNA Polymerase I Promoter Escape
|
28
|
2.96e-01
|
5.16e-01
|
0.18900
|
1.37e-01
|
0.129000
|
2.09e-01
|
2.36e-01
|
Signaling by ALK fusions and activated point mutants
|
51
|
4.20e-02
|
1.42e-01
|
0.18800
|
-4.78e-02
|
0.182000
|
5.55e-01
|
2.44e-02
|
Signaling by ALK in cancer
|
51
|
4.20e-02
|
1.42e-01
|
0.18800
|
-4.78e-02
|
0.182000
|
5.55e-01
|
2.44e-02
|
Eicosanoid ligand-binding receptors
|
14
|
3.83e-01
|
5.94e-01
|
0.18800
|
-1.29e-01
|
0.137000
|
4.03e-01
|
3.75e-01
|
Signaling by FGFR4 in disease
|
11
|
5.90e-01
|
7.54e-01
|
0.18800
|
-1.77e-01
|
-0.063200
|
3.09e-01
|
7.17e-01
|
Telomere Maintenance
|
62
|
6.26e-02
|
1.89e-01
|
0.18800
|
9.55e-02
|
0.162000
|
1.93e-01
|
2.74e-02
|
Translocation of SLC2A4 (GLUT4) to the plasma membrane
|
51
|
3.76e-02
|
1.31e-01
|
0.18800
|
-6.96e-02
|
0.175000
|
3.90e-01
|
3.10e-02
|
Response to metal ions
|
14
|
5.12e-01
|
7.00e-01
|
0.18800
|
6.20e-02
|
0.177000
|
6.88e-01
|
2.51e-01
|
Metabolism of amino acids and derivatives
|
344
|
2.78e-07
|
4.88e-06
|
0.18800
|
1.60e-01
|
0.097800
|
3.22e-07
|
1.81e-03
|
Signaling by FLT3 ITD and TKD mutants
|
16
|
4.31e-01
|
6.36e-01
|
0.18700
|
2.21e-02
|
0.186000
|
8.79e-01
|
1.97e-01
|
Integrin signaling
|
27
|
1.87e-01
|
3.82e-01
|
0.18700
|
-1.80e-01
|
0.053000
|
1.06e-01
|
6.34e-01
|
Dissolution of Fibrin Clot
|
13
|
5.72e-01
|
7.43e-01
|
0.18700
|
1.22e-01
|
0.142000
|
4.47e-01
|
3.75e-01
|
FLT3 signaling in disease
|
28
|
2.51e-01
|
4.66e-01
|
0.18700
|
4.60e-02
|
0.181000
|
6.73e-01
|
9.65e-02
|
Citric acid cycle (TCA cycle)
|
21
|
4.09e-01
|
6.16e-01
|
0.18600
|
1.25e-01
|
0.139000
|
3.23e-01
|
2.71e-01
|
Signaling by FGFR4
|
40
|
1.62e-01
|
3.54e-01
|
0.18600
|
7.54e-02
|
0.170000
|
4.09e-01
|
6.24e-02
|
O-linked glycosylation of mucins
|
62
|
5.73e-02
|
1.77e-01
|
0.18600
|
-1.73e-01
|
-0.068100
|
1.84e-02
|
3.53e-01
|
Triglyceride biosynthesis
|
13
|
4.28e-01
|
6.33e-01
|
0.18600
|
9.38e-02
|
-0.160000
|
5.58e-01
|
3.16e-01
|
Zinc transporters
|
17
|
4.88e-01
|
6.83e-01
|
0.18600
|
1.27e-01
|
0.135000
|
3.64e-01
|
3.34e-01
|
Gap junction assembly
|
18
|
3.14e-01
|
5.31e-01
|
0.18600
|
8.42e-02
|
-0.165000
|
5.36e-01
|
2.25e-01
|
Uptake and function of anthrax toxins
|
11
|
6.28e-01
|
7.88e-01
|
0.18500
|
-1.19e-01
|
-0.142000
|
4.94e-01
|
4.14e-01
|
DNA Double-Strand Break Repair
|
129
|
4.23e-03
|
2.42e-02
|
0.18500
|
1.10e-01
|
0.149000
|
3.10e-02
|
3.42e-03
|
NOTCH2 Activation and Transmission of Signal to the Nucleus
|
22
|
3.59e-01
|
5.73e-01
|
0.18500
|
1.75e-01
|
0.060200
|
1.55e-01
|
6.25e-01
|
SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs
|
11
|
6.21e-01
|
7.81e-01
|
0.18500
|
9.42e-02
|
0.159000
|
5.88e-01
|
3.60e-01
|
Insulin processing
|
26
|
3.37e-01
|
5.52e-01
|
0.18500
|
-1.37e-01
|
-0.125000
|
2.28e-01
|
2.71e-01
|
Platelet sensitization by LDL
|
17
|
3.53e-01
|
5.69e-01
|
0.18400
|
-6.21e-02
|
0.173000
|
6.57e-01
|
2.16e-01
|
Regulation of NPAS4 gene expression
|
13
|
5.83e-01
|
7.49e-01
|
0.18400
|
-1.20e-01
|
-0.139000
|
4.53e-01
|
3.84e-01
|
Signaling by FGFR
|
85
|
3.04e-02
|
1.12e-01
|
0.18300
|
1.24e-01
|
0.135000
|
4.79e-02
|
3.12e-02
|
Regulation of beta-cell development
|
41
|
1.82e-01
|
3.80e-01
|
0.18300
|
1.10e-01
|
0.147000
|
2.22e-01
|
1.04e-01
|
Glutathione synthesis and recycling
|
12
|
5.24e-01
|
7.07e-01
|
0.18300
|
-5.69e-03
|
0.183000
|
9.73e-01
|
2.72e-01
|
Transcriptional regulation of white adipocyte differentiation
|
81
|
3.13e-02
|
1.15e-01
|
0.18300
|
8.83e-02
|
0.160000
|
1.69e-01
|
1.25e-02
|
RHOV GTPase cycle
|
36
|
1.50e-01
|
3.39e-01
|
0.18300
|
-1.83e-01
|
-0.001430
|
5.74e-02
|
9.88e-01
|
ABC-family proteins mediated transport
|
98
|
1.57e-02
|
6.71e-02
|
0.18300
|
1.58e-01
|
0.091400
|
6.72e-03
|
1.18e-01
|
Beta-oxidation of very long chain fatty acids
|
10
|
5.63e-01
|
7.39e-01
|
0.18300
|
-3.68e-02
|
0.179000
|
8.40e-01
|
3.27e-01
|
Mitotic Telophase/Cytokinesis
|
10
|
5.25e-01
|
7.07e-01
|
0.18300
|
-1.37e-01
|
0.120000
|
4.53e-01
|
5.09e-01
|
RNA Polymerase I Transcription Initiation
|
42
|
1.63e-01
|
3.56e-01
|
0.18200
|
7.95e-02
|
0.164000
|
3.72e-01
|
6.56e-02
|
Phospholipase C-mediated cascade; FGFR2
|
17
|
5.01e-01
|
6.92e-01
|
0.18200
|
1.24e-01
|
0.134000
|
3.76e-01
|
3.40e-01
|
Negative regulation of NMDA receptor-mediated neuronal transmission
|
20
|
4.20e-01
|
6.25e-01
|
0.18200
|
-7.68e-02
|
-0.165000
|
5.52e-01
|
2.01e-01
|
HDR through Single Strand Annealing (SSA)
|
36
|
2.22e-01
|
4.24e-01
|
0.18200
|
9.15e-02
|
0.157000
|
3.42e-01
|
1.03e-01
|
HCMV Early Events
|
55
|
7.79e-02
|
2.17e-01
|
0.18100
|
4.15e-02
|
0.176000
|
5.94e-01
|
2.39e-02
|
FRS-mediated FGFR3 signaling
|
19
|
3.79e-01
|
5.90e-01
|
0.18100
|
4.23e-03
|
0.181000
|
9.75e-01
|
1.73e-01
|
Synthesis of PA
|
35
|
2.08e-01
|
4.04e-01
|
0.18000
|
-4.90e-02
|
-0.173000
|
6.16e-01
|
7.70e-02
|
Prefoldin mediated transfer of substrate to CCT/TriC
|
27
|
3.15e-01
|
5.31e-01
|
0.17900
|
1.66e-01
|
0.065800
|
1.34e-01
|
5.54e-01
|
Synthesis of PIPs at the early endosome membrane
|
15
|
4.50e-01
|
6.57e-01
|
0.17800
|
-1.77e-01
|
0.024000
|
2.36e-01
|
8.72e-01
|
SHC-mediated cascade:FGFR2
|
22
|
3.42e-01
|
5.59e-01
|
0.17800
|
1.17e-02
|
0.178000
|
9.25e-01
|
1.48e-01
|
Disassembly of the destruction complex and recruitment of AXIN to the membrane
|
30
|
2.53e-01
|
4.66e-01
|
0.17800
|
3.51e-02
|
0.175000
|
7.39e-01
|
9.75e-02
|
Regulation of TP53 Activity through Acetylation
|
29
|
1.95e-01
|
3.94e-01
|
0.17800
|
-5.15e-02
|
0.170000
|
6.31e-01
|
1.12e-01
|
SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription
|
36
|
2.51e-01
|
4.66e-01
|
0.17700
|
1.31e-01
|
0.119000
|
1.75e-01
|
2.15e-01
|
Maturation of spike protein 9694548
|
35
|
1.28e-01
|
3.08e-01
|
0.17600
|
-8.89e-02
|
0.152000
|
3.63e-01
|
1.19e-01
|
Regulation of TP53 Activity
|
154
|
1.62e-03
|
1.10e-02
|
0.17600
|
6.08e-02
|
0.166000
|
1.93e-01
|
3.88e-04
|
NOTCH2 intracellular domain regulates transcription
|
11
|
6.55e-01
|
8.02e-01
|
0.17600
|
1.42e-01
|
0.105000
|
4.16e-01
|
5.48e-01
|
Heme signaling
|
45
|
1.43e-01
|
3.31e-01
|
0.17600
|
-1.70e-01
|
-0.046900
|
4.89e-02
|
5.86e-01
|
Aggrephagy
|
23
|
3.67e-01
|
5.81e-01
|
0.17600
|
1.70e-01
|
0.044000
|
1.57e-01
|
7.15e-01
|
O-linked glycosylation
|
107
|
1.75e-02
|
7.34e-02
|
0.17600
|
-1.33e-01
|
-0.115000
|
1.71e-02
|
4.03e-02
|
Signaling by NTRKs
|
133
|
3.49e-03
|
2.08e-02
|
0.17500
|
4.74e-02
|
0.169000
|
3.45e-01
|
7.83e-04
|
RHOU GTPase cycle
|
37
|
1.54e-01
|
3.43e-01
|
0.17500
|
-1.73e-01
|
0.020300
|
6.78e-02
|
8.31e-01
|
Interleukin-35 Signalling
|
12
|
5.37e-01
|
7.19e-01
|
0.17400
|
3.05e-02
|
-0.172000
|
8.55e-01
|
3.03e-01
|
Gene expression (Transcription)
|
1420
|
2.57e-24
|
7.94e-22
|
0.17400
|
6.47e-02
|
0.162000
|
3.99e-05
|
1.09e-24
|
RHOQ GTPase cycle
|
57
|
8.22e-02
|
2.28e-01
|
0.17400
|
-1.71e-01
|
-0.032200
|
2.55e-02
|
6.74e-01
|
Interleukin-2 signaling
|
11
|
5.45e-01
|
7.24e-01
|
0.17400
|
1.61e-01
|
-0.064900
|
3.54e-01
|
7.09e-01
|
RNA Polymerase II Transcription
|
1284
|
9.70e-22
|
2.50e-19
|
0.17400
|
7.26e-02
|
0.158000
|
1.13e-05
|
1.12e-21
|
Antimicrobial peptides
|
78
|
1.24e-02
|
5.58e-02
|
0.17400
|
1.55e-01
|
-0.078500
|
1.79e-02
|
2.31e-01
|
Diseases associated with visual transduction
|
11
|
6.65e-01
|
8.07e-01
|
0.17400
|
-1.33e-01
|
-0.111000
|
4.45e-01
|
5.22e-01
|
Diseases of the neuronal system
|
11
|
6.65e-01
|
8.07e-01
|
0.17400
|
-1.33e-01
|
-0.111000
|
4.45e-01
|
5.22e-01
|
Retinoid cycle disease events
|
11
|
6.65e-01
|
8.07e-01
|
0.17400
|
-1.33e-01
|
-0.111000
|
4.45e-01
|
5.22e-01
|
APC truncation mutants have impaired AXIN binding
|
13
|
4.93e-01
|
6.85e-01
|
0.17300
|
-5.98e-02
|
0.163000
|
7.09e-01
|
3.10e-01
|
AXIN missense mutants destabilize the destruction complex
|
13
|
4.93e-01
|
6.85e-01
|
0.17300
|
-5.98e-02
|
0.163000
|
7.09e-01
|
3.10e-01
|
Signaling by AMER1 mutants
|
13
|
4.93e-01
|
6.85e-01
|
0.17300
|
-5.98e-02
|
0.163000
|
7.09e-01
|
3.10e-01
|
Signaling by APC mutants
|
13
|
4.93e-01
|
6.85e-01
|
0.17300
|
-5.98e-02
|
0.163000
|
7.09e-01
|
3.10e-01
|
Signaling by AXIN mutants
|
13
|
4.93e-01
|
6.85e-01
|
0.17300
|
-5.98e-02
|
0.163000
|
7.09e-01
|
3.10e-01
|
Truncations of AMER1 destabilize the destruction complex
|
13
|
4.93e-01
|
6.85e-01
|
0.17300
|
-5.98e-02
|
0.163000
|
7.09e-01
|
3.10e-01
|
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein
|
74
|
5.64e-02
|
1.75e-01
|
0.17300
|
7.37e-02
|
0.156000
|
2.73e-01
|
2.01e-02
|
Processive synthesis on the lagging strand
|
14
|
5.87e-01
|
7.52e-01
|
0.17200
|
8.17e-02
|
0.152000
|
5.97e-01
|
3.25e-01
|
GRB2 events in ERBB2 signaling
|
16
|
4.71e-01
|
6.72e-01
|
0.17200
|
-1.72e-01
|
0.000783
|
2.32e-01
|
9.96e-01
|
TCF dependent signaling in response to WNT
|
168
|
1.90e-03
|
1.24e-02
|
0.17200
|
8.82e-02
|
0.148000
|
4.84e-02
|
9.38e-04
|
ERBB2 Activates PTK6 Signaling
|
13
|
5.59e-01
|
7.37e-01
|
0.17200
|
-1.65e-02
|
-0.171000
|
9.18e-01
|
2.85e-01
|
TP53 Regulates Transcription of Genes Involved in Cytochrome C Release
|
19
|
4.12e-01
|
6.18e-01
|
0.17200
|
-1.00e-04
|
0.172000
|
9.99e-01
|
1.95e-01
|
Acyl chain remodelling of PC
|
26
|
2.64e-01
|
4.78e-01
|
0.17200
|
4.01e-02
|
-0.167000
|
7.24e-01
|
1.41e-01
|
Thrombin signalling through proteinase activated receptors (PARs)
|
32
|
1.78e-01
|
3.76e-01
|
0.17100
|
-6.65e-02
|
0.158000
|
5.15e-01
|
1.22e-01
|
Signaling by Hedgehog
|
133
|
8.67e-03
|
4.23e-02
|
0.17100
|
1.15e-01
|
0.126000
|
2.16e-02
|
1.18e-02
|
Acyl chain remodelling of PS
|
21
|
3.81e-01
|
5.92e-01
|
0.17000
|
6.00e-04
|
-0.170000
|
9.96e-01
|
1.76e-01
|
Signaling by the B Cell Receptor (BCR)
|
105
|
2.44e-02
|
9.41e-02
|
0.17000
|
1.21e-01
|
0.120000
|
3.26e-02
|
3.32e-02
|
Extracellular matrix organization
|
287
|
4.48e-05
|
4.36e-04
|
0.17000
|
-1.19e-01
|
-0.121000
|
5.09e-04
|
4.16e-04
|
CTNNB1 S33 mutants aren’t phosphorylated
|
14
|
4.62e-01
|
6.68e-01
|
0.16900
|
-1.06e-01
|
0.131000
|
4.91e-01
|
3.94e-01
|
CTNNB1 S37 mutants aren’t phosphorylated
|
14
|
4.62e-01
|
6.68e-01
|
0.16900
|
-1.06e-01
|
0.131000
|
4.91e-01
|
3.94e-01
|
CTNNB1 S45 mutants aren’t phosphorylated
|
14
|
4.62e-01
|
6.68e-01
|
0.16900
|
-1.06e-01
|
0.131000
|
4.91e-01
|
3.94e-01
|
CTNNB1 T41 mutants aren’t phosphorylated
|
14
|
4.62e-01
|
6.68e-01
|
0.16900
|
-1.06e-01
|
0.131000
|
4.91e-01
|
3.94e-01
|
Signaling by CTNNB1 phospho-site mutants
|
14
|
4.62e-01
|
6.68e-01
|
0.16900
|
-1.06e-01
|
0.131000
|
4.91e-01
|
3.94e-01
|
Signaling by GSK3beta mutants
|
14
|
4.62e-01
|
6.68e-01
|
0.16900
|
-1.06e-01
|
0.131000
|
4.91e-01
|
3.94e-01
|
TRP channels
|
24
|
3.60e-01
|
5.74e-01
|
0.16900
|
-2.09e-02
|
-0.168000
|
8.60e-01
|
1.55e-01
|
Activated point mutants of FGFR2
|
16
|
5.72e-01
|
7.44e-01
|
0.16900
|
1.18e-01
|
0.120000
|
4.12e-01
|
4.04e-01
|
EGR2 and SOX10-mediated initiation of Schwann cell myelination
|
27
|
2.82e-01
|
5.02e-01
|
0.16900
|
1.59e-02
|
-0.168000
|
8.86e-01
|
1.31e-01
|
Activated NOTCH1 Transmits Signal to the Nucleus
|
30
|
2.37e-01
|
4.46e-01
|
0.16900
|
1.67e-01
|
-0.026100
|
1.14e-01
|
8.04e-01
|
Mitochondrial biogenesis
|
69
|
6.59e-02
|
1.96e-01
|
0.16900
|
4.67e-02
|
0.162000
|
5.02e-01
|
2.00e-02
|
GRB2:SOS provides linkage to MAPK signaling for Integrins
|
15
|
4.42e-01
|
6.50e-01
|
0.16800
|
-1.30e-01
|
0.106000
|
3.84e-01
|
4.76e-01
|
Infectious disease
|
830
|
3.74e-13
|
1.84e-11
|
0.16800
|
8.67e-02
|
0.144000
|
2.07e-05
|
1.77e-12
|
Ethanol oxidation
|
12
|
5.41e-01
|
7.22e-01
|
0.16700
|
6.23e-02
|
-0.155000
|
7.08e-01
|
3.51e-01
|
Generic Transcription Pathway
|
1163
|
1.59e-18
|
2.04e-16
|
0.16700
|
6.69e-02
|
0.153000
|
1.12e-04
|
8.91e-19
|
Assembly of collagen fibrils and other multimeric structures
|
56
|
1.12e-01
|
2.82e-01
|
0.16700
|
-4.34e-02
|
-0.161000
|
5.74e-01
|
3.66e-02
|
Metabolism of nucleotides
|
95
|
1.26e-02
|
5.64e-02
|
0.16700
|
-1.79e-02
|
0.166000
|
7.63e-01
|
5.15e-03
|
ECM proteoglycans
|
55
|
1.53e-01
|
3.43e-01
|
0.16700
|
-1.08e-01
|
-0.127000
|
1.67e-01
|
1.02e-01
|
SHC-mediated cascade:FGFR4
|
19
|
4.06e-01
|
6.14e-01
|
0.16700
|
-3.06e-02
|
0.164000
|
8.18e-01
|
2.16e-01
|
Meiotic synapsis
|
32
|
1.86e-01
|
3.81e-01
|
0.16600
|
-1.42e-01
|
0.087500
|
1.66e-01
|
3.92e-01
|
SARS-CoV-2-host interactions
|
183
|
1.48e-03
|
1.01e-02
|
0.16600
|
7.19e-02
|
0.150000
|
9.32e-02
|
4.80e-04
|
Signaling by PDGFRA extracellular domain mutants
|
12
|
5.59e-01
|
7.37e-01
|
0.16600
|
-1.59e-01
|
0.045200
|
3.39e-01
|
7.86e-01
|
Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants
|
12
|
5.59e-01
|
7.37e-01
|
0.16600
|
-1.59e-01
|
0.045200
|
3.39e-01
|
7.86e-01
|
RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function
|
38
|
1.82e-01
|
3.80e-01
|
0.16500
|
-1.65e-01
|
0.014000
|
7.85e-02
|
8.81e-01
|
Downstream signaling of activated FGFR3
|
24
|
3.72e-01
|
5.85e-01
|
0.16500
|
1.65e-02
|
0.164000
|
8.89e-01
|
1.63e-01
|
RHOBTB2 GTPase cycle
|
22
|
4.74e-01
|
6.74e-01
|
0.16500
|
1.35e-01
|
0.095900
|
2.75e-01
|
4.36e-01
|
Acyl chain remodelling of PE
|
24
|
3.12e-01
|
5.29e-01
|
0.16500
|
4.82e-02
|
-0.158000
|
6.83e-01
|
1.80e-01
|
Nicotinamide salvaging
|
17
|
4.20e-01
|
6.25e-01
|
0.16500
|
7.69e-02
|
-0.146000
|
5.83e-01
|
2.97e-01
|
Creation of C4 and C2 activators
|
14
|
5.96e-01
|
7.59e-01
|
0.16500
|
-5.41e-02
|
-0.156000
|
7.26e-01
|
3.13e-01
|
Activation of Matrix Metalloproteinases
|
31
|
3.28e-01
|
5.45e-01
|
0.16500
|
-6.43e-02
|
-0.152000
|
5.36e-01
|
1.44e-01
|
Impaired BRCA2 binding to RAD51
|
33
|
3.29e-01
|
5.45e-01
|
0.16500
|
9.63e-02
|
0.134000
|
3.39e-01
|
1.84e-01
|
DDX58/IFIH1-mediated induction of interferon-alpha/beta
|
75
|
4.76e-02
|
1.57e-01
|
0.16400
|
1.59e-02
|
0.163000
|
8.11e-01
|
1.44e-02
|
Deubiquitination
|
226
|
4.98e-04
|
3.91e-03
|
0.16400
|
8.43e-02
|
0.140000
|
2.88e-02
|
2.73e-04
|
mRNA decay by 5’ to 3’ exoribonuclease
|
15
|
5.67e-01
|
7.43e-01
|
0.16400
|
3.95e-02
|
0.159000
|
7.91e-01
|
2.87e-01
|
Sealing of the nuclear envelope (NE) by ESCRT-III
|
31
|
3.49e-01
|
5.65e-01
|
0.16300
|
8.01e-02
|
0.142000
|
4.40e-01
|
1.71e-01
|
Non-integrin membrane-ECM interactions
|
40
|
2.63e-01
|
4.78e-01
|
0.16300
|
-1.38e-01
|
-0.087500
|
1.32e-01
|
3.38e-01
|
Signaling by NODAL
|
21
|
3.91e-01
|
6.00e-01
|
0.16200
|
1.60e-01
|
-0.026600
|
2.04e-01
|
8.33e-01
|
Maturation of nucleoprotein 9694631
|
15
|
4.70e-01
|
6.71e-01
|
0.16200
|
9.18e-02
|
-0.134000
|
5.38e-01
|
3.69e-01
|
Downstream signaling of activated FGFR1
|
31
|
3.43e-01
|
5.59e-01
|
0.16200
|
6.64e-02
|
0.148000
|
5.22e-01
|
1.54e-01
|
MAP2K and MAPK activation
|
36
|
1.87e-01
|
3.82e-01
|
0.16200
|
-4.71e-02
|
0.155000
|
6.25e-01
|
1.08e-01
|
CS/DS degradation
|
12
|
5.46e-01
|
7.25e-01
|
0.16200
|
-1.01e-01
|
0.127000
|
5.46e-01
|
4.48e-01
|
Potential therapeutics for SARS
|
92
|
1.95e-02
|
7.99e-02
|
0.16200
|
-1.44e-02
|
0.161000
|
8.12e-01
|
7.59e-03
|
Regulation of FZD by ubiquitination
|
21
|
5.11e-01
|
7.00e-01
|
0.16200
|
1.09e-01
|
0.119000
|
3.87e-01
|
3.44e-01
|
Negative regulation of MET activity
|
20
|
4.40e-01
|
6.48e-01
|
0.16200
|
1.78e-03
|
0.162000
|
9.89e-01
|
2.11e-01
|
Reversible hydration of carbon dioxide
|
11
|
7.04e-01
|
8.35e-01
|
0.16200
|
1.12e-01
|
0.117000
|
5.22e-01
|
5.02e-01
|
Defective homologous recombination repair (HRR) due to BRCA2 loss of function
|
39
|
2.90e-01
|
5.09e-01
|
0.16100
|
1.21e-01
|
0.106000
|
1.90e-01
|
2.53e-01
|
Diseases of DNA Double-Strand Break Repair
|
39
|
2.90e-01
|
5.09e-01
|
0.16100
|
1.21e-01
|
0.106000
|
1.90e-01
|
2.53e-01
|
NPAS4 regulates expression of target genes
|
21
|
4.81e-01
|
6.78e-01
|
0.16100
|
1.51e-01
|
0.054400
|
2.31e-01
|
6.66e-01
|
Rab regulation of trafficking
|
113
|
6.12e-03
|
3.33e-02
|
0.16000
|
-4.17e-02
|
0.155000
|
4.44e-01
|
4.42e-03
|
Translesion synthesis by REV1
|
16
|
6.03e-01
|
7.64e-01
|
0.16000
|
1.02e-01
|
0.124000
|
4.80e-01
|
3.91e-01
|
Defective HDR through Homologous Recombination (HRR) due to BRCA1 loss-of-function
|
23
|
4.84e-01
|
6.78e-01
|
0.16000
|
1.22e-01
|
0.104000
|
3.11e-01
|
3.88e-01
|
Defective HDR through Homologous Recombination (HRR) due to PALB2 loss of function
|
23
|
4.84e-01
|
6.78e-01
|
0.16000
|
1.22e-01
|
0.104000
|
3.11e-01
|
3.88e-01
|
Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function
|
23
|
4.84e-01
|
6.78e-01
|
0.16000
|
1.22e-01
|
0.104000
|
3.11e-01
|
3.88e-01
|
Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function
|
23
|
4.84e-01
|
6.78e-01
|
0.16000
|
1.22e-01
|
0.104000
|
3.11e-01
|
3.88e-01
|
Impaired BRCA2 binding to PALB2
|
23
|
4.84e-01
|
6.78e-01
|
0.16000
|
1.22e-01
|
0.104000
|
3.11e-01
|
3.88e-01
|
Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation
|
35
|
2.89e-01
|
5.09e-01
|
0.16000
|
4.46e-02
|
0.154000
|
6.48e-01
|
1.16e-01
|
Butyrophilin (BTN) family interactions
|
12
|
6.30e-01
|
7.89e-01
|
0.16000
|
1.59e-01
|
0.015900
|
3.40e-01
|
9.24e-01
|
Defects of contact activation system (CAS) and kallikrein/kinin system (KKS)
|
14
|
6.35e-01
|
7.92e-01
|
0.15900
|
-1.39e-01
|
-0.077700
|
3.68e-01
|
6.15e-01
|
Diseases of hemostasis
|
14
|
6.35e-01
|
7.92e-01
|
0.15900
|
-1.39e-01
|
-0.077700
|
3.68e-01
|
6.15e-01
|
NCAM1 interactions
|
36
|
1.73e-01
|
3.70e-01
|
0.15900
|
1.24e-01
|
-0.099500
|
1.98e-01
|
3.01e-01
|
Translesion synthesis by POLI
|
17
|
5.77e-01
|
7.47e-01
|
0.15900
|
1.40e-01
|
0.075800
|
3.18e-01
|
5.88e-01
|
FGFR1 mutant receptor activation
|
30
|
3.62e-01
|
5.76e-01
|
0.15900
|
5.73e-02
|
0.148000
|
5.87e-01
|
1.60e-01
|
RHOB GTPase cycle
|
66
|
9.65e-02
|
2.52e-01
|
0.15900
|
-1.54e-01
|
-0.040300
|
3.07e-02
|
5.71e-01
|
LGI-ADAM interactions
|
14
|
6.15e-01
|
7.74e-01
|
0.15900
|
4.63e-02
|
0.152000
|
7.64e-01
|
3.25e-01
|
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding
|
32
|
3.74e-01
|
5.85e-01
|
0.15800
|
1.09e-01
|
0.115000
|
2.85e-01
|
2.61e-01
|
Programmed Cell Death
|
192
|
2.48e-03
|
1.56e-02
|
0.15800
|
8.54e-02
|
0.133000
|
4.10e-02
|
1.44e-03
|
Telomere C-strand (Lagging Strand) Synthesis
|
32
|
2.81e-01
|
5.01e-01
|
0.15800
|
-1.82e-03
|
0.158000
|
9.86e-01
|
1.22e-01
|
Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants
|
54
|
1.84e-01
|
3.80e-01
|
0.15700
|
8.00e-02
|
0.136000
|
3.09e-01
|
8.49e-02
|
Constitutive Signaling by NOTCH1 PEST Domain Mutants
|
54
|
1.84e-01
|
3.80e-01
|
0.15700
|
8.00e-02
|
0.136000
|
3.09e-01
|
8.49e-02
|
Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer
|
54
|
1.84e-01
|
3.80e-01
|
0.15700
|
8.00e-02
|
0.136000
|
3.09e-01
|
8.49e-02
|
Signaling by NOTCH1 PEST Domain Mutants in Cancer
|
54
|
1.84e-01
|
3.80e-01
|
0.15700
|
8.00e-02
|
0.136000
|
3.09e-01
|
8.49e-02
|
Signaling by NOTCH1 in Cancer
|
54
|
1.84e-01
|
3.80e-01
|
0.15700
|
8.00e-02
|
0.136000
|
3.09e-01
|
8.49e-02
|
Early SARS-CoV-2 Infection Events
|
34
|
2.68e-01
|
4.83e-01
|
0.15700
|
3.07e-03
|
0.157000
|
9.75e-01
|
1.12e-01
|
Glutathione conjugation
|
36
|
2.37e-01
|
4.46e-01
|
0.15700
|
-1.00e-02
|
0.157000
|
9.17e-01
|
1.04e-01
|
RHOH GTPase cycle
|
36
|
1.85e-01
|
3.81e-01
|
0.15700
|
-8.45e-02
|
0.132000
|
3.80e-01
|
1.70e-01
|
Cell junction organization
|
79
|
8.88e-02
|
2.37e-01
|
0.15700
|
-8.80e-02
|
-0.130000
|
1.76e-01
|
4.59e-02
|
PI Metabolism
|
79
|
2.96e-02
|
1.10e-01
|
0.15600
|
-1.44e-01
|
0.060500
|
2.71e-02
|
3.52e-01
|
Retrograde neurotrophin signalling
|
14
|
6.59e-01
|
8.03e-01
|
0.15600
|
1.03e-01
|
0.117000
|
5.03e-01
|
4.49e-01
|
Removal of the Flap Intermediate
|
13
|
6.81e-01
|
8.20e-01
|
0.15500
|
1.03e-01
|
0.116000
|
5.19e-01
|
4.69e-01
|
Extension of Telomeres
|
48
|
1.89e-01
|
3.83e-01
|
0.15500
|
3.00e-02
|
0.152000
|
7.19e-01
|
6.79e-02
|
Apoptosis
|
164
|
7.94e-03
|
3.97e-02
|
0.15500
|
9.35e-02
|
0.123000
|
3.88e-02
|
6.33e-03
|
MyD88:MAL(TIRAP) cascade initiated on plasma membrane
|
106
|
1.77e-02
|
7.34e-02
|
0.15500
|
-3.97e-03
|
0.155000
|
9.44e-01
|
5.94e-03
|
Toll Like Receptor 2 (TLR2) Cascade
|
106
|
1.77e-02
|
7.34e-02
|
0.15500
|
-3.97e-03
|
0.155000
|
9.44e-01
|
5.94e-03
|
Toll Like Receptor TLR1:TLR2 Cascade
|
106
|
1.77e-02
|
7.34e-02
|
0.15500
|
-3.97e-03
|
0.155000
|
9.44e-01
|
5.94e-03
|
Toll Like Receptor TLR6:TLR2 Cascade
|
106
|
1.77e-02
|
7.34e-02
|
0.15500
|
-3.97e-03
|
0.155000
|
9.44e-01
|
5.94e-03
|
Transcriptional activation of mitochondrial biogenesis
|
51
|
2.12e-01
|
4.08e-01
|
0.15500
|
7.57e-02
|
0.135000
|
3.50e-01
|
9.57e-02
|
SUMOylation of transcription cofactors
|
43
|
1.96e-01
|
3.94e-01
|
0.15500
|
-2.09e-03
|
0.155000
|
9.81e-01
|
7.95e-02
|
Telomere Extension By Telomerase
|
22
|
4.69e-01
|
6.71e-01
|
0.15400
|
2.99e-02
|
0.152000
|
8.08e-01
|
2.18e-01
|
Homologous DNA Pairing and Strand Exchange
|
41
|
3.03e-01
|
5.18e-01
|
0.15400
|
1.08e-01
|
0.111000
|
2.33e-01
|
2.20e-01
|
Regulation of Complement cascade
|
45
|
2.70e-01
|
4.86e-01
|
0.15400
|
-9.68e-02
|
-0.120000
|
2.61e-01
|
1.65e-01
|
tRNA modification in the nucleus and cytosol
|
38
|
3.24e-01
|
5.42e-01
|
0.15400
|
8.42e-02
|
0.129000
|
3.69e-01
|
1.70e-01
|
NR1H2 and NR1H3-mediated signaling
|
53
|
2.00e-01
|
3.99e-01
|
0.15400
|
-1.36e-01
|
-0.071000
|
8.60e-02
|
3.71e-01
|
Regulation of TP53 Expression and Degradation
|
37
|
3.23e-01
|
5.41e-01
|
0.15300
|
6.69e-02
|
0.138000
|
4.81e-01
|
1.46e-01
|
Signaling by NTRK3 (TRKC)
|
17
|
4.72e-01
|
6.73e-01
|
0.15300
|
-7.27e-02
|
0.135000
|
6.04e-01
|
3.35e-01
|
Asparagine N-linked glycosylation
|
278
|
1.15e-04
|
1.03e-03
|
0.15300
|
3.70e-02
|
0.148000
|
2.87e-01
|
2.07e-05
|
Signaling by FGFR2 in disease
|
42
|
3.02e-01
|
5.18e-01
|
0.15300
|
1.03e-01
|
0.113000
|
2.48e-01
|
2.06e-01
|
Sphingolipid de novo biosynthesis
|
41
|
2.32e-01
|
4.39e-01
|
0.15300
|
-1.52e-01
|
-0.010300
|
9.13e-02
|
9.09e-01
|
G-protein activation
|
24
|
3.41e-01
|
5.58e-01
|
0.15200
|
-1.09e-01
|
0.106000
|
3.55e-01
|
3.68e-01
|
MASTL Facilitates Mitotic Progression
|
10
|
6.49e-01
|
8.01e-01
|
0.15100
|
-7.61e-02
|
0.131000
|
6.77e-01
|
4.74e-01
|
Stimuli-sensing channels
|
96
|
6.73e-02
|
1.98e-01
|
0.15100
|
-9.24e-02
|
-0.120000
|
1.17e-01
|
4.28e-02
|
Cell-extracellular matrix interactions
|
14
|
6.33e-01
|
7.91e-01
|
0.15100
|
1.48e-01
|
0.031400
|
3.39e-01
|
8.39e-01
|
Toll Like Receptor 4 (TLR4) Cascade
|
135
|
8.28e-03
|
4.08e-02
|
0.15100
|
3.09e-03
|
0.151000
|
9.51e-01
|
2.45e-03
|
Synthesis of substrates in N-glycan biosythesis
|
60
|
1.75e-01
|
3.73e-01
|
0.15100
|
7.37e-02
|
0.132000
|
3.23e-01
|
7.75e-02
|
Regulation of commissural axon pathfinding by SLIT and ROBO
|
10
|
7.57e-01
|
8.65e-01
|
0.15100
|
-1.08e-01
|
-0.105000
|
5.53e-01
|
5.65e-01
|
Signaling by NOTCH
|
182
|
6.19e-03
|
3.34e-02
|
0.15100
|
8.92e-02
|
0.121000
|
3.77e-02
|
4.73e-03
|
Glucose metabolism
|
87
|
6.83e-02
|
2.00e-01
|
0.15100
|
4.81e-02
|
0.143000
|
4.38e-01
|
2.13e-02
|
Glycosphingolipid metabolism
|
40
|
2.91e-01
|
5.10e-01
|
0.15000
|
4.76e-02
|
0.143000
|
6.02e-01
|
1.18e-01
|
SARS-CoV Infections
|
387
|
5.81e-06
|
7.08e-05
|
0.15000
|
3.98e-02
|
0.145000
|
1.78e-01
|
9.38e-07
|
Gap junction trafficking
|
27
|
4.03e-01
|
6.11e-01
|
0.15000
|
-1.87e-02
|
-0.149000
|
8.66e-01
|
1.80e-01
|
Organic cation transport
|
10
|
6.72e-01
|
8.11e-01
|
0.15000
|
-4.09e-02
|
0.144000
|
8.23e-01
|
4.30e-01
|
ALK mutants bind TKIs
|
12
|
6.45e-01
|
8.00e-01
|
0.15000
|
-1.49e-01
|
0.010500
|
3.70e-01
|
9.50e-01
|
Signalling to ERKs
|
34
|
2.40e-01
|
4.51e-01
|
0.15000
|
-7.01e-02
|
0.132000
|
4.79e-01
|
1.82e-01
|
Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA)
|
25
|
5.06e-01
|
6.97e-01
|
0.14900
|
1.04e-01
|
0.107000
|
3.69e-01
|
3.54e-01
|
Regulation of TP53 Degradation
|
36
|
3.34e-01
|
5.50e-01
|
0.14900
|
4.57e-02
|
0.142000
|
6.35e-01
|
1.41e-01
|
Visual phototransduction
|
93
|
5.28e-02
|
1.68e-01
|
0.14900
|
-3.21e-02
|
-0.145000
|
5.93e-01
|
1.53e-02
|
Toll Like Receptor 9 (TLR9) Cascade
|
100
|
3.90e-02
|
1.34e-01
|
0.14900
|
2.36e-02
|
0.147000
|
6.83e-01
|
1.10e-02
|
VEGFA-VEGFR2 Pathway
|
93
|
2.27e-02
|
8.93e-02
|
0.14900
|
-1.35e-01
|
0.062000
|
2.44e-02
|
3.01e-01
|
Presynaptic phase of homologous DNA pairing and strand exchange
|
38
|
3.55e-01
|
5.71e-01
|
0.14800
|
8.92e-02
|
0.119000
|
3.41e-01
|
2.05e-01
|
Platelet Aggregation (Plug Formation)
|
37
|
2.26e-01
|
4.31e-01
|
0.14800
|
-1.37e-01
|
0.056400
|
1.49e-01
|
5.53e-01
|
Degradation of the extracellular matrix
|
108
|
5.16e-02
|
1.66e-01
|
0.14800
|
-7.91e-02
|
-0.125000
|
1.55e-01
|
2.46e-02
|
MyD88 dependent cascade initiated on endosome
|
96
|
5.04e-02
|
1.64e-01
|
0.14700
|
3.03e-02
|
0.144000
|
6.08e-01
|
1.45e-02
|
Toll Like Receptor 7/8 (TLR7/8) Cascade
|
96
|
5.04e-02
|
1.64e-01
|
0.14700
|
3.03e-02
|
0.144000
|
6.08e-01
|
1.45e-02
|
Vitamin B5 (pantothenate) metabolism
|
16
|
6.50e-01
|
8.01e-01
|
0.14700
|
8.69e-02
|
0.119000
|
5.47e-01
|
4.10e-01
|
Interleukin-1 family signaling
|
145
|
2.21e-02
|
8.76e-02
|
0.14700
|
1.05e-01
|
0.103000
|
2.93e-02
|
3.22e-02
|
InlB-mediated entry of Listeria monocytogenes into host cell
|
14
|
6.90e-01
|
8.28e-01
|
0.14700
|
1.15e-01
|
0.090700
|
4.56e-01
|
5.57e-01
|
G beta:gamma signalling through PI3Kgamma
|
25
|
3.71e-01
|
5.84e-01
|
0.14700
|
-1.33e-01
|
0.060900
|
2.49e-01
|
5.98e-01
|
FCERI mediated MAPK activation
|
29
|
3.04e-01
|
5.19e-01
|
0.14600
|
-1.20e-01
|
0.084500
|
2.65e-01
|
4.31e-01
|
RNA Polymerase III Transcription Termination
|
23
|
5.48e-01
|
7.27e-01
|
0.14600
|
1.05e-01
|
0.102000
|
3.84e-01
|
3.98e-01
|
Fc epsilon receptor (FCERI) signaling
|
126
|
3.55e-02
|
1.26e-01
|
0.14600
|
8.23e-02
|
0.121000
|
1.11e-01
|
1.93e-02
|
Amino acids regulate mTORC1
|
52
|
1.30e-01
|
3.10e-01
|
0.14600
|
-5.96e-02
|
0.133000
|
4.57e-01
|
9.68e-02
|
Activated NTRK2 signals through FRS2 and FRS3
|
11
|
6.44e-01
|
7.99e-01
|
0.14600
|
-7.18e-02
|
0.127000
|
6.80e-01
|
4.66e-01
|
GPVI-mediated activation cascade
|
32
|
3.01e-01
|
5.18e-01
|
0.14600
|
-4.07e-02
|
0.140000
|
6.90e-01
|
1.71e-01
|
Phase II - Conjugation of compounds
|
106
|
4.37e-02
|
1.47e-01
|
0.14500
|
-1.41e-01
|
-0.034800
|
1.24e-02
|
5.36e-01
|
Myogenesis
|
29
|
3.28e-01
|
5.45e-01
|
0.14500
|
-1.33e-01
|
0.057100
|
2.15e-01
|
5.94e-01
|
Interleukin-4 and Interleukin-13 signaling
|
104
|
7.18e-02
|
2.07e-01
|
0.14400
|
9.74e-02
|
0.106000
|
8.58e-02
|
6.14e-02
|
Phenylalanine and tyrosine metabolism
|
10
|
7.11e-01
|
8.39e-01
|
0.14400
|
-1.44e-01
|
0.012500
|
4.32e-01
|
9.45e-01
|
Deactivation of the beta-catenin transactivating complex
|
39
|
2.97e-01
|
5.16e-01
|
0.14400
|
1.63e-02
|
0.143000
|
8.60e-01
|
1.22e-01
|
Metabolism of Angiotensinogen to Angiotensins
|
15
|
6.84e-01
|
8.23e-01
|
0.14400
|
-9.61e-02
|
-0.107000
|
5.19e-01
|
4.74e-01
|
Branched-chain amino acid catabolism
|
20
|
5.92e-01
|
7.56e-01
|
0.14300
|
6.88e-02
|
0.126000
|
5.94e-01
|
3.31e-01
|
Antigen processing: Ubiquitination & Proteasome degradation
|
293
|
2.72e-04
|
2.26e-03
|
0.14200
|
3.76e-02
|
0.137000
|
2.68e-01
|
5.18e-05
|
Reduction of cytosolic Ca++ levels
|
11
|
6.70e-01
|
8.11e-01
|
0.14200
|
1.34e-01
|
-0.047300
|
4.42e-01
|
7.86e-01
|
TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation
|
95
|
6.37e-02
|
1.92e-01
|
0.14200
|
2.80e-02
|
0.139000
|
6.37e-01
|
1.90e-02
|
Processive synthesis on the C-strand of the telomere
|
19
|
4.92e-01
|
6.85e-01
|
0.14200
|
-6.24e-02
|
0.127000
|
6.38e-01
|
3.37e-01
|
Apoptotic cleavage of cellular proteins
|
35
|
2.79e-01
|
4.98e-01
|
0.14200
|
-1.32e-01
|
0.051100
|
1.76e-01
|
6.01e-01
|
Late endosomal microautophagy
|
32
|
4.46e-01
|
6.54e-01
|
0.14200
|
7.47e-02
|
0.120000
|
4.64e-01
|
2.39e-01
|
Retinoid metabolism and transport
|
42
|
2.56e-01
|
4.71e-01
|
0.14100
|
8.49e-03
|
-0.141000
|
9.24e-01
|
1.13e-01
|
Disorders of transmembrane transporters
|
167
|
1.61e-02
|
6.83e-02
|
0.14100
|
1.17e-01
|
0.079400
|
9.21e-03
|
7.64e-02
|
WNT5A-dependent internalization of FZD2, FZD5 and ROR2
|
13
|
7.26e-01
|
8.47e-01
|
0.14100
|
8.44e-02
|
0.113000
|
5.98e-01
|
4.81e-01
|
Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal
|
89
|
9.16e-02
|
2.43e-01
|
0.14100
|
4.67e-02
|
0.133000
|
4.46e-01
|
3.01e-02
|
Amplification of signal from the kinetochores
|
89
|
9.16e-02
|
2.43e-01
|
0.14100
|
4.67e-02
|
0.133000
|
4.46e-01
|
3.01e-02
|
Retrograde transport at the Trans-Golgi-Network
|
47
|
2.60e-01
|
4.74e-01
|
0.14100
|
2.62e-02
|
0.138000
|
7.56e-01
|
1.01e-01
|
NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux
|
43
|
3.15e-01
|
5.31e-01
|
0.14100
|
-1.33e-01
|
-0.046000
|
1.31e-01
|
6.02e-01
|
Formation of the cornified envelope
|
73
|
1.72e-01
|
3.69e-01
|
0.14100
|
-9.74e-02
|
-0.101000
|
1.50e-01
|
1.35e-01
|
Neurexins and neuroligins
|
52
|
2.86e-01
|
5.05e-01
|
0.14000
|
-9.71e-02
|
-0.102000
|
2.26e-01
|
2.05e-01
|
Signaling by VEGF
|
101
|
2.72e-02
|
1.03e-01
|
0.14000
|
-1.31e-01
|
0.050400
|
2.29e-02
|
3.81e-01
|
G alpha (s) signalling events
|
153
|
2.43e-02
|
9.41e-02
|
0.14000
|
-1.14e-01
|
-0.082100
|
1.51e-02
|
7.95e-02
|
Lagging Strand Synthesis
|
19
|
6.17e-01
|
7.76e-01
|
0.14000
|
6.26e-02
|
0.125000
|
6.37e-01
|
3.44e-01
|
Golgi Associated Vesicle Biogenesis
|
51
|
1.44e-01
|
3.31e-01
|
0.14000
|
-9.77e-02
|
0.100000
|
2.27e-01
|
2.15e-01
|
Caspase-mediated cleavage of cytoskeletal proteins
|
12
|
7.17e-01
|
8.43e-01
|
0.14000
|
3.29e-02
|
0.136000
|
8.43e-01
|
4.15e-01
|
Translesion synthesis by POLK
|
17
|
6.54e-01
|
8.01e-01
|
0.14000
|
6.77e-02
|
0.122000
|
6.29e-01
|
3.82e-01
|
Interferon Signaling
|
191
|
1.05e-02
|
4.88e-02
|
0.14000
|
8.96e-02
|
0.107000
|
3.27e-02
|
1.05e-02
|
Signaling by high-kinase activity BRAF mutants
|
32
|
2.99e-01
|
5.16e-01
|
0.14000
|
-9.56e-02
|
0.102000
|
3.49e-01
|
3.18e-01
|
Complement cascade
|
56
|
2.58e-01
|
4.73e-01
|
0.14000
|
-8.13e-02
|
-0.113000
|
2.93e-01
|
1.42e-01
|
Other semaphorin interactions
|
18
|
5.79e-01
|
7.47e-01
|
0.13900
|
-1.39e-01
|
-0.003970
|
3.06e-01
|
9.77e-01
|
Toll-like Receptor Cascades
|
154
|
8.67e-03
|
4.23e-02
|
0.13900
|
-3.47e-03
|
0.139000
|
9.41e-01
|
2.84e-03
|
Metallothioneins bind metals
|
11
|
7.61e-01
|
8.67e-01
|
0.13900
|
6.67e-02
|
0.122000
|
7.02e-01
|
4.83e-01
|
Downregulation of ERBB2 signaling
|
28
|
5.08e-01
|
6.98e-01
|
0.13900
|
1.16e-01
|
0.077700
|
2.90e-01
|
4.77e-01
|
Trafficking and processing of endosomal TLR
|
11
|
7.66e-01
|
8.69e-01
|
0.13900
|
7.85e-02
|
0.115000
|
6.52e-01
|
5.09e-01
|
Synthesis of PIPs at the Golgi membrane
|
17
|
5.41e-01
|
7.22e-01
|
0.13900
|
-1.24e-01
|
0.062800
|
3.75e-01
|
6.54e-01
|
Elevation of cytosolic Ca2+ levels
|
16
|
5.68e-01
|
7.43e-01
|
0.13900
|
-1.29e-01
|
0.053000
|
3.73e-01
|
7.13e-01
|
Phospholipase C-mediated cascade; FGFR4
|
14
|
7.18e-01
|
8.43e-01
|
0.13900
|
9.08e-02
|
0.105000
|
5.56e-01
|
4.96e-01
|
Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell
|
120
|
2.01e-02
|
8.18e-02
|
0.13900
|
1.37e-01
|
-0.022800
|
9.53e-03
|
6.66e-01
|
alpha-linolenic (omega3) and linoleic (omega6) acid metabolism
|
12
|
7.21e-01
|
8.44e-01
|
0.13900
|
3.30e-02
|
0.135000
|
8.43e-01
|
4.19e-01
|
alpha-linolenic acid (ALA) metabolism
|
12
|
7.21e-01
|
8.44e-01
|
0.13900
|
3.30e-02
|
0.135000
|
8.43e-01
|
4.19e-01
|
Cell-Cell communication
|
112
|
7.22e-02
|
2.08e-01
|
0.13900
|
-1.03e-01
|
-0.092500
|
5.87e-02
|
9.08e-02
|
Gap junction trafficking and regulation
|
29
|
4.65e-01
|
6.70e-01
|
0.13900
|
-4.20e-02
|
-0.132000
|
6.95e-01
|
2.18e-01
|
MAP kinase activation
|
58
|
2.00e-01
|
3.99e-01
|
0.13800
|
2.30e-02
|
0.136000
|
7.62e-01
|
7.34e-02
|
Downstream signal transduction
|
29
|
3.46e-01
|
5.62e-01
|
0.13800
|
-1.01e-01
|
0.093400
|
3.47e-01
|
3.84e-01
|
Pre-NOTCH Expression and Processing
|
61
|
1.24e-01
|
2.99e-01
|
0.13700
|
-5.17e-02
|
0.127000
|
4.85e-01
|
8.66e-02
|
SLBP independent Processing of Histone Pre-mRNAs
|
10
|
7.95e-01
|
8.80e-01
|
0.13700
|
9.95e-02
|
0.094000
|
5.86e-01
|
6.07e-01
|
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane
|
10
|
7.06e-01
|
8.36e-01
|
0.13700
|
-5.98e-02
|
0.123000
|
7.43e-01
|
5.00e-01
|
Amine ligand-binding receptors
|
41
|
2.43e-01
|
4.55e-01
|
0.13700
|
-1.24e-01
|
0.056800
|
1.69e-01
|
5.29e-01
|
Activation of gene expression by SREBF (SREBP)
|
42
|
3.15e-01
|
5.31e-01
|
0.13600
|
1.85e-02
|
0.135000
|
8.35e-01
|
1.30e-01
|
FOXO-mediated transcription
|
65
|
1.57e-01
|
3.47e-01
|
0.13600
|
1.36e-01
|
0.007350
|
5.80e-02
|
9.18e-01
|
Chondroitin sulfate biosynthesis
|
18
|
5.25e-01
|
7.07e-01
|
0.13600
|
-1.02e-01
|
0.089900
|
4.53e-01
|
5.09e-01
|
Beta-catenin independent WNT signaling
|
144
|
3.89e-02
|
1.34e-01
|
0.13600
|
9.39e-02
|
0.098500
|
5.16e-02
|
4.12e-02
|
Regulation of cholesterol biosynthesis by SREBP (SREBF)
|
54
|
2.20e-01
|
4.23e-01
|
0.13600
|
1.06e-02
|
0.135000
|
8.93e-01
|
8.55e-02
|
Transcriptional Regulation by MECP2
|
60
|
1.45e-01
|
3.31e-01
|
0.13600
|
-1.31e-01
|
0.034600
|
7.90e-02
|
6.43e-01
|
Signaling by EGFR in Cancer
|
25
|
5.28e-01
|
7.08e-01
|
0.13500
|
3.47e-02
|
0.131000
|
7.64e-01
|
2.59e-01
|
Glutamate Neurotransmitter Release Cycle
|
23
|
5.40e-01
|
7.21e-01
|
0.13500
|
1.33e-01
|
0.019600
|
2.68e-01
|
8.70e-01
|
Resolution of Sister Chromatid Cohesion
|
98
|
7.55e-02
|
2.13e-01
|
0.13500
|
2.35e-02
|
0.133000
|
6.88e-01
|
2.32e-02
|
Activation of the AP-1 family of transcription factors
|
10
|
8.01e-01
|
8.80e-01
|
0.13400
|
1.02e-01
|
0.087400
|
5.76e-01
|
6.32e-01
|
Sema4D induced cell migration and growth-cone collapse
|
20
|
6.10e-01
|
7.71e-01
|
0.13400
|
4.05e-02
|
0.128000
|
7.54e-01
|
3.22e-01
|
Class I MHC mediated antigen processing & presentation
|
361
|
9.62e-05
|
8.74e-04
|
0.13400
|
2.50e-02
|
0.132000
|
4.15e-01
|
1.72e-05
|
ER to Golgi Anterograde Transport
|
134
|
2.46e-02
|
9.47e-02
|
0.13400
|
4.74e-03
|
0.134000
|
9.25e-01
|
7.56e-03
|
FGFRL1 modulation of FGFR1 signaling
|
13
|
7.20e-01
|
8.44e-01
|
0.13400
|
3.13e-02
|
0.130000
|
8.45e-01
|
4.18e-01
|
Oxidative Stress Induced Senescence
|
66
|
1.29e-01
|
3.08e-01
|
0.13300
|
-3.26e-02
|
0.129000
|
6.47e-01
|
6.89e-02
|
CLEC7A (Dectin-1) induces NFAT activation
|
11
|
7.66e-01
|
8.69e-01
|
0.13300
|
-4.30e-02
|
-0.126000
|
8.05e-01
|
4.68e-01
|
Post-translational protein phosphorylation
|
100
|
1.14e-01
|
2.85e-01
|
0.13300
|
-1.02e-01
|
-0.085200
|
7.71e-02
|
1.41e-01
|
Removal of the Flap Intermediate from the C-strand
|
17
|
5.96e-01
|
7.59e-01
|
0.13300
|
-2.67e-02
|
0.130000
|
8.49e-01
|
3.52e-01
|
Activation of BH3-only proteins
|
30
|
3.60e-01
|
5.74e-01
|
0.13300
|
-1.05e-01
|
0.081500
|
3.19e-01
|
4.40e-01
|
VEGFR2 mediated cell proliferation
|
19
|
5.43e-01
|
7.24e-01
|
0.13300
|
-1.23e-01
|
0.048800
|
3.51e-01
|
7.12e-01
|
PIP3 activates AKT signaling
|
275
|
5.54e-04
|
4.32e-03
|
0.13300
|
3.09e-03
|
0.133000
|
9.30e-01
|
1.50e-04
|
Gamma carboxylation, hypusine formation and arylsulfatase activation
|
34
|
4.81e-01
|
6.78e-01
|
0.13300
|
8.68e-02
|
0.100000
|
3.81e-01
|
3.12e-01
|
FOXO-mediated transcription of cell cycle genes
|
16
|
6.94e-01
|
8.29e-01
|
0.13200
|
1.20e-01
|
0.055700
|
4.06e-01
|
7.00e-01
|
FRS-mediated FGFR2 signaling
|
24
|
5.24e-01
|
7.07e-01
|
0.13200
|
6.35e-03
|
0.132000
|
9.57e-01
|
2.63e-01
|
Arachidonic acid metabolism
|
56
|
2.99e-01
|
5.16e-01
|
0.13200
|
1.08e-01
|
0.076100
|
1.64e-01
|
3.25e-01
|
Defective EXT1 causes exostoses 1, TRPS2 and CHDS
|
12
|
7.46e-01
|
8.60e-01
|
0.13100
|
-3.16e-02
|
-0.127000
|
8.50e-01
|
4.44e-01
|
Defective EXT2 causes exostoses 2
|
12
|
7.46e-01
|
8.60e-01
|
0.13100
|
-3.16e-02
|
-0.127000
|
8.50e-01
|
4.44e-01
|
RHO GTPases Activate Formins
|
114
|
6.70e-02
|
1.98e-01
|
0.13100
|
3.80e-02
|
0.126000
|
4.83e-01
|
2.04e-02
|
HDMs demethylate histones
|
18
|
5.79e-01
|
7.47e-01
|
0.13100
|
-3.49e-02
|
0.127000
|
7.98e-01
|
3.53e-01
|
HDR through MMEJ (alt-NHEJ)
|
11
|
7.62e-01
|
8.67e-01
|
0.13100
|
2.69e-02
|
0.128000
|
8.77e-01
|
4.61e-01
|
Signal transduction by L1
|
20
|
6.07e-01
|
7.68e-01
|
0.13000
|
1.29e-01
|
0.020700
|
3.19e-01
|
8.73e-01
|
PI3K events in ERBB4 signaling
|
10
|
8.11e-01
|
8.87e-01
|
0.13000
|
-1.03e-01
|
-0.079900
|
5.74e-01
|
6.62e-01
|
Axon guidance
|
503
|
2.16e-05
|
2.18e-04
|
0.13000
|
1.15e-01
|
0.061100
|
9.73e-06
|
1.88e-02
|
Caspase activation via extrinsic apoptotic signalling pathway
|
25
|
5.88e-01
|
7.53e-01
|
0.13000
|
6.99e-02
|
0.110000
|
5.45e-01
|
3.42e-01
|
Integrin cell surface interactions
|
66
|
2.27e-01
|
4.32e-01
|
0.13000
|
-1.20e-01
|
-0.049000
|
9.04e-02
|
4.91e-01
|
Defective B3GALT6 causes EDSP2 and SEMDJL1
|
17
|
6.54e-01
|
8.01e-01
|
0.13000
|
-1.83e-02
|
-0.129000
|
8.96e-01
|
3.58e-01
|
PI-3K cascade:FGFR3
|
17
|
7.03e-01
|
8.35e-01
|
0.13000
|
8.24e-02
|
0.100000
|
5.57e-01
|
4.73e-01
|
Gastrulation
|
21
|
5.18e-01
|
7.04e-01
|
0.12900
|
-1.14e-01
|
0.061400
|
3.67e-01
|
6.26e-01
|
Ca2+ pathway
|
62
|
2.83e-01
|
5.03e-01
|
0.12900
|
-8.23e-02
|
-0.099100
|
2.62e-01
|
1.77e-01
|
RORA activates gene expression
|
17
|
5.86e-01
|
7.52e-01
|
0.12900
|
-1.09e-01
|
0.068300
|
4.36e-01
|
6.26e-01
|
ERBB2 Regulates Cell Motility
|
15
|
7.31e-01
|
8.52e-01
|
0.12800
|
-1.11e-01
|
-0.064800
|
4.58e-01
|
6.64e-01
|
EML4 and NUDC in mitotic spindle formation
|
93
|
1.19e-01
|
2.95e-01
|
0.12800
|
3.42e-02
|
0.124000
|
5.69e-01
|
3.95e-02
|
Death Receptor Signalling
|
134
|
6.73e-02
|
1.98e-01
|
0.12800
|
1.01e-01
|
0.078400
|
4.29e-02
|
1.17e-01
|
HuR (ELAVL1) binds and stabilizes mRNA
|
10
|
7.39e-01
|
8.57e-01
|
0.12800
|
-5.23e-02
|
0.117000
|
7.75e-01
|
5.22e-01
|
Nonhomologous End-Joining (NHEJ)
|
32
|
5.27e-01
|
7.08e-01
|
0.12800
|
8.69e-02
|
0.093900
|
3.95e-01
|
3.58e-01
|
Downstream signaling of activated FGFR2
|
29
|
4.93e-01
|
6.85e-01
|
0.12800
|
1.61e-02
|
0.127000
|
8.80e-01
|
2.37e-01
|
Common Pathway of Fibrin Clot Formation
|
21
|
6.45e-01
|
8.00e-01
|
0.12800
|
-6.30e-02
|
-0.111000
|
6.17e-01
|
3.77e-01
|
Protein-protein interactions at synapses
|
78
|
2.00e-01
|
3.99e-01
|
0.12800
|
-6.38e-02
|
-0.110000
|
3.30e-01
|
9.17e-02
|
G-protein beta:gamma signalling
|
30
|
4.13e-01
|
6.18e-01
|
0.12700
|
-1.19e-01
|
0.045500
|
2.59e-01
|
6.66e-01
|
The role of Nef in HIV-1 replication and disease pathogenesis
|
27
|
5.77e-01
|
7.47e-01
|
0.12700
|
1.08e-01
|
0.067800
|
3.33e-01
|
5.42e-01
|
RND3 GTPase cycle
|
41
|
4.13e-01
|
6.18e-01
|
0.12700
|
-1.18e-01
|
-0.045700
|
1.89e-01
|
6.12e-01
|
SARS-CoV-2 Infection
|
276
|
2.82e-03
|
1.74e-02
|
0.12700
|
4.71e-02
|
0.118000
|
1.78e-01
|
7.42e-04
|
p130Cas linkage to MAPK signaling for integrins
|
15
|
6.54e-01
|
8.01e-01
|
0.12700
|
-1.22e-01
|
0.033700
|
4.13e-01
|
8.21e-01
|
Cobalamin (Cbl, vitamin B12) transport and metabolism
|
20
|
5.45e-01
|
7.24e-01
|
0.12700
|
6.60e-02
|
-0.108000
|
6.09e-01
|
4.03e-01
|
Signaling by Erythropoietin
|
25
|
4.70e-01
|
6.71e-01
|
0.12600
|
-6.38e-02
|
0.109000
|
5.81e-01
|
3.44e-01
|
Depolymerisation of the Nuclear Lamina
|
14
|
7.27e-01
|
8.47e-01
|
0.12600
|
2.76e-02
|
0.123000
|
8.58e-01
|
4.24e-01
|
PLC beta mediated events
|
47
|
3.50e-01
|
5.66e-01
|
0.12600
|
-1.22e-01
|
-0.031900
|
1.48e-01
|
7.05e-01
|
Diseases of signal transduction by growth factor receptors and second messengers
|
410
|
8.42e-05
|
7.70e-04
|
0.12600
|
1.87e-02
|
0.124000
|
5.16e-01
|
1.57e-05
|
Gastrin-CREB signalling pathway via PKC and MAPK
|
17
|
6.25e-01
|
7.85e-01
|
0.12500
|
-1.21e-01
|
0.032700
|
3.87e-01
|
8.15e-01
|
SARS-CoV-2 targets host intracellular signalling and regulatory pathways
|
12
|
7.83e-01
|
8.74e-01
|
0.12500
|
-1.12e-01
|
-0.056100
|
5.01e-01
|
7.36e-01
|
Resolution of D-loop Structures through Holliday Junction Intermediates
|
30
|
5.62e-01
|
7.39e-01
|
0.12500
|
8.86e-02
|
0.088700
|
4.01e-01
|
4.00e-01
|
SARS-CoV-2 activates/modulates innate and adaptive immune responses
|
110
|
5.52e-02
|
1.72e-01
|
0.12500
|
-1.86e-02
|
0.124000
|
7.36e-01
|
2.47e-02
|
Interleukin-12 signaling
|
43
|
3.69e-01
|
5.83e-01
|
0.12500
|
1.80e-02
|
0.124000
|
8.38e-01
|
1.59e-01
|
Formation of Senescence-Associated Heterochromatin Foci (SAHF)
|
11
|
7.23e-01
|
8.45e-01
|
0.12500
|
-5.99e-02
|
0.110000
|
7.31e-01
|
5.27e-01
|
MyD88 cascade initiated on plasma membrane
|
91
|
1.45e-01
|
3.31e-01
|
0.12500
|
4.06e-02
|
0.118000
|
5.03e-01
|
5.10e-02
|
Toll Like Receptor 10 (TLR10) Cascade
|
91
|
1.45e-01
|
3.31e-01
|
0.12500
|
4.06e-02
|
0.118000
|
5.03e-01
|
5.10e-02
|
Toll Like Receptor 5 (TLR5) Cascade
|
91
|
1.45e-01
|
3.31e-01
|
0.12500
|
4.06e-02
|
0.118000
|
5.03e-01
|
5.10e-02
|
Condensation of Prophase Chromosomes
|
12
|
7.06e-01
|
8.36e-01
|
0.12500
|
-5.28e-02
|
0.113000
|
7.52e-01
|
4.97e-01
|
Sensory processing of sound by outer hair cells of the cochlea
|
49
|
3.57e-01
|
5.72e-01
|
0.12500
|
-4.30e-02
|
-0.117000
|
6.02e-01
|
1.55e-01
|
Regulation of actin dynamics for phagocytic cup formation
|
59
|
3.17e-01
|
5.33e-01
|
0.12500
|
1.04e-01
|
0.069400
|
1.67e-01
|
3.57e-01
|
Role of phospholipids in phagocytosis
|
23
|
6.13e-01
|
7.74e-01
|
0.12500
|
-3.96e-02
|
-0.118000
|
7.42e-01
|
3.26e-01
|
Azathioprine ADME
|
22
|
5.18e-01
|
7.04e-01
|
0.12500
|
-9.76e-02
|
0.077500
|
4.28e-01
|
5.29e-01
|
GAB1 signalosome
|
17
|
6.13e-01
|
7.74e-01
|
0.12500
|
-1.13e-01
|
0.053400
|
4.22e-01
|
7.03e-01
|
Sodium/Calcium exchangers
|
11
|
7.19e-01
|
8.44e-01
|
0.12500
|
8.14e-02
|
-0.094200
|
6.40e-01
|
5.88e-01
|
HS-GAG biosynthesis
|
28
|
5.86e-01
|
7.52e-01
|
0.12400
|
-7.76e-02
|
-0.097300
|
4.77e-01
|
3.73e-01
|
Unblocking of NMDA receptors, glutamate binding and activation
|
19
|
6.30e-01
|
7.89e-01
|
0.12400
|
-9.28e-04
|
-0.124000
|
9.94e-01
|
3.48e-01
|
Inositol phosphate metabolism
|
45
|
4.13e-01
|
6.18e-01
|
0.12400
|
-1.08e-01
|
-0.061300
|
2.10e-01
|
4.77e-01
|
N-glycan antennae elongation in the medial/trans-Golgi
|
26
|
5.12e-01
|
7.00e-01
|
0.12400
|
-1.23e-01
|
0.016800
|
2.78e-01
|
8.82e-01
|
Interleukin-12 family signaling
|
53
|
3.11e-01
|
5.28e-01
|
0.12400
|
2.50e-02
|
0.121000
|
7.53e-01
|
1.26e-01
|
Mitotic Prometaphase
|
174
|
1.81e-02
|
7.49e-02
|
0.12400
|
1.18e-02
|
0.123000
|
7.89e-01
|
5.00e-03
|
RND2 GTPase cycle
|
42
|
4.16e-01
|
6.20e-01
|
0.12400
|
-1.18e-01
|
-0.038100
|
1.87e-01
|
6.69e-01
|
Metabolism of proteins
|
1767
|
1.32e-14
|
1.02e-12
|
0.12300
|
6.07e-02
|
0.107000
|
1.99e-05
|
4.39e-14
|
G-protein mediated events
|
52
|
3.12e-01
|
5.28e-01
|
0.12300
|
-1.22e-01
|
-0.017800
|
1.28e-01
|
8.24e-01
|
Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer
|
49
|
3.65e-01
|
5.79e-01
|
0.12300
|
4.00e-02
|
0.116000
|
6.28e-01
|
1.59e-01
|
COPI-mediated anterograde transport
|
83
|
2.09e-01
|
4.05e-01
|
0.12300
|
6.90e-02
|
0.102000
|
2.77e-01
|
1.09e-01
|
Plasma lipoprotein clearance
|
37
|
5.00e-01
|
6.92e-01
|
0.12300
|
1.01e-01
|
0.070600
|
2.90e-01
|
4.58e-01
|
Resolution of D-Loop Structures
|
31
|
5.64e-01
|
7.40e-01
|
0.12300
|
8.01e-02
|
0.093000
|
4.40e-01
|
3.70e-01
|
RAC2 GTPase cycle
|
80
|
1.15e-01
|
2.87e-01
|
0.12300
|
-1.16e-01
|
0.040100
|
7.27e-02
|
5.35e-01
|
Notch-HLH transcription pathway
|
24
|
4.98e-01
|
6.91e-01
|
0.12300
|
-7.96e-02
|
0.093400
|
5.00e-01
|
4.28e-01
|
Keratan sulfate/keratin metabolism
|
33
|
3.91e-01
|
5.99e-01
|
0.12200
|
-6.71e-02
|
0.102000
|
5.05e-01
|
3.09e-01
|
C-type lectin receptors (CLRs)
|
137
|
6.86e-02
|
2.00e-01
|
0.12200
|
4.96e-02
|
0.112000
|
3.16e-01
|
2.39e-02
|
Nervous system development
|
527
|
3.96e-05
|
3.90e-04
|
0.12200
|
1.12e-01
|
0.049500
|
1.11e-05
|
5.15e-02
|
Antigen activates B Cell Receptor (BCR) leading to generation of second messengers
|
28
|
5.89e-01
|
7.53e-01
|
0.12200
|
-1.06e-01
|
-0.061100
|
3.33e-01
|
5.76e-01
|
RHOC GTPase cycle
|
69
|
1.83e-01
|
3.80e-01
|
0.12200
|
-1.21e-01
|
0.013800
|
8.20e-02
|
8.42e-01
|
Cytokine Signaling in Immune system
|
670
|
7.01e-06
|
8.27e-05
|
0.12200
|
7.92e-02
|
0.092400
|
4.60e-04
|
4.34e-05
|
TRAF6 mediated IRF7 activation
|
26
|
4.77e-01
|
6.76e-01
|
0.12100
|
-8.25e-02
|
0.088900
|
4.66e-01
|
4.32e-01
|
RHOBTB GTPase Cycle
|
34
|
5.44e-01
|
7.24e-01
|
0.12100
|
9.18e-02
|
0.078500
|
3.54e-01
|
4.28e-01
|
FLT3 Signaling
|
38
|
4.95e-01
|
6.88e-01
|
0.12100
|
1.05e-01
|
0.060200
|
2.64e-01
|
5.20e-01
|
YAP1- and WWTR1 (TAZ)-stimulated gene expression
|
15
|
6.89e-01
|
8.28e-01
|
0.12100
|
1.19e-01
|
-0.022000
|
4.27e-01
|
8.83e-01
|
Listeria monocytogenes entry into host cells
|
19
|
6.58e-01
|
8.03e-01
|
0.12000
|
9.36e-03
|
0.120000
|
9.44e-01
|
3.65e-01
|
Miscellaneous transport and binding events
|
21
|
6.63e-01
|
8.07e-01
|
0.12000
|
-4.07e-02
|
-0.113000
|
7.47e-01
|
3.69e-01
|
Downregulation of SMAD2/3:SMAD4 transcriptional activity
|
29
|
4.84e-01
|
6.78e-01
|
0.12000
|
-2.64e-02
|
0.117000
|
8.05e-01
|
2.74e-01
|
Signaling by FGFR1 in disease
|
37
|
4.04e-01
|
6.12e-01
|
0.12000
|
-2.02e-02
|
0.118000
|
8.32e-01
|
2.12e-01
|
BMAL1:CLOCK,NPAS2 activates circadian gene expression
|
27
|
5.80e-01
|
7.47e-01
|
0.12000
|
-3.12e-02
|
-0.116000
|
7.79e-01
|
2.97e-01
|
Disease
|
1567
|
6.99e-13
|
3.00e-11
|
0.11900
|
4.19e-02
|
0.111000
|
5.41e-03
|
1.43e-13
|
Phase I - Functionalization of compounds
|
100
|
6.70e-02
|
1.98e-01
|
0.11900
|
7.07e-02
|
-0.095500
|
2.22e-01
|
9.88e-02
|
FGFR4 ligand binding and activation
|
13
|
7.99e-01
|
8.80e-01
|
0.11900
|
8.13e-02
|
0.086600
|
6.12e-01
|
5.89e-01
|
Synthesis of very long-chain fatty acyl-CoAs
|
23
|
6.39e-01
|
7.94e-01
|
0.11900
|
-3.41e-02
|
-0.114000
|
7.77e-01
|
3.45e-01
|
Glucagon signaling in metabolic regulation
|
33
|
4.07e-01
|
6.15e-01
|
0.11900
|
-8.42e-02
|
0.083600
|
4.02e-01
|
4.06e-01
|
Iron uptake and transport
|
57
|
3.53e-01
|
5.69e-01
|
0.11800
|
4.85e-02
|
0.108000
|
5.27e-01
|
1.59e-01
|
Elastic fibre formation
|
40
|
3.83e-01
|
5.94e-01
|
0.11800
|
-1.16e-01
|
0.024100
|
2.06e-01
|
7.92e-01
|
IL-6-type cytokine receptor ligand interactions
|
17
|
7.49e-01
|
8.60e-01
|
0.11800
|
-8.58e-02
|
-0.081000
|
5.40e-01
|
5.63e-01
|
LDL clearance
|
19
|
6.65e-01
|
8.07e-01
|
0.11800
|
1.18e-01
|
0.005110
|
3.75e-01
|
9.69e-01
|
Metal ion SLC transporters
|
25
|
6.04e-01
|
7.66e-01
|
0.11800
|
2.02e-02
|
0.116000
|
8.61e-01
|
3.16e-01
|
Signaling by cytosolic FGFR1 fusion mutants
|
17
|
6.38e-01
|
7.94e-01
|
0.11700
|
-9.62e-02
|
0.067400
|
4.92e-01
|
6.30e-01
|
Organic cation/anion/zwitterion transport
|
15
|
6.94e-01
|
8.29e-01
|
0.11700
|
3.21e-02
|
-0.113000
|
8.30e-01
|
4.49e-01
|
Heme biosynthesis
|
13
|
7.87e-01
|
8.77e-01
|
0.11700
|
-4.28e-02
|
-0.109000
|
7.89e-01
|
4.95e-01
|
FRS-mediated FGFR4 signaling
|
21
|
6.00e-01
|
7.62e-01
|
0.11700
|
-3.26e-02
|
0.113000
|
7.96e-01
|
3.71e-01
|
Interferon alpha/beta signaling
|
69
|
2.94e-01
|
5.13e-01
|
0.11700
|
1.06e-01
|
0.050400
|
1.30e-01
|
4.69e-01
|
ADP signalling through P2Y purinoceptor 12
|
22
|
5.81e-01
|
7.47e-01
|
0.11700
|
-1.10e-01
|
0.040200
|
3.73e-01
|
7.44e-01
|
Transport to the Golgi and subsequent modification
|
165
|
2.37e-02
|
9.29e-02
|
0.11700
|
-1.54e-02
|
0.116000
|
7.33e-01
|
1.03e-02
|
Formation of tubulin folding intermediates by CCT/TriC
|
26
|
6.36e-01
|
7.92e-01
|
0.11600
|
1.03e-01
|
0.054200
|
3.63e-01
|
6.33e-01
|
Gene Silencing by RNA
|
80
|
1.46e-01
|
3.32e-01
|
0.11600
|
-3.43e-02
|
0.111000
|
5.96e-01
|
8.56e-02
|
RND1 GTPase cycle
|
41
|
4.03e-01
|
6.11e-01
|
0.11600
|
-1.16e-01
|
0.010400
|
2.00e-01
|
9.09e-01
|
Sema4D in semaphorin signaling
|
24
|
6.35e-01
|
7.92e-01
|
0.11600
|
2.97e-02
|
0.112000
|
8.01e-01
|
3.41e-01
|
Erythropoietin activates Phosphoinositide-3-kinase (PI3K)
|
12
|
7.78e-01
|
8.74e-01
|
0.11600
|
-1.16e-01
|
-0.004720
|
4.87e-01
|
9.77e-01
|
Estrogen-dependent gene expression
|
91
|
2.06e-01
|
4.02e-01
|
0.11600
|
5.23e-02
|
0.104000
|
3.88e-01
|
8.75e-02
|
Netrin-1 signaling
|
49
|
4.23e-01
|
6.29e-01
|
0.11600
|
-4.95e-02
|
-0.105000
|
5.49e-01
|
2.04e-01
|
Regulation of KIT signaling
|
16
|
7.66e-01
|
8.69e-01
|
0.11600
|
-6.63e-02
|
-0.094600
|
6.46e-01
|
5.12e-01
|
RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known
|
37
|
3.89e-01
|
5.98e-01
|
0.11500
|
-9.28e-02
|
0.068500
|
3.29e-01
|
4.71e-01
|
CRMPs in Sema3A signaling
|
15
|
6.80e-01
|
8.20e-01
|
0.11500
|
8.09e-02
|
-0.082000
|
5.87e-01
|
5.82e-01
|
Endogenous sterols
|
26
|
6.53e-01
|
8.01e-01
|
0.11500
|
-6.99e-02
|
-0.091600
|
5.37e-01
|
4.19e-01
|
N-Glycan antennae elongation
|
15
|
7.09e-01
|
8.38e-01
|
0.11500
|
-2.54e-02
|
0.112000
|
8.65e-01
|
4.52e-01
|
EGFR downregulation
|
30
|
5.94e-01
|
7.58e-01
|
0.11500
|
1.05e-01
|
0.046600
|
3.19e-01
|
6.59e-01
|
Association of TriC/CCT with target proteins during biosynthesis
|
38
|
5.45e-01
|
7.24e-01
|
0.11400
|
8.03e-02
|
0.081400
|
3.91e-01
|
3.85e-01
|
Other interleukin signaling
|
24
|
6.69e-01
|
8.10e-01
|
0.11400
|
4.91e-02
|
0.102000
|
6.77e-01
|
3.85e-01
|
Sensory processing of sound
|
69
|
2.85e-01
|
5.05e-01
|
0.11300
|
-2.60e-02
|
-0.110000
|
7.08e-01
|
1.13e-01
|
Signaling by Interleukins
|
434
|
1.16e-03
|
8.27e-03
|
0.11300
|
7.00e-02
|
0.089100
|
1.23e-02
|
1.44e-03
|
Regulation of PLK1 Activity at G2/M Transition
|
83
|
2.26e-01
|
4.31e-01
|
0.11300
|
2.79e-02
|
0.109000
|
6.60e-01
|
8.48e-02
|
Intrinsic Pathway for Apoptosis
|
52
|
4.45e-01
|
6.53e-01
|
0.11200
|
8.96e-02
|
0.067700
|
2.63e-01
|
3.99e-01
|
Signaling by Leptin
|
11
|
8.35e-01
|
9.01e-01
|
0.11200
|
4.89e-02
|
0.101000
|
7.79e-01
|
5.62e-01
|
Synthesis of PC
|
27
|
5.63e-01
|
7.39e-01
|
0.11200
|
-1.88e-02
|
0.111000
|
8.66e-01
|
3.20e-01
|
Factors involved in megakaryocyte development and platelet production
|
128
|
5.16e-02
|
1.66e-01
|
0.11200
|
-1.01e-01
|
0.048000
|
4.81e-02
|
3.48e-01
|
RAB GEFs exchange GTP for GDP on RABs
|
82
|
1.38e-01
|
3.22e-01
|
0.11200
|
-7.86e-02
|
0.079700
|
2.18e-01
|
2.12e-01
|
Downstream signaling of activated FGFR4
|
26
|
5.82e-01
|
7.49e-01
|
0.11200
|
-1.42e-02
|
0.111000
|
9.00e-01
|
3.28e-01
|
Metabolism of fat-soluble vitamins
|
46
|
3.63e-01
|
5.77e-01
|
0.11200
|
3.14e-02
|
-0.107000
|
7.13e-01
|
2.09e-01
|
Intracellular signaling by second messengers
|
313
|
2.11e-03
|
1.36e-02
|
0.11100
|
-3.70e-03
|
0.111000
|
9.10e-01
|
6.91e-04
|
Signaling by NTRK2 (TRKB)
|
25
|
5.78e-01
|
7.47e-01
|
0.11100
|
-3.11e-02
|
0.107000
|
7.88e-01
|
3.55e-01
|
FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes
|
29
|
5.06e-01
|
6.97e-01
|
0.11100
|
9.32e-02
|
-0.060300
|
3.85e-01
|
5.74e-01
|
Sensory processing of sound by inner hair cells of the cochlea
|
62
|
2.99e-01
|
5.16e-01
|
0.11100
|
1.33e-03
|
-0.111000
|
9.86e-01
|
1.31e-01
|
Synthesis of IP3 and IP4 in the cytosol
|
25
|
6.50e-01
|
8.01e-01
|
0.11100
|
-2.82e-02
|
-0.107000
|
8.07e-01
|
3.54e-01
|
DSCAM interactions
|
11
|
8.25e-01
|
8.99e-01
|
0.11100
|
-1.08e-01
|
-0.024300
|
5.36e-01
|
8.89e-01
|
RHOF GTPase cycle
|
40
|
5.50e-01
|
7.29e-01
|
0.11000
|
-8.35e-02
|
-0.072300
|
3.61e-01
|
4.29e-01
|
Apoptotic execution phase
|
43
|
3.75e-01
|
5.85e-01
|
0.11000
|
-9.76e-02
|
0.051700
|
2.68e-01
|
5.58e-01
|
MAP3K8 (TPL2)-dependent MAPK1/3 activation
|
15
|
7.70e-01
|
8.70e-01
|
0.11000
|
1.08e-01
|
0.023100
|
4.69e-01
|
8.77e-01
|
Signaling by WNT
|
263
|
1.52e-02
|
6.55e-02
|
0.11000
|
4.30e-02
|
0.102000
|
2.30e-01
|
4.56e-03
|
PI3K events in ERBB2 signaling
|
16
|
7.68e-01
|
8.70e-01
|
0.11000
|
-3.40e-02
|
-0.104000
|
8.14e-01
|
4.70e-01
|
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
|
117
|
1.40e-01
|
3.26e-01
|
0.10900
|
-2.73e-02
|
-0.106000
|
6.10e-01
|
4.75e-02
|
Growth hormone receptor signaling
|
24
|
6.00e-01
|
7.62e-01
|
0.10900
|
3.20e-02
|
-0.105000
|
7.86e-01
|
3.75e-01
|
Chromatin modifying enzymes
|
186
|
2.64e-02
|
1.00e-01
|
0.10900
|
-1.07e-02
|
0.109000
|
8.01e-01
|
1.05e-02
|
Chromatin organization
|
186
|
2.64e-02
|
1.00e-01
|
0.10900
|
-1.07e-02
|
0.109000
|
8.01e-01
|
1.05e-02
|
Blood group systems biosynthesis
|
22
|
7.04e-01
|
8.35e-01
|
0.10900
|
-1.02e-01
|
-0.039500
|
4.09e-01
|
7.49e-01
|
Signaling by FGFR in disease
|
61
|
3.98e-01
|
6.08e-01
|
0.10900
|
5.17e-02
|
0.095500
|
4.85e-01
|
1.97e-01
|
Post-chaperonin tubulin folding pathway
|
23
|
6.56e-01
|
8.02e-01
|
0.10900
|
3.49e-03
|
0.108000
|
9.77e-01
|
3.68e-01
|
Signaling by ERBB2 ECD mutants
|
15
|
7.77e-01
|
8.74e-01
|
0.10800
|
2.27e-02
|
0.106000
|
8.79e-01
|
4.77e-01
|
Ion channel transport
|
168
|
9.01e-02
|
2.40e-01
|
0.10800
|
-6.50e-02
|
-0.086200
|
1.46e-01
|
5.39e-02
|
Defective B3GAT3 causes JDSSDHD
|
17
|
7.68e-01
|
8.70e-01
|
0.10700
|
-3.76e-02
|
-0.101000
|
7.88e-01
|
4.72e-01
|
Interleukin-17 signaling
|
66
|
2.71e-01
|
4.87e-01
|
0.10700
|
-2.21e-02
|
0.105000
|
7.56e-01
|
1.40e-01
|
Ion transport by P-type ATPases
|
51
|
3.99e-01
|
6.08e-01
|
0.10700
|
-1.32e-03
|
-0.107000
|
9.87e-01
|
1.85e-01
|
Metabolism of nitric oxide: NOS3 activation and regulation
|
15
|
8.09e-01
|
8.85e-01
|
0.10700
|
-8.28e-02
|
-0.068000
|
5.79e-01
|
6.49e-01
|
Lewis blood group biosynthesis
|
18
|
7.32e-01
|
8.53e-01
|
0.10700
|
-1.06e-01
|
-0.010000
|
4.34e-01
|
9.41e-01
|
Serotonin receptors
|
11
|
8.52e-01
|
9.08e-01
|
0.10700
|
-5.15e-02
|
-0.093600
|
7.67e-01
|
5.91e-01
|
Transport of inorganic cations/anions and amino acids/oligopeptides
|
101
|
1.61e-01
|
3.54e-01
|
0.10700
|
2.05e-03
|
-0.107000
|
9.72e-01
|
6.40e-02
|
Innate Immune System
|
999
|
5.84e-08
|
1.28e-06
|
0.10600
|
6.89e-03
|
0.106000
|
7.12e-01
|
1.24e-08
|
FCGR3A-mediated phagocytosis
|
57
|
4.55e-01
|
6.63e-01
|
0.10600
|
8.10e-02
|
0.068600
|
2.90e-01
|
3.71e-01
|
Leishmania phagocytosis
|
57
|
4.55e-01
|
6.63e-01
|
0.10600
|
8.10e-02
|
0.068600
|
2.90e-01
|
3.71e-01
|
Parasite infection
|
57
|
4.55e-01
|
6.63e-01
|
0.10600
|
8.10e-02
|
0.068600
|
2.90e-01
|
3.71e-01
|
Prostacyclin signalling through prostacyclin receptor
|
19
|
6.65e-01
|
8.07e-01
|
0.10600
|
-5.85e-02
|
0.088400
|
6.59e-01
|
5.05e-01
|
Signaling by KIT in disease
|
20
|
6.51e-01
|
8.01e-01
|
0.10600
|
-6.07e-02
|
0.086800
|
6.38e-01
|
5.02e-01
|
Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants
|
20
|
6.51e-01
|
8.01e-01
|
0.10600
|
-6.07e-02
|
0.086800
|
6.38e-01
|
5.02e-01
|
Regulation of signaling by CBL
|
18
|
7.57e-01
|
8.65e-01
|
0.10600
|
-3.08e-02
|
-0.101000
|
8.21e-01
|
4.57e-01
|
Ras activation upon Ca2+ influx through NMDA receptor
|
19
|
7.72e-01
|
8.71e-01
|
0.10600
|
-7.12e-02
|
-0.078000
|
5.91e-01
|
5.56e-01
|
Cytochrome P450 - arranged by substrate type
|
64
|
3.01e-01
|
5.17e-01
|
0.10500
|
1.73e-02
|
-0.104000
|
8.11e-01
|
1.50e-01
|
Recycling pathway of L1
|
23
|
6.45e-01
|
8.00e-01
|
0.10500
|
-1.03e-01
|
0.020700
|
3.91e-01
|
8.64e-01
|
Incretin synthesis, secretion, and inactivation
|
23
|
6.13e-01
|
7.74e-01
|
0.10500
|
-6.13e-02
|
0.085700
|
6.11e-01
|
4.77e-01
|
Glycogen breakdown (glycogenolysis)
|
11
|
7.96e-01
|
8.80e-01
|
0.10500
|
-8.98e-02
|
0.053500
|
6.06e-01
|
7.59e-01
|
NOD1/2 Signaling Pathway
|
29
|
5.72e-01
|
7.43e-01
|
0.10400
|
-3.14e-02
|
0.099100
|
7.69e-01
|
3.56e-01
|
Reproduction
|
82
|
3.30e-01
|
5.45e-01
|
0.10400
|
-8.78e-02
|
-0.055500
|
1.69e-01
|
3.85e-01
|
RHO GTPases activate PAKs
|
19
|
7.13e-01
|
8.40e-01
|
0.10400
|
1.09e-02
|
-0.103000
|
9.35e-01
|
4.36e-01
|
Molecules associated with elastic fibres
|
29
|
6.31e-01
|
7.90e-01
|
0.10400
|
-1.03e-01
|
-0.014600
|
3.39e-01
|
8.92e-01
|
RHOBTB1 GTPase cycle
|
22
|
7.49e-01
|
8.60e-01
|
0.10400
|
7.14e-02
|
0.075100
|
5.62e-01
|
5.42e-01
|
Interleukin-37 signaling
|
20
|
6.97e-01
|
8.31e-01
|
0.10400
|
-1.02e-01
|
0.015000
|
4.27e-01
|
9.07e-01
|
Scavenging by Class A Receptors
|
19
|
7.80e-01
|
8.74e-01
|
0.10300
|
-7.24e-02
|
-0.073900
|
5.85e-01
|
5.77e-01
|
Diseases associated with glycosaminoglycan metabolism
|
38
|
5.98e-01
|
7.60e-01
|
0.10300
|
-8.96e-02
|
-0.051300
|
3.39e-01
|
5.84e-01
|
Signaling by Hippo
|
19
|
7.80e-01
|
8.74e-01
|
0.10300
|
-7.59e-02
|
-0.070000
|
5.67e-01
|
5.97e-01
|
Mitochondrial Fatty Acid Beta-Oxidation
|
35
|
5.24e-01
|
7.07e-01
|
0.10300
|
-2.42e-02
|
0.100000
|
8.04e-01
|
3.05e-01
|
activated TAK1 mediates p38 MAPK activation
|
16
|
7.23e-01
|
8.45e-01
|
0.10300
|
-6.54e-02
|
0.079000
|
6.51e-01
|
5.84e-01
|
Centrosome maturation
|
76
|
2.93e-01
|
5.12e-01
|
0.10200
|
4.75e-03
|
0.102000
|
9.43e-01
|
1.23e-01
|
Recruitment of mitotic centrosome proteins and complexes
|
76
|
2.93e-01
|
5.12e-01
|
0.10200
|
4.75e-03
|
0.102000
|
9.43e-01
|
1.23e-01
|
AURKA Activation by TPX2
|
68
|
3.77e-01
|
5.88e-01
|
0.10200
|
3.04e-02
|
0.097500
|
6.65e-01
|
1.64e-01
|
mRNA Editing
|
10
|
8.78e-01
|
9.26e-01
|
0.10200
|
8.56e-02
|
0.055600
|
6.39e-01
|
7.61e-01
|
EPH-ephrin mediated repulsion of cells
|
48
|
4.49e-01
|
6.57e-01
|
0.10200
|
-3.55e-03
|
0.102000
|
9.66e-01
|
2.21e-01
|
RAF/MAP kinase cascade
|
264
|
3.40e-02
|
1.22e-01
|
0.10200
|
5.89e-02
|
0.083300
|
9.94e-02
|
1.97e-02
|
Recruitment of NuMA to mitotic centrosomes
|
75
|
2.91e-01
|
5.10e-01
|
0.10200
|
-1.47e-03
|
0.102000
|
9.82e-01
|
1.27e-01
|
Transcriptional regulation by RUNX1
|
183
|
5.79e-02
|
1.79e-01
|
0.10200
|
1.01e-02
|
0.101000
|
8.13e-01
|
1.79e-02
|
SHC1 events in ERBB2 signaling
|
22
|
6.50e-01
|
8.01e-01
|
0.10200
|
-8.71e-02
|
0.052500
|
4.79e-01
|
6.70e-01
|
Post-translational protein modification
|
1289
|
1.33e-08
|
3.45e-07
|
0.10200
|
2.17e-02
|
0.099300
|
1.88e-01
|
1.72e-09
|
Glucagon-like Peptide-1 (GLP1) regulates insulin secretion
|
42
|
4.33e-01
|
6.39e-01
|
0.10100
|
-7.27e-02
|
0.070800
|
4.15e-01
|
4.27e-01
|
Pyruvate metabolism and Citric Acid (TCA) cycle
|
52
|
5.11e-01
|
7.00e-01
|
0.10100
|
5.42e-02
|
0.085700
|
4.99e-01
|
2.85e-01
|
Tight junction interactions
|
28
|
6.95e-01
|
8.29e-01
|
0.10100
|
-8.79e-02
|
-0.049900
|
4.21e-01
|
6.48e-01
|
RHO GTPase Effectors
|
232
|
3.02e-02
|
1.12e-01
|
0.10100
|
1.26e-02
|
0.100000
|
7.42e-01
|
8.50e-03
|
Signaling by EGFR
|
49
|
4.78e-01
|
6.77e-01
|
0.10100
|
1.43e-02
|
0.099900
|
8.63e-01
|
2.26e-01
|
CaMK IV-mediated phosphorylation of CREB
|
10
|
8.41e-01
|
9.03e-01
|
0.10100
|
1.96e-02
|
-0.098600
|
9.14e-01
|
5.89e-01
|
Signaling by FGFR3 in disease
|
21
|
7.15e-01
|
8.41e-01
|
0.10000
|
-1.01e-03
|
0.100000
|
9.94e-01
|
4.26e-01
|
Translation of Structural Proteins 9683701
|
29
|
6.93e-01
|
8.29e-01
|
0.10000
|
5.37e-02
|
0.084600
|
6.17e-01
|
4.30e-01
|
Interleukin-7 signaling
|
21
|
6.93e-01
|
8.29e-01
|
0.10000
|
9.73e-02
|
-0.023400
|
4.40e-01
|
8.53e-01
|
Signaling by BRAF and RAF1 fusions
|
60
|
3.27e-01
|
5.45e-01
|
0.09970
|
-8.77e-02
|
0.047400
|
2.40e-01
|
5.26e-01
|
Protein folding
|
96
|
2.52e-01
|
4.66e-01
|
0.09960
|
1.82e-02
|
0.097900
|
7.57e-01
|
9.71e-02
|
MAPK1/MAPK3 signaling
|
270
|
3.75e-02
|
1.31e-01
|
0.09960
|
5.92e-02
|
0.080100
|
9.38e-02
|
2.34e-02
|
TP53 Regulates Transcription of Caspase Activators and Caspases
|
12
|
8.38e-01
|
9.02e-01
|
0.09950
|
-9.86e-02
|
-0.013400
|
5.54e-01
|
9.36e-01
|
Pre-NOTCH Transcription and Translation
|
45
|
4.77e-01
|
6.76e-01
|
0.09940
|
-1.20e-02
|
0.098700
|
8.90e-01
|
2.52e-01
|
RHO GTPases activate CIT
|
19
|
7.42e-01
|
8.59e-01
|
0.09920
|
9.92e-02
|
-0.002010
|
4.54e-01
|
9.88e-01
|
Processing of SMDT1
|
15
|
7.63e-01
|
8.68e-01
|
0.09920
|
3.79e-02
|
-0.091700
|
7.99e-01
|
5.39e-01
|
Regulation of MECP2 expression and activity
|
30
|
6.05e-01
|
7.66e-01
|
0.09860
|
-9.66e-02
|
0.020100
|
3.60e-01
|
8.49e-01
|
Cell surface interactions at the vascular wall
|
127
|
9.32e-02
|
2.46e-01
|
0.09850
|
-7.09e-02
|
0.068300
|
1.67e-01
|
1.84e-01
|
Activation of BAD and translocation to mitochondria
|
15
|
7.78e-01
|
8.74e-01
|
0.09840
|
-9.61e-02
|
0.021000
|
5.19e-01
|
8.88e-01
|
Regulation of IFNG signaling
|
14
|
7.73e-01
|
8.72e-01
|
0.09840
|
-5.36e-02
|
0.082400
|
7.28e-01
|
5.93e-01
|
Neurotransmitter release cycle
|
47
|
4.65e-01
|
6.70e-01
|
0.09830
|
9.72e-02
|
-0.015000
|
2.49e-01
|
8.59e-01
|
PECAM1 interactions
|
12
|
8.65e-01
|
9.16e-01
|
0.09810
|
5.20e-02
|
0.083100
|
7.55e-01
|
6.18e-01
|
Extra-nuclear estrogen signaling
|
73
|
2.65e-01
|
4.79e-01
|
0.09800
|
-8.33e-02
|
0.051700
|
2.19e-01
|
4.45e-01
|
Basigin interactions
|
24
|
7.49e-01
|
8.60e-01
|
0.09790
|
5.32e-02
|
0.082200
|
6.52e-01
|
4.86e-01
|
ADORA2B mediated anti-inflammatory cytokines production
|
42
|
5.12e-01
|
7.00e-01
|
0.09790
|
-9.72e-02
|
0.011900
|
2.76e-01
|
8.94e-01
|
Signaling by SCF-KIT
|
43
|
4.96e-01
|
6.88e-01
|
0.09780
|
-9.62e-02
|
0.017700
|
2.75e-01
|
8.41e-01
|
Defects in vitamin and cofactor metabolism
|
20
|
7.83e-01
|
8.74e-01
|
0.09770
|
4.59e-02
|
0.086200
|
7.22e-01
|
5.04e-01
|
GPER1 signaling
|
44
|
4.49e-01
|
6.57e-01
|
0.09750
|
-7.94e-02
|
0.056500
|
3.62e-01
|
5.17e-01
|
Regulation of gene expression in beta cells
|
21
|
7.83e-01
|
8.74e-01
|
0.09730
|
6.22e-02
|
0.074800
|
6.22e-01
|
5.53e-01
|
Nuclear Receptor transcription pathway
|
51
|
4.27e-01
|
6.33e-01
|
0.09710
|
-9.32e-02
|
0.027300
|
2.50e-01
|
7.36e-01
|
Constitutive Signaling by AKT1 E17K in Cancer
|
25
|
6.47e-01
|
8.01e-01
|
0.09670
|
-4.34e-02
|
0.086400
|
7.07e-01
|
4.55e-01
|
Class B/2 (Secretin family receptors)
|
94
|
2.08e-01
|
4.04e-01
|
0.09660
|
-3.13e-02
|
0.091400
|
5.99e-01
|
1.26e-01
|
Synaptic adhesion-like molecules
|
19
|
7.12e-01
|
8.39e-01
|
0.09650
|
7.79e-02
|
-0.057000
|
5.56e-01
|
6.67e-01
|
RMTs methylate histone arginines
|
30
|
6.71e-01
|
8.11e-01
|
0.09640
|
2.03e-02
|
0.094200
|
8.48e-01
|
3.72e-01
|
HATs acetylate histones
|
71
|
3.70e-01
|
5.84e-01
|
0.09620
|
8.80e-03
|
0.095800
|
8.98e-01
|
1.62e-01
|
Opioid Signalling
|
88
|
2.76e-01
|
4.93e-01
|
0.09620
|
-9.62e-02
|
0.000823
|
1.19e-01
|
9.89e-01
|
RUNX2 regulates osteoblast differentiation
|
22
|
7.37e-01
|
8.55e-01
|
0.09620
|
1.04e-02
|
0.095600
|
9.33e-01
|
4.37e-01
|
Signaling by PDGF
|
52
|
5.16e-01
|
7.04e-01
|
0.09600
|
-9.19e-02
|
-0.027700
|
2.52e-01
|
7.29e-01
|
Deadenylation of mRNA
|
25
|
7.03e-01
|
8.35e-01
|
0.09580
|
-9.56e-02
|
-0.006240
|
4.08e-01
|
9.57e-01
|
Ca-dependent events
|
35
|
6.76e-01
|
8.15e-01
|
0.09560
|
-6.49e-02
|
-0.070200
|
5.06e-01
|
4.72e-01
|
Hyaluronan metabolism
|
17
|
7.66e-01
|
8.69e-01
|
0.09560
|
-1.92e-02
|
0.093700
|
8.91e-01
|
5.04e-01
|
RAS processing
|
19
|
7.91e-01
|
8.79e-01
|
0.09470
|
-9.03e-02
|
-0.028600
|
4.96e-01
|
8.29e-01
|
Aquaporin-mediated transport
|
51
|
5.72e-01
|
7.43e-01
|
0.09430
|
-7.47e-02
|
-0.057500
|
3.56e-01
|
4.78e-01
|
Translation of Structural Proteins 9694635
|
55
|
4.68e-01
|
6.71e-01
|
0.09430
|
2.91e-03
|
0.094200
|
9.70e-01
|
2.27e-01
|
G beta:gamma signalling through PLC beta
|
20
|
7.34e-01
|
8.54e-01
|
0.09420
|
-9.17e-02
|
0.021700
|
4.78e-01
|
8.66e-01
|
Signaling by NOTCH1
|
69
|
4.68e-01
|
6.71e-01
|
0.09420
|
5.43e-02
|
0.077000
|
4.35e-01
|
2.69e-01
|
RHOG GTPase cycle
|
69
|
4.29e-01
|
6.34e-01
|
0.09410
|
-9.04e-02
|
-0.026000
|
1.94e-01
|
7.09e-01
|
PI-3K cascade:FGFR2
|
22
|
7.90e-01
|
8.78e-01
|
0.09370
|
6.69e-02
|
0.065600
|
5.87e-01
|
5.94e-01
|
Long-term potentiation
|
22
|
7.58e-01
|
8.66e-01
|
0.09360
|
-1.89e-02
|
-0.091600
|
8.78e-01
|
4.57e-01
|
PKMTs methylate histone lysines
|
37
|
5.60e-01
|
7.37e-01
|
0.09320
|
-8.75e-02
|
0.031900
|
3.57e-01
|
7.37e-01
|
Fatty acid metabolism
|
167
|
1.54e-01
|
3.43e-01
|
0.09300
|
3.99e-02
|
0.084000
|
3.73e-01
|
6.08e-02
|
Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1)
|
20
|
7.41e-01
|
8.58e-01
|
0.09300
|
-2.08e-02
|
0.090700
|
8.72e-01
|
4.83e-01
|
Attachment and Entry 9694614
|
16
|
8.34e-01
|
9.01e-01
|
0.09250
|
-8.56e-02
|
-0.034900
|
5.53e-01
|
8.09e-01
|
SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion
|
13
|
8.38e-01
|
9.02e-01
|
0.09230
|
-1.71e-03
|
0.092300
|
9.91e-01
|
5.65e-01
|
Glutamate binding, activation of AMPA receptors and synaptic plasticity
|
29
|
6.90e-01
|
8.28e-01
|
0.09220
|
9.17e-02
|
0.009200
|
3.93e-01
|
9.32e-01
|
Trafficking of AMPA receptors
|
29
|
6.90e-01
|
8.28e-01
|
0.09220
|
9.17e-02
|
0.009200
|
3.93e-01
|
9.32e-01
|
MAPK3 (ERK1) activation
|
10
|
8.49e-01
|
9.07e-01
|
0.09210
|
6.41e-02
|
-0.066100
|
7.25e-01
|
7.17e-01
|
Chaperonin-mediated protein folding
|
90
|
3.36e-01
|
5.52e-01
|
0.09210
|
1.93e-02
|
0.090000
|
7.51e-01
|
1.40e-01
|
Dermatan sulfate biosynthesis
|
10
|
8.85e-01
|
9.31e-01
|
0.09200
|
-1.80e-02
|
-0.090200
|
9.22e-01
|
6.21e-01
|
CD28 co-stimulation
|
32
|
6.32e-01
|
7.90e-01
|
0.09180
|
-9.04e-02
|
0.016300
|
3.76e-01
|
8.73e-01
|
Signaling by ERBB2 TMD/JMD mutants
|
21
|
7.17e-01
|
8.43e-01
|
0.09180
|
-4.39e-02
|
0.080600
|
7.28e-01
|
5.22e-01
|
Pregnenolone biosynthesis
|
10
|
8.96e-01
|
9.36e-01
|
0.09140
|
8.30e-02
|
0.038300
|
6.49e-01
|
8.34e-01
|
Integration of energy metabolism
|
106
|
1.83e-01
|
3.80e-01
|
0.09130
|
-5.69e-02
|
0.071400
|
3.11e-01
|
2.04e-01
|
RA biosynthesis pathway
|
22
|
7.10e-01
|
8.39e-01
|
0.09120
|
-4.21e-02
|
0.080800
|
7.32e-01
|
5.12e-01
|
Carboxyterminal post-translational modifications of tubulin
|
40
|
5.56e-01
|
7.35e-01
|
0.09110
|
8.76e-02
|
-0.025100
|
3.38e-01
|
7.84e-01
|
Regulation of insulin secretion
|
77
|
2.97e-01
|
5.16e-01
|
0.09110
|
-4.89e-02
|
0.076900
|
4.58e-01
|
2.43e-01
|
MHC class II antigen presentation
|
104
|
3.45e-01
|
5.61e-01
|
0.09050
|
4.95e-02
|
0.075800
|
3.83e-01
|
1.82e-01
|
CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling
|
25
|
7.73e-01
|
8.72e-01
|
0.09030
|
-7.69e-02
|
-0.047300
|
5.05e-01
|
6.82e-01
|
Signaling by MET
|
66
|
3.68e-01
|
5.81e-01
|
0.09010
|
-8.02e-02
|
0.041100
|
2.59e-01
|
5.64e-01
|
Estrogen-dependent nuclear events downstream of ESR-membrane signaling
|
23
|
7.03e-01
|
8.35e-01
|
0.09010
|
-7.80e-02
|
0.045200
|
5.17e-01
|
7.07e-01
|
GABA synthesis, release, reuptake and degradation
|
19
|
7.52e-01
|
8.62e-01
|
0.08950
|
7.91e-02
|
-0.042000
|
5.51e-01
|
7.51e-01
|
G alpha (i) signalling events
|
305
|
5.19e-02
|
1.66e-01
|
0.08940
|
-6.74e-02
|
-0.058700
|
4.26e-02
|
7.74e-02
|
GABA receptor activation
|
57
|
5.19e-01
|
7.04e-01
|
0.08940
|
-8.77e-02
|
-0.017200
|
2.52e-01
|
8.22e-01
|
Interleukin receptor SHC signaling
|
24
|
7.70e-01
|
8.70e-01
|
0.08910
|
-8.50e-02
|
-0.026800
|
4.71e-01
|
8.20e-01
|
Immune System
|
1870
|
4.57e-09
|
1.36e-07
|
0.08900
|
2.39e-02
|
0.085800
|
8.51e-02
|
6.08e-10
|
GPCR downstream signalling
|
603
|
2.91e-03
|
1.78e-02
|
0.08890
|
-7.46e-02
|
-0.048400
|
1.72e-03
|
4.21e-02
|
Signaling by ERBB2
|
49
|
5.32e-01
|
7.13e-01
|
0.08890
|
-6.89e-03
|
0.088600
|
9.34e-01
|
2.83e-01
|
CREB1 phosphorylation through the activation of Adenylate Cyclase
|
11
|
8.53e-01
|
9.09e-01
|
0.08860
|
-3.45e-02
|
0.081600
|
8.43e-01
|
6.39e-01
|
Defects in cobalamin (B12) metabolism
|
12
|
8.89e-01
|
9.31e-01
|
0.08850
|
4.80e-02
|
0.074400
|
7.73e-01
|
6.56e-01
|
EPHA-mediated growth cone collapse
|
15
|
7.99e-01
|
8.80e-01
|
0.08830
|
5.03e-02
|
-0.072600
|
7.36e-01
|
6.26e-01
|
Meiosis
|
56
|
4.62e-01
|
6.68e-01
|
0.08830
|
-8.47e-02
|
0.025000
|
2.73e-01
|
7.47e-01
|
TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain
|
21
|
8.09e-01
|
8.85e-01
|
0.08800
|
7.98e-02
|
0.037200
|
5.27e-01
|
7.68e-01
|
A tetrasaccharide linker sequence is required for GAG synthesis
|
23
|
8.00e-01
|
8.80e-01
|
0.08770
|
-4.53e-02
|
-0.075100
|
7.07e-01
|
5.33e-01
|
Inwardly rectifying K+ channels
|
35
|
7.11e-01
|
8.39e-01
|
0.08760
|
-4.34e-02
|
-0.076100
|
6.57e-01
|
4.36e-01
|
CD209 (DC-SIGN) signaling
|
20
|
8.33e-01
|
9.01e-01
|
0.08640
|
-6.37e-02
|
-0.058400
|
6.22e-01
|
6.51e-01
|
Loss of Nlp from mitotic centrosomes
|
65
|
4.73e-01
|
6.73e-01
|
0.08610
|
2.86e-03
|
0.086000
|
9.68e-01
|
2.30e-01
|
Loss of proteins required for interphase microtubule organization from the centrosome
|
65
|
4.73e-01
|
6.73e-01
|
0.08610
|
2.86e-03
|
0.086000
|
9.68e-01
|
2.30e-01
|
ROS and RNS production in phagocytes
|
35
|
6.25e-01
|
7.85e-01
|
0.08590
|
-3.17e-02
|
0.079800
|
7.46e-01
|
4.14e-01
|
RHO GTPase cycle
|
420
|
4.74e-03
|
2.67e-02
|
0.08520
|
-8.12e-02
|
0.025800
|
4.27e-03
|
3.64e-01
|
Pyroptosis
|
26
|
7.60e-01
|
8.67e-01
|
0.08490
|
1.35e-02
|
0.083800
|
9.05e-01
|
4.59e-01
|
RAC1 GTPase cycle
|
170
|
1.41e-01
|
3.27e-01
|
0.08480
|
-8.47e-02
|
0.004130
|
5.67e-02
|
9.26e-01
|
Sphingolipid metabolism
|
81
|
3.28e-01
|
5.45e-01
|
0.08460
|
-5.37e-02
|
0.065400
|
4.03e-01
|
3.09e-01
|
MAPK family signaling cascades
|
311
|
6.32e-02
|
1.91e-01
|
0.08460
|
4.58e-02
|
0.071200
|
1.65e-01
|
3.08e-02
|
Organelle biogenesis and maintenance
|
243
|
8.66e-02
|
2.36e-01
|
0.08440
|
1.87e-02
|
0.082300
|
6.15e-01
|
2.70e-02
|
G beta:gamma signalling through BTK
|
17
|
7.92e-01
|
8.80e-01
|
0.08440
|
-6.63e-02
|
0.052300
|
6.36e-01
|
7.09e-01
|
Adaptive Immune System
|
709
|
1.69e-03
|
1.12e-02
|
0.08430
|
3.63e-02
|
0.076100
|
9.92e-02
|
5.42e-04
|
Metabolic disorders of biological oxidation enzymes
|
32
|
7.56e-01
|
8.65e-01
|
0.08420
|
-5.32e-02
|
-0.065300
|
6.03e-01
|
5.22e-01
|
L1CAM interactions
|
92
|
3.95e-01
|
6.04e-01
|
0.08410
|
-1.75e-02
|
-0.082200
|
7.71e-01
|
1.73e-01
|
NRAGE signals death through JNK
|
53
|
6.34e-01
|
7.92e-01
|
0.08390
|
-6.14e-02
|
-0.057200
|
4.39e-01
|
4.71e-01
|
Effects of PIP2 hydrolysis
|
26
|
7.99e-01
|
8.80e-01
|
0.08390
|
-6.32e-02
|
-0.055100
|
5.77e-01
|
6.27e-01
|
Regulation of lipid metabolism by PPARalpha
|
116
|
2.62e-01
|
4.76e-01
|
0.08360
|
-9.50e-03
|
0.083100
|
8.60e-01
|
1.22e-01
|
Glucagon-type ligand receptors
|
33
|
6.57e-01
|
8.03e-01
|
0.08360
|
-7.78e-02
|
0.030500
|
4.39e-01
|
7.62e-01
|
Metabolism of carbohydrates
|
275
|
4.12e-02
|
1.41e-01
|
0.08330
|
-1.31e-02
|
0.082200
|
7.09e-01
|
1.88e-02
|
Diseases of glycosylation
|
137
|
2.98e-01
|
5.16e-01
|
0.08320
|
-7.33e-02
|
-0.039400
|
1.38e-01
|
4.26e-01
|
Insulin receptor recycling
|
26
|
7.46e-01
|
8.60e-01
|
0.08320
|
-5.69e-03
|
0.083000
|
9.60e-01
|
4.64e-01
|
Defective B4GALT7 causes EDS, progeroid type
|
17
|
8.66e-01
|
9.17e-01
|
0.08310
|
-5.43e-02
|
-0.063000
|
6.99e-01
|
6.53e-01
|
Membrane Trafficking
|
585
|
1.20e-03
|
8.50e-03
|
0.08310
|
-1.45e-02
|
0.081800
|
5.49e-01
|
6.99e-04
|
Biotin transport and metabolism
|
10
|
9.01e-01
|
9.38e-01
|
0.08300
|
7.47e-03
|
0.082700
|
9.67e-01
|
6.51e-01
|
G alpha (q) signalling events
|
206
|
1.21e-01
|
2.97e-01
|
0.08300
|
-8.25e-02
|
-0.009350
|
4.12e-02
|
8.17e-01
|
Muscle contraction
|
193
|
1.03e-01
|
2.65e-01
|
0.08300
|
1.68e-02
|
-0.081200
|
6.87e-01
|
5.15e-02
|
Keratan sulfate biosynthesis
|
28
|
6.94e-01
|
8.29e-01
|
0.08280
|
-7.00e-02
|
0.044200
|
5.21e-01
|
6.85e-01
|
Synthesis, secretion, and deacylation of Ghrelin
|
19
|
8.38e-01
|
9.02e-01
|
0.08270
|
7.80e-02
|
0.027400
|
5.56e-01
|
8.36e-01
|
NCAM signaling for neurite out-growth
|
57
|
4.77e-01
|
6.76e-01
|
0.08240
|
6.73e-02
|
-0.047600
|
3.79e-01
|
5.35e-01
|
Adenylate cyclase activating pathway
|
10
|
8.88e-01
|
9.31e-01
|
0.08220
|
2.05e-02
|
-0.079600
|
9.11e-01
|
6.63e-01
|
Smooth Muscle Contraction
|
43
|
5.71e-01
|
7.43e-01
|
0.08220
|
6.28e-02
|
-0.053000
|
4.76e-01
|
5.48e-01
|
Prolonged ERK activation events
|
14
|
8.91e-01
|
9.32e-01
|
0.08170
|
-6.57e-02
|
-0.048500
|
6.70e-01
|
7.53e-01
|
Syndecan interactions
|
19
|
7.89e-01
|
8.78e-01
|
0.08160
|
-7.25e-02
|
0.037500
|
5.84e-01
|
7.77e-01
|
ESR-mediated signaling
|
160
|
1.73e-01
|
3.70e-01
|
0.08100
|
-1.16e-02
|
0.080200
|
8.01e-01
|
7.99e-02
|
Plasma lipoprotein assembly, remodeling, and clearance
|
73
|
4.02e-01
|
6.11e-01
|
0.08100
|
4.52e-02
|
-0.067200
|
5.04e-01
|
3.21e-01
|
Heparan sulfate/heparin (HS-GAG) metabolism
|
49
|
6.69e-01
|
8.10e-01
|
0.08090
|
-6.85e-02
|
-0.042900
|
4.07e-01
|
6.03e-01
|
PPARA activates gene expression
|
114
|
2.85e-01
|
5.05e-01
|
0.08030
|
-1.53e-02
|
0.078800
|
7.77e-01
|
1.46e-01
|
Germ layer formation at gastrulation
|
16
|
8.33e-01
|
9.01e-01
|
0.08030
|
-7.68e-02
|
0.023300
|
5.95e-01
|
8.72e-01
|
Cardiac conduction
|
123
|
2.68e-01
|
4.84e-01
|
0.07990
|
1.14e-02
|
-0.079100
|
8.27e-01
|
1.29e-01
|
Interleukin-6 family signaling
|
24
|
8.24e-01
|
8.98e-01
|
0.07990
|
-4.07e-02
|
-0.068700
|
7.30e-01
|
5.60e-01
|
Metabolism of steroids
|
148
|
2.38e-01
|
4.47e-01
|
0.07980
|
-5.63e-03
|
-0.079600
|
9.06e-01
|
9.43e-02
|
Phospholipid metabolism
|
192
|
1.14e-01
|
2.84e-01
|
0.07940
|
-7.45e-02
|
0.027500
|
7.50e-02
|
5.11e-01
|
Hemostasis
|
555
|
1.73e-03
|
1.14e-02
|
0.07920
|
-7.07e-02
|
0.035700
|
4.32e-03
|
1.50e-01
|
Intraflagellar transport
|
36
|
6.94e-01
|
8.29e-01
|
0.07900
|
-5.23e-03
|
0.078800
|
9.57e-01
|
4.13e-01
|
Sema3A PAK dependent Axon repulsion
|
14
|
8.98e-01
|
9.37e-01
|
0.07860
|
-6.33e-02
|
-0.046500
|
6.82e-01
|
7.63e-01
|
Anti-inflammatory response favouring Leishmania parasite infection
|
75
|
5.70e-01
|
7.43e-01
|
0.07840
|
-5.67e-02
|
-0.054100
|
3.96e-01
|
4.17e-01
|
Leishmania parasite growth and survival
|
75
|
5.70e-01
|
7.43e-01
|
0.07840
|
-5.67e-02
|
-0.054100
|
3.96e-01
|
4.17e-01
|
EPH-Ephrin signaling
|
90
|
5.11e-01
|
7.00e-01
|
0.07810
|
5.16e-02
|
0.058700
|
3.98e-01
|
3.36e-01
|
FCERI mediated Ca+2 mobilization
|
27
|
8.19e-01
|
8.94e-01
|
0.07770
|
-5.44e-02
|
-0.055500
|
6.25e-01
|
6.17e-01
|
DAG and IP3 signaling
|
39
|
7.42e-01
|
8.59e-01
|
0.07740
|
-6.75e-02
|
-0.038000
|
4.66e-01
|
6.82e-01
|
Pyruvate metabolism
|
29
|
7.75e-01
|
8.73e-01
|
0.07740
|
1.20e-02
|
0.076400
|
9.11e-01
|
4.76e-01
|
Metabolism of folate and pterines
|
16
|
8.47e-01
|
9.07e-01
|
0.07670
|
-2.00e-02
|
0.074000
|
8.90e-01
|
6.08e-01
|
Signaling by ALK
|
26
|
7.82e-01
|
8.74e-01
|
0.07660
|
7.65e-02
|
-0.003530
|
4.99e-01
|
9.75e-01
|
Prolactin receptor signaling
|
15
|
8.57e-01
|
9.12e-01
|
0.07630
|
-2.07e-02
|
0.073400
|
8.90e-01
|
6.23e-01
|
Oncogenic MAPK signaling
|
76
|
4.31e-01
|
6.36e-01
|
0.07590
|
-5.90e-02
|
0.047800
|
3.74e-01
|
4.71e-01
|
Glyoxylate metabolism and glycine degradation
|
30
|
7.98e-01
|
8.80e-01
|
0.07570
|
3.06e-02
|
0.069200
|
7.72e-01
|
5.12e-01
|
Crosslinking of collagen fibrils
|
10
|
9.21e-01
|
9.53e-01
|
0.07530
|
7.42e-02
|
0.013000
|
6.85e-01
|
9.43e-01
|
Constitutive Signaling by EGFRvIII
|
15
|
9.01e-01
|
9.38e-01
|
0.07530
|
5.48e-02
|
0.051600
|
7.13e-01
|
7.29e-01
|
Signaling by EGFRvIII in Cancer
|
15
|
9.01e-01
|
9.38e-01
|
0.07530
|
5.48e-02
|
0.051600
|
7.13e-01
|
7.29e-01
|
Signaling by TGF-beta Receptor Complex
|
90
|
4.56e-01
|
6.64e-01
|
0.07520
|
3.39e-03
|
0.075100
|
9.56e-01
|
2.18e-01
|
Clathrin-mediated endocytosis
|
135
|
3.73e-01
|
5.85e-01
|
0.07520
|
3.29e-02
|
0.067600
|
5.09e-01
|
1.75e-01
|
Platelet activation, signaling and aggregation
|
245
|
7.32e-02
|
2.10e-01
|
0.07470
|
-5.77e-02
|
0.047500
|
1.20e-01
|
2.00e-01
|
Metabolism
|
1963
|
1.13e-06
|
1.70e-05
|
0.07470
|
2.54e-02
|
0.070300
|
6.11e-02
|
2.19e-07
|
G alpha (12/13) signalling events
|
74
|
5.25e-01
|
7.07e-01
|
0.07420
|
-7.42e-02
|
0.000371
|
2.69e-01
|
9.96e-01
|
Vasopressin regulates renal water homeostasis via Aquaporins
|
42
|
6.72e-01
|
8.11e-01
|
0.07420
|
-7.27e-02
|
0.014800
|
4.15e-01
|
8.68e-01
|
Peptide hormone metabolism
|
83
|
5.28e-01
|
7.08e-01
|
0.07420
|
-7.17e-02
|
-0.018800
|
2.58e-01
|
7.67e-01
|
Peptide ligand-binding receptors
|
190
|
1.41e-01
|
3.27e-01
|
0.07350
|
5.79e-02
|
-0.045300
|
1.68e-01
|
2.82e-01
|
Cargo trafficking to the periciliary membrane
|
49
|
6.53e-01
|
8.01e-01
|
0.07340
|
7.33e-02
|
-0.003890
|
3.75e-01
|
9.62e-01
|
RAC3 GTPase cycle
|
84
|
4.63e-01
|
6.68e-01
|
0.07320
|
-7.18e-02
|
0.014300
|
2.55e-01
|
8.20e-01
|
FCGR3A-mediated IL10 synthesis
|
37
|
7.35e-01
|
8.55e-01
|
0.07300
|
-1.64e-03
|
-0.072900
|
9.86e-01
|
4.43e-01
|
Fcgamma receptor (FCGR) dependent phagocytosis
|
82
|
5.77e-01
|
7.47e-01
|
0.07290
|
3.72e-02
|
0.062700
|
5.60e-01
|
3.26e-01
|
Interleukin-27 signaling
|
11
|
8.96e-01
|
9.36e-01
|
0.07230
|
6.02e-02
|
-0.040200
|
7.30e-01
|
8.18e-01
|
Vesicle-mediated transport
|
623
|
3.09e-03
|
1.88e-02
|
0.07220
|
-2.65e-02
|
0.067100
|
2.57e-01
|
4.14e-03
|
Rap1 signalling
|
16
|
8.68e-01
|
9.18e-01
|
0.07200
|
-1.26e-02
|
0.070900
|
9.31e-01
|
6.23e-01
|
Hyaluronan uptake and degradation
|
12
|
9.26e-01
|
9.56e-01
|
0.07180
|
5.85e-02
|
0.041600
|
7.26e-01
|
8.03e-01
|
Phase 4 - resting membrane potential
|
19
|
8.41e-01
|
9.03e-01
|
0.07150
|
2.16e-02
|
-0.068200
|
8.71e-01
|
6.07e-01
|
Platelet homeostasis
|
85
|
5.88e-01
|
7.53e-01
|
0.07120
|
-5.61e-02
|
-0.043900
|
3.71e-01
|
4.84e-01
|
G beta:gamma signalling through CDC42
|
19
|
8.34e-01
|
9.01e-01
|
0.07120
|
-3.46e-02
|
0.062300
|
7.94e-01
|
6.38e-01
|
Glycosaminoglycan metabolism
|
116
|
3.48e-01
|
5.64e-01
|
0.07080
|
-6.60e-02
|
0.025600
|
2.19e-01
|
6.33e-01
|
Signaling by Retinoic Acid
|
41
|
7.05e-01
|
8.36e-01
|
0.07060
|
-1.29e-02
|
0.069500
|
8.87e-01
|
4.41e-01
|
Signaling by Insulin receptor
|
77
|
5.17e-01
|
7.04e-01
|
0.07040
|
-1.57e-02
|
0.068600
|
8.12e-01
|
2.98e-01
|
Glycogen metabolism
|
22
|
8.24e-01
|
8.98e-01
|
0.06980
|
-2.28e-02
|
0.066000
|
8.53e-01
|
5.92e-01
|
Nuclear signaling by ERBB4
|
32
|
7.82e-01
|
8.74e-01
|
0.06910
|
3.22e-03
|
-0.069100
|
9.75e-01
|
4.99e-01
|
Cargo recognition for clathrin-mediated endocytosis
|
98
|
5.67e-01
|
7.43e-01
|
0.06890
|
4.80e-02
|
0.049500
|
4.12e-01
|
3.97e-01
|
Leishmania infection
|
156
|
3.58e-01
|
5.73e-01
|
0.06820
|
1.52e-02
|
0.066500
|
7.43e-01
|
1.52e-01
|
Phase 2 - plateau phase
|
14
|
8.87e-01
|
9.31e-01
|
0.06810
|
6.20e-02
|
-0.028200
|
6.88e-01
|
8.55e-01
|
Biological oxidations
|
213
|
2.96e-01
|
5.16e-01
|
0.06790
|
-3.80e-02
|
-0.056200
|
3.38e-01
|
1.57e-01
|
Sulfur amino acid metabolism
|
27
|
8.50e-01
|
9.07e-01
|
0.06780
|
2.83e-02
|
0.061700
|
7.99e-01
|
5.79e-01
|
Neurotoxicity of clostridium toxins
|
10
|
9.45e-01
|
9.66e-01
|
0.06770
|
5.09e-02
|
0.044600
|
7.80e-01
|
8.07e-01
|
COPI-independent Golgi-to-ER retrograde traffic
|
34
|
7.47e-01
|
8.60e-01
|
0.06760
|
5.96e-02
|
-0.032000
|
5.48e-01
|
7.47e-01
|
RUNX2 regulates bone development
|
29
|
8.40e-01
|
9.03e-01
|
0.06760
|
2.69e-02
|
0.062100
|
8.02e-01
|
5.63e-01
|
Interferon gamma signaling
|
89
|
5.97e-01
|
7.59e-01
|
0.06760
|
3.33e-02
|
0.058800
|
5.87e-01
|
3.37e-01
|
Presynaptic function of Kainate receptors
|
21
|
8.57e-01
|
9.12e-01
|
0.06720
|
-6.71e-02
|
0.003910
|
5.94e-01
|
9.75e-01
|
CaM pathway
|
33
|
8.34e-01
|
9.01e-01
|
0.06690
|
-4.46e-02
|
-0.049900
|
6.57e-01
|
6.20e-01
|
Calmodulin induced events
|
33
|
8.34e-01
|
9.01e-01
|
0.06690
|
-4.46e-02
|
-0.049900
|
6.57e-01
|
6.20e-01
|
Signaling by Rho GTPases, Miro GTPases and RHOBTB3
|
603
|
6.96e-03
|
3.59e-02
|
0.06650
|
-3.67e-02
|
0.055400
|
1.23e-01
|
1.98e-02
|
Signaling by Rho GTPases
|
589
|
8.48e-03
|
4.16e-02
|
0.06560
|
-4.08e-02
|
0.051300
|
8.98e-02
|
3.30e-02
|
IGF1R signaling cascade
|
51
|
6.61e-01
|
8.05e-01
|
0.06530
|
-3.56e-02
|
0.054800
|
6.60e-01
|
4.98e-01
|
Circadian Clock
|
69
|
5.70e-01
|
7.43e-01
|
0.06490
|
-4.44e-02
|
0.047400
|
5.24e-01
|
4.96e-01
|
Signaling by Nuclear Receptors
|
237
|
1.64e-01
|
3.58e-01
|
0.06490
|
-2.44e-02
|
0.060100
|
5.17e-01
|
1.10e-01
|
Post-translational modification: synthesis of GPI-anchored proteins
|
89
|
5.18e-01
|
7.04e-01
|
0.06470
|
1.80e-02
|
-0.062100
|
7.68e-01
|
3.11e-01
|
eNOS activation
|
11
|
9.43e-01
|
9.65e-01
|
0.06460
|
-3.25e-02
|
-0.055800
|
8.52e-01
|
7.49e-01
|
Kinesins
|
42
|
7.80e-01
|
8.74e-01
|
0.06460
|
-6.28e-02
|
-0.015100
|
4.81e-01
|
8.65e-01
|
Signaling by Receptor Tyrosine Kinases
|
493
|
3.18e-02
|
1.16e-01
|
0.06450
|
-1.23e-02
|
0.063300
|
6.39e-01
|
1.59e-02
|
Antigen Presentation: Folding, assembly and peptide loading of class I MHC
|
29
|
8.05e-01
|
8.82e-01
|
0.06430
|
-2.17e-02
|
0.060500
|
8.40e-01
|
5.72e-01
|
Signaling by Non-Receptor Tyrosine Kinases
|
55
|
6.50e-01
|
8.01e-01
|
0.06390
|
-5.22e-02
|
0.037000
|
5.03e-01
|
6.35e-01
|
Signaling by PTK6
|
55
|
6.50e-01
|
8.01e-01
|
0.06390
|
-5.22e-02
|
0.037000
|
5.03e-01
|
6.35e-01
|
Glycogen storage diseases
|
14
|
9.32e-01
|
9.59e-01
|
0.06380
|
4.95e-02
|
0.040300
|
7.49e-01
|
7.94e-01
|
Surfactant metabolism
|
28
|
8.05e-01
|
8.82e-01
|
0.06340
|
-4.94e-02
|
0.039600
|
6.51e-01
|
7.17e-01
|
CDC42 GTPase cycle
|
143
|
3.84e-01
|
5.94e-01
|
0.06260
|
-6.13e-02
|
0.012400
|
2.05e-01
|
7.97e-01
|
CTLA4 inhibitory signaling
|
21
|
8.66e-01
|
9.17e-01
|
0.06250
|
-6.04e-02
|
0.015900
|
6.32e-01
|
9.00e-01
|
Transferrin endocytosis and recycling
|
30
|
7.98e-01
|
8.80e-01
|
0.06240
|
-4.32e-02
|
0.045000
|
6.82e-01
|
6.70e-01
|
Assembly and cell surface presentation of NMDA receptors
|
23
|
8.94e-01
|
9.35e-01
|
0.06190
|
-3.13e-02
|
-0.053400
|
7.95e-01
|
6.57e-01
|
DARPP-32 events
|
24
|
8.46e-01
|
9.07e-01
|
0.06180
|
-2.29e-02
|
0.057400
|
8.46e-01
|
6.27e-01
|
Serotonin Neurotransmitter Release Cycle
|
16
|
9.22e-01
|
9.53e-01
|
0.06170
|
-5.73e-02
|
-0.022800
|
6.92e-01
|
8.74e-01
|
Signaling by GPCR
|
670
|
4.50e-02
|
1.50e-01
|
0.06100
|
-5.34e-02
|
-0.029400
|
1.82e-02
|
1.93e-01
|
Anchoring of the basal body to the plasma membrane
|
92
|
5.76e-01
|
7.47e-01
|
0.06050
|
-5.27e-03
|
0.060300
|
9.30e-01
|
3.17e-01
|
Vitamin D (calciferol) metabolism
|
12
|
9.32e-01
|
9.59e-01
|
0.06050
|
-6.05e-02
|
0.001340
|
7.17e-01
|
9.94e-01
|
DAP12 signaling
|
28
|
8.26e-01
|
8.99e-01
|
0.06040
|
-5.33e-02
|
0.028400
|
6.26e-01
|
7.95e-01
|
Amyloid fiber formation
|
53
|
7.49e-01
|
8.60e-01
|
0.06020
|
5.99e-02
|
0.005940
|
4.51e-01
|
9.40e-01
|
Negative regulation of the PI3K/AKT network
|
111
|
4.69e-01
|
6.71e-01
|
0.05990
|
-3.34e-02
|
0.049700
|
5.43e-01
|
3.65e-01
|
IRS-mediated signalling
|
47
|
7.23e-01
|
8.45e-01
|
0.05980
|
-3.73e-02
|
0.046800
|
6.59e-01
|
5.79e-01
|
Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R)
|
52
|
7.00e-01
|
8.34e-01
|
0.05970
|
-4.72e-02
|
0.036600
|
5.56e-01
|
6.48e-01
|
Peptide hormone biosynthesis
|
11
|
9.27e-01
|
9.57e-01
|
0.05960
|
-4.29e-02
|
0.041300
|
8.05e-01
|
8.12e-01
|
Intra-Golgi traffic
|
43
|
7.80e-01
|
8.74e-01
|
0.05880
|
-7.35e-03
|
0.058400
|
9.34e-01
|
5.08e-01
|
Chondroitin sulfate/dermatan sulfate metabolism
|
45
|
7.43e-01
|
8.59e-01
|
0.05870
|
-3.48e-02
|
0.047300
|
6.87e-01
|
5.83e-01
|
Adenylate cyclase inhibitory pathway
|
14
|
9.40e-01
|
9.65e-01
|
0.05830
|
-2.62e-02
|
-0.052000
|
8.65e-01
|
7.36e-01
|
Ephrin signaling
|
17
|
9.08e-01
|
9.43e-01
|
0.05810
|
-5.73e-02
|
0.009380
|
6.83e-01
|
9.47e-01
|
Interleukin-3, Interleukin-5 and GM-CSF signaling
|
41
|
8.34e-01
|
9.01e-01
|
0.05770
|
-5.33e-02
|
-0.022000
|
5.55e-01
|
8.07e-01
|
SLC-mediated transmembrane transport
|
238
|
2.58e-01
|
4.73e-01
|
0.05750
|
1.32e-02
|
-0.055900
|
7.25e-01
|
1.37e-01
|
Nicotinate metabolism
|
29
|
8.58e-01
|
9.12e-01
|
0.05720
|
5.71e-02
|
-0.002870
|
5.94e-01
|
9.79e-01
|
Fatty acyl-CoA biosynthesis
|
36
|
8.27e-01
|
8.99e-01
|
0.05720
|
3.07e-03
|
-0.057100
|
9.75e-01
|
5.53e-01
|
Activation of GABAB receptors
|
43
|
8.36e-01
|
9.01e-01
|
0.05660
|
-2.42e-02
|
-0.051100
|
7.84e-01
|
5.62e-01
|
GABA B receptor activation
|
43
|
8.36e-01
|
9.01e-01
|
0.05660
|
-2.42e-02
|
-0.051100
|
7.84e-01
|
5.62e-01
|
Signaling by RAF1 mutants
|
37
|
7.98e-01
|
8.80e-01
|
0.05640
|
-3.31e-02
|
0.045600
|
7.28e-01
|
6.31e-01
|
Paradoxical activation of RAF signaling by kinase inactive BRAF
|
41
|
8.00e-01
|
8.80e-01
|
0.05630
|
-1.13e-02
|
0.055100
|
9.00e-01
|
5.41e-01
|
Signaling by RAS mutants
|
41
|
8.00e-01
|
8.80e-01
|
0.05630
|
-1.13e-02
|
0.055100
|
9.00e-01
|
5.41e-01
|
Signaling by moderate kinase activity BRAF mutants
|
41
|
8.00e-01
|
8.80e-01
|
0.05630
|
-1.13e-02
|
0.055100
|
9.00e-01
|
5.41e-01
|
Signaling downstream of RAS mutants
|
41
|
8.00e-01
|
8.80e-01
|
0.05630
|
-1.13e-02
|
0.055100
|
9.00e-01
|
5.41e-01
|
Insulin receptor signalling cascade
|
53
|
7.41e-01
|
8.59e-01
|
0.05620
|
-1.74e-02
|
0.053400
|
8.26e-01
|
5.01e-01
|
Aflatoxin activation and detoxification
|
19
|
9.21e-01
|
9.53e-01
|
0.05570
|
-1.51e-02
|
-0.053600
|
9.09e-01
|
6.86e-01
|
Activation of G protein gated Potassium channels
|
29
|
8.89e-01
|
9.31e-01
|
0.05570
|
-2.32e-02
|
-0.050600
|
8.29e-01
|
6.37e-01
|
G protein gated Potassium channels
|
29
|
8.89e-01
|
9.31e-01
|
0.05570
|
-2.32e-02
|
-0.050600
|
8.29e-01
|
6.37e-01
|
Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits
|
29
|
8.89e-01
|
9.31e-01
|
0.05570
|
-2.32e-02
|
-0.050600
|
8.29e-01
|
6.37e-01
|
EPHB-mediated forward signaling
|
34
|
8.54e-01
|
9.10e-01
|
0.05540
|
5.37e-03
|
0.055100
|
9.57e-01
|
5.78e-01
|
Glycogen synthesis
|
13
|
9.43e-01
|
9.65e-01
|
0.05510
|
5.46e-02
|
0.007370
|
7.33e-01
|
9.63e-01
|
Signal attenuation
|
10
|
9.55e-01
|
9.73e-01
|
0.05500
|
4.34e-03
|
0.054800
|
9.81e-01
|
7.64e-01
|
RET signaling
|
41
|
7.90e-01
|
8.78e-01
|
0.05500
|
-4.57e-02
|
0.030600
|
6.13e-01
|
7.35e-01
|
Deadenylation-dependent mRNA decay
|
56
|
8.14e-01
|
8.90e-01
|
0.05470
|
4.09e-02
|
0.036400
|
5.97e-01
|
6.37e-01
|
Striated Muscle Contraction
|
33
|
8.84e-01
|
9.30e-01
|
0.05470
|
-2.94e-02
|
-0.046100
|
7.70e-01
|
6.47e-01
|
Cell death signalling via NRAGE, NRIF and NADE
|
69
|
7.80e-01
|
8.74e-01
|
0.05430
|
4.07e-02
|
0.035900
|
5.58e-01
|
6.06e-01
|
GPCR ligand binding
|
443
|
2.05e-01
|
4.02e-01
|
0.05350
|
-4.63e-02
|
-0.026900
|
9.45e-02
|
3.31e-01
|
Formation of the beta-catenin:TCF transactivating complex
|
32
|
8.65e-01
|
9.16e-01
|
0.05330
|
5.33e-02
|
-0.001350
|
6.02e-01
|
9.89e-01
|
Signaling by ERBB2 KD Mutants
|
24
|
8.80e-01
|
9.28e-01
|
0.05260
|
-3.46e-02
|
0.039600
|
7.69e-01
|
7.37e-01
|
Signaling by ERBB4
|
57
|
8.23e-01
|
8.98e-01
|
0.05250
|
3.07e-02
|
0.042500
|
6.88e-01
|
5.78e-01
|
IRS-related events triggered by IGF1R
|
50
|
7.67e-01
|
8.69e-01
|
0.05240
|
-3.65e-02
|
0.037600
|
6.56e-01
|
6.45e-01
|
Interleukin-15 signaling
|
13
|
9.55e-01
|
9.73e-01
|
0.05240
|
4.63e-02
|
0.024500
|
7.73e-01
|
8.78e-01
|
Transport of small molecules
|
689
|
5.71e-02
|
1.77e-01
|
0.05230
|
-1.56e-03
|
-0.052300
|
9.44e-01
|
1.90e-02
|
Regulation of pyruvate dehydrogenase (PDH) complex
|
14
|
9.42e-01
|
9.65e-01
|
0.05190
|
5.19e-02
|
-0.000172
|
7.37e-01
|
9.99e-01
|
Post NMDA receptor activation events
|
58
|
7.81e-01
|
8.74e-01
|
0.05170
|
-5.17e-02
|
0.001160
|
4.96e-01
|
9.88e-01
|
Activation of kainate receptors upon glutamate binding
|
29
|
9.11e-01
|
9.45e-01
|
0.05120
|
-3.88e-02
|
-0.033500
|
7.18e-01
|
7.55e-01
|
RAF activation
|
33
|
8.50e-01
|
9.07e-01
|
0.05100
|
-2.55e-02
|
0.044200
|
8.00e-01
|
6.60e-01
|
CD28 dependent PI3K/Akt signaling
|
22
|
9.03e-01
|
9.38e-01
|
0.05100
|
-4.85e-02
|
0.015900
|
6.94e-01
|
8.97e-01
|
Cilium Assembly
|
174
|
5.19e-01
|
7.04e-01
|
0.05070
|
7.47e-03
|
0.050200
|
8.65e-01
|
2.53e-01
|
RHO GTPases activate PKNs
|
34
|
8.49e-01
|
9.07e-01
|
0.05010
|
-3.01e-02
|
0.040100
|
7.61e-01
|
6.86e-01
|
DAP12 interactions
|
40
|
8.82e-01
|
9.29e-01
|
0.04950
|
-4.33e-02
|
-0.023900
|
6.35e-01
|
7.94e-01
|
Transcriptional Regulation by NPAS4
|
33
|
8.77e-01
|
9.26e-01
|
0.04890
|
4.86e-02
|
-0.005750
|
6.29e-01
|
9.54e-01
|
Nucleotide catabolism
|
35
|
8.80e-01
|
9.28e-01
|
0.04840
|
-4.84e-02
|
-0.001650
|
6.20e-01
|
9.87e-01
|
PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling
|
104
|
6.59e-01
|
8.03e-01
|
0.04820
|
-1.08e-02
|
0.046900
|
8.50e-01
|
4.08e-01
|
Activation of NMDA receptors and postsynaptic events
|
69
|
7.96e-01
|
8.80e-01
|
0.04770
|
-4.70e-02
|
-0.008450
|
5.00e-01
|
9.03e-01
|
PI-3K cascade:FGFR4
|
19
|
9.49e-01
|
9.69e-01
|
0.04750
|
3.34e-02
|
0.033800
|
8.01e-01
|
7.99e-01
|
The canonical retinoid cycle in rods (twilight vision)
|
23
|
9.37e-01
|
9.63e-01
|
0.04740
|
-3.96e-02
|
-0.026000
|
7.42e-01
|
8.29e-01
|
Metabolism of water-soluble vitamins and cofactors
|
118
|
7.04e-01
|
8.35e-01
|
0.04700
|
1.60e-02
|
0.044200
|
7.64e-01
|
4.07e-01
|
Diseases of metabolism
|
234
|
5.01e-01
|
6.92e-01
|
0.04680
|
-4.43e-02
|
-0.015100
|
2.43e-01
|
6.91e-01
|
Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding
|
38
|
8.89e-01
|
9.31e-01
|
0.04670
|
1.08e-02
|
0.045500
|
9.09e-01
|
6.27e-01
|
Late SARS-CoV-2 Infection Events
|
67
|
7.57e-01
|
8.65e-01
|
0.04670
|
-2.61e-02
|
0.038700
|
7.12e-01
|
5.83e-01
|
RHOA GTPase cycle
|
140
|
5.69e-01
|
7.43e-01
|
0.04610
|
-3.86e-02
|
0.025300
|
4.31e-01
|
6.06e-01
|
Voltage gated Potassium channels
|
42
|
8.48e-01
|
9.07e-01
|
0.04600
|
-2.05e-02
|
0.041200
|
8.18e-01
|
6.44e-01
|
VxPx cargo-targeting to cilium
|
20
|
9.43e-01
|
9.65e-01
|
0.04590
|
-1.18e-02
|
-0.044300
|
9.27e-01
|
7.31e-01
|
Repression of WNT target genes
|
13
|
9.49e-01
|
9.69e-01
|
0.04550
|
3.56e-02
|
-0.028400
|
8.24e-01
|
8.59e-01
|
Downregulation of TGF-beta receptor signaling
|
26
|
9.26e-01
|
9.56e-01
|
0.04530
|
8.61e-03
|
0.044400
|
9.39e-01
|
6.95e-01
|
p75 NTR receptor-mediated signalling
|
89
|
8.05e-01
|
8.82e-01
|
0.04400
|
3.76e-02
|
0.022800
|
5.39e-01
|
7.10e-01
|
Platelet degranulation
|
115
|
7.46e-01
|
8.60e-01
|
0.04260
|
-4.13e-02
|
-0.010300
|
4.44e-01
|
8.48e-01
|
Neuronal System
|
371
|
4.48e-01
|
6.57e-01
|
0.04230
|
-2.77e-02
|
-0.031900
|
3.58e-01
|
2.91e-01
|
Sialic acid metabolism
|
33
|
9.28e-01
|
9.57e-01
|
0.04180
|
1.82e-02
|
0.037600
|
8.56e-01
|
7.09e-01
|
Gluconeogenesis
|
32
|
9.20e-01
|
9.53e-01
|
0.04170
|
4.77e-03
|
0.041500
|
9.63e-01
|
6.85e-01
|
Semaphorin interactions
|
61
|
8.49e-01
|
9.07e-01
|
0.04150
|
1.39e-03
|
0.041500
|
9.85e-01
|
5.75e-01
|
Signal Transduction
|
2409
|
1.28e-03
|
8.96e-03
|
0.04080
|
-1.59e-02
|
0.037500
|
1.97e-01
|
2.40e-03
|
Tandem pore domain potassium channels
|
12
|
9.76e-01
|
9.84e-01
|
0.04070
|
2.84e-02
|
0.029200
|
8.65e-01
|
8.61e-01
|
PI3K/AKT Signaling in Cancer
|
103
|
7.60e-01
|
8.67e-01
|
0.03990
|
-5.42e-03
|
0.039600
|
9.24e-01
|
4.88e-01
|
PKA-mediated phosphorylation of CREB
|
19
|
9.58e-01
|
9.75e-01
|
0.03990
|
-3.89e-02
|
-0.009130
|
7.69e-01
|
9.45e-01
|
Potassium Channels
|
102
|
8.28e-01
|
8.99e-01
|
0.03900
|
-2.78e-02
|
-0.027300
|
6.27e-01
|
6.33e-01
|
MicroRNA (miRNA) biogenesis
|
26
|
9.30e-01
|
9.58e-01
|
0.03880
|
-1.58e-02
|
0.035500
|
8.89e-01
|
7.54e-01
|
Signaling by TGFB family members
|
118
|
8.01e-01
|
8.80e-01
|
0.03870
|
3.28e-02
|
0.020600
|
5.39e-01
|
6.99e-01
|
G alpha (z) signalling events
|
48
|
8.77e-01
|
9.26e-01
|
0.03810
|
-3.34e-02
|
0.018300
|
6.89e-01
|
8.27e-01
|
Signaling by ERBB2 in Cancer
|
25
|
9.45e-01
|
9.66e-01
|
0.03720
|
-2.38e-03
|
0.037100
|
9.84e-01
|
7.48e-01
|
Physiological factors
|
14
|
9.65e-01
|
9.79e-01
|
0.03690
|
1.81e-02
|
-0.032100
|
9.07e-01
|
8.35e-01
|
Metabolism of vitamins and cofactors
|
181
|
7.36e-01
|
8.55e-01
|
0.03670
|
3.16e-02
|
0.018600
|
4.63e-01
|
6.66e-01
|
PI3K Cascade
|
43
|
9.09e-01
|
9.44e-01
|
0.03650
|
-4.44e-03
|
0.036200
|
9.60e-01
|
6.81e-01
|
Intra-Golgi and retrograde Golgi-to-ER traffic
|
181
|
7.55e-01
|
8.65e-01
|
0.03540
|
2.03e-02
|
0.029000
|
6.37e-01
|
5.01e-01
|
Developmental Biology
|
1027
|
2.05e-01
|
4.02e-01
|
0.03530
|
3.13e-02
|
0.016400
|
8.87e-02
|
3.71e-01
|
COPI-dependent Golgi-to-ER retrograde traffic
|
81
|
8.36e-01
|
9.01e-01
|
0.03440
|
-1.63e-02
|
0.030200
|
7.99e-01
|
6.38e-01
|
Acetylcholine Neurotransmitter Release Cycle
|
16
|
9.65e-01
|
9.79e-01
|
0.03410
|
2.90e-02
|
-0.017900
|
8.41e-01
|
9.01e-01
|
Frs2-mediated activation
|
12
|
9.74e-01
|
9.84e-01
|
0.03370
|
2.75e-02
|
-0.019400
|
8.69e-01
|
9.07e-01
|
PKA activation in glucagon signalling
|
17
|
9.75e-01
|
9.84e-01
|
0.03350
|
-3.03e-02
|
-0.014500
|
8.29e-01
|
9.18e-01
|
RHOD GTPase cycle
|
48
|
9.14e-01
|
9.48e-01
|
0.03320
|
-3.28e-02
|
0.005450
|
6.94e-01
|
9.48e-01
|
HS-GAG degradation
|
18
|
9.71e-01
|
9.83e-01
|
0.03240
|
7.65e-04
|
0.032300
|
9.96e-01
|
8.12e-01
|
Amino acid transport across the plasma membrane
|
30
|
9.41e-01
|
9.65e-01
|
0.03230
|
2.40e-02
|
-0.021500
|
8.20e-01
|
8.39e-01
|
Adrenaline,noradrenaline inhibits insulin secretion
|
28
|
9.64e-01
|
9.79e-01
|
0.03220
|
-1.74e-02
|
-0.027100
|
8.73e-01
|
8.04e-01
|
SARS-CoV-1 targets host intracellular signalling and regulatory pathways
|
16
|
9.75e-01
|
9.84e-01
|
0.03170
|
1.32e-03
|
0.031600
|
9.93e-01
|
8.27e-01
|
Synthesis of IP2, IP, and Ins in the cytosol
|
13
|
9.85e-01
|
9.89e-01
|
0.02950
|
-1.04e-02
|
-0.027600
|
9.48e-01
|
8.63e-01
|
Response to elevated platelet cytosolic Ca2+
|
120
|
8.59e-01
|
9.13e-01
|
0.02880
|
-2.87e-02
|
-0.001870
|
5.87e-01
|
9.72e-01
|
Glycerophospholipid biosynthesis
|
114
|
8.63e-01
|
9.16e-01
|
0.02790
|
-2.76e-02
|
0.003500
|
6.10e-01
|
9.49e-01
|
SLC transporter disorders
|
92
|
9.02e-01
|
9.38e-01
|
0.02780
|
4.81e-03
|
0.027400
|
9.36e-01
|
6.50e-01
|
Uptake and actions of bacterial toxins
|
29
|
9.58e-01
|
9.75e-01
|
0.02760
|
2.07e-02
|
-0.018300
|
8.47e-01
|
8.64e-01
|
RHO GTPases Activate ROCKs
|
19
|
9.75e-01
|
9.84e-01
|
0.02650
|
1.63e-02
|
-0.020900
|
9.02e-01
|
8.74e-01
|
Ion homeostasis
|
50
|
9.58e-01
|
9.75e-01
|
0.02650
|
-1.92e-02
|
-0.018200
|
8.14e-01
|
8.23e-01
|
Trafficking of GluR2-containing AMPA receptors
|
15
|
9.80e-01
|
9.86e-01
|
0.02650
|
1.33e-02
|
-0.022900
|
9.29e-01
|
8.78e-01
|
Constitutive Signaling by Aberrant PI3K in Cancer
|
77
|
9.34e-01
|
9.60e-01
|
0.02490
|
4.95e-03
|
0.024400
|
9.40e-01
|
7.11e-01
|
Neurotransmitter receptors and postsynaptic signal transmission
|
175
|
8.45e-01
|
9.07e-01
|
0.02490
|
-2.49e-02
|
-0.000632
|
5.70e-01
|
9.88e-01
|
Platelet calcium homeostasis
|
27
|
9.69e-01
|
9.82e-01
|
0.02480
|
-2.16e-02
|
0.012200
|
8.46e-01
|
9.13e-01
|
Metabolism of lipids
|
696
|
4.80e-01
|
6.78e-01
|
0.02420
|
-2.18e-02
|
0.010400
|
3.25e-01
|
6.41e-01
|
PIWI-interacting RNA (piRNA) biogenesis
|
29
|
9.75e-01
|
9.84e-01
|
0.02360
|
2.36e-02
|
-0.000603
|
8.26e-01
|
9.96e-01
|
Meiotic recombination
|
26
|
9.83e-01
|
9.89e-01
|
0.02150
|
-6.15e-03
|
-0.020600
|
9.57e-01
|
8.56e-01
|
Mitochondrial calcium ion transport
|
22
|
9.88e-01
|
9.90e-01
|
0.02120
|
1.16e-02
|
0.017700
|
9.25e-01
|
8.86e-01
|
Dopamine Neurotransmitter Release Cycle
|
20
|
9.87e-01
|
9.90e-01
|
0.02100
|
-2.09e-02
|
-0.002740
|
8.72e-01
|
9.83e-01
|
Interleukin-2 family signaling
|
40
|
9.79e-01
|
9.85e-01
|
0.02100
|
-1.38e-02
|
-0.015800
|
8.80e-01
|
8.62e-01
|
PKA activation
|
18
|
9.89e-01
|
9.91e-01
|
0.02050
|
-5.23e-03
|
-0.019800
|
9.69e-01
|
8.84e-01
|
Norepinephrine Neurotransmitter Release Cycle
|
16
|
9.93e-01
|
9.94e-01
|
0.01770
|
-1.63e-02
|
-0.007050
|
9.10e-01
|
9.61e-01
|
Diseases of carbohydrate metabolism
|
30
|
9.87e-01
|
9.90e-01
|
0.01540
|
-7.67e-03
|
0.013400
|
9.42e-01
|
8.99e-01
|
Transport of bile salts and organic acids, metal ions and amine compounds
|
84
|
9.70e-01
|
9.82e-01
|
0.01440
|
4.06e-03
|
-0.013800
|
9.49e-01
|
8.27e-01
|
Costimulation by the CD28 family
|
65
|
9.78e-01
|
9.85e-01
|
0.01340
|
9.17e-03
|
-0.009810
|
8.98e-01
|
8.91e-01
|
Golgi-to-ER retrograde transport
|
115
|
9.74e-01
|
9.84e-01
|
0.01330
|
6.16e-03
|
0.011800
|
9.09e-01
|
8.26e-01
|
Transmission across Chemical Synapses
|
237
|
9.60e-01
|
9.76e-01
|
0.01140
|
-1.05e-02
|
-0.004450
|
7.80e-01
|
9.06e-01
|
Class A/1 (Rhodopsin-like receptors)
|
311
|
9.29e-01
|
9.58e-01
|
0.01110
|
8.08e-03
|
-0.007640
|
8.06e-01
|
8.17e-01
|
Transport of vitamins, nucleosides, and related molecules
|
38
|
9.93e-01
|
9.94e-01
|
0.01060
|
1.33e-03
|
-0.010500
|
9.89e-01
|
9.11e-01
|
TGF-beta receptor signaling activates SMADs
|
45
|
9.94e-01
|
9.94e-01
|
0.00892
|
8.33e-03
|
-0.003190
|
9.23e-01
|
9.70e-01
|