Peptide chain elongation
|
87
|
7.78e-50
|
2.35e-47
|
0.93400
|
0.740000
|
-5.70e-01
|
6.05e-33
|
3.91e-20
|
SARS-CoV-1 modulates host translation machinery
|
36
|
5.10e-21
|
1.97e-19
|
0.93400
|
0.761000
|
-5.42e-01
|
2.71e-15
|
1.83e-08
|
Eukaryotic Translation Elongation
|
92
|
2.53e-52
|
3.71e-49
|
0.93100
|
0.731000
|
-5.77e-01
|
6.43e-34
|
1.11e-21
|
Viral mRNA Translation
|
87
|
4.69e-48
|
8.61e-46
|
0.91700
|
0.725000
|
-5.62e-01
|
1.17e-31
|
1.27e-19
|
Formation of a pool of free 40S subunits
|
99
|
4.01e-51
|
2.33e-48
|
0.88700
|
0.705000
|
-5.38e-01
|
5.90e-34
|
2.01e-20
|
Selenocysteine synthesis
|
91
|
2.61e-46
|
3.49e-44
|
0.88000
|
0.707000
|
-5.25e-01
|
1.90e-31
|
4.65e-18
|
Eukaryotic Translation Termination
|
91
|
8.08e-46
|
9.89e-44
|
0.87600
|
0.682000
|
-5.49e-01
|
2.03e-29
|
1.33e-19
|
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC)
|
93
|
3.46e-45
|
3.91e-43
|
0.86000
|
0.673000
|
-5.36e-01
|
2.81e-29
|
4.21e-19
|
L13a-mediated translational silencing of Ceruloplasmin expression
|
109
|
4.75e-51
|
2.33e-48
|
0.84500
|
0.664000
|
-5.24e-01
|
4.22e-33
|
3.29e-21
|
GTP hydrolysis and joining of the 60S ribosomal subunit
|
110
|
7.99e-50
|
2.35e-47
|
0.83100
|
0.652000
|
-5.16e-01
|
3.00e-32
|
8.03e-21
|
Response of EIF2AK4 (GCN2) to amino acid deficiency
|
99
|
9.95e-45
|
1.04e-42
|
0.83000
|
0.652000
|
-5.13e-01
|
3.07e-29
|
1.12e-18
|
Formation of the ternary complex, and subsequently, the 43S complex
|
51
|
5.47e-23
|
2.51e-21
|
0.82200
|
0.656000
|
-4.95e-01
|
4.84e-16
|
9.59e-10
|
Cap-dependent Translation Initiation
|
117
|
2.09e-48
|
4.38e-46
|
0.79500
|
0.612000
|
-5.07e-01
|
2.63e-30
|
2.45e-21
|
Eukaryotic Translation Initiation
|
117
|
2.09e-48
|
4.38e-46
|
0.79500
|
0.612000
|
-5.07e-01
|
2.63e-30
|
2.45e-21
|
SRP-dependent cotranslational protein targeting to membrane
|
110
|
2.40e-42
|
2.21e-40
|
0.76600
|
0.553000
|
-5.30e-01
|
1.09e-23
|
7.90e-22
|
FCGR activation
|
19
|
5.24e-08
|
6.75e-07
|
0.76500
|
-0.707000
|
-2.90e-01
|
9.31e-08
|
2.85e-02
|
Translation initiation complex formation
|
58
|
1.73e-22
|
7.71e-21
|
0.76200
|
0.598000
|
-4.72e-01
|
3.09e-15
|
4.82e-10
|
Selenoamino acid metabolism
|
113
|
6.20e-43
|
6.07e-41
|
0.76100
|
0.579000
|
-4.94e-01
|
1.90e-26
|
1.17e-19
|
Gluconeogenesis
|
27
|
6.66e-11
|
1.53e-09
|
0.75700
|
-0.507000
|
-5.63e-01
|
5.09e-06
|
4.18e-07
|
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S
|
59
|
2.15e-22
|
9.27e-21
|
0.75400
|
0.582000
|
-4.80e-01
|
9.88e-15
|
1.86e-10
|
Ribosomal scanning and start codon recognition
|
58
|
8.44e-22
|
3.54e-20
|
0.75000
|
0.581000
|
-4.75e-01
|
1.94e-14
|
3.87e-10
|
Classical antibody-mediated complement activation
|
13
|
1.63e-05
|
1.09e-04
|
0.75000
|
-0.713000
|
-2.32e-01
|
8.45e-06
|
1.48e-01
|
Formation of tubulin folding intermediates by CCT/TriC
|
21
|
3.16e-08
|
4.38e-07
|
0.74300
|
0.355000
|
-6.53e-01
|
4.82e-03
|
2.21e-07
|
Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane
|
13
|
2.92e-05
|
1.86e-04
|
0.73400
|
0.252000
|
-6.89e-01
|
1.15e-01
|
1.68e-05
|
SARS-CoV-2 modulates host translation machinery
|
49
|
1.95e-17
|
5.85e-16
|
0.72700
|
0.608000
|
-3.98e-01
|
1.70e-13
|
1.47e-06
|
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC)
|
113
|
6.45e-39
|
4.99e-37
|
0.72400
|
0.561000
|
-4.58e-01
|
6.39e-25
|
4.17e-17
|
Nonsense-Mediated Decay (NMD)
|
113
|
6.45e-39
|
4.99e-37
|
0.72400
|
0.561000
|
-4.58e-01
|
6.39e-25
|
4.17e-17
|
Expression and translocation of olfactory receptors
|
21
|
9.15e-08
|
1.08e-06
|
0.71500
|
0.677000
|
2.31e-01
|
7.80e-08
|
6.63e-02
|
Prefoldin mediated transfer of substrate to CCT/TriC
|
25
|
1.07e-08
|
1.63e-07
|
0.70300
|
0.375000
|
-5.94e-01
|
1.17e-03
|
2.70e-07
|
Scavenging of heme from plasma
|
13
|
1.00e-04
|
5.79e-04
|
0.68400
|
-0.517000
|
-4.48e-01
|
1.24e-03
|
5.20e-03
|
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding
|
28
|
3.46e-09
|
6.12e-08
|
0.68400
|
0.355000
|
-5.85e-01
|
1.16e-03
|
8.39e-08
|
Folding of actin by CCT/TriC
|
10
|
1.12e-03
|
5.34e-03
|
0.67600
|
0.301000
|
-6.05e-01
|
9.88e-02
|
9.30e-04
|
Erythrocytes take up carbon dioxide and release oxygen
|
10
|
1.14e-03
|
5.42e-03
|
0.67500
|
0.374000
|
-5.62e-01
|
4.04e-02
|
2.10e-03
|
O2/CO2 exchange in erythrocytes
|
10
|
1.14e-03
|
5.42e-03
|
0.67500
|
0.374000
|
-5.62e-01
|
4.04e-02
|
2.10e-03
|
Creation of C4 and C2 activators
|
16
|
3.29e-05
|
2.05e-04
|
0.65400
|
-0.624000
|
-1.97e-01
|
1.54e-05
|
1.73e-01
|
Transport of connexons to the plasma membrane
|
14
|
1.49e-04
|
8.38e-04
|
0.64900
|
0.168000
|
-6.27e-01
|
2.76e-01
|
4.82e-05
|
Phosphorylation of CD3 and TCR zeta chains
|
11
|
1.18e-03
|
5.57e-03
|
0.63700
|
-0.518000
|
-3.70e-01
|
2.92e-03
|
3.36e-02
|
Downregulation of ERBB2:ERBB3 signaling
|
13
|
5.59e-04
|
2.85e-03
|
0.62300
|
0.386000
|
-4.88e-01
|
1.59e-02
|
2.29e-03
|
IRE1alpha activates chaperones
|
49
|
4.70e-13
|
1.28e-11
|
0.61900
|
-0.389000
|
-4.82e-01
|
2.51e-06
|
5.31e-09
|
PD-1 signaling
|
11
|
1.77e-03
|
7.86e-03
|
0.61700
|
-0.465000
|
-4.06e-01
|
7.56e-03
|
1.98e-02
|
XBP1(S) activates chaperone genes
|
47
|
2.08e-12
|
5.17e-11
|
0.61500
|
-0.394000
|
-4.72e-01
|
2.90e-06
|
2.10e-08
|
Regulation of glycolysis by fructose 2,6-bisphosphate metabolism
|
10
|
3.63e-03
|
1.46e-02
|
0.61000
|
-0.359000
|
-4.92e-01
|
4.91e-02
|
7.02e-03
|
Olfactory Signaling Pathway
|
25
|
1.04e-06
|
9.52e-06
|
0.60500
|
0.582000
|
1.64e-01
|
4.65e-07
|
1.55e-01
|
FGFR2 ligand binding and activation
|
10
|
4.42e-03
|
1.73e-02
|
0.60400
|
0.354000
|
-4.89e-01
|
5.24e-02
|
7.41e-03
|
Initial triggering of complement
|
23
|
3.97e-06
|
3.19e-05
|
0.59900
|
-0.582000
|
-1.44e-01
|
1.36e-06
|
2.32e-01
|
Transferrin endocytosis and recycling
|
28
|
2.54e-07
|
2.69e-06
|
0.59900
|
-0.377000
|
-4.65e-01
|
5.47e-04
|
2.05e-05
|
Josephin domain DUBs
|
10
|
4.81e-03
|
1.86e-02
|
0.59800
|
0.177000
|
-5.71e-01
|
3.34e-01
|
1.75e-03
|
TP53 Regulates Transcription of Death Receptors and Ligands
|
10
|
4.88e-03
|
1.87e-02
|
0.59700
|
0.193000
|
-5.65e-01
|
2.91e-01
|
1.96e-03
|
Regulation of expression of SLITs and ROBOs
|
162
|
1.79e-37
|
1.31e-35
|
0.59400
|
0.408000
|
-4.32e-01
|
3.26e-19
|
2.32e-21
|
Insulin receptor recycling
|
26
|
9.61e-07
|
9.01e-06
|
0.59400
|
-0.373000
|
-4.62e-01
|
1.01e-03
|
4.51e-05
|
Influenza Viral RNA Transcription and Replication
|
134
|
1.13e-30
|
6.14e-29
|
0.59000
|
0.461000
|
-3.67e-01
|
3.06e-20
|
2.11e-13
|
Crosslinking of collagen fibrils
|
14
|
7.07e-04
|
3.55e-03
|
0.58600
|
-0.290000
|
-5.09e-01
|
6.01e-02
|
9.84e-04
|
Mucopolysaccharidoses
|
11
|
3.73e-03
|
1.48e-02
|
0.58300
|
-0.578000
|
7.90e-02
|
9.08e-04
|
6.50e-01
|
Keratan sulfate degradation
|
13
|
1.35e-03
|
6.23e-03
|
0.58000
|
-0.275000
|
-5.11e-01
|
8.65e-02
|
1.43e-03
|
Interleukin-2 signaling
|
11
|
4.46e-03
|
1.73e-02
|
0.57000
|
-0.450000
|
-3.51e-01
|
9.78e-03
|
4.40e-02
|
Keratan sulfate biosynthesis
|
26
|
4.42e-06
|
3.47e-05
|
0.56300
|
0.044300
|
-5.61e-01
|
6.96e-01
|
7.28e-07
|
NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10
|
12
|
3.49e-03
|
1.41e-02
|
0.56200
|
-0.170000
|
5.36e-01
|
3.08e-01
|
1.30e-03
|
Glycogen synthesis
|
12
|
3.58e-03
|
1.44e-02
|
0.56200
|
0.321000
|
-4.61e-01
|
5.42e-02
|
5.67e-03
|
STAT3 nuclear events downstream of ALK signaling
|
10
|
9.06e-03
|
3.18e-02
|
0.55900
|
-0.136000
|
-5.42e-01
|
4.56e-01
|
2.99e-03
|
ABC transporters in lipid homeostasis
|
12
|
4.06e-03
|
1.61e-02
|
0.55600
|
-0.461000
|
3.10e-01
|
5.70e-03
|
6.28e-02
|
Packaging Of Telomere Ends
|
12
|
4.21e-03
|
1.66e-02
|
0.55400
|
0.434000
|
-3.45e-01
|
9.31e-03
|
3.87e-02
|
Cellular response to starvation
|
149
|
7.89e-30
|
3.99e-28
|
0.55100
|
0.359000
|
-4.19e-01
|
4.08e-14
|
1.12e-18
|
Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters
|
19
|
1.64e-04
|
9.21e-04
|
0.55100
|
-0.493000
|
-2.46e-01
|
1.97e-04
|
6.37e-02
|
Activation of Matrix Metalloproteinases
|
23
|
3.64e-05
|
2.24e-04
|
0.54300
|
-0.169000
|
-5.16e-01
|
1.62e-01
|
1.81e-05
|
WNT5A-dependent internalization of FZD2, FZD5 and ROR2
|
13
|
3.46e-03
|
1.40e-02
|
0.53700
|
-0.462000
|
-2.74e-01
|
3.92e-03
|
8.74e-02
|
Syndecan interactions
|
26
|
1.38e-05
|
9.31e-05
|
0.53600
|
-0.020100
|
-5.35e-01
|
8.59e-01
|
2.29e-06
|
Major pathway of rRNA processing in the nucleolus and cytosol
|
179
|
8.49e-33
|
5.20e-31
|
0.52900
|
0.404000
|
-3.40e-01
|
1.08e-20
|
4.03e-15
|
Suppression of phagosomal maturation
|
13
|
4.56e-03
|
1.77e-02
|
0.52600
|
0.038800
|
-5.25e-01
|
8.08e-01
|
1.05e-03
|
Trafficking and processing of endosomal TLR
|
12
|
7.14e-03
|
2.60e-02
|
0.52500
|
-0.507000
|
1.37e-01
|
2.35e-03
|
4.11e-01
|
Membrane binding and targetting of GAG proteins
|
14
|
3.17e-03
|
1.30e-02
|
0.52500
|
0.196000
|
-4.87e-01
|
2.05e-01
|
1.59e-03
|
Synthesis And Processing Of GAG, GAGPOL Polyproteins
|
14
|
3.17e-03
|
1.30e-02
|
0.52500
|
0.196000
|
-4.87e-01
|
2.05e-01
|
1.59e-03
|
Influenza Infection
|
153
|
1.18e-27
|
5.80e-26
|
0.52400
|
0.406000
|
-3.31e-01
|
4.57e-18
|
1.69e-12
|
Response of EIF2AK1 (HRI) to heme deficiency
|
14
|
3.34e-03
|
1.36e-02
|
0.52300
|
0.187000
|
-4.88e-01
|
2.25e-01
|
1.57e-03
|
Free fatty acids regulate insulin secretion
|
10
|
1.73e-02
|
5.56e-02
|
0.52200
|
-0.387000
|
3.50e-01
|
3.39e-02
|
5.50e-02
|
Chondroitin sulfate biosynthesis
|
16
|
1.43e-03
|
6.50e-03
|
0.52200
|
-0.057300
|
-5.19e-01
|
6.92e-01
|
3.25e-04
|
Collagen degradation
|
54
|
2.71e-10
|
5.61e-09
|
0.52000
|
-0.277000
|
-4.40e-01
|
4.41e-04
|
2.18e-08
|
rRNA processing in the nucleus and cytosol
|
189
|
2.19e-33
|
1.46e-31
|
0.51900
|
0.397000
|
-3.35e-01
|
5.24e-21
|
2.09e-15
|
Role of LAT2/NTAL/LAB on calcium mobilization
|
20
|
3.63e-04
|
1.92e-03
|
0.51300
|
-0.498000
|
-1.24e-01
|
1.16e-04
|
3.38e-01
|
The role of GTSE1 in G2/M progression after G2 checkpoint
|
70
|
1.23e-12
|
3.11e-11
|
0.51300
|
0.093000
|
-5.04e-01
|
1.79e-01
|
3.00e-13
|
Striated Muscle Contraction
|
30
|
7.21e-06
|
5.37e-05
|
0.51100
|
-0.314000
|
-4.03e-01
|
2.92e-03
|
1.32e-04
|
Formation of ATP by chemiosmotic coupling
|
16
|
1.97e-03
|
8.63e-03
|
0.51100
|
0.114000
|
-4.98e-01
|
4.30e-01
|
5.65e-04
|
ATF6 (ATF6-alpha) activates chaperones
|
12
|
9.39e-03
|
3.28e-02
|
0.50900
|
-0.052400
|
-5.06e-01
|
7.53e-01
|
2.39e-03
|
Role of phospholipids in phagocytosis
|
30
|
9.25e-06
|
6.53e-05
|
0.50600
|
-0.451000
|
-2.30e-01
|
1.93e-05
|
2.92e-02
|
Aggrephagy
|
34
|
2.50e-06
|
2.13e-05
|
0.50500
|
0.326000
|
-3.86e-01
|
1.00e-03
|
9.70e-05
|
Collagen biosynthesis and modifying enzymes
|
60
|
9.42e-11
|
2.10e-09
|
0.50500
|
-0.220000
|
-4.55e-01
|
3.26e-03
|
1.08e-09
|
Interleukin-10 signaling
|
35
|
1.80e-06
|
1.58e-05
|
0.50000
|
-0.288000
|
-4.09e-01
|
3.14e-03
|
2.87e-05
|
Transcriptional regulation of pluripotent stem cells
|
16
|
2.57e-03
|
1.08e-02
|
0.50000
|
0.488000
|
-1.07e-01
|
7.24e-04
|
4.60e-01
|
HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand
|
49
|
1.35e-08
|
1.98e-07
|
0.49900
|
0.373000
|
-3.32e-01
|
6.23e-06
|
5.90e-05
|
Translation
|
291
|
8.07e-47
|
1.32e-44
|
0.49800
|
0.295000
|
-4.01e-01
|
4.61e-18
|
5.85e-32
|
Ubiquitin-dependent degradation of Cyclin D
|
50
|
9.45e-09
|
1.46e-07
|
0.49700
|
0.047300
|
-4.95e-01
|
5.63e-01
|
1.39e-09
|
Keratan sulfate/keratin metabolism
|
32
|
7.04e-06
|
5.28e-05
|
0.49700
|
-0.098000
|
-4.87e-01
|
3.38e-01
|
1.87e-06
|
rRNA processing
|
199
|
3.82e-32
|
2.25e-30
|
0.49600
|
0.379000
|
-3.21e-01
|
3.34e-20
|
6.04e-15
|
Diseases associated with glycosaminoglycan metabolism
|
38
|
9.32e-07
|
8.93e-06
|
0.49400
|
-0.014800
|
-4.94e-01
|
8.74e-01
|
1.39e-07
|
Diseases associated with glycosylation precursor biosynthesis
|
15
|
4.42e-03
|
1.73e-02
|
0.49000
|
-0.064900
|
-4.86e-01
|
6.63e-01
|
1.11e-03
|
Post-chaperonin tubulin folding pathway
|
18
|
1.77e-03
|
7.86e-03
|
0.48600
|
0.207000
|
-4.40e-01
|
1.28e-01
|
1.23e-03
|
Zinc transporters
|
10
|
2.83e-02
|
8.24e-02
|
0.48600
|
-0.205000
|
-4.41e-01
|
2.62e-01
|
1.58e-02
|
TRAF3-dependent IRF activation pathway
|
13
|
1.05e-02
|
3.58e-02
|
0.48500
|
-0.438000
|
2.08e-01
|
6.21e-03
|
1.93e-01
|
Regulation of RUNX3 expression and activity
|
55
|
4.03e-09
|
7.05e-08
|
0.48400
|
-0.035800
|
-4.83e-01
|
6.46e-01
|
5.78e-10
|
TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway
|
13
|
1.03e-02
|
3.53e-02
|
0.48200
|
-0.365000
|
-3.16e-01
|
2.28e-02
|
4.89e-02
|
Signaling by ROBO receptors
|
201
|
2.55e-30
|
1.34e-28
|
0.48000
|
0.313000
|
-3.63e-01
|
1.95e-14
|
7.41e-19
|
The canonical retinoid cycle in rods (twilight vision)
|
11
|
2.37e-02
|
7.13e-02
|
0.47800
|
-0.157000
|
4.51e-01
|
3.68e-01
|
9.57e-03
|
SARS-CoV-2 modulates autophagy
|
11
|
2.34e-02
|
7.09e-02
|
0.47700
|
-0.477000
|
1.46e-02
|
6.14e-03
|
9.33e-01
|
Assembly of active LPL and LIPC lipase complexes
|
12
|
1.61e-02
|
5.19e-02
|
0.47700
|
-0.282000
|
-3.85e-01
|
9.08e-02
|
2.10e-02
|
Diseases associated with N-glycosylation of proteins
|
20
|
1.04e-03
|
5.03e-03
|
0.47700
|
-0.395000
|
-2.67e-01
|
2.21e-03
|
3.90e-02
|
Regulation of ornithine decarboxylase (ODC)
|
48
|
8.51e-08
|
1.02e-06
|
0.47600
|
0.019200
|
-4.76e-01
|
8.19e-01
|
1.17e-08
|
Assembly Of The HIV Virion
|
16
|
4.46e-03
|
1.73e-02
|
0.47600
|
0.124000
|
-4.60e-01
|
3.89e-01
|
1.46e-03
|
Ubiquitin Mediated Degradation of Phosphorylated Cdc25A
|
49
|
6.54e-08
|
8.01e-07
|
0.47500
|
0.024600
|
-4.74e-01
|
7.66e-01
|
9.10e-09
|
p53-Independent DNA Damage Response
|
49
|
6.54e-08
|
8.01e-07
|
0.47500
|
0.024600
|
-4.74e-01
|
7.66e-01
|
9.10e-09
|
p53-Independent G1/S DNA damage checkpoint
|
49
|
6.54e-08
|
8.01e-07
|
0.47500
|
0.024600
|
-4.74e-01
|
7.66e-01
|
9.10e-09
|
Regulation of activated PAK-2p34 by proteasome mediated degradation
|
48
|
9.44e-08
|
1.11e-06
|
0.47500
|
0.044200
|
-4.73e-01
|
5.96e-01
|
1.45e-08
|
ATF6 (ATF6-alpha) activates chaperone genes
|
10
|
3.56e-02
|
9.82e-02
|
0.47200
|
0.005660
|
-4.72e-01
|
9.75e-01
|
9.79e-03
|
TNFs bind their physiological receptors
|
19
|
1.70e-03
|
7.60e-03
|
0.47200
|
-0.431000
|
-1.92e-01
|
1.15e-03
|
1.47e-01
|
Defective CFTR causes cystic fibrosis
|
58
|
4.19e-09
|
7.16e-08
|
0.47100
|
-0.006000
|
-4.71e-01
|
9.37e-01
|
5.30e-10
|
Hh mutants are degraded by ERAD
|
53
|
2.25e-08
|
3.17e-07
|
0.47100
|
-0.009150
|
-4.71e-01
|
9.08e-01
|
2.98e-09
|
Scavenging by Class A Receptors
|
16
|
4.84e-03
|
1.86e-02
|
0.47100
|
-0.468000
|
-5.23e-02
|
1.19e-03
|
7.17e-01
|
SUMOylation of immune response proteins
|
11
|
2.58e-02
|
7.64e-02
|
0.46900
|
-0.236000
|
-4.05e-01
|
1.74e-01
|
2.00e-02
|
Synthesis of PIPs at the Golgi membrane
|
15
|
7.40e-03
|
2.67e-02
|
0.46900
|
-0.406000
|
2.34e-01
|
6.42e-03
|
1.17e-01
|
Autodegradation of the E3 ubiquitin ligase COP1
|
49
|
1.04e-07
|
1.20e-06
|
0.46800
|
0.032000
|
-4.67e-01
|
6.99e-01
|
1.51e-08
|
FBXL7 down-regulates AURKA during mitotic entry and in early mitosis
|
53
|
3.15e-08
|
4.38e-07
|
0.46700
|
0.037700
|
-4.65e-01
|
6.35e-01
|
4.56e-09
|
HSF1 activation
|
25
|
3.07e-04
|
1.65e-03
|
0.46700
|
0.302000
|
-3.56e-01
|
8.99e-03
|
2.06e-03
|
RUNX3 regulates p14-ARF
|
10
|
3.84e-02
|
1.04e-01
|
0.46400
|
-0.245000
|
-3.95e-01
|
1.80e-01
|
3.07e-02
|
Degradation of DVL
|
55
|
2.08e-08
|
2.97e-07
|
0.46400
|
0.043000
|
-4.62e-01
|
5.82e-01
|
3.09e-09
|
Chemokine receptors bind chemokines
|
36
|
8.90e-06
|
6.32e-05
|
0.46300
|
-0.131000
|
-4.44e-01
|
1.73e-01
|
3.96e-06
|
Vif-mediated degradation of APOBEC3G
|
52
|
6.16e-08
|
7.74e-07
|
0.46200
|
0.057700
|
-4.59e-01
|
4.72e-01
|
1.04e-08
|
AUF1 (hnRNP D0) binds and destabilizes mRNA
|
53
|
5.51e-08
|
7.04e-07
|
0.46000
|
0.076700
|
-4.53e-01
|
3.34e-01
|
1.14e-08
|
The role of Nef in HIV-1 replication and disease pathogenesis
|
26
|
2.57e-04
|
1.40e-03
|
0.46000
|
-0.447000
|
-1.08e-01
|
8.01e-05
|
3.41e-01
|
Retrograde neurotrophin signalling
|
14
|
1.18e-02
|
3.99e-02
|
0.45800
|
-0.421000
|
-1.82e-01
|
6.43e-03
|
2.38e-01
|
FGFR2 mutant receptor activation
|
24
|
5.75e-04
|
2.92e-03
|
0.45700
|
0.173000
|
-4.23e-01
|
1.43e-01
|
3.34e-04
|
Defective Intrinsic Pathway for Apoptosis
|
21
|
1.37e-03
|
6.31e-03
|
0.45700
|
-0.105000
|
-4.44e-01
|
4.04e-01
|
4.23e-04
|
ROS and RNS production in phagocytes
|
31
|
5.76e-05
|
3.42e-04
|
0.45600
|
-0.333000
|
-3.12e-01
|
1.31e-03
|
2.67e-03
|
Negative regulation of NOTCH4 signaling
|
54
|
5.00e-08
|
6.50e-07
|
0.45600
|
0.032900
|
-4.55e-01
|
6.76e-01
|
7.16e-09
|
SHC-mediated cascade:FGFR3
|
12
|
2.42e-02
|
7.22e-02
|
0.45600
|
0.085500
|
-4.48e-01
|
6.08e-01
|
7.27e-03
|
Assembly of collagen fibrils and other multimeric structures
|
54
|
4.76e-08
|
6.24e-07
|
0.45500
|
-0.209000
|
-4.04e-01
|
8.01e-03
|
2.73e-07
|
Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3
|
11
|
3.37e-02
|
9.37e-02
|
0.45500
|
0.421000
|
-1.73e-01
|
1.57e-02
|
3.20e-01
|
Hh mutants abrogate ligand secretion
|
55
|
4.31e-08
|
5.80e-07
|
0.45400
|
0.008800
|
-4.54e-01
|
9.10e-01
|
5.75e-09
|
Maturation of spike protein 9694548
|
37
|
1.02e-05
|
7.08e-05
|
0.45300
|
-0.300000
|
-3.40e-01
|
1.61e-03
|
3.41e-04
|
Collagen chain trimerization
|
38
|
8.01e-06
|
5.84e-05
|
0.45300
|
-0.175000
|
-4.17e-01
|
6.13e-02
|
8.53e-06
|
Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha
|
64
|
3.33e-09
|
5.96e-08
|
0.45200
|
0.064300
|
-4.48e-01
|
3.74e-01
|
5.92e-10
|
Antimicrobial peptides
|
26
|
3.63e-04
|
1.92e-03
|
0.45100
|
0.058700
|
-4.48e-01
|
6.05e-01
|
7.78e-05
|
Vpu mediated degradation of CD4
|
50
|
2.43e-07
|
2.61e-06
|
0.45100
|
0.020000
|
-4.51e-01
|
8.07e-01
|
3.48e-08
|
GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2
|
52
|
1.37e-07
|
1.52e-06
|
0.45100
|
0.021100
|
-4.50e-01
|
7.92e-01
|
1.93e-08
|
Metabolism of polyamines
|
56
|
4.40e-08
|
5.87e-07
|
0.45000
|
0.010000
|
-4.50e-01
|
8.97e-01
|
5.88e-09
|
Collagen formation
|
81
|
2.12e-11
|
5.04e-10
|
0.44900
|
-0.197000
|
-4.04e-01
|
2.24e-03
|
3.39e-10
|
Binding and Uptake of Ligands by Scavenger Receptors
|
38
|
9.86e-06
|
6.93e-05
|
0.44900
|
-0.414000
|
-1.74e-01
|
1.03e-05
|
6.36e-02
|
SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs
|
11
|
3.82e-02
|
1.03e-01
|
0.44600
|
0.194000
|
-4.02e-01
|
2.65e-01
|
2.09e-02
|
SCF-beta-TrCP mediated degradation of Emi1
|
53
|
1.37e-07
|
1.52e-06
|
0.44600
|
-0.002710
|
-4.46e-01
|
9.73e-01
|
1.89e-08
|
Attenuation phase
|
22
|
1.51e-03
|
6.82e-03
|
0.44600
|
0.294000
|
-3.35e-01
|
1.71e-02
|
6.46e-03
|
SLBP independent Processing of Histone Pre-mRNAs
|
10
|
5.20e-02
|
1.30e-01
|
0.44600
|
0.219000
|
-3.88e-01
|
2.30e-01
|
3.35e-02
|
Cross-presentation of soluble exogenous antigens (endosomes)
|
46
|
1.14e-06
|
1.04e-05
|
0.44500
|
-0.045800
|
-4.43e-01
|
5.91e-01
|
2.01e-07
|
Regulation of NPAS4 gene expression
|
12
|
2.76e-02
|
8.12e-02
|
0.44500
|
0.208000
|
3.93e-01
|
2.12e-01
|
1.83e-02
|
Dectin-1 mediated noncanonical NF-kB signaling
|
58
|
3.45e-08
|
4.73e-07
|
0.44500
|
-0.010600
|
-4.45e-01
|
8.89e-01
|
4.65e-09
|
Insertion of tail-anchored proteins into the endoplasmic reticulum membrane
|
22
|
1.55e-03
|
6.97e-03
|
0.44200
|
-0.072900
|
-4.36e-01
|
5.54e-01
|
3.97e-04
|
E3 ubiquitin ligases ubiquitinate target proteins
|
43
|
3.82e-06
|
3.11e-05
|
0.44200
|
0.289000
|
-3.35e-01
|
1.04e-03
|
1.47e-04
|
cGMP effects
|
13
|
2.15e-02
|
6.66e-02
|
0.44200
|
0.347000
|
2.74e-01
|
3.03e-02
|
8.76e-02
|
Cristae formation
|
29
|
2.30e-04
|
1.25e-03
|
0.44000
|
0.049000
|
-4.37e-01
|
6.48e-01
|
4.66e-05
|
Metabolism of Angiotensinogen to Angiotensins
|
13
|
2.28e-02
|
6.94e-02
|
0.43900
|
-0.135000
|
-4.18e-01
|
3.99e-01
|
9.05e-03
|
SHC-mediated cascade:FGFR4
|
11
|
4.24e-02
|
1.12e-01
|
0.43900
|
0.151000
|
-4.12e-01
|
3.86e-01
|
1.79e-02
|
NIK–>noncanonical NF-kB signaling
|
57
|
7.45e-08
|
9.04e-07
|
0.43900
|
-0.011000
|
-4.38e-01
|
8.86e-01
|
1.03e-08
|
Pexophagy
|
11
|
4.53e-02
|
1.17e-01
|
0.43500
|
0.326000
|
-2.88e-01
|
6.13e-02
|
9.77e-02
|
Stabilization of p53
|
54
|
2.35e-07
|
2.55e-06
|
0.43500
|
0.017600
|
-4.34e-01
|
8.23e-01
|
3.34e-08
|
Cohesin Loading onto Chromatin
|
10
|
5.85e-02
|
1.42e-01
|
0.43300
|
0.250000
|
3.54e-01
|
1.70e-01
|
5.28e-02
|
Dectin-2 family
|
14
|
2.02e-02
|
6.29e-02
|
0.43300
|
-0.251000
|
3.53e-01
|
1.05e-01
|
2.21e-02
|
Signaling by FGFR2 IIIa TM
|
19
|
5.01e-03
|
1.91e-02
|
0.43300
|
0.149000
|
-4.06e-01
|
2.61e-01
|
2.18e-03
|
Generation of second messenger molecules
|
21
|
2.64e-03
|
1.10e-02
|
0.43200
|
-0.321000
|
-2.90e-01
|
1.09e-02
|
2.16e-02
|
Cytosolic tRNA aminoacylation
|
24
|
1.18e-03
|
5.57e-03
|
0.43200
|
-0.099700
|
-4.20e-01
|
3.98e-01
|
3.64e-04
|
Regulation of BACH1 activity
|
11
|
4.70e-02
|
1.20e-01
|
0.43100
|
0.087000
|
-4.23e-01
|
6.17e-01
|
1.52e-02
|
GLI3 is processed to GLI3R by the proteasome
|
57
|
1.34e-07
|
1.52e-06
|
0.43100
|
-0.017800
|
-4.30e-01
|
8.17e-01
|
1.93e-08
|
Regulation of Apoptosis
|
51
|
7.46e-07
|
7.36e-06
|
0.43000
|
0.034400
|
-4.29e-01
|
6.71e-01
|
1.17e-07
|
DARPP-32 events
|
22
|
2.42e-03
|
1.03e-02
|
0.42800
|
0.019100
|
-4.27e-01
|
8.77e-01
|
5.23e-04
|
Cargo concentration in the ER
|
28
|
4.45e-04
|
2.30e-03
|
0.42700
|
-0.178000
|
-3.89e-01
|
1.03e-01
|
3.72e-04
|
TICAM1-dependent activation of IRF3/IRF7
|
12
|
3.74e-02
|
1.01e-01
|
0.42600
|
-0.142000
|
-4.02e-01
|
3.95e-01
|
1.59e-02
|
Unfolded Protein Response (UPR)
|
91
|
2.13e-11
|
5.04e-10
|
0.42400
|
-0.185000
|
-3.81e-01
|
2.27e-03
|
3.36e-10
|
SCF(Skp2)-mediated degradation of p27/p21
|
59
|
1.36e-07
|
1.52e-06
|
0.42400
|
0.037400
|
-4.22e-01
|
6.19e-01
|
2.07e-08
|
NF-kB is activated and signals survival
|
13
|
3.06e-02
|
8.77e-02
|
0.42300
|
0.017400
|
-4.23e-01
|
9.14e-01
|
8.31e-03
|
Gap junction assembly
|
21
|
3.65e-03
|
1.46e-02
|
0.42300
|
0.079700
|
-4.15e-01
|
5.27e-01
|
9.82e-04
|
Plasma lipoprotein assembly
|
11
|
5.39e-02
|
1.33e-01
|
0.42200
|
-0.370000
|
2.05e-01
|
3.38e-02
|
2.40e-01
|
SHC1 events in EGFR signaling
|
11
|
5.38e-02
|
1.33e-01
|
0.42100
|
-0.418000
|
5.14e-02
|
1.63e-02
|
7.68e-01
|
Degradation of GLI2 by the proteasome
|
57
|
2.66e-07
|
2.79e-06
|
0.42100
|
-0.004520
|
-4.21e-01
|
9.53e-01
|
3.76e-08
|
Phase 4 - resting membrane potential
|
11
|
5.51e-02
|
1.34e-01
|
0.42000
|
0.085200
|
-4.11e-01
|
6.25e-01
|
1.82e-02
|
Regulation of RUNX2 expression and activity
|
70
|
1.10e-08
|
1.66e-07
|
0.41900
|
0.008860
|
-4.18e-01
|
8.98e-01
|
1.41e-09
|
PINK1-PRKN Mediated Mitophagy
|
21
|
4.26e-03
|
1.67e-02
|
0.41800
|
0.219000
|
-3.56e-01
|
8.28e-02
|
4.69e-03
|
Anchoring fibril formation
|
11
|
5.48e-02
|
1.34e-01
|
0.41800
|
-0.183000
|
-3.76e-01
|
2.95e-01
|
3.07e-02
|
Pentose phosphate pathway
|
13
|
3.28e-02
|
9.18e-02
|
0.41800
|
-0.090900
|
-4.08e-01
|
5.71e-01
|
1.09e-02
|
Hedgehog ligand biogenesis
|
60
|
1.57e-07
|
1.73e-06
|
0.41800
|
-0.001760
|
-4.18e-01
|
9.81e-01
|
2.17e-08
|
Inhibition of DNA recombination at telomere
|
26
|
1.28e-03
|
5.94e-03
|
0.41500
|
0.260000
|
-3.24e-01
|
2.17e-02
|
4.26e-03
|
Regulation of Complement cascade
|
37
|
7.03e-05
|
4.14e-04
|
0.41400
|
-0.364000
|
-1.96e-01
|
1.26e-04
|
3.87e-02
|
Cleavage of the damaged purine
|
15
|
2.22e-02
|
6.79e-02
|
0.41400
|
0.301000
|
-2.83e-01
|
4.34e-02
|
5.75e-02
|
Depurination
|
15
|
2.22e-02
|
6.79e-02
|
0.41400
|
0.301000
|
-2.83e-01
|
4.34e-02
|
5.75e-02
|
Recognition and association of DNA glycosylase with site containing an affected purine
|
15
|
2.22e-02
|
6.79e-02
|
0.41400
|
0.301000
|
-2.83e-01
|
4.34e-02
|
5.75e-02
|
Activation of NF-kappaB in B cells
|
65
|
6.13e-08
|
7.74e-07
|
0.41300
|
0.007050
|
-4.13e-01
|
9.22e-01
|
8.26e-09
|
Beta-catenin phosphorylation cascade
|
17
|
1.33e-02
|
4.36e-02
|
0.41200
|
0.020700
|
-4.11e-01
|
8.83e-01
|
3.31e-03
|
Downstream TCR signaling
|
82
|
1.02e-09
|
2.00e-08
|
0.41100
|
-0.013600
|
-4.11e-01
|
8.31e-01
|
1.29e-10
|
Glucose metabolism
|
82
|
8.95e-10
|
1.80e-08
|
0.41100
|
-0.335000
|
-2.37e-01
|
1.53e-07
|
2.09e-04
|
Cellular response to hypoxia
|
72
|
1.41e-08
|
2.05e-07
|
0.41000
|
0.040300
|
-4.08e-01
|
5.54e-01
|
2.11e-09
|
Nuclear events mediated by NFE2L2
|
76
|
5.02e-09
|
8.48e-08
|
0.41000
|
0.000878
|
-4.10e-01
|
9.89e-01
|
6.33e-10
|
Other semaphorin interactions
|
19
|
8.22e-03
|
2.92e-02
|
0.41000
|
-0.406000
|
-5.86e-02
|
2.19e-03
|
6.58e-01
|
WNT5A-dependent internalization of FZD4
|
14
|
2.85e-02
|
8.26e-02
|
0.41000
|
-0.327000
|
-2.48e-01
|
3.43e-02
|
1.09e-01
|
Post-translational protein phosphorylation
|
78
|
2.89e-09
|
5.24e-08
|
0.40900
|
-0.180000
|
-3.68e-01
|
6.06e-03
|
2.00e-08
|
Sealing of the nuclear envelope (NE) by ESCRT-III
|
24
|
2.51e-03
|
1.06e-02
|
0.40900
|
0.111000
|
-3.94e-01
|
3.47e-01
|
8.44e-04
|
Degradation of GLI1 by the proteasome
|
57
|
6.47e-07
|
6.51e-06
|
0.40900
|
-0.011200
|
-4.09e-01
|
8.84e-01
|
9.53e-08
|
Degradation of cysteine and homocysteine
|
12
|
4.90e-02
|
1.25e-01
|
0.40800
|
-0.188000
|
-3.62e-01
|
2.59e-01
|
3.00e-02
|
Degradation of beta-catenin by the destruction complex
|
83
|
1.15e-09
|
2.23e-08
|
0.40800
|
0.057800
|
-4.04e-01
|
3.63e-01
|
2.03e-10
|
Interconversion of nucleotide di- and triphosphates
|
27
|
1.26e-03
|
5.89e-03
|
0.40700
|
0.107000
|
-3.93e-01
|
3.36e-01
|
4.09e-04
|
Assembly and cell surface presentation of NMDA receptors
|
34
|
2.29e-04
|
1.25e-03
|
0.40700
|
0.168000
|
-3.71e-01
|
8.94e-02
|
1.84e-04
|
SHC-mediated cascade:FGFR2
|
14
|
3.13e-02
|
8.90e-02
|
0.40700
|
0.089000
|
-3.97e-01
|
5.64e-01
|
1.01e-02
|
Activation of AMPK downstream of NMDARs
|
21
|
5.71e-03
|
2.14e-02
|
0.40700
|
0.277000
|
-2.98e-01
|
2.82e-02
|
1.79e-02
|
TRAF6 mediated IRF7 activation
|
15
|
2.51e-02
|
7.46e-02
|
0.40600
|
-0.366000
|
1.77e-01
|
1.42e-02
|
2.34e-01
|
Interleukin-15 signaling
|
14
|
3.08e-02
|
8.81e-02
|
0.40500
|
-0.314000
|
-2.57e-01
|
4.21e-02
|
9.64e-02
|
Regulation of IFNA/IFNB signaling
|
12
|
5.09e-02
|
1.28e-01
|
0.40500
|
-0.316000
|
-2.54e-01
|
5.82e-02
|
1.28e-01
|
Asymmetric localization of PCP proteins
|
61
|
3.45e-07
|
3.57e-06
|
0.40400
|
-0.017600
|
-4.03e-01
|
8.12e-01
|
5.10e-08
|
GAB1 signalosome
|
14
|
3.38e-02
|
9.38e-02
|
0.40300
|
-0.368000
|
1.65e-01
|
1.72e-02
|
2.84e-01
|
YAP1- and WWTR1 (TAZ)-stimulated gene expression
|
11
|
6.99e-02
|
1.63e-01
|
0.40300
|
0.141000
|
-3.77e-01
|
4.18e-01
|
3.02e-02
|
Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell
|
95
|
8.75e-11
|
1.98e-09
|
0.40300
|
-0.358000
|
-1.85e-01
|
1.73e-09
|
1.84e-03
|
Degradation of AXIN
|
53
|
2.75e-06
|
2.32e-05
|
0.40200
|
0.013500
|
-4.02e-01
|
8.65e-01
|
4.22e-07
|
COPI-mediated anterograde transport
|
92
|
2.26e-10
|
4.74e-09
|
0.40200
|
-0.026700
|
-4.01e-01
|
6.58e-01
|
3.01e-11
|
Processing and activation of SUMO
|
10
|
9.13e-02
|
1.99e-01
|
0.40100
|
0.256000
|
-3.10e-01
|
1.62e-01
|
9.01e-02
|
Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer’s disease models
|
18
|
1.28e-02
|
4.22e-02
|
0.40100
|
-0.078000
|
-3.94e-01
|
5.67e-01
|
3.84e-03
|
Neurodegenerative Diseases
|
18
|
1.28e-02
|
4.22e-02
|
0.40100
|
-0.078000
|
-3.94e-01
|
5.67e-01
|
3.84e-03
|
Cholesterol biosynthesis
|
26
|
2.03e-03
|
8.87e-03
|
0.40100
|
0.333000
|
-2.23e-01
|
3.30e-03
|
4.94e-02
|
Other interleukin signaling
|
20
|
7.99e-03
|
2.85e-02
|
0.40000
|
-0.369000
|
-1.55e-01
|
4.30e-03
|
2.30e-01
|
TP53 Regulates Transcription of Caspase Activators and Caspases
|
10
|
9.28e-02
|
2.01e-01
|
0.40000
|
-0.253000
|
3.10e-01
|
1.66e-01
|
8.99e-02
|
The activation of arylsulfatases
|
10
|
9.08e-02
|
1.99e-01
|
0.39900
|
-0.149000
|
-3.70e-01
|
4.14e-01
|
4.29e-02
|
P2Y receptors
|
11
|
7.14e-02
|
1.65e-01
|
0.39800
|
0.207000
|
3.41e-01
|
2.35e-01
|
5.04e-02
|
FOXO-mediated transcription of cell cycle genes
|
15
|
2.85e-02
|
8.26e-02
|
0.39800
|
0.393000
|
-6.46e-02
|
8.38e-03
|
6.65e-01
|
Pausing and recovery of Tat-mediated HIV elongation
|
30
|
8.17e-04
|
4.04e-03
|
0.39800
|
0.068500
|
-3.92e-01
|
5.16e-01
|
1.99e-04
|
Tat-mediated HIV elongation arrest and recovery
|
30
|
8.17e-04
|
4.04e-03
|
0.39800
|
0.068500
|
-3.92e-01
|
5.16e-01
|
1.99e-04
|
Nitric oxide stimulates guanylate cyclase
|
16
|
2.20e-02
|
6.78e-02
|
0.39700
|
0.314000
|
2.44e-01
|
2.97e-02
|
9.17e-02
|
Signaling by ALK
|
26
|
2.18e-03
|
9.46e-03
|
0.39600
|
-0.115000
|
-3.79e-01
|
3.12e-01
|
8.29e-04
|
NGF-stimulated transcription
|
35
|
2.94e-04
|
1.59e-03
|
0.39600
|
0.227000
|
-3.24e-01
|
2.00e-02
|
9.15e-04
|
Mitochondrial translation elongation
|
88
|
1.46e-09
|
2.79e-08
|
0.39500
|
0.212000
|
-3.33e-01
|
5.98e-04
|
6.48e-08
|
Regulation of KIT signaling
|
16
|
2.40e-02
|
7.19e-02
|
0.39400
|
-0.389000
|
-5.89e-02
|
7.01e-03
|
6.84e-01
|
Regulation of TP53 Activity through Association with Co-factors
|
10
|
9.65e-02
|
2.07e-01
|
0.39400
|
-0.155000
|
-3.62e-01
|
3.95e-01
|
4.77e-02
|
TNFR2 non-canonical NF-kB pathway
|
87
|
1.62e-09
|
3.06e-08
|
0.39300
|
-0.134000
|
-3.70e-01
|
3.13e-02
|
2.43e-09
|
Complement cascade
|
41
|
7.05e-05
|
4.14e-04
|
0.39300
|
-0.358000
|
-1.62e-01
|
7.20e-05
|
7.23e-02
|
GRB2 events in EGFR signaling
|
10
|
1.01e-01
|
2.15e-01
|
0.39200
|
-0.364000
|
1.45e-01
|
4.62e-02
|
4.26e-01
|
PI-3K cascade:FGFR4
|
11
|
8.07e-02
|
1.82e-01
|
0.39200
|
0.355000
|
-1.67e-01
|
4.17e-02
|
3.37e-01
|
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
|
87
|
1.92e-09
|
3.58e-08
|
0.39200
|
-0.129000
|
-3.70e-01
|
3.70e-02
|
2.49e-09
|
p53-Dependent G1 DNA Damage Response
|
62
|
6.75e-07
|
6.70e-06
|
0.39100
|
0.002630
|
-3.91e-01
|
9.71e-01
|
9.78e-08
|
p53-Dependent G1/S DNA damage checkpoint
|
62
|
6.75e-07
|
6.70e-06
|
0.39100
|
0.002630
|
-3.91e-01
|
9.71e-01
|
9.78e-08
|
Complex I biogenesis
|
51
|
1.05e-05
|
7.26e-05
|
0.38900
|
0.167000
|
-3.51e-01
|
3.91e-02
|
1.43e-05
|
RUNX1 regulates transcription of genes involved in differentiation of HSCs
|
69
|
1.89e-07
|
2.07e-06
|
0.38800
|
0.087700
|
-3.78e-01
|
2.08e-01
|
5.59e-08
|
Orc1 removal from chromatin
|
67
|
3.05e-07
|
3.18e-06
|
0.38700
|
0.045900
|
-3.85e-01
|
5.16e-01
|
5.19e-08
|
Antigen Presentation: Folding, assembly and peptide loading of class I MHC
|
23
|
5.46e-03
|
2.06e-02
|
0.38700
|
-0.309000
|
-2.33e-01
|
1.03e-02
|
5.31e-02
|
FCGR3A-mediated IL10 synthesis
|
43
|
6.20e-05
|
3.67e-04
|
0.38700
|
-0.361000
|
-1.39e-01
|
4.18e-05
|
1.16e-01
|
Unwinding of DNA
|
11
|
8.52e-02
|
1.90e-01
|
0.38700
|
0.015100
|
-3.86e-01
|
9.31e-01
|
2.65e-02
|
Assembly of the ORC complex at the origin of replication
|
14
|
4.43e-02
|
1.16e-01
|
0.38600
|
0.374000
|
-9.61e-02
|
1.54e-02
|
5.34e-01
|
Cellular hexose transport
|
13
|
5.47e-02
|
1.34e-01
|
0.38500
|
-0.377000
|
-8.16e-02
|
1.87e-02
|
6.10e-01
|
KEAP1-NFE2L2 pathway
|
101
|
1.87e-10
|
3.98e-09
|
0.38500
|
-0.028800
|
-3.84e-01
|
6.17e-01
|
2.56e-11
|
Mitochondrial translation termination
|
88
|
4.11e-09
|
7.10e-08
|
0.38500
|
0.215000
|
-3.19e-01
|
4.89e-04
|
2.29e-07
|
Mitochondrial iron-sulfur cluster biogenesis
|
13
|
5.80e-02
|
1.41e-01
|
0.38400
|
0.176000
|
-3.41e-01
|
2.73e-01
|
3.32e-02
|
Protein methylation
|
15
|
3.75e-02
|
1.02e-01
|
0.38300
|
0.351000
|
-1.53e-01
|
1.84e-02
|
3.04e-01
|
G1/S DNA Damage Checkpoints
|
63
|
1.01e-06
|
9.29e-06
|
0.38300
|
0.004120
|
-3.83e-01
|
9.55e-01
|
1.48e-07
|
Iron uptake and transport
|
55
|
5.66e-06
|
4.35e-05
|
0.38200
|
-0.133000
|
-3.58e-01
|
8.90e-02
|
4.31e-06
|
Maturation of nucleoprotein 9683610
|
11
|
9.13e-02
|
1.99e-01
|
0.38200
|
-0.377000
|
6.03e-02
|
3.05e-02
|
7.29e-01
|
Chondroitin sulfate/dermatan sulfate metabolism
|
45
|
5.38e-05
|
3.22e-04
|
0.38100
|
-0.140000
|
-3.54e-01
|
1.05e-01
|
3.92e-05
|
Formation of annular gap junctions
|
11
|
9.09e-02
|
1.99e-01
|
0.38000
|
-0.354000
|
-1.38e-01
|
4.19e-02
|
4.28e-01
|
Defects in cobalamin (B12) metabolism
|
12
|
7.32e-02
|
1.68e-01
|
0.38000
|
0.337000
|
1.76e-01
|
4.33e-02
|
2.93e-01
|
Metal ion SLC transporters
|
18
|
1.98e-02
|
6.24e-02
|
0.38000
|
-0.173000
|
-3.38e-01
|
2.05e-01
|
1.29e-02
|
N-Glycan antennae elongation
|
13
|
6.14e-02
|
1.48e-01
|
0.37900
|
0.069500
|
-3.73e-01
|
6.65e-01
|
2.00e-02
|
Mitochondrial translation initiation
|
88
|
7.74e-09
|
1.24e-07
|
0.37900
|
0.212000
|
-3.13e-01
|
5.81e-04
|
3.76e-07
|
Mitochondrial protein import
|
63
|
1.49e-06
|
1.34e-05
|
0.37800
|
0.052600
|
-3.74e-01
|
4.70e-01
|
2.81e-07
|
COPI-dependent Golgi-to-ER retrograde traffic
|
85
|
1.26e-08
|
1.88e-07
|
0.37800
|
-0.083000
|
-3.68e-01
|
1.86e-01
|
4.31e-09
|
Interleukin receptor SHC signaling
|
22
|
9.10e-03
|
3.19e-02
|
0.37700
|
-0.373000
|
-5.38e-02
|
2.44e-03
|
6.62e-01
|
Synthesis of bile acids and bile salts via 24-hydroxycholesterol
|
10
|
1.18e-01
|
2.40e-01
|
0.37700
|
0.367000
|
8.46e-02
|
4.45e-02
|
6.43e-01
|
Golgi Cisternae Pericentriolar Stack Reorganization
|
14
|
5.02e-02
|
1.27e-01
|
0.37600
|
-0.267000
|
-2.64e-01
|
8.32e-02
|
8.71e-02
|
TP53 Regulates Transcription of Genes Involved in Cytochrome C Release
|
17
|
2.80e-02
|
8.18e-02
|
0.37400
|
-0.356000
|
-1.12e-01
|
1.10e-02
|
4.23e-01
|
MASTL Facilitates Mitotic Progression
|
10
|
1.25e-01
|
2.47e-01
|
0.37400
|
0.103000
|
-3.59e-01
|
5.71e-01
|
4.94e-02
|
FCERI mediated NF-kB activation
|
81
|
4.49e-08
|
5.94e-07
|
0.37300
|
-0.065600
|
-3.68e-01
|
3.07e-01
|
1.08e-08
|
Late SARS-CoV-2 Infection Events
|
66
|
9.57e-07
|
9.01e-06
|
0.37300
|
-0.262000
|
-2.66e-01
|
2.37e-04
|
1.88e-04
|
Translation of Structural Proteins 9683701
|
29
|
2.29e-03
|
9.91e-03
|
0.37300
|
-0.202000
|
-3.13e-01
|
5.98e-02
|
3.53e-03
|
Plasma lipoprotein remodeling
|
19
|
1.88e-02
|
6.00e-02
|
0.37200
|
-0.338000
|
-1.56e-01
|
1.07e-02
|
2.41e-01
|
Regulation of PTEN stability and activity
|
67
|
9.78e-07
|
9.09e-06
|
0.37200
|
0.042300
|
-3.70e-01
|
5.50e-01
|
1.68e-07
|
COPII-mediated vesicle transport
|
63
|
2.02e-06
|
1.76e-05
|
0.37200
|
-0.192000
|
-3.18e-01
|
8.49e-03
|
1.25e-05
|
Somitogenesis
|
50
|
3.31e-05
|
2.06e-04
|
0.37100
|
-0.012500
|
-3.71e-01
|
8.78e-01
|
5.68e-06
|
Interleukin-4 and Interleukin-13 signaling
|
90
|
9.36e-09
|
1.46e-07
|
0.37000
|
-0.042400
|
-3.68e-01
|
4.87e-01
|
1.60e-09
|
Translation of Structural Proteins 9694635
|
57
|
7.52e-06
|
5.58e-05
|
0.37000
|
-0.248000
|
-2.75e-01
|
1.22e-03
|
3.25e-04
|
APC/C:Cdc20 mediated degradation of Securin
|
66
|
1.37e-06
|
1.24e-05
|
0.37000
|
0.047600
|
-3.67e-01
|
5.04e-01
|
2.48e-07
|
Negative regulation of FGFR3 signaling
|
23
|
9.13e-03
|
3.19e-02
|
0.37000
|
0.118000
|
-3.51e-01
|
3.27e-01
|
3.58e-03
|
ABC transporter disorders
|
68
|
9.36e-07
|
8.93e-06
|
0.36900
|
-0.046200
|
-3.66e-01
|
5.11e-01
|
1.77e-07
|
Budding and maturation of HIV virion
|
27
|
4.25e-03
|
1.67e-02
|
0.36900
|
0.175000
|
-3.25e-01
|
1.16e-01
|
3.48e-03
|
Interleukin-2 family signaling
|
36
|
6.52e-04
|
3.30e-03
|
0.36800
|
-0.362000
|
-6.70e-02
|
1.70e-04
|
4.87e-01
|
Autodegradation of Cdh1 by Cdh1:APC/C
|
64
|
2.40e-06
|
2.07e-05
|
0.36800
|
0.047500
|
-3.65e-01
|
5.11e-01
|
4.41e-07
|
Transcriptional regulation by RUNX3
|
94
|
5.89e-09
|
9.81e-08
|
0.36800
|
0.042400
|
-3.65e-01
|
4.78e-01
|
9.28e-10
|
Abortive elongation of HIV-1 transcript in the absence of Tat
|
23
|
9.72e-03
|
3.37e-02
|
0.36700
|
0.058500
|
-3.63e-01
|
6.27e-01
|
2.62e-03
|
DCC mediated attractive signaling
|
13
|
7.07e-02
|
1.64e-01
|
0.36700
|
0.246000
|
2.73e-01
|
1.25e-01
|
8.87e-02
|
Hyaluronan metabolism
|
16
|
3.97e-02
|
1.06e-01
|
0.36700
|
-0.365000
|
-3.10e-02
|
1.14e-02
|
8.30e-01
|
RHO GTPases activate PKNs
|
36
|
7.25e-04
|
3.62e-03
|
0.36600
|
0.366000
|
-1.99e-02
|
1.46e-04
|
8.37e-01
|
Lysosome Vesicle Biogenesis
|
33
|
1.29e-03
|
5.99e-03
|
0.36600
|
-0.352000
|
-9.94e-02
|
4.63e-04
|
3.23e-01
|
Common Pathway of Fibrin Clot Formation
|
10
|
1.35e-01
|
2.60e-01
|
0.36500
|
-0.086200
|
-3.55e-01
|
6.37e-01
|
5.21e-02
|
Formation of Senescence-Associated Heterochromatin Foci (SAHF)
|
11
|
1.11e-01
|
2.29e-01
|
0.36500
|
-0.081300
|
-3.56e-01
|
6.41e-01
|
4.12e-02
|
RHO GTPases activate IQGAPs
|
24
|
8.57e-03
|
3.03e-02
|
0.36500
|
0.092500
|
-3.53e-01
|
4.33e-01
|
2.78e-03
|
HSF1-dependent transactivation
|
32
|
1.86e-03
|
8.20e-03
|
0.36400
|
0.209000
|
-2.98e-01
|
4.05e-02
|
3.59e-03
|
Respiratory electron transport
|
93
|
1.17e-08
|
1.75e-07
|
0.36400
|
0.117000
|
-3.44e-01
|
5.20e-02
|
9.46e-09
|
Synthesis of PE
|
12
|
9.39e-02
|
2.03e-01
|
0.36300
|
-0.353000
|
8.45e-02
|
3.40e-02
|
6.12e-01
|
ER to Golgi Anterograde Transport
|
141
|
8.50e-13
|
2.19e-11
|
0.36300
|
-0.067700
|
-3.57e-01
|
1.66e-01
|
2.62e-13
|
Negative regulation of FGFR4 signaling
|
22
|
1.36e-02
|
4.45e-02
|
0.36200
|
0.152000
|
-3.29e-01
|
2.17e-01
|
7.60e-03
|
TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest
|
17
|
3.48e-02
|
9.63e-02
|
0.36200
|
-0.288000
|
-2.19e-01
|
4.00e-02
|
1.18e-01
|
TNFR1-induced proapoptotic signaling
|
25
|
7.66e-03
|
2.76e-02
|
0.35900
|
-0.301000
|
-1.96e-01
|
9.20e-03
|
8.99e-02
|
Mitochondrial translation
|
94
|
1.60e-08
|
2.31e-07
|
0.35900
|
0.202000
|
-2.97e-01
|
7.22e-04
|
6.53e-07
|
VLDLR internalisation and degradation
|
15
|
5.41e-02
|
1.33e-01
|
0.35900
|
-0.226000
|
-2.79e-01
|
1.31e-01
|
6.16e-02
|
Glycosphingolipid metabolism
|
36
|
9.55e-04
|
4.68e-03
|
0.35800
|
-0.310000
|
-1.79e-01
|
1.31e-03
|
6.25e-02
|
Transcriptional regulation by RUNX2
|
114
|
3.52e-10
|
7.19e-09
|
0.35800
|
-0.021000
|
-3.57e-01
|
6.99e-01
|
4.62e-11
|
Integrin cell surface interactions
|
73
|
8.34e-07
|
8.11e-06
|
0.35700
|
-0.082700
|
-3.48e-01
|
2.22e-01
|
2.79e-07
|
Response of Mtb to phagocytosis
|
23
|
1.22e-02
|
4.10e-02
|
0.35700
|
-0.065100
|
-3.51e-01
|
5.89e-01
|
3.56e-03
|
Glycolysis
|
65
|
4.23e-06
|
3.36e-05
|
0.35500
|
-0.294000
|
-1.99e-01
|
4.09e-05
|
5.51e-03
|
p75NTR signals via NF-kB
|
16
|
4.93e-02
|
1.25e-01
|
0.35400
|
0.016200
|
-3.54e-01
|
9.11e-01
|
1.42e-02
|
RAS processing
|
21
|
2.00e-02
|
6.26e-02
|
0.35400
|
0.215000
|
-2.81e-01
|
8.79e-02
|
2.57e-02
|
Caspase-mediated cleavage of cytoskeletal proteins
|
12
|
1.07e-01
|
2.24e-01
|
0.35300
|
-0.038200
|
3.51e-01
|
8.19e-01
|
3.54e-02
|
Mitophagy
|
28
|
5.66e-03
|
2.13e-02
|
0.35200
|
0.113000
|
-3.34e-01
|
3.02e-01
|
2.24e-03
|
Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins.
|
113
|
9.48e-10
|
1.88e-08
|
0.35200
|
0.108000
|
-3.35e-01
|
4.80e-02
|
7.63e-10
|
PI-3K cascade:FGFR3
|
12
|
1.10e-01
|
2.29e-01
|
0.35200
|
0.272000
|
-2.23e-01
|
1.03e-01
|
1.81e-01
|
TCR signaling
|
102
|
6.54e-09
|
1.06e-07
|
0.35100
|
-0.072500
|
-3.44e-01
|
2.06e-01
|
2.02e-09
|
Establishment of Sister Chromatid Cohesion
|
11
|
1.29e-01
|
2.53e-01
|
0.35100
|
0.215000
|
2.77e-01
|
2.17e-01
|
1.11e-01
|
alpha-linolenic (omega3) and linoleic (omega6) acid metabolism
|
11
|
1.30e-01
|
2.54e-01
|
0.35100
|
-0.341000
|
-8.33e-02
|
5.04e-02
|
6.32e-01
|
alpha-linolenic acid (ALA) metabolism
|
11
|
1.30e-01
|
2.54e-01
|
0.35100
|
-0.341000
|
-8.33e-02
|
5.04e-02
|
6.32e-01
|
Negative regulation of FGFR2 signaling
|
25
|
1.03e-02
|
3.53e-02
|
0.35100
|
0.117000
|
-3.30e-01
|
3.10e-01
|
4.24e-03
|
CS/DS degradation
|
11
|
1.32e-01
|
2.56e-01
|
0.35000
|
-0.096500
|
-3.36e-01
|
5.80e-01
|
5.35e-02
|
Translesion Synthesis by POLH
|
18
|
3.85e-02
|
1.04e-01
|
0.34900
|
0.224000
|
-2.68e-01
|
9.98e-02
|
4.94e-02
|
IL-6-type cytokine receptor ligand interactions
|
13
|
9.48e-02
|
2.04e-01
|
0.34800
|
0.077500
|
-3.40e-01
|
6.29e-01
|
3.40e-02
|
CTNNB1 S33 mutants aren’t phosphorylated
|
15
|
6.65e-02
|
1.57e-01
|
0.34800
|
0.071200
|
-3.40e-01
|
6.33e-01
|
2.24e-02
|
CTNNB1 S37 mutants aren’t phosphorylated
|
15
|
6.65e-02
|
1.57e-01
|
0.34800
|
0.071200
|
-3.40e-01
|
6.33e-01
|
2.24e-02
|
CTNNB1 S45 mutants aren’t phosphorylated
|
15
|
6.65e-02
|
1.57e-01
|
0.34800
|
0.071200
|
-3.40e-01
|
6.33e-01
|
2.24e-02
|
CTNNB1 T41 mutants aren’t phosphorylated
|
15
|
6.65e-02
|
1.57e-01
|
0.34800
|
0.071200
|
-3.40e-01
|
6.33e-01
|
2.24e-02
|
Signaling by CTNNB1 phospho-site mutants
|
15
|
6.65e-02
|
1.57e-01
|
0.34800
|
0.071200
|
-3.40e-01
|
6.33e-01
|
2.24e-02
|
Signaling by GSK3beta mutants
|
15
|
6.65e-02
|
1.57e-01
|
0.34800
|
0.071200
|
-3.40e-01
|
6.33e-01
|
2.24e-02
|
Downstream signaling events of B Cell Receptor (BCR)
|
78
|
9.26e-07
|
8.93e-06
|
0.34600
|
0.058500
|
-3.41e-01
|
3.72e-01
|
1.96e-07
|
CD28 dependent Vav1 pathway
|
11
|
1.41e-01
|
2.70e-01
|
0.34500
|
-0.339000
|
6.32e-02
|
5.14e-02
|
7.17e-01
|
N-glycan antennae elongation in the medial/trans-Golgi
|
20
|
2.77e-02
|
8.12e-02
|
0.34500
|
-0.149000
|
-3.11e-01
|
2.49e-01
|
1.61e-02
|
Protein ubiquitination
|
63
|
1.50e-05
|
1.01e-04
|
0.34500
|
0.159000
|
-3.06e-01
|
2.92e-02
|
2.70e-05
|
Interleukin-6 family signaling
|
20
|
2.92e-02
|
8.42e-02
|
0.34400
|
0.097100
|
-3.30e-01
|
4.52e-01
|
1.06e-02
|
Signalling to RAS
|
20
|
2.80e-02
|
8.18e-02
|
0.34400
|
-0.225000
|
-2.60e-01
|
8.10e-02
|
4.44e-02
|
Selective autophagy
|
71
|
4.11e-06
|
3.28e-05
|
0.34300
|
0.201000
|
-2.78e-01
|
3.34e-03
|
5.14e-05
|
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1
|
72
|
3.26e-06
|
2.72e-05
|
0.34300
|
0.005210
|
-3.43e-01
|
9.39e-01
|
5.00e-07
|
HIV elongation arrest and recovery
|
32
|
3.68e-03
|
1.46e-02
|
0.34300
|
0.059500
|
-3.37e-01
|
5.61e-01
|
9.58e-04
|
Pausing and recovery of HIV elongation
|
32
|
3.68e-03
|
1.46e-02
|
0.34300
|
0.059500
|
-3.37e-01
|
5.61e-01
|
9.58e-04
|
Glycosaminoglycan metabolism
|
108
|
5.95e-09
|
9.81e-08
|
0.34200
|
-0.162000
|
-3.01e-01
|
3.71e-03
|
6.66e-08
|
Assembly of the pre-replicative complex
|
88
|
2.40e-07
|
2.59e-06
|
0.34100
|
0.101000
|
-3.26e-01
|
1.00e-01
|
1.26e-07
|
Polo-like kinase mediated events
|
14
|
8.50e-02
|
1.90e-01
|
0.34100
|
-0.214000
|
-2.66e-01
|
1.67e-01
|
8.46e-02
|
Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects
|
17
|
5.18e-02
|
1.30e-01
|
0.34100
|
-0.002040
|
-3.41e-01
|
9.88e-01
|
1.50e-02
|
Defective binding of RB1 mutants to E2F1,(E2F2, E2F3)
|
17
|
5.18e-02
|
1.30e-01
|
0.34100
|
-0.002040
|
-3.41e-01
|
9.88e-01
|
1.50e-02
|
SARS-CoV-1-host interactions
|
94
|
1.02e-07
|
1.19e-06
|
0.34000
|
0.268000
|
-2.10e-01
|
7.25e-06
|
4.43e-04
|
Processing of Intronless Pre-mRNAs
|
20
|
3.30e-02
|
9.23e-02
|
0.33900
|
-0.204000
|
2.70e-01
|
1.13e-01
|
3.65e-02
|
Elastic fibre formation
|
40
|
1.02e-03
|
4.97e-03
|
0.33800
|
-0.125000
|
-3.14e-01
|
1.70e-01
|
5.91e-04
|
Endosomal Sorting Complex Required For Transport (ESCRT)
|
30
|
6.14e-03
|
2.26e-02
|
0.33800
|
0.141000
|
-3.07e-01
|
1.81e-01
|
3.62e-03
|
Interleukin-1 signaling
|
109
|
8.80e-09
|
1.39e-07
|
0.33800
|
-0.028000
|
-3.36e-01
|
6.13e-01
|
1.32e-09
|
MECP2 regulates neuronal receptors and channels
|
15
|
7.90e-02
|
1.79e-01
|
0.33800
|
0.219000
|
-2.57e-01
|
1.42e-01
|
8.52e-02
|
Gastrin-CREB signalling pathway via PKC and MAPK
|
16
|
6.74e-02
|
1.58e-01
|
0.33700
|
-0.273000
|
1.98e-01
|
5.89e-02
|
1.71e-01
|
DNA methylation
|
10
|
1.85e-01
|
3.29e-01
|
0.33700
|
0.287000
|
-1.76e-01
|
1.16e-01
|
3.34e-01
|
Signaling by BMP
|
23
|
1.99e-02
|
6.25e-02
|
0.33700
|
0.332000
|
5.27e-02
|
5.78e-03
|
6.62e-01
|
NR1H2 and NR1H3-mediated signaling
|
39
|
1.42e-03
|
6.48e-03
|
0.33700
|
-0.292000
|
1.68e-01
|
1.63e-03
|
6.96e-02
|
rRNA modification in the nucleus and cytosol
|
59
|
5.20e-05
|
3.13e-04
|
0.33600
|
0.208000
|
-2.64e-01
|
5.73e-03
|
4.62e-04
|
Lewis blood group biosynthesis
|
10
|
1.86e-01
|
3.30e-01
|
0.33600
|
0.100000
|
-3.20e-01
|
5.83e-01
|
7.95e-02
|
Transport to the Golgi and subsequent modification
|
166
|
7.41e-13
|
1.98e-11
|
0.33600
|
-0.087800
|
-3.24e-01
|
5.13e-02
|
6.17e-13
|
Long-term potentiation
|
19
|
4.14e-02
|
1.10e-01
|
0.33500
|
0.103000
|
-3.19e-01
|
4.39e-01
|
1.60e-02
|
CDK-mediated phosphorylation and removal of Cdc6
|
70
|
8.03e-06
|
5.84e-05
|
0.33500
|
0.034700
|
-3.33e-01
|
6.16e-01
|
1.42e-06
|
Pyrimidine salvage
|
10
|
1.84e-01
|
3.27e-01
|
0.33500
|
-0.123000
|
-3.12e-01
|
4.99e-01
|
8.79e-02
|
Serotonin Neurotransmitter Release Cycle
|
15
|
8.00e-02
|
1.80e-01
|
0.33500
|
-0.040400
|
-3.32e-01
|
7.86e-01
|
2.58e-02
|
APC/C:Cdc20 mediated degradation of mitotic proteins
|
72
|
5.94e-06
|
4.50e-05
|
0.33500
|
0.019600
|
-3.34e-01
|
7.74e-01
|
9.59e-07
|
Acetylcholine Neurotransmitter Release Cycle
|
13
|
1.14e-01
|
2.35e-01
|
0.33400
|
-0.026600
|
-3.33e-01
|
8.68e-01
|
3.77e-02
|
Late endosomal microautophagy
|
31
|
5.83e-03
|
2.17e-02
|
0.33400
|
0.113000
|
-3.14e-01
|
2.78e-01
|
2.46e-03
|
Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins
|
73
|
5.27e-06
|
4.10e-05
|
0.33400
|
0.008640
|
-3.34e-01
|
8.99e-01
|
8.24e-07
|
Acyl chain remodelling of PC
|
17
|
6.10e-02
|
1.48e-01
|
0.33300
|
-0.145000
|
2.99e-01
|
3.00e-01
|
3.28e-02
|
Disassembly of the destruction complex and recruitment of AXIN to the membrane
|
27
|
1.16e-02
|
3.95e-02
|
0.33200
|
0.009420
|
-3.32e-01
|
9.32e-01
|
2.84e-03
|
Glycogen storage diseases
|
13
|
1.18e-01
|
2.40e-01
|
0.33200
|
0.042000
|
-3.29e-01
|
7.93e-01
|
3.99e-02
|
G-protein beta:gamma signalling
|
27
|
1.26e-02
|
4.20e-02
|
0.33000
|
-0.249000
|
2.17e-01
|
2.51e-02
|
5.08e-02
|
Interleukin-35 Signalling
|
10
|
1.92e-01
|
3.38e-01
|
0.33000
|
-0.223000
|
-2.44e-01
|
2.22e-01
|
1.82e-01
|
Inactivation of CSF3 (G-CSF) signaling
|
24
|
1.98e-02
|
6.24e-02
|
0.33000
|
0.003240
|
-3.30e-01
|
9.78e-01
|
5.11e-03
|
LDL clearance
|
17
|
6.31e-02
|
1.52e-01
|
0.33000
|
-0.321000
|
7.62e-02
|
2.19e-02
|
5.87e-01
|
Regulation of RAS by GAPs
|
65
|
2.62e-05
|
1.71e-04
|
0.33000
|
0.033400
|
-3.28e-01
|
6.41e-01
|
4.80e-06
|
APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint
|
70
|
1.19e-05
|
8.04e-05
|
0.32900
|
0.022600
|
-3.29e-01
|
7.44e-01
|
1.99e-06
|
Cdc20:Phospho-APC/C mediated degradation of Cyclin A
|
70
|
1.19e-05
|
8.04e-05
|
0.32900
|
0.022600
|
-3.29e-01
|
7.44e-01
|
1.99e-06
|
CTLA4 inhibitory signaling
|
19
|
4.48e-02
|
1.16e-01
|
0.32900
|
-0.126000
|
-3.04e-01
|
3.40e-01
|
2.18e-02
|
Dopamine Neurotransmitter Release Cycle
|
20
|
3.93e-02
|
1.06e-01
|
0.32900
|
0.038100
|
-3.27e-01
|
7.68e-01
|
1.14e-02
|
Gamma carboxylation, hypusine formation and arylsulfatase activation
|
33
|
4.94e-03
|
1.89e-02
|
0.32700
|
-0.079800
|
-3.17e-01
|
4.28e-01
|
1.61e-03
|
Unblocking of NMDA receptors, glutamate binding and activation
|
17
|
6.71e-02
|
1.58e-01
|
0.32700
|
0.156000
|
-2.88e-01
|
2.67e-01
|
4.01e-02
|
Cyclin E associated events during G1/S transition
|
81
|
2.45e-06
|
2.11e-05
|
0.32700
|
0.010700
|
-3.27e-01
|
8.68e-01
|
3.74e-07
|
Calnexin/calreticulin cycle
|
26
|
1.59e-02
|
5.14e-02
|
0.32500
|
-0.129000
|
-2.98e-01
|
2.53e-01
|
8.50e-03
|
Costimulation by the CD28 family
|
53
|
2.20e-04
|
1.21e-03
|
0.32500
|
-0.277000
|
-1.69e-01
|
4.78e-04
|
3.38e-02
|
Metabolism of amino acids and derivatives
|
315
|
1.01e-21
|
4.13e-20
|
0.32400
|
0.170000
|
-2.76e-01
|
2.28e-07
|
4.43e-17
|
Cleavage of the damaged pyrimidine
|
20
|
4.46e-02
|
1.16e-01
|
0.32400
|
0.244000
|
-2.13e-01
|
5.91e-02
|
9.94e-02
|
Depyrimidination
|
20
|
4.46e-02
|
1.16e-01
|
0.32400
|
0.244000
|
-2.13e-01
|
5.91e-02
|
9.94e-02
|
Recognition and association of DNA glycosylase with site containing an affected pyrimidine
|
20
|
4.46e-02
|
1.16e-01
|
0.32400
|
0.244000
|
-2.13e-01
|
5.91e-02
|
9.94e-02
|
PI-3K cascade:FGFR2
|
14
|
1.15e-01
|
2.38e-01
|
0.32200
|
0.249000
|
-2.05e-01
|
1.07e-01
|
1.85e-01
|
Asparagine N-linked glycosylation
|
278
|
2.60e-19
|
9.31e-18
|
0.32200
|
-0.118000
|
-2.99e-01
|
7.42e-04
|
9.43e-18
|
Amino acid transport across the plasma membrane
|
20
|
4.45e-02
|
1.16e-01
|
0.32100
|
-0.265000
|
-1.81e-01
|
4.02e-02
|
1.61e-01
|
Synthesis of PIPs at the early endosome membrane
|
16
|
8.62e-02
|
1.91e-01
|
0.32100
|
-0.151000
|
2.83e-01
|
2.94e-01
|
5.01e-02
|
Infection with Mycobacterium tuberculosis
|
27
|
1.55e-02
|
5.03e-02
|
0.32000
|
-0.087000
|
-3.08e-01
|
4.34e-01
|
5.57e-03
|
PCP/CE pathway
|
87
|
1.61e-06
|
1.44e-05
|
0.32000
|
-0.052200
|
-3.16e-01
|
4.01e-01
|
3.60e-07
|
Lysine catabolism
|
11
|
1.86e-01
|
3.30e-01
|
0.32000
|
-0.049300
|
3.16e-01
|
7.77e-01
|
6.96e-02
|
Amino acids regulate mTORC1
|
50
|
4.45e-04
|
2.30e-03
|
0.32000
|
-0.224000
|
-2.28e-01
|
6.06e-03
|
5.35e-03
|
RHOBTB1 GTPase cycle
|
23
|
2.87e-02
|
8.30e-02
|
0.32000
|
0.249000
|
2.00e-01
|
3.88e-02
|
9.61e-02
|
Metabolism of carbohydrates
|
254
|
1.68e-17
|
5.14e-16
|
0.31900
|
-0.187000
|
-2.59e-01
|
3.18e-07
|
1.27e-12
|
COPI-independent Golgi-to-ER retrograde traffic
|
45
|
1.11e-03
|
5.33e-03
|
0.31900
|
0.130000
|
-2.91e-01
|
1.31e-01
|
7.33e-04
|
Base-Excision Repair, AP Site Formation
|
22
|
3.66e-02
|
1.00e-01
|
0.31800
|
0.214000
|
-2.35e-01
|
8.20e-02
|
5.62e-02
|
Cyclin A:Cdk2-associated events at S phase entry
|
83
|
3.69e-06
|
3.03e-05
|
0.31800
|
-0.001100
|
-3.18e-01
|
9.86e-01
|
5.69e-07
|
N-glycan trimming in the ER and Calnexin/Calreticulin cycle
|
35
|
4.94e-03
|
1.89e-02
|
0.31700
|
-0.127000
|
-2.91e-01
|
1.95e-01
|
2.90e-03
|
AKT phosphorylates targets in the cytosol
|
14
|
1.21e-01
|
2.42e-01
|
0.31700
|
-0.018000
|
-3.17e-01
|
9.07e-01
|
4.02e-02
|
Regulation of APC/C activators between G1/S and early anaphase
|
78
|
8.46e-06
|
6.06e-05
|
0.31600
|
-0.018900
|
-3.16e-01
|
7.73e-01
|
1.42e-06
|
GPVI-mediated activation cascade
|
32
|
8.22e-03
|
2.92e-02
|
0.31600
|
-0.315000
|
-2.75e-02
|
2.04e-03
|
7.88e-01
|
A tetrasaccharide linker sequence is required for GAG synthesis
|
22
|
3.64e-02
|
9.98e-02
|
0.31600
|
-0.089900
|
-3.03e-01
|
4.66e-01
|
1.38e-02
|
Formation of the beta-catenin:TCF transactivating complex
|
36
|
4.80e-03
|
1.86e-02
|
0.31600
|
0.185000
|
-2.56e-01
|
5.47e-02
|
7.80e-03
|
Gap junction degradation
|
12
|
1.65e-01
|
3.06e-01
|
0.31600
|
-0.309000
|
-6.39e-02
|
6.37e-02
|
7.01e-01
|
TCF dependent signaling in response to WNT
|
160
|
5.56e-11
|
1.30e-09
|
0.31600
|
0.073200
|
-3.07e-01
|
1.11e-01
|
2.11e-11
|
Trafficking of GluR2-containing AMPA receptors
|
14
|
1.25e-01
|
2.47e-01
|
0.31400
|
-0.277000
|
-1.48e-01
|
7.30e-02
|
3.37e-01
|
Elevation of cytosolic Ca2+ levels
|
13
|
1.46e-01
|
2.77e-01
|
0.31300
|
-0.180000
|
-2.56e-01
|
2.60e-01
|
1.10e-01
|
Cell surface interactions at the vascular wall
|
111
|
7.74e-08
|
9.32e-07
|
0.31300
|
-0.219000
|
-2.23e-01
|
6.53e-05
|
4.87e-05
|
Synthesis of active ubiquitin: roles of E1 and E2 enzymes
|
30
|
1.25e-02
|
4.20e-02
|
0.31300
|
0.060700
|
-3.07e-01
|
5.65e-01
|
3.63e-03
|
Downregulation of TGF-beta receptor signaling
|
26
|
2.33e-02
|
7.08e-02
|
0.31200
|
0.227000
|
-2.14e-01
|
4.54e-02
|
5.84e-02
|
Cobalamin (Cbl, vitamin B12) transport and metabolism
|
15
|
1.10e-01
|
2.29e-01
|
0.31200
|
0.250000
|
1.87e-01
|
9.41e-02
|
2.09e-01
|
Golgi-to-ER retrograde transport
|
118
|
3.54e-08
|
4.81e-07
|
0.31200
|
-0.042900
|
-3.09e-01
|
4.21e-01
|
6.84e-09
|
tRNA Aminoacylation
|
42
|
2.19e-03
|
9.48e-03
|
0.31100
|
-0.141000
|
-2.77e-01
|
1.14e-01
|
1.89e-03
|
Maturation of nucleoprotein 9694631
|
15
|
1.14e-01
|
2.35e-01
|
0.31100
|
-0.310000
|
-1.85e-02
|
3.76e-02
|
9.01e-01
|
NPAS4 regulates expression of target genes
|
18
|
7.57e-02
|
1.73e-01
|
0.31100
|
0.189000
|
-2.47e-01
|
1.65e-01
|
7.01e-02
|
Hedgehog ‘on’ state
|
82
|
7.65e-06
|
5.64e-05
|
0.31000
|
-0.013000
|
-3.10e-01
|
8.39e-01
|
1.25e-06
|
ER-Phagosome pathway
|
79
|
1.16e-05
|
7.96e-05
|
0.30900
|
-0.116000
|
-2.87e-01
|
7.55e-02
|
1.05e-05
|
NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux
|
32
|
1.08e-02
|
3.67e-02
|
0.30900
|
-0.232000
|
2.04e-01
|
2.30e-02
|
4.63e-02
|
TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition)
|
15
|
1.20e-01
|
2.41e-01
|
0.30800
|
0.048900
|
-3.04e-01
|
7.43e-01
|
4.17e-02
|
Senescence-Associated Secretory Phenotype (SASP)
|
56
|
3.79e-04
|
2.00e-03
|
0.30800
|
0.097000
|
-2.92e-01
|
2.09e-01
|
1.59e-04
|
Chaperone Mediated Autophagy
|
19
|
6.97e-02
|
1.62e-01
|
0.30700
|
0.214000
|
-2.20e-01
|
1.06e-01
|
9.66e-02
|
Transport of bile salts and organic acids, metal ions and amine compounds
|
46
|
1.43e-03
|
6.51e-03
|
0.30700
|
-0.152000
|
-2.67e-01
|
7.51e-02
|
1.72e-03
|
MET activates RAP1 and RAC1
|
11
|
2.10e-01
|
3.61e-01
|
0.30700
|
0.097000
|
2.91e-01
|
5.77e-01
|
9.46e-02
|
Norepinephrine Neurotransmitter Release Cycle
|
15
|
1.21e-01
|
2.42e-01
|
0.30600
|
-0.021700
|
-3.06e-01
|
8.84e-01
|
4.05e-02
|
Switching of origins to a post-replicative state
|
88
|
4.60e-06
|
3.60e-05
|
0.30600
|
0.054900
|
-3.01e-01
|
3.74e-01
|
1.03e-06
|
CLEC7A (Dectin-1) signaling
|
95
|
1.67e-06
|
1.49e-05
|
0.30600
|
-0.043700
|
-3.03e-01
|
4.62e-01
|
3.42e-07
|
Inflammasomes
|
21
|
5.21e-02
|
1.30e-01
|
0.30500
|
-0.255000
|
-1.68e-01
|
4.32e-02
|
1.83e-01
|
Peroxisomal lipid metabolism
|
26
|
2.83e-02
|
8.24e-02
|
0.30400
|
-0.132000
|
2.73e-01
|
2.43e-01
|
1.59e-02
|
TRP channels
|
20
|
6.48e-02
|
1.55e-01
|
0.30400
|
-0.210000
|
2.19e-01
|
1.04e-01
|
8.99e-02
|
Negative regulation of MAPK pathway
|
42
|
3.12e-03
|
1.29e-02
|
0.30400
|
0.064200
|
-2.97e-01
|
4.71e-01
|
8.81e-04
|
Caspase activation via extrinsic apoptotic signalling pathway
|
23
|
4.13e-02
|
1.10e-01
|
0.30400
|
-0.295000
|
-7.33e-02
|
1.45e-02
|
5.43e-01
|
Pregnenolone biosynthesis
|
10
|
2.50e-01
|
4.10e-01
|
0.30300
|
-0.248000
|
-1.74e-01
|
1.74e-01
|
3.41e-01
|
FRS-mediated FGFR4 signaling
|
13
|
1.70e-01
|
3.11e-01
|
0.30300
|
0.230000
|
-1.97e-01
|
1.50e-01
|
2.20e-01
|
Regulation of CDH11 gene transcription
|
10
|
2.51e-01
|
4.11e-01
|
0.30200
|
-0.208000
|
-2.19e-01
|
2.55e-01
|
2.30e-01
|
Degradation of the extracellular matrix
|
110
|
3.56e-07
|
3.65e-06
|
0.30000
|
-0.175000
|
-2.43e-01
|
1.54e-03
|
1.06e-05
|
Interleukin-7 signaling
|
19
|
7.81e-02
|
1.77e-01
|
0.30000
|
0.025100
|
-2.98e-01
|
8.50e-01
|
2.43e-02
|
Ras activation upon Ca2+ influx through NMDA receptor
|
16
|
1.18e-01
|
2.40e-01
|
0.29900
|
0.128000
|
-2.70e-01
|
3.75e-01
|
6.11e-02
|
APC truncation mutants have impaired AXIN binding
|
14
|
1.55e-01
|
2.90e-01
|
0.29800
|
0.023200
|
-2.97e-01
|
8.81e-01
|
5.40e-02
|
AXIN missense mutants destabilize the destruction complex
|
14
|
1.55e-01
|
2.90e-01
|
0.29800
|
0.023200
|
-2.97e-01
|
8.81e-01
|
5.40e-02
|
Signaling by AMER1 mutants
|
14
|
1.55e-01
|
2.90e-01
|
0.29800
|
0.023200
|
-2.97e-01
|
8.81e-01
|
5.40e-02
|
Signaling by APC mutants
|
14
|
1.55e-01
|
2.90e-01
|
0.29800
|
0.023200
|
-2.97e-01
|
8.81e-01
|
5.40e-02
|
Signaling by AXIN mutants
|
14
|
1.55e-01
|
2.90e-01
|
0.29800
|
0.023200
|
-2.97e-01
|
8.81e-01
|
5.40e-02
|
Truncations of AMER1 destabilize the destruction complex
|
14
|
1.55e-01
|
2.90e-01
|
0.29800
|
0.023200
|
-2.97e-01
|
8.81e-01
|
5.40e-02
|
Nucleotide salvage
|
21
|
6.07e-02
|
1.47e-01
|
0.29800
|
-0.040500
|
-2.95e-01
|
7.48e-01
|
1.92e-02
|
MAP3K8 (TPL2)-dependent MAPK1/3 activation
|
16
|
1.19e-01
|
2.40e-01
|
0.29800
|
-0.025200
|
-2.97e-01
|
8.61e-01
|
3.99e-02
|
Defective B4GALT7 causes EDS, progeroid type
|
17
|
1.05e-01
|
2.21e-01
|
0.29800
|
0.021700
|
-2.97e-01
|
8.77e-01
|
3.42e-02
|
ECM proteoglycans
|
61
|
3.22e-04
|
1.72e-03
|
0.29700
|
0.004080
|
-2.97e-01
|
9.56e-01
|
6.07e-05
|
Extracellular matrix organization
|
250
|
6.33e-15
|
1.75e-13
|
0.29600
|
-0.089400
|
-2.83e-01
|
1.51e-02
|
1.48e-14
|
Activation of the AP-1 family of transcription factors
|
10
|
2.70e-01
|
4.31e-01
|
0.29600
|
0.278000
|
-1.04e-01
|
1.28e-01
|
5.71e-01
|
Metalloprotease DUBs
|
19
|
8.39e-02
|
1.88e-01
|
0.29600
|
0.182000
|
-2.34e-01
|
1.70e-01
|
7.77e-02
|
Competing endogenous RNAs (ceRNAs) regulate PTEN translation
|
10
|
2.67e-01
|
4.28e-01
|
0.29600
|
0.129000
|
2.66e-01
|
4.80e-01
|
1.45e-01
|
Sema4D induced cell migration and growth-cone collapse
|
19
|
8.52e-02
|
1.90e-01
|
0.29500
|
0.256000
|
-1.47e-01
|
5.35e-02
|
2.66e-01
|
FRS-mediated FGFR3 signaling
|
14
|
1.63e-01
|
3.04e-01
|
0.29500
|
0.169000
|
-2.42e-01
|
2.75e-01
|
1.17e-01
|
LGI-ADAM interactions
|
10
|
2.74e-01
|
4.35e-01
|
0.29400
|
-0.291000
|
4.49e-02
|
1.11e-01
|
8.06e-01
|
Apoptotic cleavage of cellular proteins
|
34
|
1.18e-02
|
3.98e-02
|
0.29400
|
0.225000
|
1.90e-01
|
2.35e-02
|
5.52e-02
|
Signaling by Insulin receptor
|
65
|
2.15e-04
|
1.19e-03
|
0.29400
|
-0.141000
|
-2.57e-01
|
4.88e-02
|
3.33e-04
|
MAPK6/MAPK4 signaling
|
83
|
2.42e-05
|
1.58e-04
|
0.29400
|
0.092000
|
-2.79e-01
|
1.48e-01
|
1.13e-05
|
Azathioprine ADME
|
18
|
9.58e-02
|
2.06e-01
|
0.29400
|
-0.235000
|
-1.76e-01
|
8.45e-02
|
1.96e-01
|
Paracetamol ADME
|
19
|
8.89e-02
|
1.95e-01
|
0.29300
|
-0.233000
|
1.78e-01
|
7.91e-02
|
1.80e-01
|
RHO GTPases activate CIT
|
18
|
9.98e-02
|
2.12e-01
|
0.29300
|
0.291000
|
-2.67e-02
|
3.24e-02
|
8.45e-01
|
Carboxyterminal post-translational modifications of tubulin
|
30
|
2.26e-02
|
6.92e-02
|
0.29200
|
0.163000
|
-2.42e-01
|
1.23e-01
|
2.19e-02
|
NFE2L2 regulating anti-oxidant/detoxification enzymes
|
14
|
1.69e-01
|
3.11e-01
|
0.29200
|
0.083800
|
-2.79e-01
|
5.87e-01
|
7.04e-02
|
Hedgehog ‘off’ state
|
105
|
1.74e-06
|
1.54e-05
|
0.29200
|
0.065000
|
-2.84e-01
|
2.50e-01
|
4.91e-07
|
Negative regulation of NMDA receptor-mediated neuronal transmission
|
16
|
1.31e-01
|
2.56e-01
|
0.29100
|
0.056000
|
-2.86e-01
|
6.98e-01
|
4.77e-02
|
Regulation of FZD by ubiquitination
|
16
|
1.33e-01
|
2.58e-01
|
0.29100
|
0.237000
|
-1.70e-01
|
1.01e-01
|
2.40e-01
|
Defective B3GALT6 causes EDSP2 and SEMDJL1
|
17
|
1.18e-01
|
2.40e-01
|
0.29000
|
0.025500
|
-2.89e-01
|
8.56e-01
|
3.93e-02
|
Defective B3GAT3 causes JDSSDHD
|
17
|
1.18e-01
|
2.40e-01
|
0.29000
|
0.034200
|
-2.88e-01
|
8.07e-01
|
4.00e-02
|
Hyaluronan uptake and degradation
|
11
|
2.50e-01
|
4.10e-01
|
0.28900
|
-0.266000
|
-1.12e-01
|
1.26e-01
|
5.19e-01
|
APC/C-mediated degradation of cell cycle proteins
|
84
|
2.78e-05
|
1.78e-04
|
0.28900
|
-0.028600
|
-2.88e-01
|
6.51e-01
|
5.26e-06
|
Regulation of mitotic cell cycle
|
84
|
2.78e-05
|
1.78e-04
|
0.28900
|
-0.028600
|
-2.88e-01
|
6.51e-01
|
5.26e-06
|
Citric acid cycle (TCA cycle)
|
22
|
6.34e-02
|
1.52e-01
|
0.28800
|
-0.214000
|
-1.93e-01
|
8.29e-02
|
1.17e-01
|
Uptake and actions of bacterial toxins
|
25
|
4.40e-02
|
1.16e-01
|
0.28800
|
-0.102000
|
-2.69e-01
|
3.76e-01
|
1.98e-02
|
UCH proteinases
|
85
|
2.71e-05
|
1.75e-04
|
0.28800
|
-0.000648
|
-2.88e-01
|
9.92e-01
|
4.51e-06
|
Formation of paraxial mesoderm
|
62
|
4.73e-04
|
2.42e-03
|
0.28700
|
-0.011000
|
-2.87e-01
|
8.81e-01
|
9.27e-05
|
Cellular response to chemical stress
|
183
|
1.79e-10
|
3.87e-09
|
0.28700
|
-0.049600
|
-2.83e-01
|
2.48e-01
|
4.45e-11
|
Purine catabolism
|
13
|
2.05e-01
|
3.54e-01
|
0.28600
|
0.164000
|
-2.35e-01
|
3.07e-01
|
1.42e-01
|
NOTCH4 Intracellular Domain Regulates Transcription
|
19
|
9.67e-02
|
2.07e-01
|
0.28500
|
0.117000
|
2.61e-01
|
3.79e-01
|
4.93e-02
|
Repression of WNT target genes
|
14
|
1.84e-01
|
3.27e-01
|
0.28500
|
0.230000
|
-1.69e-01
|
1.36e-01
|
2.75e-01
|
CLEC7A (Dectin-1) induces NFAT activation
|
11
|
2.65e-01
|
4.26e-01
|
0.28500
|
0.170000
|
-2.29e-01
|
3.30e-01
|
1.88e-01
|
RHO GTPases Activate ROCKs
|
18
|
1.15e-01
|
2.38e-01
|
0.28300
|
0.278000
|
-5.41e-02
|
4.10e-02
|
6.91e-01
|
DNA Replication Pre-Initiation
|
102
|
5.30e-06
|
4.10e-05
|
0.28300
|
0.081400
|
-2.71e-01
|
1.56e-01
|
2.22e-06
|
The citric acid (TCA) cycle and respiratory electron transport
|
160
|
6.24e-09
|
1.02e-07
|
0.28200
|
0.030200
|
-2.80e-01
|
5.11e-01
|
9.52e-10
|
Acyl chain remodelling of PE
|
17
|
1.35e-01
|
2.60e-01
|
0.28200
|
-0.187000
|
2.11e-01
|
1.83e-01
|
1.32e-01
|
DAP12 interactions
|
35
|
1.57e-02
|
5.08e-02
|
0.28100
|
-0.278000
|
-4.09e-02
|
4.39e-03
|
6.75e-01
|
Antigen processing-Cross presentation
|
92
|
1.90e-05
|
1.26e-04
|
0.28000
|
-0.170000
|
-2.23e-01
|
4.83e-03
|
2.25e-04
|
Regulation of mRNA stability by proteins that bind AU-rich elements
|
87
|
3.90e-05
|
2.38e-04
|
0.28000
|
0.029800
|
-2.78e-01
|
6.31e-01
|
7.30e-06
|
Signaling by FGFR2 in disease
|
34
|
1.94e-02
|
6.17e-02
|
0.27900
|
0.161000
|
-2.29e-01
|
1.05e-01
|
2.11e-02
|
IRAK2 mediated activation of TAK1 complex
|
10
|
3.12e-01
|
4.70e-01
|
0.27900
|
0.080900
|
-2.67e-01
|
6.58e-01
|
1.43e-01
|
Non-integrin membrane-ECM interactions
|
54
|
1.90e-03
|
8.36e-03
|
0.27900
|
0.060300
|
-2.72e-01
|
4.43e-01
|
5.35e-04
|
Aspirin ADME
|
14
|
1.94e-01
|
3.41e-01
|
0.27900
|
-0.274000
|
-5.10e-02
|
7.56e-02
|
7.41e-01
|
Receptor Mediated Mitophagy
|
11
|
2.75e-01
|
4.35e-01
|
0.27900
|
-0.158000
|
-2.30e-01
|
3.65e-01
|
1.87e-01
|
Regulation of PTEN mRNA translation
|
11
|
2.75e-01
|
4.35e-01
|
0.27900
|
0.198000
|
1.96e-01
|
2.56e-01
|
2.60e-01
|
Germ layer formation at gastrulation
|
10
|
3.14e-01
|
4.71e-01
|
0.27900
|
0.268000
|
-7.56e-02
|
1.42e-01
|
6.79e-01
|
Mismatch Repair
|
14
|
1.99e-01
|
3.46e-01
|
0.27900
|
0.149000
|
-2.35e-01
|
3.35e-01
|
1.27e-01
|
EGR2 and SOX10-mediated initiation of Schwann cell myelination
|
23
|
7.08e-02
|
1.64e-01
|
0.27800
|
0.218000
|
-1.73e-01
|
7.05e-02
|
1.50e-01
|
Formation of the cornified envelope
|
23
|
6.77e-02
|
1.58e-01
|
0.27800
|
-0.180000
|
-2.12e-01
|
1.35e-01
|
7.83e-02
|
Keratinization
|
23
|
6.77e-02
|
1.58e-01
|
0.27800
|
-0.180000
|
-2.12e-01
|
1.35e-01
|
7.83e-02
|
Insulin processing
|
21
|
8.62e-02
|
1.91e-01
|
0.27800
|
-0.256000
|
-1.09e-01
|
4.24e-02
|
3.86e-01
|
Cellular responses to stimuli
|
702
|
1.37e-34
|
9.61e-33
|
0.27800
|
0.069900
|
-2.69e-01
|
1.71e-03
|
9.16e-34
|
Interferon gamma signaling
|
74
|
1.95e-04
|
1.09e-03
|
0.27800
|
-0.278000
|
7.48e-03
|
3.59e-05
|
9.11e-01
|
Diseases associated with the TLR signaling cascade
|
27
|
4.43e-02
|
1.16e-01
|
0.27800
|
-0.277000
|
2.12e-02
|
1.27e-02
|
8.49e-01
|
Diseases of Immune System
|
27
|
4.43e-02
|
1.16e-01
|
0.27800
|
-0.277000
|
2.12e-02
|
1.27e-02
|
8.49e-01
|
Initiation of Nuclear Envelope (NE) Reformation
|
19
|
1.13e-01
|
2.34e-01
|
0.27800
|
0.121000
|
-2.50e-01
|
3.61e-01
|
5.92e-02
|
Cytochrome c-mediated apoptotic response
|
13
|
2.25e-01
|
3.81e-01
|
0.27700
|
-0.120000
|
2.50e-01
|
4.53e-01
|
1.18e-01
|
Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha)
|
13
|
2.27e-01
|
3.83e-01
|
0.27700
|
0.191000
|
-2.01e-01
|
2.34e-01
|
2.09e-01
|
Peptide ligand-binding receptors
|
79
|
1.17e-04
|
6.62e-04
|
0.27700
|
-0.053900
|
-2.71e-01
|
4.08e-01
|
3.09e-05
|
Interferon alpha/beta signaling
|
57
|
1.42e-03
|
6.48e-03
|
0.27600
|
-0.253000
|
-1.12e-01
|
9.74e-04
|
1.43e-01
|
FRS-mediated FGFR2 signaling
|
16
|
1.64e-01
|
3.04e-01
|
0.27600
|
0.161000
|
-2.24e-01
|
2.64e-01
|
1.21e-01
|
Pre-NOTCH Processing in Golgi
|
18
|
1.26e-01
|
2.50e-01
|
0.27600
|
-0.202000
|
-1.88e-01
|
1.39e-01
|
1.67e-01
|
Regulation of TP53 Expression and Degradation
|
36
|
1.69e-02
|
5.42e-02
|
0.27500
|
-0.008350
|
-2.75e-01
|
9.31e-01
|
4.30e-03
|
Translesion synthesis by REV1
|
16
|
1.68e-01
|
3.09e-01
|
0.27400
|
0.175000
|
-2.11e-01
|
2.25e-01
|
1.44e-01
|
TNFR1-induced NF-kappa-B signaling pathway
|
33
|
2.37e-02
|
7.13e-02
|
0.27400
|
-0.190000
|
-1.98e-01
|
5.92e-02
|
4.96e-02
|
Neutrophil degranulation
|
423
|
4.48e-21
|
1.78e-19
|
0.27400
|
-0.188000
|
-1.99e-01
|
3.84e-11
|
2.51e-12
|
Biosynthesis of specialized proresolving mediators (SPMs)
|
13
|
2.35e-01
|
3.93e-01
|
0.27400
|
-0.255000
|
9.97e-02
|
1.12e-01
|
5.34e-01
|
ERKs are inactivated
|
13
|
2.34e-01
|
3.92e-01
|
0.27300
|
-0.029300
|
-2.71e-01
|
8.55e-01
|
9.04e-02
|
RORA activates gene expression
|
18
|
1.37e-01
|
2.63e-01
|
0.27300
|
-0.137000
|
2.36e-01
|
3.15e-01
|
8.31e-02
|
Apoptotic execution phase
|
42
|
8.96e-03
|
3.16e-02
|
0.27300
|
0.211000
|
1.72e-01
|
1.79e-02
|
5.33e-02
|
Cellular responses to stress
|
693
|
7.77e-33
|
4.96e-31
|
0.27200
|
0.071800
|
-2.63e-01
|
1.34e-03
|
6.67e-32
|
Signaling by FGFR4 in disease
|
10
|
3.27e-01
|
4.82e-01
|
0.27200
|
0.131000
|
2.38e-01
|
4.73e-01
|
1.92e-01
|
Attachment and Entry 9694614
|
16
|
1.68e-01
|
3.09e-01
|
0.27200
|
-0.157000
|
-2.22e-01
|
2.78e-01
|
1.24e-01
|
Gap junction trafficking
|
32
|
2.89e-02
|
8.35e-02
|
0.27200
|
-0.045600
|
-2.68e-01
|
6.55e-01
|
8.79e-03
|
Telomere Extension By Telomerase
|
21
|
9.91e-02
|
2.11e-01
|
0.27100
|
0.044900
|
-2.68e-01
|
7.22e-01
|
3.37e-02
|
TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest
|
11
|
2.95e-01
|
4.57e-01
|
0.27100
|
-0.177000
|
-2.05e-01
|
3.10e-01
|
2.38e-01
|
Cardiogenesis
|
18
|
1.39e-01
|
2.67e-01
|
0.27100
|
0.267000
|
-4.67e-02
|
4.99e-02
|
7.32e-01
|
Spry regulation of FGF signaling
|
16
|
1.73e-01
|
3.13e-01
|
0.27100
|
0.021500
|
-2.70e-01
|
8.82e-01
|
6.15e-02
|
Signaling by CSF3 (G-CSF)
|
29
|
4.12e-02
|
1.10e-01
|
0.27100
|
-0.051700
|
-2.66e-01
|
6.30e-01
|
1.33e-02
|
Cyclin D associated events in G1
|
47
|
5.85e-03
|
2.17e-02
|
0.27000
|
-0.016400
|
-2.70e-01
|
8.46e-01
|
1.38e-03
|
G1 Phase
|
47
|
5.85e-03
|
2.17e-02
|
0.27000
|
-0.016400
|
-2.70e-01
|
8.46e-01
|
1.38e-03
|
RNA Polymerase III Chain Elongation
|
18
|
1.43e-01
|
2.72e-01
|
0.27000
|
0.167000
|
-2.12e-01
|
2.20e-01
|
1.19e-01
|
Fcgamma receptor (FCGR) dependent phagocytosis
|
90
|
5.43e-05
|
3.24e-04
|
0.26900
|
-0.240000
|
-1.23e-01
|
8.41e-05
|
4.46e-02
|
Signaling by PDGFRA extracellular domain mutants
|
12
|
2.68e-01
|
4.29e-01
|
0.26900
|
-0.166000
|
-2.12e-01
|
3.20e-01
|
2.03e-01
|
Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants
|
12
|
2.68e-01
|
4.29e-01
|
0.26900
|
-0.166000
|
-2.12e-01
|
3.20e-01
|
2.03e-01
|
Platelet Adhesion to exposed collagen
|
11
|
3.05e-01
|
4.66e-01
|
0.26900
|
0.033500
|
-2.67e-01
|
8.47e-01
|
1.26e-01
|
Metabolism of folate and pterines
|
16
|
1.74e-01
|
3.16e-01
|
0.26900
|
-0.207000
|
-1.71e-01
|
1.52e-01
|
2.35e-01
|
Regulation of actin dynamics for phagocytic cup formation
|
67
|
6.86e-04
|
3.45e-03
|
0.26900
|
-0.236000
|
-1.29e-01
|
8.61e-04
|
6.71e-02
|
RIP-mediated NFkB activation via ZBP1
|
17
|
1.58e-01
|
2.94e-01
|
0.26800
|
-0.158000
|
-2.17e-01
|
2.59e-01
|
1.22e-01
|
Mitotic G1 phase and G1/S transition
|
143
|
2.49e-07
|
2.65e-06
|
0.26700
|
-0.013100
|
-2.67e-01
|
7.86e-01
|
3.68e-08
|
AKT phosphorylates targets in the nucleus
|
10
|
3.44e-01
|
4.99e-01
|
0.26700
|
0.013300
|
-2.67e-01
|
9.42e-01
|
1.44e-01
|
Alpha-protein kinase 1 signaling pathway
|
11
|
3.11e-01
|
4.70e-01
|
0.26700
|
0.072500
|
-2.57e-01
|
6.77e-01
|
1.40e-01
|
Blood group systems biosynthesis
|
13
|
2.55e-01
|
4.15e-01
|
0.26600
|
0.210000
|
-1.63e-01
|
1.90e-01
|
3.08e-01
|
EPH-ephrin mediated repulsion of cells
|
44
|
9.52e-03
|
3.31e-02
|
0.26500
|
-0.261000
|
-4.97e-02
|
2.77e-03
|
5.68e-01
|
Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells
|
12
|
2.83e-01
|
4.46e-01
|
0.26500
|
-0.057400
|
2.59e-01
|
7.31e-01
|
1.20e-01
|
Chaperonin-mediated protein folding
|
77
|
3.29e-04
|
1.75e-03
|
0.26500
|
0.120000
|
-2.36e-01
|
6.90e-02
|
3.38e-04
|
Nuclear events stimulated by ALK signaling in cancer
|
18
|
1.50e-01
|
2.83e-01
|
0.26500
|
-0.040400
|
-2.62e-01
|
7.67e-01
|
5.45e-02
|
Formation of HIV-1 elongation complex containing HIV-1 Tat
|
42
|
1.28e-02
|
4.22e-02
|
0.26400
|
0.095200
|
-2.46e-01
|
2.86e-01
|
5.75e-03
|
HIV Transcription Elongation
|
42
|
1.28e-02
|
4.22e-02
|
0.26400
|
0.095200
|
-2.46e-01
|
2.86e-01
|
5.75e-03
|
Tat-mediated elongation of the HIV-1 transcript
|
42
|
1.28e-02
|
4.22e-02
|
0.26400
|
0.095200
|
-2.46e-01
|
2.86e-01
|
5.75e-03
|
Nuclear Events (kinase and transcription factor activation)
|
57
|
2.84e-03
|
1.18e-02
|
0.26300
|
0.148000
|
-2.18e-01
|
5.30e-02
|
4.48e-03
|
ABC-family proteins mediated transport
|
90
|
8.69e-05
|
5.06e-04
|
0.26300
|
-0.101000
|
-2.43e-01
|
9.89e-02
|
6.83e-05
|
Nucleotide biosynthesis
|
12
|
2.85e-01
|
4.49e-01
|
0.26300
|
-0.144000
|
-2.20e-01
|
3.89e-01
|
1.86e-01
|
CD28 dependent PI3K/Akt signaling
|
21
|
1.13e-01
|
2.33e-01
|
0.26300
|
-0.252000
|
-7.44e-02
|
4.55e-02
|
5.55e-01
|
Nucleotide-like (purinergic) receptors
|
15
|
2.13e-01
|
3.65e-01
|
0.26200
|
0.030600
|
2.60e-01
|
8.37e-01
|
8.10e-02
|
Pyruvate metabolism
|
27
|
6.23e-02
|
1.50e-01
|
0.26100
|
-0.139000
|
-2.21e-01
|
2.11e-01
|
4.72e-02
|
Intra-Golgi traffic
|
41
|
1.50e-02
|
4.89e-02
|
0.26100
|
-0.250000
|
-7.40e-02
|
5.57e-03
|
4.13e-01
|
Interleukin-1 family signaling
|
137
|
9.63e-07
|
9.01e-06
|
0.26000
|
-0.028000
|
-2.59e-01
|
5.72e-01
|
1.71e-07
|
Signaling by FGFR3 in disease
|
16
|
2.00e-01
|
3.47e-01
|
0.26000
|
0.216000
|
-1.45e-01
|
1.35e-01
|
3.15e-01
|
Signaling by the B Cell Receptor (BCR)
|
109
|
1.61e-05
|
1.08e-04
|
0.26000
|
-0.038700
|
-2.57e-01
|
4.86e-01
|
3.49e-06
|
CD28 co-stimulation
|
32
|
3.92e-02
|
1.05e-01
|
0.25900
|
-0.250000
|
-7.05e-02
|
1.45e-02
|
4.90e-01
|
Antigen activates B Cell Receptor (BCR) leading to generation of second messengers
|
32
|
3.96e-02
|
1.06e-01
|
0.25900
|
-0.253000
|
-5.68e-02
|
1.34e-02
|
5.78e-01
|
Glycogen metabolism
|
23
|
1.04e-01
|
2.19e-01
|
0.25800
|
0.148000
|
-2.11e-01
|
2.19e-01
|
8.03e-02
|
Cytosolic iron-sulfur cluster assembly
|
13
|
2.75e-01
|
4.35e-01
|
0.25700
|
-0.257000
|
-6.93e-03
|
1.08e-01
|
9.66e-01
|
Regulation of TP53 Degradation
|
35
|
3.12e-02
|
8.89e-02
|
0.25700
|
-0.012500
|
-2.57e-01
|
8.99e-01
|
8.56e-03
|
Gap junction trafficking and regulation
|
34
|
3.43e-02
|
9.51e-02
|
0.25700
|
-0.037800
|
-2.54e-01
|
7.03e-01
|
1.03e-02
|
Peptide hormone metabolism
|
51
|
6.37e-03
|
2.34e-02
|
0.25700
|
-0.092600
|
-2.39e-01
|
2.53e-01
|
3.11e-03
|
Signaling by Interleukins
|
388
|
5.09e-17
|
1.46e-15
|
0.25600
|
-0.085600
|
-2.41e-01
|
3.92e-03
|
3.97e-16
|
Interleukin-12 family signaling
|
47
|
9.79e-03
|
3.38e-02
|
0.25600
|
-0.095800
|
-2.37e-01
|
2.56e-01
|
4.93e-03
|
PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases
|
14
|
2.53e-01
|
4.12e-01
|
0.25600
|
0.048200
|
2.51e-01
|
7.55e-01
|
1.04e-01
|
Regulation of TNFR1 signaling
|
48
|
8.94e-03
|
3.16e-02
|
0.25500
|
-0.156000
|
-2.02e-01
|
6.08e-02
|
1.57e-02
|
SARS-CoV-1 targets host intracellular signalling and regulatory pathways
|
16
|
2.08e-01
|
3.58e-01
|
0.25500
|
0.110000
|
2.30e-01
|
4.44e-01
|
1.11e-01
|
Sema4D in semaphorin signaling
|
23
|
1.09e-01
|
2.27e-01
|
0.25400
|
0.241000
|
-8.13e-02
|
4.54e-02
|
5.00e-01
|
Condensation of Prometaphase Chromosomes
|
11
|
3.42e-01
|
4.98e-01
|
0.25400
|
-0.213000
|
-1.39e-01
|
2.22e-01
|
4.24e-01
|
Molecules associated with elastic fibres
|
33
|
4.05e-02
|
1.08e-01
|
0.25400
|
-0.106000
|
-2.31e-01
|
2.94e-01
|
2.17e-02
|
Disorders of Developmental Biology
|
11
|
3.49e-01
|
5.04e-01
|
0.25200
|
-0.192000
|
-1.63e-01
|
2.70e-01
|
3.50e-01
|
Disorders of Nervous System Development
|
11
|
3.49e-01
|
5.04e-01
|
0.25200
|
-0.192000
|
-1.63e-01
|
2.70e-01
|
3.50e-01
|
Loss of function of MECP2 in Rett syndrome
|
11
|
3.49e-01
|
5.04e-01
|
0.25200
|
-0.192000
|
-1.63e-01
|
2.70e-01
|
3.50e-01
|
Pervasive developmental disorders
|
11
|
3.49e-01
|
5.04e-01
|
0.25200
|
-0.192000
|
-1.63e-01
|
2.70e-01
|
3.50e-01
|
Platelet sensitization by LDL
|
17
|
1.98e-01
|
3.45e-01
|
0.25100
|
-0.103000
|
-2.29e-01
|
4.63e-01
|
1.01e-01
|
Formation of RNA Pol II elongation complex
|
56
|
5.24e-03
|
1.98e-02
|
0.25100
|
0.090500
|
-2.34e-01
|
2.42e-01
|
2.43e-03
|
RNA Polymerase II Transcription Elongation
|
56
|
5.24e-03
|
1.98e-02
|
0.25100
|
0.090500
|
-2.34e-01
|
2.42e-01
|
2.43e-03
|
MHC class II antigen presentation
|
97
|
1.02e-04
|
5.85e-04
|
0.25100
|
-0.145000
|
-2.05e-01
|
1.39e-02
|
4.86e-04
|
FCERI mediated Ca+2 mobilization
|
35
|
3.62e-02
|
9.94e-02
|
0.25100
|
-0.229000
|
-1.01e-01
|
1.89e-02
|
2.99e-01
|
Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta)
|
13
|
2.98e-01
|
4.60e-01
|
0.25100
|
0.146000
|
-2.03e-01
|
3.61e-01
|
2.04e-01
|
Platelet degranulation
|
110
|
3.13e-05
|
1.97e-04
|
0.25100
|
-0.129000
|
-2.15e-01
|
1.93e-02
|
1.02e-04
|
G1/S Transition
|
125
|
8.50e-06
|
6.06e-05
|
0.25000
|
0.001500
|
-2.50e-01
|
9.77e-01
|
1.35e-06
|
Signaling by CSF1 (M-CSF) in myeloid cells
|
31
|
5.41e-02
|
1.33e-01
|
0.25000
|
-0.239000
|
-7.48e-02
|
2.15e-02
|
4.71e-01
|
RAF-independent MAPK1/3 activation
|
22
|
1.30e-01
|
2.54e-01
|
0.25000
|
0.153000
|
-1.98e-01
|
2.15e-01
|
1.08e-01
|
Plasma lipoprotein assembly, remodeling, and clearance
|
55
|
5.86e-03
|
2.17e-02
|
0.24900
|
-0.241000
|
-6.49e-02
|
2.01e-03
|
4.05e-01
|
CASP8 activity is inhibited
|
10
|
3.95e-01
|
5.51e-01
|
0.24900
|
-0.012200
|
-2.48e-01
|
9.47e-01
|
1.74e-01
|
Dimerization of procaspase-8
|
10
|
3.95e-01
|
5.51e-01
|
0.24900
|
-0.012200
|
-2.48e-01
|
9.47e-01
|
1.74e-01
|
Regulation by c-FLIP
|
10
|
3.95e-01
|
5.51e-01
|
0.24900
|
-0.012200
|
-2.48e-01
|
9.47e-01
|
1.74e-01
|
FCGR3A-mediated phagocytosis
|
65
|
2.40e-03
|
1.02e-02
|
0.24900
|
-0.234000
|
-8.27e-02
|
1.09e-03
|
2.49e-01
|
Leishmania phagocytosis
|
65
|
2.40e-03
|
1.02e-02
|
0.24900
|
-0.234000
|
-8.27e-02
|
1.09e-03
|
2.49e-01
|
Parasite infection
|
65
|
2.40e-03
|
1.02e-02
|
0.24900
|
-0.234000
|
-8.27e-02
|
1.09e-03
|
2.49e-01
|
Constitutive Signaling by NOTCH1 HD Domain Mutants
|
15
|
2.50e-01
|
4.10e-01
|
0.24800
|
0.248000
|
-1.69e-04
|
9.60e-02
|
9.99e-01
|
Signaling by NOTCH1 HD Domain Mutants in Cancer
|
15
|
2.50e-01
|
4.10e-01
|
0.24800
|
0.248000
|
-1.69e-04
|
9.60e-02
|
9.99e-01
|
GABA synthesis, release, reuptake and degradation
|
13
|
3.02e-01
|
4.64e-01
|
0.24800
|
-0.007960
|
-2.48e-01
|
9.60e-01
|
1.22e-01
|
Anti-inflammatory response favouring Leishmania parasite infection
|
74
|
1.07e-03
|
5.16e-03
|
0.24800
|
-0.227000
|
-9.92e-02
|
7.32e-04
|
1.40e-01
|
Leishmania parasite growth and survival
|
74
|
1.07e-03
|
5.16e-03
|
0.24800
|
-0.227000
|
-9.92e-02
|
7.32e-04
|
1.40e-01
|
Biosynthesis of DHA-derived SPMs
|
11
|
3.68e-01
|
5.22e-01
|
0.24700
|
-0.206000
|
1.37e-01
|
2.37e-01
|
4.32e-01
|
Gastrulation
|
85
|
4.64e-04
|
2.39e-03
|
0.24600
|
0.060800
|
-2.39e-01
|
3.33e-01
|
1.42e-04
|
Platelet calcium homeostasis
|
22
|
1.34e-01
|
2.59e-01
|
0.24600
|
-0.091800
|
-2.28e-01
|
4.56e-01
|
6.37e-02
|
Smooth Muscle Contraction
|
37
|
3.58e-02
|
9.85e-02
|
0.24600
|
0.217000
|
-1.16e-01
|
2.23e-02
|
2.23e-01
|
Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation
|
34
|
4.58e-02
|
1.18e-01
|
0.24600
|
-0.022000
|
-2.45e-01
|
8.24e-01
|
1.35e-02
|
Nervous system development
|
506
|
6.26e-20
|
2.36e-18
|
0.24600
|
0.117000
|
-2.16e-01
|
7.16e-06
|
1.05e-16
|
Diseases of carbohydrate metabolism
|
28
|
7.79e-02
|
1.77e-01
|
0.24600
|
-0.158000
|
-1.88e-01
|
1.47e-01
|
8.56e-02
|
NOTCH2 intracellular domain regulates transcription
|
10
|
4.08e-01
|
5.62e-01
|
0.24600
|
-0.219000
|
1.12e-01
|
2.31e-01
|
5.41e-01
|
Fc epsilon receptor (FCERI) signaling
|
131
|
7.68e-06
|
5.64e-05
|
0.24500
|
-0.068600
|
-2.35e-01
|
1.76e-01
|
3.35e-06
|
Protein folding
|
83
|
6.57e-04
|
3.32e-03
|
0.24400
|
0.110000
|
-2.18e-01
|
8.42e-02
|
6.00e-04
|
Defective EXT1 causes exostoses 1, TRPS2 and CHDS
|
14
|
2.86e-01
|
4.49e-01
|
0.24400
|
-0.061400
|
-2.36e-01
|
6.91e-01
|
1.27e-01
|
Defective EXT2 causes exostoses 2
|
14
|
2.86e-01
|
4.49e-01
|
0.24400
|
-0.061400
|
-2.36e-01
|
6.91e-01
|
1.27e-01
|
Formation of the Early Elongation Complex
|
33
|
5.44e-02
|
1.33e-01
|
0.24400
|
0.091300
|
-2.26e-01
|
3.64e-01
|
2.48e-02
|
Formation of the HIV-1 Early Elongation Complex
|
33
|
5.44e-02
|
1.33e-01
|
0.24400
|
0.091300
|
-2.26e-01
|
3.64e-01
|
2.48e-02
|
Activation of BAD and translocation to mitochondria
|
15
|
2.67e-01
|
4.28e-01
|
0.24300
|
0.124000
|
-2.09e-01
|
4.05e-01
|
1.61e-01
|
Axon guidance
|
486
|
8.66e-19
|
2.89e-17
|
0.24300
|
0.111000
|
-2.16e-01
|
2.95e-05
|
3.92e-16
|
Integrin signaling
|
23
|
1.30e-01
|
2.54e-01
|
0.24300
|
-0.234000
|
-6.56e-02
|
5.21e-02
|
5.86e-01
|
RNA Pol II CTD phosphorylation and interaction with CE
|
27
|
9.42e-02
|
2.03e-01
|
0.24300
|
0.104000
|
-2.19e-01
|
3.52e-01
|
4.85e-02
|
RNA Pol II CTD phosphorylation and interaction with CE during HIV infection
|
27
|
9.42e-02
|
2.03e-01
|
0.24300
|
0.104000
|
-2.19e-01
|
3.52e-01
|
4.85e-02
|
Activation of IRF3, IRF7 mediated by TBK1, IKBKE
|
17
|
2.21e-01
|
3.75e-01
|
0.24200
|
-0.152000
|
-1.88e-01
|
2.77e-01
|
1.79e-01
|
p75NTR recruits signalling complexes
|
13
|
3.20e-01
|
4.74e-01
|
0.24200
|
0.030500
|
-2.40e-01
|
8.49e-01
|
1.34e-01
|
Bacterial Infection Pathways
|
65
|
3.33e-03
|
1.36e-02
|
0.24100
|
-0.122000
|
-2.09e-01
|
9.03e-02
|
3.65e-03
|
IRAK1 recruits IKK complex
|
14
|
2.98e-01
|
4.60e-01
|
0.24100
|
0.217000
|
-1.05e-01
|
1.59e-01
|
4.97e-01
|
IRAK1 recruits IKK complex upon TLR7/8 or 9 stimulation
|
14
|
2.98e-01
|
4.60e-01
|
0.24100
|
0.217000
|
-1.05e-01
|
1.59e-01
|
4.97e-01
|
Response to elevated platelet cytosolic Ca2+
|
114
|
4.75e-05
|
2.88e-04
|
0.24100
|
-0.124000
|
-2.07e-01
|
2.27e-02
|
1.36e-04
|
Signaling by FGFR3
|
34
|
5.29e-02
|
1.32e-01
|
0.24100
|
0.098300
|
-2.20e-01
|
3.22e-01
|
2.63e-02
|
Regulation of pyruvate dehydrogenase (PDH) complex
|
15
|
2.68e-01
|
4.29e-01
|
0.24100
|
-0.190000
|
-1.47e-01
|
2.02e-01
|
3.23e-01
|
Transcriptional regulation by RUNX1
|
164
|
7.71e-07
|
7.55e-06
|
0.24100
|
0.059000
|
-2.33e-01
|
1.93e-01
|
2.54e-07
|
Heparan sulfate/heparin (HS-GAG) metabolism
|
43
|
2.34e-02
|
7.09e-02
|
0.24000
|
-0.176000
|
-1.64e-01
|
4.60e-02
|
6.30e-02
|
The phototransduction cascade
|
19
|
1.96e-01
|
3.43e-01
|
0.24000
|
0.197000
|
-1.37e-01
|
1.37e-01
|
3.00e-01
|
HS-GAG degradation
|
22
|
1.50e-01
|
2.83e-01
|
0.24000
|
-0.240000
|
1.60e-02
|
5.17e-02
|
8.97e-01
|
Signaling by NOTCH4
|
81
|
9.55e-04
|
4.68e-03
|
0.24000
|
0.034800
|
-2.38e-01
|
5.88e-01
|
2.20e-04
|
Innate Immune System
|
870
|
4.42e-32
|
2.50e-30
|
0.24000
|
-0.180000
|
-1.59e-01
|
2.94e-19
|
2.92e-15
|
TAK1-dependent IKK and NF-kappa-B activation
|
43
|
2.45e-02
|
7.30e-02
|
0.23900
|
-0.090200
|
-2.22e-01
|
3.06e-01
|
1.19e-02
|
Metabolism of nucleotides
|
81
|
9.83e-04
|
4.80e-03
|
0.23900
|
-0.008120
|
-2.39e-01
|
9.00e-01
|
2.01e-04
|
Synthesis of PIPs at the late endosome membrane
|
11
|
3.94e-01
|
5.51e-01
|
0.23800
|
-0.115000
|
2.09e-01
|
5.09e-01
|
2.30e-01
|
Translesion synthesis by POLI
|
17
|
2.38e-01
|
3.95e-01
|
0.23800
|
0.193000
|
-1.40e-01
|
1.69e-01
|
3.16e-01
|
Translesion synthesis by POLK
|
17
|
2.39e-01
|
3.96e-01
|
0.23800
|
0.169000
|
-1.68e-01
|
2.28e-01
|
2.31e-01
|
Detoxification of Reactive Oxygen Species
|
33
|
6.12e-02
|
1.48e-01
|
0.23700
|
-0.068000
|
-2.27e-01
|
4.99e-01
|
2.39e-02
|
Nuclear Pore Complex (NPC) Disassembly
|
36
|
4.99e-02
|
1.27e-01
|
0.23700
|
-0.189000
|
1.43e-01
|
4.95e-02
|
1.39e-01
|
Inactivation, recovery and regulation of the phototransduction cascade
|
18
|
2.24e-01
|
3.79e-01
|
0.23600
|
0.198000
|
-1.29e-01
|
1.46e-01
|
3.42e-01
|
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein
|
72
|
2.36e-03
|
1.01e-02
|
0.23600
|
-0.128000
|
-1.99e-01
|
6.11e-02
|
3.57e-03
|
Signaling by Hedgehog
|
139
|
9.90e-06
|
6.93e-05
|
0.23600
|
0.014000
|
-2.36e-01
|
7.76e-01
|
1.63e-06
|
Glutamate binding, activation of AMPA receptors and synaptic plasticity
|
24
|
1.32e-01
|
2.57e-01
|
0.23600
|
-0.181000
|
-1.52e-01
|
1.26e-01
|
1.97e-01
|
Trafficking of AMPA receptors
|
24
|
1.32e-01
|
2.57e-01
|
0.23600
|
-0.181000
|
-1.52e-01
|
1.26e-01
|
1.97e-01
|
RHOBTB GTPase Cycle
|
35
|
5.35e-02
|
1.32e-01
|
0.23600
|
0.210000
|
1.08e-01
|
3.20e-02
|
2.71e-01
|
Signaling by FGFR4
|
32
|
7.18e-02
|
1.65e-01
|
0.23500
|
0.121000
|
-2.02e-01
|
2.35e-01
|
4.84e-02
|
SHC-mediated cascade:FGFR1
|
13
|
3.42e-01
|
4.98e-01
|
0.23500
|
0.061000
|
-2.27e-01
|
7.03e-01
|
1.56e-01
|
Signaling by Activin
|
13
|
3.41e-01
|
4.97e-01
|
0.23500
|
0.235000
|
-4.59e-03
|
1.42e-01
|
9.77e-01
|
Early Phase of HIV Life Cycle
|
14
|
3.12e-01
|
4.70e-01
|
0.23500
|
-0.229000
|
-5.12e-02
|
1.37e-01
|
7.40e-01
|
RNA Polymerase II Pre-transcription Events
|
77
|
1.84e-03
|
8.12e-03
|
0.23500
|
0.113000
|
-2.06e-01
|
8.71e-02
|
1.78e-03
|
PIWI-interacting RNA (piRNA) biogenesis
|
22
|
1.64e-01
|
3.04e-01
|
0.23500
|
0.077800
|
-2.22e-01
|
5.28e-01
|
7.20e-02
|
Regulation of TP53 Activity through Acetylation
|
29
|
9.12e-02
|
1.99e-01
|
0.23400
|
-0.074200
|
-2.22e-01
|
4.89e-01
|
3.84e-02
|
PI-3K cascade:FGFR1
|
13
|
3.44e-01
|
5.00e-01
|
0.23400
|
0.233000
|
-1.98e-02
|
1.45e-01
|
9.02e-01
|
HS-GAG biosynthesis
|
23
|
1.52e-01
|
2.86e-01
|
0.23400
|
-0.019700
|
-2.33e-01
|
8.70e-01
|
5.31e-02
|
Kinesins
|
46
|
2.35e-02
|
7.09e-02
|
0.23400
|
0.026900
|
-2.32e-01
|
7.53e-01
|
6.46e-03
|
NS1 Mediated Effects on Host Pathways
|
40
|
3.97e-02
|
1.06e-01
|
0.23300
|
-0.124000
|
1.97e-01
|
1.74e-01
|
3.09e-02
|
Leading Strand Synthesis
|
14
|
3.19e-01
|
4.74e-01
|
0.23300
|
0.032200
|
2.31e-01
|
8.35e-01
|
1.35e-01
|
Polymerase switching
|
14
|
3.19e-01
|
4.74e-01
|
0.23300
|
0.032200
|
2.31e-01
|
8.35e-01
|
1.35e-01
|
ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression
|
22
|
1.72e-01
|
3.13e-01
|
0.23200
|
0.152000
|
-1.76e-01
|
2.17e-01
|
1.54e-01
|
DNA Replication
|
127
|
3.95e-05
|
2.41e-04
|
0.23200
|
0.052300
|
-2.26e-01
|
3.09e-01
|
1.10e-05
|
Diseases of glycosylation
|
127
|
3.58e-05
|
2.22e-04
|
0.23200
|
-0.128000
|
-1.93e-01
|
1.29e-02
|
1.71e-04
|
ZBP1(DAI) mediated induction of type I IFNs
|
20
|
1.98e-01
|
3.45e-01
|
0.23200
|
-0.165000
|
-1.63e-01
|
2.02e-01
|
2.08e-01
|
Synthesis of substrates in N-glycan biosythesis
|
57
|
1.01e-02
|
3.46e-02
|
0.23100
|
-0.110000
|
-2.04e-01
|
1.50e-01
|
7.88e-03
|
Intraflagellar transport
|
49
|
2.00e-02
|
6.25e-02
|
0.23100
|
0.228000
|
-3.73e-02
|
5.69e-03
|
6.51e-01
|
Transport of Ribonucleoproteins into the Host Nucleus
|
32
|
7.87e-02
|
1.78e-01
|
0.23100
|
-0.158000
|
1.69e-01
|
1.23e-01
|
9.72e-02
|
TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain
|
11
|
4.19e-01
|
5.72e-01
|
0.23100
|
0.145000
|
-1.80e-01
|
4.06e-01
|
3.02e-01
|
Synthesis of DNA
|
116
|
1.08e-04
|
6.13e-04
|
0.23000
|
0.042000
|
-2.26e-01
|
4.35e-01
|
2.56e-05
|
Formation of HIV elongation complex in the absence of HIV Tat
|
44
|
3.13e-02
|
8.90e-02
|
0.23000
|
0.087500
|
-2.13e-01
|
3.16e-01
|
1.46e-02
|
Uptake and function of anthrax toxins
|
11
|
4.17e-01
|
5.70e-01
|
0.23000
|
-0.037100
|
-2.27e-01
|
8.31e-01
|
1.92e-01
|
Autophagy
|
138
|
2.12e-05
|
1.40e-04
|
0.23000
|
0.120000
|
-1.96e-01
|
1.48e-02
|
7.21e-05
|
Signaling by FGFR2
|
61
|
8.45e-03
|
3.00e-02
|
0.23000
|
0.098500
|
-2.07e-01
|
1.83e-01
|
5.10e-03
|
DAP12 signaling
|
27
|
1.20e-01
|
2.41e-01
|
0.22900
|
-0.222000
|
5.70e-02
|
4.58e-02
|
6.08e-01
|
Regulation of IFNG signaling
|
13
|
3.56e-01
|
5.11e-01
|
0.22900
|
-0.136000
|
-1.84e-01
|
3.96e-01
|
2.50e-01
|
Association of TriC/CCT with target proteins during biosynthesis
|
35
|
6.46e-02
|
1.54e-01
|
0.22900
|
0.056800
|
-2.22e-01
|
5.61e-01
|
2.31e-02
|
Surfactant metabolism
|
18
|
2.41e-01
|
3.98e-01
|
0.22900
|
0.071300
|
2.18e-01
|
6.00e-01
|
1.10e-01
|
VEGFR2 mediated cell proliferation
|
19
|
2.25e-01
|
3.80e-01
|
0.22800
|
-0.069900
|
-2.17e-01
|
5.98e-01
|
1.01e-01
|
MET activates PTK2 signaling
|
30
|
9.60e-02
|
2.06e-01
|
0.22800
|
-0.036200
|
-2.25e-01
|
7.31e-01
|
3.28e-02
|
Metabolic disorders of biological oxidation enzymes
|
23
|
1.64e-01
|
3.04e-01
|
0.22800
|
-0.122000
|
-1.93e-01
|
3.12e-01
|
1.10e-01
|
Processive synthesis on the C-strand of the telomere
|
19
|
2.31e-01
|
3.89e-01
|
0.22800
|
0.113000
|
-1.98e-01
|
3.94e-01
|
1.36e-01
|
RA biosynthesis pathway
|
15
|
3.10e-01
|
4.70e-01
|
0.22800
|
0.062600
|
2.19e-01
|
6.74e-01
|
1.42e-01
|
RHOBTB2 GTPase cycle
|
23
|
1.69e-01
|
3.10e-01
|
0.22800
|
0.224000
|
-4.14e-02
|
6.32e-02
|
7.31e-01
|
p38MAPK events
|
13
|
3.61e-01
|
5.16e-01
|
0.22800
|
-0.172000
|
-1.49e-01
|
2.82e-01
|
3.53e-01
|
TRAF6 mediated IRF7 activation in TLR7/8 or 9 signaling
|
13
|
3.64e-01
|
5.17e-01
|
0.22700
|
-0.057200
|
-2.20e-01
|
7.21e-01
|
1.70e-01
|
Erythropoietin activates Phosphoinositide-3-kinase (PI3K)
|
11
|
4.30e-01
|
5.84e-01
|
0.22700
|
-0.176000
|
1.44e-01
|
3.12e-01
|
4.10e-01
|
SARS-CoV-1 Infection
|
136
|
3.21e-05
|
2.01e-04
|
0.22700
|
0.124000
|
-1.90e-01
|
1.27e-02
|
1.30e-04
|
HIV Transcription Initiation
|
45
|
3.22e-02
|
9.06e-02
|
0.22700
|
0.151000
|
-1.70e-01
|
8.04e-02
|
4.90e-02
|
RNA Polymerase II HIV Promoter Escape
|
45
|
3.22e-02
|
9.06e-02
|
0.22700
|
0.151000
|
-1.70e-01
|
8.04e-02
|
4.90e-02
|
RNA Polymerase II Promoter Escape
|
45
|
3.22e-02
|
9.06e-02
|
0.22700
|
0.151000
|
-1.70e-01
|
8.04e-02
|
4.90e-02
|
RNA Polymerase II Transcription Initiation
|
45
|
3.22e-02
|
9.06e-02
|
0.22700
|
0.151000
|
-1.70e-01
|
8.04e-02
|
4.90e-02
|
RNA Polymerase II Transcription Initiation And Promoter Clearance
|
45
|
3.22e-02
|
9.06e-02
|
0.22700
|
0.151000
|
-1.70e-01
|
8.04e-02
|
4.90e-02
|
RNA Polymerase II Transcription Pre-Initiation And Promoter Opening
|
45
|
3.22e-02
|
9.06e-02
|
0.22700
|
0.151000
|
-1.70e-01
|
8.04e-02
|
4.90e-02
|
The NLRP3 inflammasome
|
16
|
2.90e-01
|
4.53e-01
|
0.22600
|
-0.154000
|
-1.66e-01
|
2.86e-01
|
2.52e-01
|
Signaling by PDGF
|
53
|
1.75e-02
|
5.60e-02
|
0.22500
|
-0.139000
|
-1.77e-01
|
8.03e-02
|
2.59e-02
|
Nuclear Envelope (NE) Reassembly
|
68
|
6.03e-03
|
2.23e-02
|
0.22500
|
0.074900
|
-2.12e-01
|
2.86e-01
|
2.50e-03
|
Incretin synthesis, secretion, and inactivation
|
12
|
4.04e-01
|
5.58e-01
|
0.22500
|
0.049200
|
-2.19e-01
|
7.68e-01
|
1.88e-01
|
Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1)
|
12
|
4.04e-01
|
5.58e-01
|
0.22500
|
0.049200
|
-2.19e-01
|
7.68e-01
|
1.88e-01
|
Synthesis of bile acids and bile salts via 27-hydroxycholesterol
|
10
|
4.71e-01
|
6.20e-01
|
0.22400
|
0.224000
|
1.40e-02
|
2.21e-01
|
9.39e-01
|
PTEN Regulation
|
137
|
3.82e-05
|
2.35e-04
|
0.22400
|
0.048400
|
-2.18e-01
|
3.28e-01
|
1.02e-05
|
NRIF signals cell death from the nucleus
|
16
|
3.04e-01
|
4.65e-01
|
0.22400
|
0.103000
|
-1.99e-01
|
4.77e-01
|
1.69e-01
|
G2/M Checkpoints
|
124
|
1.00e-04
|
5.79e-04
|
0.22400
|
0.030900
|
-2.21e-01
|
5.53e-01
|
2.08e-05
|
Interleukin-3, Interleukin-5 and GM-CSF signaling
|
43
|
4.19e-02
|
1.11e-01
|
0.22200
|
-0.222000
|
7.98e-04
|
1.18e-02
|
9.93e-01
|
PECAM1 interactions
|
12
|
4.12e-01
|
5.66e-01
|
0.22200
|
-0.220000
|
-2.69e-02
|
1.87e-01
|
8.72e-01
|
FGFR2 alternative splicing
|
24
|
1.72e-01
|
3.13e-01
|
0.22200
|
0.056100
|
-2.15e-01
|
6.34e-01
|
6.88e-02
|
Transport of the SLBP independent Mature mRNA
|
35
|
7.79e-02
|
1.77e-01
|
0.22200
|
-0.138000
|
1.74e-01
|
1.58e-01
|
7.55e-02
|
Transport of Mature mRNA Derived from an Intronless Transcript
|
42
|
4.74e-02
|
1.21e-01
|
0.22100
|
-0.145000
|
1.67e-01
|
1.04e-01
|
6.12e-02
|
Downstream signaling of activated FGFR4
|
18
|
2.71e-01
|
4.31e-01
|
0.22100
|
0.182000
|
-1.25e-01
|
1.80e-01
|
3.60e-01
|
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks
|
42
|
4.68e-02
|
1.20e-01
|
0.22100
|
0.019800
|
-2.20e-01
|
8.25e-01
|
1.36e-02
|
Host Interactions of HIV factors
|
127
|
9.27e-05
|
5.38e-04
|
0.22100
|
-0.098400
|
-1.98e-01
|
5.56e-02
|
1.21e-04
|
DNA Double Strand Break Response
|
43
|
4.40e-02
|
1.16e-01
|
0.22100
|
0.024700
|
-2.19e-01
|
7.80e-01
|
1.29e-02
|
Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding
|
32
|
1.03e-01
|
2.18e-01
|
0.21900
|
0.141000
|
-1.68e-01
|
1.68e-01
|
1.01e-01
|
Constitutive Signaling by AKT1 E17K in Cancer
|
26
|
1.55e-01
|
2.90e-01
|
0.21800
|
-0.032600
|
-2.16e-01
|
7.73e-01
|
5.67e-02
|
MyD88 deficiency (TLR2/4)
|
14
|
3.70e-01
|
5.24e-01
|
0.21800
|
-0.216000
|
3.04e-02
|
1.62e-01
|
8.44e-01
|
C-type lectin receptors (CLRs)
|
122
|
1.74e-04
|
9.74e-04
|
0.21800
|
-0.070000
|
-2.06e-01
|
1.82e-01
|
8.56e-05
|
trans-Golgi Network Vesicle Budding
|
70
|
7.00e-03
|
2.55e-02
|
0.21700
|
-0.214000
|
-3.80e-02
|
1.96e-03
|
5.83e-01
|
Immune System
|
1632
|
1.35e-46
|
1.99e-44
|
0.21700
|
-0.163000
|
-1.44e-01
|
2.58e-27
|
1.13e-21
|
Regulation of gene expression by Hypoxia-inducible Factor
|
10
|
4.95e-01
|
6.41e-01
|
0.21700
|
0.045000
|
-2.12e-01
|
8.05e-01
|
2.45e-01
|
Receptor-type tyrosine-protein phosphatases
|
12
|
4.32e-01
|
5.85e-01
|
0.21700
|
0.108000
|
-1.88e-01
|
5.17e-01
|
2.60e-01
|
Erythropoietin activates RAS
|
13
|
3.99e-01
|
5.54e-01
|
0.21700
|
-0.214000
|
-3.66e-02
|
1.82e-01
|
8.19e-01
|
Transcription of the HIV genome
|
67
|
9.63e-03
|
3.34e-02
|
0.21600
|
0.103000
|
-1.90e-01
|
1.45e-01
|
7.17e-03
|
TGF-beta receptor signaling activates SMADs
|
45
|
4.50e-02
|
1.16e-01
|
0.21500
|
0.069600
|
-2.04e-01
|
4.19e-01
|
1.81e-02
|
Meiotic recombination
|
26
|
1.70e-01
|
3.11e-01
|
0.21400
|
0.140000
|
-1.63e-01
|
2.17e-01
|
1.51e-01
|
Pyruvate metabolism and Citric Acid (TCA) cycle
|
51
|
2.94e-02
|
8.44e-02
|
0.21400
|
-0.148000
|
-1.55e-01
|
6.82e-02
|
5.55e-02
|
Macroautophagy
|
124
|
2.28e-04
|
1.25e-03
|
0.21400
|
0.122000
|
-1.76e-01
|
1.89e-02
|
7.34e-04
|
Intra-Golgi and retrograde Golgi-to-ER traffic
|
184
|
3.46e-06
|
2.85e-05
|
0.21400
|
-0.081300
|
-1.98e-01
|
5.75e-02
|
3.77e-06
|
TNF signaling
|
57
|
1.96e-02
|
6.18e-02
|
0.21400
|
-0.163000
|
-1.38e-01
|
3.31e-02
|
7.12e-02
|
IRAK4 deficiency (TLR2/4)
|
15
|
3.60e-01
|
5.15e-01
|
0.21400
|
-0.197000
|
8.36e-02
|
1.87e-01
|
5.75e-01
|
Downstream signaling of activated FGFR3
|
19
|
2.75e-01
|
4.35e-01
|
0.21400
|
0.139000
|
-1.62e-01
|
2.93e-01
|
2.21e-01
|
mRNA Capping
|
29
|
1.40e-01
|
2.68e-01
|
0.21400
|
0.106000
|
-1.86e-01
|
3.24e-01
|
8.37e-02
|
Mitochondrial tRNA aminoacylation
|
21
|
2.35e-01
|
3.93e-01
|
0.21400
|
-0.150000
|
-1.52e-01
|
2.34e-01
|
2.29e-01
|
Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways
|
56
|
2.15e-02
|
6.66e-02
|
0.21300
|
-0.187000
|
-1.03e-01
|
1.56e-02
|
1.83e-01
|
FCERI mediated MAPK activation
|
36
|
8.50e-02
|
1.90e-01
|
0.21300
|
-0.205000
|
-5.78e-02
|
3.30e-02
|
5.49e-01
|
Separation of Sister Chromatids
|
175
|
8.30e-06
|
5.97e-05
|
0.21300
|
0.066300
|
-2.02e-01
|
1.31e-01
|
4.05e-06
|
G alpha (i) signalling events
|
178
|
5.80e-06
|
4.42e-05
|
0.21300
|
-0.122000
|
-1.74e-01
|
5.18e-03
|
6.04e-05
|
Negative regulation of FGFR1 signaling
|
25
|
1.86e-01
|
3.29e-01
|
0.21300
|
0.072900
|
-2.00e-01
|
5.28e-01
|
8.38e-02
|
NEP/NS2 Interacts with the Cellular Export Machinery
|
32
|
1.17e-01
|
2.40e-01
|
0.21200
|
-0.128000
|
1.69e-01
|
2.09e-01
|
9.76e-02
|
Metabolism of fat-soluble vitamins
|
32
|
1.18e-01
|
2.40e-01
|
0.21200
|
0.068900
|
-2.00e-01
|
5.00e-01
|
4.98e-02
|
mRNA Splicing - Minor Pathway
|
50
|
3.57e-02
|
9.83e-02
|
0.21200
|
0.091900
|
-1.91e-01
|
2.61e-01
|
1.95e-02
|
Viral Infection Pathways
|
662
|
2.76e-19
|
9.66e-18
|
0.21200
|
0.039200
|
-2.08e-01
|
8.72e-02
|
9.07e-20
|
PERK regulates gene expression
|
32
|
1.18e-01
|
2.40e-01
|
0.21200
|
0.066600
|
-2.01e-01
|
5.15e-01
|
4.92e-02
|
Beta-oxidation of very long chain fatty acids
|
10
|
5.22e-01
|
6.64e-01
|
0.20900
|
-0.148000
|
1.48e-01
|
4.18e-01
|
4.17e-01
|
Mitotic G2-G2/M phases
|
187
|
5.69e-06
|
4.35e-05
|
0.20900
|
0.036100
|
-2.06e-01
|
3.95e-01
|
1.25e-06
|
G2/M Transition
|
185
|
6.57e-06
|
4.95e-05
|
0.20900
|
0.044300
|
-2.04e-01
|
3.00e-01
|
1.73e-06
|
SLC-mediated transmembrane transport
|
152
|
4.84e-05
|
2.93e-04
|
0.20900
|
-0.160000
|
-1.34e-01
|
6.86e-04
|
4.28e-03
|
Apoptotic factor-mediated response
|
20
|
2.73e-01
|
4.34e-01
|
0.20900
|
-0.198000
|
6.67e-02
|
1.26e-01
|
6.06e-01
|
Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors
|
29
|
1.53e-01
|
2.89e-01
|
0.20800
|
0.088100
|
-1.89e-01
|
4.12e-01
|
7.82e-02
|
Cytokine Signaling in Immune system
|
593
|
4.40e-17
|
1.29e-15
|
0.20800
|
-0.122000
|
-1.69e-01
|
3.96e-07
|
2.71e-12
|
Signaling by NTRK3 (TRKC)
|
17
|
3.28e-01
|
4.83e-01
|
0.20800
|
-0.160000
|
-1.34e-01
|
2.54e-01
|
3.40e-01
|
Ephrin signaling
|
18
|
3.13e-01
|
4.70e-01
|
0.20800
|
-0.200000
|
5.64e-02
|
1.41e-01
|
6.79e-01
|
MET activates RAS signaling
|
11
|
4.93e-01
|
6.40e-01
|
0.20800
|
-0.166000
|
1.25e-01
|
3.41e-01
|
4.71e-01
|
Transport of Mature mRNAs Derived from Intronless Transcripts
|
43
|
6.39e-02
|
1.53e-01
|
0.20800
|
-0.143000
|
1.51e-01
|
1.05e-01
|
8.77e-02
|
HIV Infection
|
223
|
6.34e-07
|
6.42e-06
|
0.20800
|
-0.039200
|
-2.04e-01
|
3.13e-01
|
1.63e-07
|
Regulation of TLR by endogenous ligand
|
15
|
3.81e-01
|
5.35e-01
|
0.20800
|
-0.205000
|
3.43e-02
|
1.70e-01
|
8.18e-01
|
GPER1 signaling
|
37
|
9.06e-02
|
1.99e-01
|
0.20700
|
-0.090500
|
-1.87e-01
|
3.41e-01
|
4.94e-02
|
Downstream signaling of activated FGFR2
|
21
|
2.62e-01
|
4.24e-01
|
0.20700
|
0.137000
|
-1.56e-01
|
2.79e-01
|
2.17e-01
|
Signaling by Hippo
|
20
|
2.77e-01
|
4.37e-01
|
0.20700
|
0.207000
|
1.33e-04
|
1.09e-01
|
9.99e-01
|
Recycling pathway of L1
|
41
|
7.13e-02
|
1.65e-01
|
0.20700
|
-0.065100
|
-1.96e-01
|
4.71e-01
|
2.96e-02
|
Signaling by FGFR
|
70
|
1.17e-02
|
3.98e-02
|
0.20700
|
0.066300
|
-1.96e-01
|
3.38e-01
|
4.63e-03
|
PI Metabolism
|
78
|
7.39e-03
|
2.67e-02
|
0.20600
|
-0.100000
|
1.80e-01
|
1.26e-01
|
6.02e-03
|
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol
|
16
|
3.62e-01
|
5.16e-01
|
0.20600
|
-0.011900
|
2.06e-01
|
9.34e-01
|
1.54e-01
|
Metabolism of proteins
|
1626
|
3.90e-41
|
3.37e-39
|
0.20500
|
0.029000
|
-2.03e-01
|
5.43e-02
|
1.18e-41
|
RNA Polymerase III Transcription Termination
|
23
|
2.37e-01
|
3.95e-01
|
0.20500
|
0.180000
|
-9.89e-02
|
1.36e-01
|
4.12e-01
|
Transport of the SLBP Dependant Mature mRNA
|
36
|
1.06e-01
|
2.22e-01
|
0.20500
|
-0.136000
|
1.54e-01
|
1.59e-01
|
1.10e-01
|
DNA Damage/Telomere Stress Induced Senescence
|
33
|
1.28e-01
|
2.52e-01
|
0.20500
|
0.110000
|
-1.73e-01
|
2.74e-01
|
8.61e-02
|
Basigin interactions
|
21
|
2.64e-01
|
4.26e-01
|
0.20500
|
-0.159000
|
-1.29e-01
|
2.07e-01
|
3.06e-01
|
O-linked glycosylation of mucins
|
42
|
7.06e-02
|
1.64e-01
|
0.20500
|
-0.088300
|
-1.85e-01
|
3.22e-01
|
3.84e-02
|
Transcription of E2F targets under negative control by DREAM complex
|
18
|
3.20e-01
|
4.75e-01
|
0.20500
|
-0.118000
|
-1.67e-01
|
3.85e-01
|
2.20e-01
|
Formation of WDR5-containing histone-modifying complexes
|
42
|
7.32e-02
|
1.68e-01
|
0.20400
|
-0.057200
|
1.96e-01
|
5.21e-01
|
2.78e-02
|
Meiotic synapsis
|
31
|
1.45e-01
|
2.77e-01
|
0.20400
|
0.194000
|
-6.58e-02
|
6.22e-02
|
5.26e-01
|
G beta:gamma signalling through PLC beta
|
15
|
3.97e-01
|
5.52e-01
|
0.20400
|
-0.107000
|
1.73e-01
|
4.74e-01
|
2.45e-01
|
Interleukin-12 signaling
|
41
|
7.74e-02
|
1.77e-01
|
0.20400
|
-0.081400
|
-1.87e-01
|
3.67e-01
|
3.88e-02
|
DNA Damage Recognition in GG-NER
|
38
|
9.67e-02
|
2.07e-01
|
0.20300
|
0.052800
|
-1.96e-01
|
5.73e-01
|
3.65e-02
|
TP53 Regulates Transcription of DNA Repair Genes
|
61
|
2.38e-02
|
7.13e-02
|
0.20300
|
0.075200
|
-1.89e-01
|
3.10e-01
|
1.08e-02
|
activated TAK1 mediates p38 MAPK activation
|
23
|
2.41e-01
|
3.98e-01
|
0.20300
|
-0.002680
|
-2.03e-01
|
9.82e-01
|
9.19e-02
|
Amyloid fiber formation
|
41
|
7.82e-02
|
1.77e-01
|
0.20300
|
-0.091800
|
-1.81e-01
|
3.09e-01
|
4.48e-02
|
SUMOylation of ubiquitinylation proteins
|
39
|
9.20e-02
|
2.00e-01
|
0.20300
|
-0.173000
|
1.06e-01
|
6.11e-02
|
2.54e-01
|
Sensory perception of taste
|
16
|
3.77e-01
|
5.30e-01
|
0.20300
|
-0.177000
|
9.90e-02
|
2.21e-01
|
4.93e-01
|
Signaling by KIT in disease
|
20
|
2.91e-01
|
4.53e-01
|
0.20200
|
-0.154000
|
-1.31e-01
|
2.34e-01
|
3.10e-01
|
Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants
|
20
|
2.91e-01
|
4.53e-01
|
0.20200
|
-0.154000
|
-1.31e-01
|
2.34e-01
|
3.10e-01
|
MET receptor recycling
|
10
|
5.43e-01
|
6.82e-01
|
0.20200
|
0.023900
|
2.00e-01
|
8.96e-01
|
2.73e-01
|
mitochondrial fatty acid beta-oxidation of saturated fatty acids
|
10
|
5.43e-01
|
6.82e-01
|
0.20200
|
0.200000
|
2.11e-02
|
2.73e-01
|
9.08e-01
|
Mitotic Anaphase
|
218
|
2.29e-06
|
1.99e-05
|
0.20100
|
0.065200
|
-1.90e-01
|
9.77e-02
|
1.34e-06
|
TICAM1, RIP1-mediated IKK complex recruitment
|
19
|
3.19e-01
|
4.74e-01
|
0.20100
|
0.117000
|
-1.64e-01
|
3.77e-01
|
2.17e-01
|
Diseases of metabolism
|
206
|
3.97e-06
|
3.19e-05
|
0.20100
|
-0.117000
|
-1.64e-01
|
3.98e-03
|
5.24e-05
|
TICAM1,TRAF6-dependent induction of TAK1 complex
|
11
|
5.14e-01
|
6.56e-01
|
0.20100
|
-0.009490
|
-2.01e-01
|
9.57e-01
|
2.49e-01
|
Regulation of CDH11 function
|
10
|
5.48e-01
|
6.86e-01
|
0.20100
|
0.041500
|
-1.96e-01
|
8.20e-01
|
2.83e-01
|
RUNX2 regulates osteoblast differentiation
|
22
|
2.63e-01
|
4.25e-01
|
0.20100
|
-0.107000
|
-1.70e-01
|
3.86e-01
|
1.68e-01
|
Negative regulators of DDX58/IFIH1 signaling
|
34
|
1.27e-01
|
2.50e-01
|
0.20000
|
-0.156000
|
-1.27e-01
|
1.17e-01
|
2.02e-01
|
Metabolism of RNA
|
693
|
7.30e-18
|
2.28e-16
|
0.20000
|
0.144000
|
-1.38e-01
|
1.23e-10
|
6.66e-10
|
Synthesis of bile acids and bile salts
|
26
|
2.09e-01
|
3.59e-01
|
0.20000
|
0.151000
|
1.30e-01
|
1.82e-01
|
2.50e-01
|
RMTs methylate histone arginines
|
33
|
1.39e-01
|
2.67e-01
|
0.19900
|
-0.060900
|
-1.90e-01
|
5.45e-01
|
5.95e-02
|
SARS-CoV-2 activates/modulates innate and adaptive immune responses
|
101
|
2.70e-03
|
1.13e-02
|
0.19900
|
-0.191000
|
5.33e-02
|
9.00e-04
|
3.55e-01
|
ER Quality Control Compartment (ERQC)
|
21
|
2.88e-01
|
4.52e-01
|
0.19900
|
-0.035700
|
-1.95e-01
|
7.77e-01
|
1.21e-01
|
Removal of the Flap Intermediate from the C-strand
|
17
|
3.70e-01
|
5.24e-01
|
0.19800
|
0.111000
|
-1.64e-01
|
4.27e-01
|
2.41e-01
|
Mitotic Metaphase and Anaphase
|
219
|
3.05e-06
|
2.56e-05
|
0.19800
|
0.065600
|
-1.87e-01
|
9.47e-02
|
1.85e-06
|
Interaction between L1 and Ankyrins
|
25
|
2.30e-01
|
3.88e-01
|
0.19800
|
0.197000
|
-1.99e-02
|
8.80e-02
|
8.63e-01
|
mRNA decay by 5’ to 3’ exoribonuclease
|
15
|
4.13e-01
|
5.67e-01
|
0.19800
|
-0.035200
|
-1.95e-01
|
8.14e-01
|
1.91e-01
|
Neurexins and neuroligins
|
41
|
8.87e-02
|
1.95e-01
|
0.19800
|
-0.133000
|
-1.47e-01
|
1.41e-01
|
1.05e-01
|
Hemostasis
|
487
|
7.53e-13
|
1.98e-11
|
0.19700
|
-0.118000
|
-1.58e-01
|
8.09e-06
|
2.70e-09
|
Transcriptional Regulation by NPAS4
|
30
|
1.75e-01
|
3.16e-01
|
0.19700
|
0.197000
|
9.44e-03
|
6.21e-02
|
9.29e-01
|
Transport of inorganic cations/anions and amino acids/oligopeptides
|
66
|
2.14e-02
|
6.66e-02
|
0.19700
|
-0.191000
|
-4.75e-02
|
7.25e-03
|
5.05e-01
|
Activation of BH3-only proteins
|
28
|
1.96e-01
|
3.43e-01
|
0.19700
|
-0.012200
|
-1.97e-01
|
9.11e-01
|
7.18e-02
|
Purine salvage
|
12
|
4.98e-01
|
6.43e-01
|
0.19700
|
0.009310
|
-1.97e-01
|
9.55e-01
|
2.38e-01
|
Protein localization
|
155
|
1.36e-04
|
7.68e-04
|
0.19600
|
-0.008260
|
-1.96e-01
|
8.59e-01
|
2.51e-05
|
Telomere Maintenance
|
69
|
1.93e-02
|
6.14e-02
|
0.19600
|
0.106000
|
-1.66e-01
|
1.29e-01
|
1.74e-02
|
Mitotic Telophase/Cytokinesis
|
13
|
4.73e-01
|
6.20e-01
|
0.19600
|
0.066700
|
1.84e-01
|
6.77e-01
|
2.51e-01
|
PLC beta mediated events
|
45
|
7.68e-02
|
1.75e-01
|
0.19600
|
-0.194000
|
2.75e-02
|
2.47e-02
|
7.50e-01
|
Deposition of new CENPA-containing nucleosomes at the centromere
|
30
|
1.83e-01
|
3.27e-01
|
0.19500
|
0.182000
|
-6.94e-02
|
8.40e-02
|
5.11e-01
|
Nucleosome assembly
|
30
|
1.83e-01
|
3.27e-01
|
0.19500
|
0.182000
|
-6.94e-02
|
8.40e-02
|
5.11e-01
|
Vpr-mediated nuclear import of PICs
|
34
|
1.47e-01
|
2.79e-01
|
0.19500
|
-0.124000
|
1.50e-01
|
2.11e-01
|
1.29e-01
|
SUMOylation of DNA replication proteins
|
46
|
7.34e-02
|
1.68e-01
|
0.19500
|
-0.195000
|
1.99e-03
|
2.23e-02
|
9.81e-01
|
Advanced glycosylation endproduct receptor signaling
|
12
|
5.03e-01
|
6.48e-01
|
0.19500
|
-0.159000
|
-1.12e-01
|
3.40e-01
|
5.02e-01
|
G beta:gamma signalling through PI3Kgamma
|
20
|
3.26e-01
|
4.81e-01
|
0.19400
|
-0.169000
|
9.49e-02
|
1.90e-01
|
4.63e-01
|
RAF/MAP kinase cascade
|
233
|
2.48e-06
|
2.12e-05
|
0.19300
|
-0.003190
|
-1.93e-01
|
9.33e-01
|
3.79e-07
|
Telomere C-strand synthesis initiation
|
13
|
4.83e-01
|
6.29e-01
|
0.19300
|
0.193000
|
2.61e-04
|
2.27e-01
|
9.99e-01
|
Oxidative Stress Induced Senescence
|
69
|
2.15e-02
|
6.66e-02
|
0.19300
|
0.031400
|
-1.91e-01
|
6.52e-01
|
6.18e-03
|
Platelet activation, signaling and aggregation
|
222
|
4.39e-06
|
3.47e-05
|
0.19300
|
-0.140000
|
-1.33e-01
|
3.29e-04
|
6.79e-04
|
Regulation of NF-kappa B signaling
|
18
|
3.64e-01
|
5.17e-01
|
0.19300
|
-0.140000
|
-1.32e-01
|
3.04e-01
|
3.31e-01
|
Toll Like Receptor 3 (TLR3) Cascade
|
103
|
3.28e-03
|
1.34e-02
|
0.19300
|
-0.045200
|
-1.87e-01
|
4.28e-01
|
1.04e-03
|
Interferon Signaling
|
166
|
1.06e-04
|
6.05e-04
|
0.19300
|
-0.192000
|
-1.10e-02
|
1.96e-05
|
8.07e-01
|
RAB geranylgeranylation
|
55
|
4.85e-02
|
1.24e-01
|
0.19200
|
0.065800
|
-1.81e-01
|
3.99e-01
|
2.04e-02
|
Developmental Biology
|
777
|
2.08e-18
|
6.64e-17
|
0.19200
|
0.097000
|
-1.66e-01
|
4.80e-06
|
5.49e-15
|
Platelet Aggregation (Plug Formation)
|
30
|
1.91e-01
|
3.36e-01
|
0.19100
|
-0.123000
|
-1.46e-01
|
2.43e-01
|
1.66e-01
|
Deactivation of the beta-catenin transactivating complex
|
39
|
1.20e-01
|
2.41e-01
|
0.19100
|
0.088900
|
-1.69e-01
|
3.37e-01
|
6.75e-02
|
Defective pyroptosis
|
19
|
3.51e-01
|
5.06e-01
|
0.19100
|
0.128000
|
1.42e-01
|
3.34e-01
|
2.85e-01
|
NCAM1 interactions
|
31
|
1.82e-01
|
3.26e-01
|
0.19100
|
-0.103000
|
-1.60e-01
|
3.20e-01
|
1.22e-01
|
G1/S-Specific Transcription
|
25
|
2.56e-01
|
4.15e-01
|
0.19000
|
-0.185000
|
-4.70e-02
|
1.10e-01
|
6.84e-01
|
Ca-dependent events
|
33
|
1.70e-01
|
3.11e-01
|
0.18900
|
-0.189000
|
9.83e-03
|
6.00e-02
|
9.22e-01
|
MAPK1/MAPK3 signaling
|
239
|
3.28e-06
|
2.72e-05
|
0.18900
|
0.001520
|
-1.89e-01
|
9.68e-01
|
5.02e-07
|
EPHA-mediated growth cone collapse
|
22
|
3.12e-01
|
4.70e-01
|
0.18900
|
0.180000
|
-5.71e-02
|
1.45e-01
|
6.43e-01
|
Biotin transport and metabolism
|
11
|
5.55e-01
|
6.90e-01
|
0.18800
|
-0.180000
|
-5.71e-02
|
3.03e-01
|
7.43e-01
|
Sensory perception of sweet, bitter, and umami (glutamate) taste
|
13
|
5.04e-01
|
6.48e-01
|
0.18800
|
-0.145000
|
1.20e-01
|
3.66e-01
|
4.53e-01
|
Potential therapeutics for SARS
|
96
|
6.05e-03
|
2.23e-02
|
0.18800
|
-0.096800
|
-1.61e-01
|
1.01e-01
|
6.34e-03
|
Adaptive Immune System
|
654
|
2.76e-15
|
7.81e-14
|
0.18800
|
-0.144000
|
-1.20e-01
|
4.17e-10
|
1.69e-07
|
Signaling by WNT
|
241
|
3.88e-06
|
3.15e-05
|
0.18700
|
0.041200
|
-1.83e-01
|
2.72e-01
|
1.06e-06
|
SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion
|
14
|
4.83e-01
|
6.29e-01
|
0.18700
|
-0.166000
|
8.64e-02
|
2.82e-01
|
5.76e-01
|
Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R)
|
40
|
1.25e-01
|
2.48e-01
|
0.18700
|
0.053500
|
-1.79e-01
|
5.58e-01
|
5.03e-02
|
Caspase activation via Death Receptors in the presence of ligand
|
15
|
4.55e-01
|
6.04e-01
|
0.18700
|
-0.175000
|
-6.51e-02
|
2.41e-01
|
6.63e-01
|
Mitochondrial Fatty Acid Beta-Oxidation
|
34
|
1.72e-01
|
3.13e-01
|
0.18600
|
0.178000
|
-5.52e-02
|
7.26e-02
|
5.78e-01
|
TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain
|
19
|
3.71e-01
|
5.25e-01
|
0.18600
|
0.183000
|
3.63e-02
|
1.68e-01
|
7.84e-01
|
Sulfur amino acid metabolism
|
23
|
2.99e-01
|
4.61e-01
|
0.18600
|
-0.149000
|
-1.12e-01
|
2.17e-01
|
3.52e-01
|
Infectious disease
|
835
|
1.34e-18
|
4.37e-17
|
0.18600
|
-0.000133
|
-1.86e-01
|
9.95e-01
|
1.17e-19
|
Regulation of localization of FOXO transcription factors
|
12
|
5.40e-01
|
6.81e-01
|
0.18600
|
0.149000
|
-1.12e-01
|
3.73e-01
|
5.03e-01
|
BBSome-mediated cargo-targeting to cilium
|
21
|
3.40e-01
|
4.97e-01
|
0.18600
|
0.175000
|
-6.29e-02
|
1.66e-01
|
6.18e-01
|
Sensory processing of sound by outer hair cells of the cochlea
|
35
|
1.64e-01
|
3.04e-01
|
0.18500
|
0.163000
|
8.75e-02
|
9.50e-02
|
3.71e-01
|
Transcriptional regulation of granulopoiesis
|
33
|
1.86e-01
|
3.30e-01
|
0.18400
|
0.002750
|
-1.84e-01
|
9.78e-01
|
6.67e-02
|
Downregulation of SMAD2/3:SMAD4 transcriptional activity
|
30
|
2.20e-01
|
3.73e-01
|
0.18400
|
0.157000
|
-9.69e-02
|
1.37e-01
|
3.59e-01
|
Retinoid metabolism and transport
|
29
|
2.31e-01
|
3.89e-01
|
0.18400
|
0.081300
|
-1.65e-01
|
4.49e-01
|
1.23e-01
|
SHC1 events in ERBB4 signaling
|
12
|
5.41e-01
|
6.81e-01
|
0.18400
|
-0.165000
|
-8.20e-02
|
3.23e-01
|
6.23e-01
|
Interleukin-20 family signaling
|
14
|
4.88e-01
|
6.35e-01
|
0.18400
|
-0.114000
|
-1.45e-01
|
4.61e-01
|
3.48e-01
|
Leishmania infection
|
154
|
4.29e-04
|
2.24e-03
|
0.18300
|
-0.172000
|
-6.38e-02
|
2.32e-04
|
1.72e-01
|
Parasitic Infection Pathways
|
154
|
4.29e-04
|
2.24e-03
|
0.18300
|
-0.172000
|
-6.38e-02
|
2.32e-04
|
1.72e-01
|
Beta-catenin independent WNT signaling
|
133
|
1.33e-03
|
6.16e-03
|
0.18300
|
0.008470
|
-1.83e-01
|
8.66e-01
|
2.77e-04
|
Regulation of RUNX1 Expression and Activity
|
18
|
4.04e-01
|
5.58e-01
|
0.18300
|
-0.065600
|
-1.71e-01
|
6.30e-01
|
2.10e-01
|
Factors involved in megakaryocyte development and platelet production
|
119
|
2.58e-03
|
1.08e-02
|
0.18300
|
-0.071600
|
-1.68e-01
|
1.77e-01
|
1.55e-03
|
Signal regulatory protein family interactions
|
11
|
5.79e-01
|
7.08e-01
|
0.18300
|
-0.168000
|
7.15e-02
|
3.35e-01
|
6.81e-01
|
Post-translational modification: synthesis of GPI-anchored proteins
|
62
|
4.48e-02
|
1.16e-01
|
0.18300
|
-0.064700
|
-1.71e-01
|
3.78e-01
|
2.02e-02
|
PKA activation in glucagon signalling
|
15
|
4.70e-01
|
6.20e-01
|
0.18200
|
-0.111000
|
-1.45e-01
|
4.58e-01
|
3.31e-01
|
Cell recruitment (pro-inflammatory response)
|
24
|
3.02e-01
|
4.64e-01
|
0.18200
|
-0.180000
|
-2.78e-02
|
1.27e-01
|
8.14e-01
|
Purinergic signaling in leishmaniasis infection
|
24
|
3.02e-01
|
4.64e-01
|
0.18200
|
-0.180000
|
-2.78e-02
|
1.27e-01
|
8.14e-01
|
EGFR downregulation
|
27
|
2.61e-01
|
4.22e-01
|
0.18200
|
-0.140000
|
-1.15e-01
|
2.08e-01
|
2.99e-01
|
STING mediated induction of host immune responses
|
15
|
4.80e-01
|
6.28e-01
|
0.18100
|
-0.084100
|
1.61e-01
|
5.73e-01
|
2.81e-01
|
PIP3 activates AKT signaling
|
242
|
8.22e-06
|
5.95e-05
|
0.18100
|
0.010600
|
-1.81e-01
|
7.76e-01
|
1.34e-06
|
PRC2 methylates histones and DNA
|
19
|
3.96e-01
|
5.52e-01
|
0.18100
|
0.168000
|
-6.69e-02
|
2.05e-01
|
6.14e-01
|
Cargo recognition for clathrin-mediated endocytosis
|
90
|
1.22e-02
|
4.10e-02
|
0.18100
|
-0.177000
|
-3.79e-02
|
3.76e-03
|
5.35e-01
|
Notch-HLH transcription pathway
|
28
|
2.57e-01
|
4.17e-01
|
0.18100
|
-0.090900
|
1.56e-01
|
4.05e-01
|
1.53e-01
|
Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function
|
24
|
3.07e-01
|
4.68e-01
|
0.18100
|
0.169000
|
6.34e-02
|
1.51e-01
|
5.91e-01
|
Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function
|
24
|
3.07e-01
|
4.68e-01
|
0.18100
|
0.169000
|
6.34e-02
|
1.51e-01
|
5.91e-01
|
Defective homologous recombination repair (HRR) due to BRCA1 loss of function
|
24
|
3.07e-01
|
4.68e-01
|
0.18100
|
0.169000
|
6.34e-02
|
1.51e-01
|
5.91e-01
|
Defective homologous recombination repair (HRR) due to PALB2 loss of function
|
24
|
3.07e-01
|
4.68e-01
|
0.18100
|
0.169000
|
6.34e-02
|
1.51e-01
|
5.91e-01
|
Ion homeostasis
|
43
|
1.23e-01
|
2.45e-01
|
0.18100
|
0.001550
|
-1.81e-01
|
9.86e-01
|
4.05e-02
|
Glutathione synthesis and recycling
|
10
|
6.13e-01
|
7.33e-01
|
0.18000
|
-0.166000
|
-7.04e-02
|
3.64e-01
|
7.00e-01
|
Disorders of transmembrane transporters
|
138
|
1.25e-03
|
5.88e-03
|
0.18000
|
-0.071100
|
-1.65e-01
|
1.50e-01
|
8.19e-04
|
Regulation of TP53 Activity through Methylation
|
19
|
3.96e-01
|
5.51e-01
|
0.18000
|
-0.117000
|
-1.36e-01
|
3.78e-01
|
3.03e-01
|
Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC)
|
32
|
2.19e-01
|
3.72e-01
|
0.17900
|
-0.126000
|
1.27e-01
|
2.17e-01
|
2.14e-01
|
Regulation of Glucokinase by Glucokinase Regulatory Protein
|
32
|
2.19e-01
|
3.72e-01
|
0.17900
|
-0.126000
|
1.27e-01
|
2.17e-01
|
2.14e-01
|
RUNX3 regulates NOTCH signaling
|
14
|
5.12e-01
|
6.55e-01
|
0.17800
|
0.012600
|
1.78e-01
|
9.35e-01
|
2.49e-01
|
Triglyceride metabolism
|
24
|
3.19e-01
|
4.74e-01
|
0.17800
|
-0.175000
|
-3.52e-02
|
1.39e-01
|
7.65e-01
|
RNA Polymerase I Promoter Escape
|
37
|
1.76e-01
|
3.18e-01
|
0.17800
|
0.173000
|
-3.92e-02
|
6.85e-02
|
6.80e-01
|
RUNX2 regulates bone development
|
28
|
2.64e-01
|
4.26e-01
|
0.17700
|
-0.082000
|
-1.57e-01
|
4.53e-01
|
1.50e-01
|
Bile acid and bile salt metabolism
|
29
|
2.52e-01
|
4.12e-01
|
0.17700
|
0.102000
|
1.45e-01
|
3.41e-01
|
1.77e-01
|
Signaling by NTRK1 (TRKA)
|
108
|
6.73e-03
|
2.46e-02
|
0.17600
|
0.009730
|
-1.76e-01
|
8.61e-01
|
1.58e-03
|
Diseases associated with O-glycosylation of proteins
|
55
|
7.94e-02
|
1.79e-01
|
0.17600
|
-0.136000
|
1.12e-01
|
8.02e-02
|
1.52e-01
|
Metabolism of cofactors
|
18
|
4.34e-01
|
5.86e-01
|
0.17600
|
0.011000
|
-1.76e-01
|
9.35e-01
|
1.97e-01
|
Miscellaneous transport and binding events
|
21
|
3.74e-01
|
5.28e-01
|
0.17600
|
-0.131000
|
-1.17e-01
|
2.98e-01
|
3.53e-01
|
Integration of energy metabolism
|
86
|
1.87e-02
|
5.96e-02
|
0.17600
|
-0.026500
|
-1.74e-01
|
6.71e-01
|
5.34e-03
|
Gap-filling DNA repair synthesis and ligation in GG-NER
|
25
|
3.18e-01
|
4.74e-01
|
0.17600
|
0.098500
|
-1.45e-01
|
3.94e-01
|
2.09e-01
|
Impaired BRCA2 binding to PALB2
|
23
|
3.44e-01
|
4.99e-01
|
0.17500
|
0.151000
|
8.89e-02
|
2.09e-01
|
4.60e-01
|
Rap1 signalling
|
13
|
5.52e-01
|
6.89e-01
|
0.17500
|
-0.100000
|
1.44e-01
|
5.30e-01
|
3.70e-01
|
SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription
|
36
|
1.94e-01
|
3.40e-01
|
0.17500
|
0.072900
|
-1.59e-01
|
4.49e-01
|
9.84e-02
|
S Phase
|
157
|
8.39e-04
|
4.14e-03
|
0.17500
|
0.044600
|
-1.69e-01
|
3.36e-01
|
2.65e-04
|
Metabolism of steroid hormones
|
21
|
3.85e-01
|
5.41e-01
|
0.17400
|
-0.169000
|
-4.17e-02
|
1.81e-01
|
7.41e-01
|
MyD88-independent TLR4 cascade
|
107
|
7.96e-03
|
2.85e-02
|
0.17400
|
-0.052600
|
-1.65e-01
|
3.47e-01
|
3.12e-03
|
TRIF(TICAM1)-mediated TLR4 signaling
|
107
|
7.96e-03
|
2.85e-02
|
0.17400
|
-0.052600
|
-1.65e-01
|
3.47e-01
|
3.12e-03
|
Cyclin A/B1/B2 associated events during G2/M transition
|
22
|
3.70e-01
|
5.24e-01
|
0.17300
|
-0.034000
|
-1.70e-01
|
7.83e-01
|
1.67e-01
|
Plasma lipoprotein clearance
|
32
|
2.38e-01
|
3.95e-01
|
0.17300
|
-0.173000
|
-3.46e-03
|
9.02e-02
|
9.73e-01
|
Signaling by ALK fusions and activated point mutants
|
54
|
8.87e-02
|
1.95e-01
|
0.17300
|
-0.033800
|
-1.70e-01
|
6.68e-01
|
3.12e-02
|
Signaling by ALK in cancer
|
54
|
8.87e-02
|
1.95e-01
|
0.17300
|
-0.033800
|
-1.70e-01
|
6.68e-01
|
3.12e-02
|
Muscle contraction
|
153
|
1.11e-03
|
5.33e-03
|
0.17300
|
-0.003770
|
-1.73e-01
|
9.36e-01
|
2.27e-04
|
Estrogen-dependent gene expression
|
89
|
1.95e-02
|
6.18e-02
|
0.17300
|
0.157000
|
-7.23e-02
|
1.06e-02
|
2.39e-01
|
Acyl chain remodelling of PS
|
12
|
5.91e-01
|
7.16e-01
|
0.17200
|
-0.084600
|
1.49e-01
|
6.12e-01
|
3.70e-01
|
APC-Cdc20 mediated degradation of Nek2A
|
25
|
3.36e-01
|
4.94e-01
|
0.17100
|
0.080800
|
-1.51e-01
|
4.85e-01
|
1.91e-01
|
Transport of small molecules
|
526
|
1.59e-10
|
3.49e-09
|
0.17100
|
-0.115000
|
-1.26e-01
|
6.63e-06
|
7.86e-07
|
Synthesis of PC
|
23
|
3.63e-01
|
5.17e-01
|
0.17100
|
-0.117000
|
-1.24e-01
|
3.31e-01
|
3.03e-01
|
Export of Viral Ribonucleoproteins from Nucleus
|
33
|
2.41e-01
|
3.98e-01
|
0.17000
|
-0.094700
|
1.42e-01
|
3.46e-01
|
1.59e-01
|
JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1
|
22
|
3.85e-01
|
5.41e-01
|
0.17000
|
0.013300
|
-1.70e-01
|
9.14e-01
|
1.68e-01
|
Heme biosynthesis
|
13
|
5.73e-01
|
7.04e-01
|
0.17000
|
0.115000
|
-1.25e-01
|
4.75e-01
|
4.34e-01
|
TP53 Regulates Transcription of Cell Death Genes
|
40
|
1.76e-01
|
3.18e-01
|
0.17000
|
-0.138000
|
-9.89e-02
|
1.32e-01
|
2.79e-01
|
Oncogene Induced Senescence
|
33
|
2.41e-01
|
3.98e-01
|
0.17000
|
-0.013700
|
-1.69e-01
|
8.92e-01
|
9.30e-02
|
NOTCH4 Activation and Transmission of Signal to the Nucleus
|
11
|
6.21e-01
|
7.38e-01
|
0.17000
|
0.062200
|
1.58e-01
|
7.21e-01
|
3.65e-01
|
Neddylation
|
223
|
8.05e-05
|
4.71e-04
|
0.16900
|
0.020900
|
-1.68e-01
|
5.90e-01
|
1.61e-05
|
Glutamate Neurotransmitter Release Cycle
|
22
|
3.91e-01
|
5.48e-01
|
0.16900
|
0.012300
|
-1.68e-01
|
9.21e-01
|
1.72e-01
|
Aberrant regulation of mitotic cell cycle due to RB1 defects
|
36
|
2.17e-01
|
3.71e-01
|
0.16800
|
0.022100
|
-1.67e-01
|
8.18e-01
|
8.30e-02
|
MAPK family signaling cascades
|
274
|
1.10e-05
|
7.55e-05
|
0.16800
|
0.024400
|
-1.66e-01
|
4.88e-01
|
2.19e-06
|
Eicosanoid ligand-binding receptors
|
14
|
5.51e-01
|
6.88e-01
|
0.16800
|
-0.129000
|
-1.07e-01
|
4.04e-01
|
4.86e-01
|
RHOV GTPase cycle
|
34
|
2.38e-01
|
3.95e-01
|
0.16800
|
0.034300
|
1.64e-01
|
7.29e-01
|
9.79e-02
|
IGF1R signaling cascade
|
39
|
1.96e-01
|
3.43e-01
|
0.16800
|
0.049600
|
-1.60e-01
|
5.92e-01
|
8.38e-02
|
SIRT1 negatively regulates rRNA expression
|
14
|
5.53e-01
|
6.89e-01
|
0.16700
|
0.156000
|
5.96e-02
|
3.11e-01
|
7.00e-01
|
Nuclear signaling by ERBB4
|
28
|
3.11e-01
|
4.70e-01
|
0.16700
|
-0.163000
|
3.77e-02
|
1.36e-01
|
7.30e-01
|
RNA Polymerase III Transcription Initiation From Type 3 Promoter
|
28
|
3.11e-01
|
4.70e-01
|
0.16700
|
0.162000
|
-4.02e-02
|
1.37e-01
|
7.13e-01
|
HCMV Infection
|
99
|
1.67e-02
|
5.37e-02
|
0.16700
|
0.052400
|
-1.59e-01
|
3.68e-01
|
6.44e-03
|
Rev-mediated nuclear export of HIV RNA
|
35
|
2.36e-01
|
3.93e-01
|
0.16700
|
-0.139000
|
9.23e-02
|
1.55e-01
|
3.45e-01
|
Synthesis of PA
|
29
|
3.02e-01
|
4.64e-01
|
0.16600
|
-0.158000
|
5.29e-02
|
1.41e-01
|
6.22e-01
|
Synaptic adhesion-like molecules
|
18
|
4.76e-01
|
6.25e-01
|
0.16600
|
0.069400
|
-1.51e-01
|
6.10e-01
|
2.67e-01
|
Intracellular signaling by second messengers
|
278
|
1.17e-05
|
7.96e-05
|
0.16600
|
-0.009550
|
-1.66e-01
|
7.84e-01
|
1.97e-06
|
G0 and Early G1
|
25
|
3.54e-01
|
5.09e-01
|
0.16600
|
-0.140000
|
-8.84e-02
|
2.24e-01
|
4.44e-01
|
PKMTs methylate histone lysines
|
42
|
1.77e-01
|
3.19e-01
|
0.16600
|
0.018100
|
1.65e-01
|
8.39e-01
|
6.45e-02
|
RND1 GTPase cycle
|
37
|
2.16e-01
|
3.68e-01
|
0.16600
|
0.147000
|
7.60e-02
|
1.21e-01
|
4.24e-01
|
RHO GTPases Activate NADPH Oxidases
|
21
|
4.21e-01
|
5.73e-01
|
0.16600
|
-0.165000
|
-9.54e-03
|
1.89e-01
|
9.40e-01
|
Golgi Associated Vesicle Biogenesis
|
55
|
1.03e-01
|
2.19e-01
|
0.16600
|
-0.156000
|
-5.62e-02
|
4.57e-02
|
4.71e-01
|
Signaling by FLT3 ITD and TKD mutants
|
15
|
5.44e-01
|
6.82e-01
|
0.16500
|
0.143000
|
-8.31e-02
|
3.38e-01
|
5.77e-01
|
Fatty acyl-CoA biosynthesis
|
30
|
2.94e-01
|
4.57e-01
|
0.16500
|
-0.036400
|
-1.61e-01
|
7.30e-01
|
1.28e-01
|
Formation of Fibrin Clot (Clotting Cascade)
|
20
|
4.45e-01
|
5.94e-01
|
0.16400
|
0.017300
|
-1.64e-01
|
8.94e-01
|
2.06e-01
|
Effects of PIP2 hydrolysis
|
22
|
4.09e-01
|
5.62e-01
|
0.16400
|
-0.156000
|
-5.07e-02
|
2.04e-01
|
6.80e-01
|
Cellular Senescence
|
132
|
5.03e-03
|
1.91e-02
|
0.16400
|
0.018000
|
-1.63e-01
|
7.21e-01
|
1.21e-03
|
Vitamin B5 (pantothenate) metabolism
|
16
|
5.22e-01
|
6.64e-01
|
0.16400
|
-0.159000
|
-3.95e-02
|
2.69e-01
|
7.85e-01
|
RHO GTPases activate PAKs
|
20
|
4.49e-01
|
5.97e-01
|
0.16400
|
0.145000
|
-7.78e-02
|
2.63e-01
|
5.47e-01
|
Sema3A PAK dependent Axon repulsion
|
16
|
5.24e-01
|
6.66e-01
|
0.16400
|
-0.164000
|
-1.17e-02
|
2.57e-01
|
9.36e-01
|
RHOU GTPase cycle
|
39
|
2.11e-01
|
3.62e-01
|
0.16400
|
-0.128000
|
1.02e-01
|
1.66e-01
|
2.69e-01
|
Growth hormone receptor signaling
|
20
|
4.45e-01
|
5.94e-01
|
0.16400
|
-0.079500
|
-1.43e-01
|
5.38e-01
|
2.68e-01
|
Signaling by Leptin
|
10
|
6.72e-01
|
7.76e-01
|
0.16400
|
0.126000
|
-1.04e-01
|
4.89e-01
|
5.69e-01
|
Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1
|
16
|
5.27e-01
|
6.67e-01
|
0.16400
|
-0.164000
|
1.70e-03
|
2.57e-01
|
9.91e-01
|
Retrograde transport at the Trans-Golgi-Network
|
49
|
1.40e-01
|
2.68e-01
|
0.16400
|
-0.161000
|
-2.80e-02
|
5.11e-02
|
7.34e-01
|
Apoptosis
|
161
|
1.72e-03
|
7.67e-03
|
0.16300
|
0.012000
|
-1.63e-01
|
7.93e-01
|
3.69e-04
|
Signaling by NODAL
|
13
|
5.93e-01
|
7.16e-01
|
0.16300
|
0.083400
|
1.40e-01
|
6.03e-01
|
3.81e-01
|
RAF activation
|
34
|
2.58e-01
|
4.18e-01
|
0.16300
|
-0.022100
|
-1.62e-01
|
8.24e-01
|
1.03e-01
|
CaM pathway
|
31
|
2.93e-01
|
4.56e-01
|
0.16300
|
-0.161000
|
2.53e-02
|
1.21e-01
|
8.08e-01
|
Calmodulin induced events
|
31
|
2.93e-01
|
4.56e-01
|
0.16300
|
-0.161000
|
2.53e-02
|
1.21e-01
|
8.08e-01
|
Formation of apoptosome
|
11
|
6.48e-01
|
7.60e-01
|
0.16300
|
-0.032000
|
1.59e-01
|
8.54e-01
|
3.60e-01
|
Regulation of the apoptosome activity
|
11
|
6.48e-01
|
7.60e-01
|
0.16300
|
-0.032000
|
1.59e-01
|
8.54e-01
|
3.60e-01
|
ADP signalling through P2Y purinoceptor 1
|
20
|
4.55e-01
|
6.04e-01
|
0.16200
|
-0.161000
|
-1.65e-02
|
2.13e-01
|
8.99e-01
|
Physiological factors
|
10
|
6.78e-01
|
7.79e-01
|
0.16200
|
0.136000
|
-8.69e-02
|
4.55e-01
|
6.34e-01
|
Diseases of programmed cell death
|
47
|
1.58e-01
|
2.94e-01
|
0.16200
|
-0.051000
|
-1.53e-01
|
5.45e-01
|
6.89e-02
|
Depolymerization of the Nuclear Lamina
|
15
|
5.54e-01
|
6.89e-01
|
0.16100
|
-0.134000
|
-9.03e-02
|
3.69e-01
|
5.45e-01
|
Base Excision Repair
|
50
|
1.44e-01
|
2.75e-01
|
0.16100
|
0.064100
|
-1.48e-01
|
4.33e-01
|
7.00e-02
|
Signaling by Erythropoietin
|
24
|
3.95e-01
|
5.51e-01
|
0.16100
|
-0.131000
|
9.39e-02
|
2.66e-01
|
4.26e-01
|
Ub-specific processing proteases
|
155
|
2.57e-03
|
1.08e-02
|
0.16100
|
0.035000
|
-1.57e-01
|
4.52e-01
|
7.32e-04
|
Pyroptosis
|
21
|
4.40e-01
|
5.91e-01
|
0.16100
|
-0.141000
|
-7.81e-02
|
2.64e-01
|
5.36e-01
|
Post-translational protein modification
|
1189
|
1.89e-19
|
6.95e-18
|
0.16100
|
-0.038800
|
-1.56e-01
|
2.54e-02
|
2.46e-19
|
IRS-related events triggered by IGF1R
|
38
|
2.35e-01
|
3.93e-01
|
0.16000
|
0.076200
|
-1.41e-01
|
4.16e-01
|
1.33e-01
|
Cytosolic sulfonation of small molecules
|
18
|
4.98e-01
|
6.43e-01
|
0.16000
|
-0.123000
|
-1.02e-01
|
3.65e-01
|
4.54e-01
|
Tryptophan catabolism
|
10
|
6.84e-01
|
7.81e-01
|
0.16000
|
-0.146000
|
6.59e-02
|
4.25e-01
|
7.18e-01
|
GRB2 events in ERBB2 signaling
|
14
|
5.87e-01
|
7.13e-01
|
0.16000
|
-0.156000
|
3.16e-02
|
3.11e-01
|
8.38e-01
|
Processing of SMDT1
|
15
|
5.68e-01
|
7.00e-01
|
0.15900
|
0.145000
|
-6.64e-02
|
3.32e-01
|
6.56e-01
|
NOD1/2 Signaling Pathway
|
36
|
2.54e-01
|
4.14e-01
|
0.15900
|
-0.152000
|
-4.76e-02
|
1.15e-01
|
6.21e-01
|
Killing mechanisms
|
10
|
6.82e-01
|
7.81e-01
|
0.15900
|
-0.122000
|
-1.02e-01
|
5.05e-01
|
5.75e-01
|
WNT5:FZD7-mediated leishmania damping
|
10
|
6.82e-01
|
7.81e-01
|
0.15900
|
-0.122000
|
-1.02e-01
|
5.05e-01
|
5.75e-01
|
NRAGE signals death through JNK
|
56
|
1.24e-01
|
2.46e-01
|
0.15800
|
-0.150000
|
4.94e-02
|
5.15e-02
|
5.23e-01
|
G beta:gamma signalling through CDC42
|
15
|
5.74e-01
|
7.04e-01
|
0.15800
|
-0.088700
|
1.30e-01
|
5.52e-01
|
3.82e-01
|
Signaling by WNT in cancer
|
28
|
3.55e-01
|
5.09e-01
|
0.15800
|
0.055000
|
-1.48e-01
|
6.15e-01
|
1.76e-01
|
APC/C:Cdc20 mediated degradation of Cyclin B
|
24
|
4.13e-01
|
5.67e-01
|
0.15700
|
0.064100
|
-1.44e-01
|
5.87e-01
|
2.23e-01
|
L1CAM interactions
|
102
|
2.35e-02
|
7.09e-02
|
0.15700
|
0.029100
|
-1.55e-01
|
6.12e-01
|
7.02e-03
|
mRNA 3’-end processing
|
57
|
1.25e-01
|
2.47e-01
|
0.15700
|
-0.081900
|
1.34e-01
|
2.85e-01
|
8.06e-02
|
Glycerophospholipid biosynthesis
|
100
|
2.56e-02
|
7.57e-02
|
0.15700
|
-0.156000
|
-1.29e-02
|
7.01e-03
|
8.24e-01
|
PI3K Cascade
|
31
|
3.23e-01
|
4.78e-01
|
0.15600
|
0.011000
|
-1.56e-01
|
9.16e-01
|
1.34e-01
|
Laminin interactions
|
27
|
3.74e-01
|
5.28e-01
|
0.15600
|
0.155000
|
-1.93e-02
|
1.64e-01
|
8.62e-01
|
FRS-mediated FGFR1 signaling
|
15
|
5.81e-01
|
7.08e-01
|
0.15600
|
0.142000
|
-6.49e-02
|
3.42e-01
|
6.63e-01
|
Signaling by FGFR1
|
40
|
2.36e-01
|
3.93e-01
|
0.15600
|
0.052600
|
-1.47e-01
|
5.65e-01
|
1.08e-01
|
RIPK1-mediated regulated necrosis
|
30
|
3.38e-01
|
4.95e-01
|
0.15600
|
0.046900
|
-1.48e-01
|
6.56e-01
|
1.59e-01
|
Regulation of necroptotic cell death
|
30
|
3.38e-01
|
4.95e-01
|
0.15600
|
0.046900
|
-1.48e-01
|
6.56e-01
|
1.59e-01
|
Sialic acid metabolism
|
27
|
3.73e-01
|
5.27e-01
|
0.15600
|
-0.056400
|
-1.45e-01
|
6.12e-01
|
1.92e-01
|
Thrombin signalling through proteinase activated receptors (PARs)
|
24
|
4.19e-01
|
5.72e-01
|
0.15600
|
-0.155000
|
7.67e-03
|
1.88e-01
|
9.48e-01
|
Chromosome Maintenance
|
92
|
3.73e-02
|
1.01e-01
|
0.15500
|
0.109000
|
-1.10e-01
|
6.97e-02
|
6.74e-02
|
RET signaling
|
32
|
3.12e-01
|
4.70e-01
|
0.15500
|
-0.133000
|
-8.09e-02
|
1.94e-01
|
4.28e-01
|
RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known
|
36
|
2.75e-01
|
4.35e-01
|
0.15400
|
-0.039100
|
-1.49e-01
|
6.85e-01
|
1.21e-01
|
Signaling by NOTCH
|
176
|
1.98e-03
|
8.66e-03
|
0.15400
|
-0.014100
|
-1.54e-01
|
7.47e-01
|
4.47e-04
|
Synthesis of Leukotrienes (LT) and Eoxins (EX)
|
12
|
6.54e-01
|
7.65e-01
|
0.15400
|
-0.129000
|
8.50e-02
|
4.40e-01
|
6.10e-01
|
Activation of NMDA receptors and postsynaptic events
|
77
|
6.68e-02
|
1.58e-01
|
0.15400
|
0.104000
|
-1.13e-01
|
1.13e-01
|
8.59e-02
|
Cytoprotection by HMOX1
|
58
|
1.26e-01
|
2.49e-01
|
0.15400
|
-0.071300
|
-1.37e-01
|
3.48e-01
|
7.20e-02
|
Phospholipid metabolism
|
177
|
2.30e-03
|
9.92e-03
|
0.15300
|
-0.133000
|
7.51e-02
|
2.32e-03
|
8.51e-02
|
Signaling by Receptor Tyrosine Kinases
|
468
|
1.11e-07
|
1.27e-06
|
0.15300
|
-0.080100
|
-1.30e-01
|
3.08e-03
|
1.62e-06
|
HDMs demethylate histones
|
21
|
4.79e-01
|
6.28e-01
|
0.15200
|
-0.140000
|
-6.02e-02
|
2.67e-01
|
6.33e-01
|
ERBB2 Activates PTK6 Signaling
|
11
|
6.84e-01
|
7.81e-01
|
0.15200
|
-0.122000
|
9.10e-02
|
4.83e-01
|
6.01e-01
|
Post NMDA receptor activation events
|
65
|
1.09e-01
|
2.27e-01
|
0.15200
|
0.083800
|
-1.26e-01
|
2.43e-01
|
7.80e-02
|
Signaling by FGFR in disease
|
53
|
1.66e-01
|
3.06e-01
|
0.15100
|
0.059900
|
-1.39e-01
|
4.51e-01
|
8.08e-02
|
Class A/1 (Rhodopsin-like receptors)
|
144
|
7.36e-03
|
2.67e-02
|
0.15100
|
-0.069000
|
-1.34e-01
|
1.53e-01
|
5.48e-03
|
MAPK targets/ Nuclear events mediated by MAP kinases
|
31
|
3.51e-01
|
5.06e-01
|
0.15100
|
0.130000
|
-7.72e-02
|
2.12e-01
|
4.57e-01
|
G-protein mediated events
|
49
|
1.90e-01
|
3.34e-01
|
0.15100
|
-0.150000
|
1.13e-02
|
6.88e-02
|
8.91e-01
|
Death Receptor Signaling
|
147
|
6.90e-03
|
2.52e-02
|
0.15000
|
-0.128000
|
-7.95e-02
|
7.68e-03
|
9.64e-02
|
PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling
|
82
|
6.28e-02
|
1.51e-01
|
0.15000
|
-0.081400
|
-1.26e-01
|
2.03e-01
|
4.92e-02
|
Vesicle-mediated transport
|
607
|
2.34e-09
|
4.30e-08
|
0.15000
|
-0.110000
|
-1.01e-01
|
3.78e-06
|
2.22e-05
|
Diseases of mitotic cell cycle
|
38
|
2.82e-01
|
4.44e-01
|
0.15000
|
0.035900
|
-1.45e-01
|
7.02e-01
|
1.21e-01
|
Late Phase of HIV Life Cycle
|
132
|
1.26e-02
|
4.22e-02
|
0.15000
|
0.041900
|
-1.44e-01
|
4.06e-01
|
4.44e-03
|
SUMOylation of SUMOylation proteins
|
35
|
3.14e-01
|
4.71e-01
|
0.14900
|
-0.105000
|
1.06e-01
|
2.80e-01
|
2.79e-01
|
Formation of TC-NER Pre-Incision Complex
|
53
|
1.74e-01
|
3.16e-01
|
0.14900
|
0.084600
|
-1.23e-01
|
2.87e-01
|
1.22e-01
|
InlB-mediated entry of Listeria monocytogenes into host cell
|
14
|
6.25e-01
|
7.41e-01
|
0.14900
|
-0.128000
|
-7.70e-02
|
4.08e-01
|
6.18e-01
|
Protein-protein interactions at synapses
|
63
|
1.23e-01
|
2.45e-01
|
0.14900
|
-0.032300
|
-1.45e-01
|
6.57e-01
|
4.60e-02
|
Metabolism
|
1726
|
5.00e-23
|
2.37e-21
|
0.14800
|
-0.011100
|
-1.48e-01
|
4.50e-01
|
5.60e-24
|
G alpha (12/13) signalling events
|
70
|
1.02e-01
|
2.15e-01
|
0.14800
|
-0.126000
|
7.83e-02
|
6.81e-02
|
2.58e-01
|
Translation of Replicase and Assembly of the Replication Transcription Complex 9679504
|
12
|
6.75e-01
|
7.77e-01
|
0.14800
|
0.116000
|
-9.30e-02
|
4.88e-01
|
5.77e-01
|
Signaling by cytosolic FGFR1 fusion mutants
|
18
|
5.55e-01
|
6.90e-01
|
0.14800
|
-0.071100
|
1.30e-01
|
6.02e-01
|
3.39e-01
|
Metabolism of nitric oxide: NOS3 activation and regulation
|
15
|
6.08e-01
|
7.29e-01
|
0.14800
|
0.115000
|
9.31e-02
|
4.40e-01
|
5.33e-01
|
DAG and IP3 signaling
|
37
|
2.97e-01
|
4.60e-01
|
0.14800
|
-0.143000
|
-3.69e-02
|
1.32e-01
|
6.98e-01
|
Signaling by SCF-KIT
|
41
|
2.63e-01
|
4.25e-01
|
0.14800
|
-0.147000
|
1.14e-02
|
1.03e-01
|
9.00e-01
|
Methylation
|
12
|
6.79e-01
|
7.80e-01
|
0.14700
|
0.076800
|
-1.26e-01
|
6.45e-01
|
4.51e-01
|
Intrinsic Pathway for Apoptosis
|
52
|
1.84e-01
|
3.28e-01
|
0.14700
|
-0.100000
|
-1.08e-01
|
2.12e-01
|
1.80e-01
|
DDX58/IFIH1-mediated induction of interferon-alpha/beta
|
66
|
1.17e-01
|
2.40e-01
|
0.14700
|
-0.108000
|
-9.96e-02
|
1.30e-01
|
1.62e-01
|
Meiosis
|
50
|
2.03e-01
|
3.51e-01
|
0.14700
|
0.126000
|
-7.53e-02
|
1.24e-01
|
3.57e-01
|
Programmed Cell Death
|
188
|
2.53e-03
|
1.07e-02
|
0.14700
|
0.011400
|
-1.46e-01
|
7.89e-01
|
5.61e-04
|
Inhibition of replication initiation of damaged DNA by RB1/E2F1
|
13
|
6.59e-01
|
7.69e-01
|
0.14600
|
-0.145000
|
2.16e-02
|
3.66e-01
|
8.93e-01
|
Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA)
|
26
|
4.32e-01
|
5.85e-01
|
0.14600
|
0.111000
|
9.49e-02
|
3.27e-01
|
4.03e-01
|
Prolactin receptor signaling
|
11
|
7.07e-01
|
7.98e-01
|
0.14600
|
-0.083900
|
1.19e-01
|
6.30e-01
|
4.94e-01
|
Regulation of FOXO transcriptional activity by acetylation
|
10
|
7.26e-01
|
8.16e-01
|
0.14600
|
0.129000
|
6.81e-02
|
4.81e-01
|
7.09e-01
|
CRMPs in Sema3A signaling
|
15
|
6.19e-01
|
7.36e-01
|
0.14600
|
-0.122000
|
-7.86e-02
|
4.12e-01
|
5.98e-01
|
Intrinsic Pathway of Fibrin Clot Formation
|
12
|
6.86e-01
|
7.81e-01
|
0.14500
|
0.111000
|
-9.39e-02
|
5.06e-01
|
5.73e-01
|
Negative regulation of FLT3
|
13
|
6.62e-01
|
7.71e-01
|
0.14500
|
-0.053200
|
-1.35e-01
|
7.40e-01
|
3.99e-01
|
Downstream signal transduction
|
28
|
4.13e-01
|
5.67e-01
|
0.14500
|
-0.076300
|
-1.23e-01
|
4.85e-01
|
2.61e-01
|
Sensory Perception
|
148
|
1.00e-02
|
3.46e-02
|
0.14400
|
0.141000
|
2.92e-02
|
3.02e-03
|
5.40e-01
|
Regulation of cholesterol biosynthesis by SREBP (SREBF)
|
55
|
1.81e-01
|
3.24e-01
|
0.14400
|
0.009120
|
-1.44e-01
|
9.07e-01
|
6.47e-02
|
Interactions of Vpr with host cellular proteins
|
37
|
3.19e-01
|
4.74e-01
|
0.14400
|
-0.113000
|
8.97e-02
|
2.35e-01
|
3.45e-01
|
GRB2:SOS provides linkage to MAPK signaling for Integrins
|
12
|
6.91e-01
|
7.85e-01
|
0.14400
|
-0.136000
|
4.70e-02
|
4.15e-01
|
7.78e-01
|
Disease
|
1472
|
6.97e-19
|
2.38e-17
|
0.14400
|
-0.021800
|
-1.42e-01
|
1.67e-01
|
1.78e-19
|
Regulation of PTEN gene transcription
|
59
|
1.64e-01
|
3.04e-01
|
0.14400
|
0.066300
|
-1.28e-01
|
3.78e-01
|
9.03e-02
|
Inwardly rectifying K+ channels
|
22
|
5.12e-01
|
6.55e-01
|
0.14300
|
0.065900
|
-1.27e-01
|
5.92e-01
|
3.02e-01
|
Recognition of DNA damage by PCNA-containing replication complex
|
30
|
3.98e-01
|
5.53e-01
|
0.14300
|
0.142000
|
1.40e-02
|
1.77e-01
|
8.94e-01
|
Cell Cycle Checkpoints
|
239
|
7.43e-04
|
3.70e-03
|
0.14300
|
0.029700
|
-1.40e-01
|
4.30e-01
|
1.99e-04
|
Signalling to ERKs
|
33
|
3.62e-01
|
5.16e-01
|
0.14300
|
-0.099200
|
-1.03e-01
|
3.24e-01
|
3.07e-01
|
Dissolution of Fibrin Clot
|
10
|
7.35e-01
|
8.20e-01
|
0.14300
|
-0.046000
|
-1.35e-01
|
8.01e-01
|
4.59e-01
|
Constitutive Signaling by EGFRvIII
|
15
|
6.34e-01
|
7.50e-01
|
0.14300
|
-0.058000
|
1.30e-01
|
6.98e-01
|
3.82e-01
|
Signaling by EGFRvIII in Cancer
|
15
|
6.34e-01
|
7.50e-01
|
0.14300
|
-0.058000
|
1.30e-01
|
6.98e-01
|
3.82e-01
|
Downregulation of ERBB2 signaling
|
27
|
4.42e-01
|
5.93e-01
|
0.14300
|
0.074200
|
-1.22e-01
|
5.04e-01
|
2.73e-01
|
Drug ADME
|
58
|
1.72e-01
|
3.13e-01
|
0.14200
|
-0.142000
|
-1.18e-02
|
6.17e-02
|
8.76e-01
|
MET promotes cell motility
|
40
|
3.01e-01
|
4.63e-01
|
0.14200
|
0.000739
|
-1.42e-01
|
9.94e-01
|
1.21e-01
|
Transport of Mature mRNA derived from an Intron-Containing Transcript
|
72
|
1.18e-01
|
2.40e-01
|
0.14200
|
-0.080700
|
1.16e-01
|
2.37e-01
|
8.76e-02
|
PI3K/AKT Signaling in Cancer
|
83
|
8.27e-02
|
1.86e-01
|
0.14100
|
-0.046500
|
-1.34e-01
|
4.64e-01
|
3.55e-02
|
NoRC negatively regulates rRNA expression
|
52
|
2.12e-01
|
3.63e-01
|
0.14100
|
0.141000
|
1.09e-03
|
7.80e-02
|
9.89e-01
|
CD209 (DC-SIGN) signaling
|
20
|
5.48e-01
|
6.86e-01
|
0.14100
|
-0.109000
|
-9.02e-02
|
4.01e-01
|
4.85e-01
|
Synthesis of IP2, IP, and Ins in the cytosol
|
12
|
7.02e-01
|
7.93e-01
|
0.14100
|
-0.051200
|
1.31e-01
|
7.59e-01
|
4.32e-01
|
EPHB-mediated forward signaling
|
39
|
3.19e-01
|
4.74e-01
|
0.14100
|
-0.112000
|
8.55e-02
|
2.28e-01
|
3.56e-01
|
ATF4 activates genes in response to endoplasmic reticulum stress
|
27
|
4.53e-01
|
6.02e-01
|
0.14000
|
0.030500
|
-1.37e-01
|
7.84e-01
|
2.19e-01
|
RNA Polymerase I Transcription Termination
|
30
|
4.15e-01
|
5.68e-01
|
0.14000
|
0.139000
|
1.42e-02
|
1.88e-01
|
8.93e-01
|
Listeria monocytogenes entry into host cells
|
18
|
5.88e-01
|
7.13e-01
|
0.14000
|
-0.109000
|
-8.78e-02
|
4.24e-01
|
5.19e-01
|
HIV Life Cycle
|
145
|
1.50e-02
|
4.88e-02
|
0.14000
|
0.014400
|
-1.39e-01
|
7.65e-01
|
3.90e-03
|
Regulation of TP53 Activity
|
149
|
1.30e-02
|
4.28e-02
|
0.14000
|
-0.035600
|
-1.35e-01
|
4.54e-01
|
4.47e-03
|
Signaling by NTRKs
|
124
|
2.76e-02
|
8.12e-02
|
0.13900
|
-0.027700
|
-1.36e-01
|
5.95e-01
|
8.77e-03
|
Transport of Mature Transcript to Cytoplasm
|
81
|
9.82e-02
|
2.09e-01
|
0.13900
|
-0.088000
|
1.08e-01
|
1.71e-01
|
9.38e-02
|
Stimuli-sensing channels
|
72
|
1.29e-01
|
2.53e-01
|
0.13900
|
-0.125000
|
6.02e-02
|
6.71e-02
|
3.77e-01
|
MyD88 cascade initiated on plasma membrane
|
94
|
6.76e-02
|
1.58e-01
|
0.13900
|
-0.011900
|
-1.38e-01
|
8.42e-01
|
2.08e-02
|
Toll Like Receptor 10 (TLR10) Cascade
|
94
|
6.76e-02
|
1.58e-01
|
0.13900
|
-0.011900
|
-1.38e-01
|
8.42e-01
|
2.08e-02
|
Toll Like Receptor 5 (TLR5) Cascade
|
94
|
6.76e-02
|
1.58e-01
|
0.13900
|
-0.011900
|
-1.38e-01
|
8.42e-01
|
2.08e-02
|
Downstream signaling of activated FGFR1
|
21
|
5.49e-01
|
6.86e-01
|
0.13800
|
0.130000
|
-4.79e-02
|
3.03e-01
|
7.04e-01
|
Signaling by EGFR
|
46
|
2.67e-01
|
4.28e-01
|
0.13800
|
-0.125000
|
-5.83e-02
|
1.42e-01
|
4.94e-01
|
Interleukin-6 signaling
|
11
|
7.32e-01
|
8.18e-01
|
0.13800
|
0.062400
|
-1.23e-01
|
7.20e-01
|
4.80e-01
|
Adherens junctions interactions
|
44
|
2.89e-01
|
4.53e-01
|
0.13800
|
0.075700
|
-1.15e-01
|
3.85e-01
|
1.86e-01
|
RHO GTPases Activate Formins
|
126
|
3.03e-02
|
8.69e-02
|
0.13700
|
0.057000
|
-1.25e-01
|
2.70e-01
|
1.58e-02
|
IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation
|
15
|
6.54e-01
|
7.65e-01
|
0.13700
|
-0.113000
|
-7.77e-02
|
4.49e-01
|
6.02e-01
|
Adrenaline,noradrenaline inhibits insulin secretion
|
23
|
5.27e-01
|
6.67e-01
|
0.13700
|
0.127000
|
-5.15e-02
|
2.93e-01
|
6.69e-01
|
SARS-CoV-1 activates/modulates innate immune responses
|
39
|
3.32e-01
|
4.88e-01
|
0.13700
|
-0.116000
|
-7.20e-02
|
2.09e-01
|
4.37e-01
|
SARS-CoV Infections
|
379
|
2.82e-05
|
1.80e-04
|
0.13700
|
-0.051100
|
-1.27e-01
|
8.87e-02
|
2.31e-05
|
Carnitine metabolism
|
13
|
6.93e-01
|
7.86e-01
|
0.13700
|
0.077400
|
1.13e-01
|
6.29e-01
|
4.82e-01
|
ERBB2 Regulates Cell Motility
|
13
|
6.98e-01
|
7.90e-01
|
0.13600
|
-0.075300
|
1.14e-01
|
6.38e-01
|
4.77e-01
|
CREB1 phosphorylation through the activation of Adenylate Cyclase
|
10
|
7.57e-01
|
8.35e-01
|
0.13600
|
-0.136000
|
3.65e-03
|
4.56e-01
|
9.84e-01
|
Ion transport by P-type ATPases
|
42
|
3.14e-01
|
4.71e-01
|
0.13600
|
0.128000
|
-4.75e-02
|
1.53e-01
|
5.94e-01
|
Toll Like Receptor 4 (TLR4) Cascade
|
137
|
2.27e-02
|
6.93e-02
|
0.13600
|
-0.057300
|
-1.23e-01
|
2.47e-01
|
1.29e-02
|
VxPx cargo-targeting to cilium
|
17
|
6.29e-01
|
7.46e-01
|
0.13600
|
-0.109000
|
8.08e-02
|
4.38e-01
|
5.64e-01
|
RNA Polymerase III Transcription Initiation From Type 1 Promoter
|
28
|
4.63e-01
|
6.13e-01
|
0.13500
|
-0.003120
|
-1.35e-01
|
9.77e-01
|
2.15e-01
|
SHC1 events in ERBB2 signaling
|
20
|
5.76e-01
|
7.05e-01
|
0.13500
|
-0.125000
|
-5.14e-02
|
3.33e-01
|
6.90e-01
|
Translation of Replicase and Assembly of the Replication Transcription Complex 9694676
|
13
|
7.03e-01
|
7.94e-01
|
0.13500
|
0.114000
|
-7.21e-02
|
4.76e-01
|
6.52e-01
|
Cytosolic sensors of pathogen-associated DNA
|
63
|
1.81e-01
|
3.24e-01
|
0.13500
|
-0.000401
|
-1.35e-01
|
9.96e-01
|
6.44e-02
|
MyD88:MAL(TIRAP) cascade initiated on plasma membrane
|
108
|
5.34e-02
|
1.32e-01
|
0.13500
|
-0.030500
|
-1.31e-01
|
5.85e-01
|
1.86e-02
|
Toll Like Receptor 2 (TLR2) Cascade
|
108
|
5.34e-02
|
1.32e-01
|
0.13500
|
-0.030500
|
-1.31e-01
|
5.85e-01
|
1.86e-02
|
Toll Like Receptor TLR1:TLR2 Cascade
|
108
|
5.34e-02
|
1.32e-01
|
0.13500
|
-0.030500
|
-1.31e-01
|
5.85e-01
|
1.86e-02
|
Toll Like Receptor TLR6:TLR2 Cascade
|
108
|
5.34e-02
|
1.32e-01
|
0.13500
|
-0.030500
|
-1.31e-01
|
5.85e-01
|
1.86e-02
|
Signaling by TGFB family members
|
112
|
5.25e-02
|
1.31e-01
|
0.13300
|
0.082800
|
-1.05e-01
|
1.30e-01
|
5.58e-02
|
Clathrin-mediated endocytosis
|
129
|
3.29e-02
|
9.21e-02
|
0.13300
|
-0.129000
|
-3.43e-02
|
1.18e-02
|
5.01e-01
|
Branched-chain amino acid catabolism
|
21
|
5.79e-01
|
7.08e-01
|
0.13200
|
-0.099700
|
8.72e-02
|
4.29e-01
|
4.89e-01
|
Formation of Incision Complex in GG-NER
|
43
|
3.29e-01
|
4.85e-01
|
0.13200
|
0.096400
|
-9.01e-02
|
2.74e-01
|
3.07e-01
|
KSRP (KHSRP) binds and destabilizes mRNA
|
17
|
6.43e-01
|
7.58e-01
|
0.13200
|
-0.131000
|
7.68e-03
|
3.48e-01
|
9.56e-01
|
NOTCH2 Activation and Transmission of Signal to the Nucleus
|
22
|
5.71e-01
|
7.02e-01
|
0.13100
|
0.070700
|
-1.10e-01
|
5.66e-01
|
3.71e-01
|
Membrane Trafficking
|
572
|
5.94e-07
|
6.06e-06
|
0.13100
|
-0.090900
|
-9.42e-02
|
2.14e-04
|
1.26e-04
|
O-linked glycosylation
|
86
|
1.10e-01
|
2.29e-01
|
0.13100
|
-0.101000
|
-8.29e-02
|
1.06e-01
|
1.84e-01
|
Nuclear import of Rev protein
|
34
|
4.23e-01
|
5.75e-01
|
0.13100
|
-0.105000
|
7.78e-02
|
2.91e-01
|
4.32e-01
|
mTORC1-mediated signalling
|
24
|
5.45e-01
|
6.83e-01
|
0.13000
|
0.079900
|
-1.03e-01
|
4.98e-01
|
3.82e-01
|
Transcriptional Regulation by TP53
|
340
|
2.06e-04
|
1.14e-03
|
0.13000
|
0.006690
|
-1.30e-01
|
8.33e-01
|
3.85e-05
|
MAP kinase activation
|
63
|
2.06e-01
|
3.56e-01
|
0.13000
|
0.018800
|
-1.28e-01
|
7.96e-01
|
7.85e-02
|
Neurotransmitter release cycle
|
37
|
3.98e-01
|
5.53e-01
|
0.12900
|
0.052800
|
-1.18e-01
|
5.79e-01
|
2.14e-01
|
Presynaptic function of Kainate receptors
|
16
|
6.72e-01
|
7.76e-01
|
0.12900
|
-0.074700
|
1.05e-01
|
6.05e-01
|
4.65e-01
|
Cardiac conduction
|
91
|
1.05e-01
|
2.21e-01
|
0.12900
|
0.023700
|
-1.27e-01
|
6.96e-01
|
3.65e-02
|
Mitochondrial biogenesis
|
85
|
1.20e-01
|
2.41e-01
|
0.12900
|
-0.027600
|
-1.26e-01
|
6.61e-01
|
4.45e-02
|
Interactions of Rev with host cellular proteins
|
37
|
4.01e-01
|
5.55e-01
|
0.12900
|
-0.116000
|
5.65e-02
|
2.22e-01
|
5.52e-01
|
IRS-mediated signalling
|
35
|
4.21e-01
|
5.73e-01
|
0.12900
|
0.030700
|
-1.25e-01
|
7.53e-01
|
2.00e-01
|
Signal amplification
|
27
|
5.09e-01
|
6.53e-01
|
0.12900
|
-0.106000
|
-7.31e-02
|
3.41e-01
|
5.11e-01
|
SARS-CoV-2 Infection
|
265
|
1.53e-03
|
6.89e-03
|
0.12800
|
-0.053100
|
-1.17e-01
|
1.37e-01
|
1.09e-03
|
G alpha (z) signalling events
|
37
|
4.06e-01
|
5.59e-01
|
0.12800
|
0.064100
|
-1.11e-01
|
5.00e-01
|
2.43e-01
|
FOXO-mediated transcription of cell death genes
|
15
|
6.92e-01
|
7.86e-01
|
0.12800
|
0.002820
|
-1.28e-01
|
9.85e-01
|
3.90e-01
|
Transport of vitamins, nucleosides, and related molecules
|
29
|
4.92e-01
|
6.39e-01
|
0.12800
|
-0.030900
|
-1.24e-01
|
7.73e-01
|
2.49e-01
|
EML4 and NUDC in mitotic spindle formation
|
103
|
8.38e-02
|
1.88e-01
|
0.12700
|
0.037700
|
-1.22e-01
|
5.09e-01
|
3.30e-02
|
MyD88 dependent cascade initiated on endosome
|
101
|
8.69e-02
|
1.92e-01
|
0.12700
|
-0.047500
|
-1.18e-01
|
4.10e-01
|
4.10e-02
|
MicroRNA (miRNA) biogenesis
|
24
|
5.65e-01
|
6.97e-01
|
0.12700
|
0.059200
|
-1.12e-01
|
6.16e-01
|
3.43e-01
|
Signaling by TGF-beta Receptor Complex
|
90
|
1.18e-01
|
2.40e-01
|
0.12600
|
0.021300
|
-1.25e-01
|
7.27e-01
|
4.13e-02
|
Class I MHC mediated antigen processing & presentation
|
343
|
3.13e-04
|
1.68e-03
|
0.12600
|
-0.080600
|
-9.68e-02
|
1.05e-02
|
2.12e-03
|
Negative regulation of the PI3K/AKT network
|
89
|
1.20e-01
|
2.41e-01
|
0.12600
|
-0.062300
|
-1.09e-01
|
3.10e-01
|
7.45e-02
|
Heme signaling
|
44
|
3.54e-01
|
5.09e-01
|
0.12600
|
-0.036900
|
1.20e-01
|
6.72e-01
|
1.67e-01
|
RND3 GTPase cycle
|
36
|
4.24e-01
|
5.75e-01
|
0.12600
|
0.089900
|
8.79e-02
|
3.51e-01
|
3.62e-01
|
TRAF6 mediated NF-kB activation
|
23
|
5.82e-01
|
7.09e-01
|
0.12600
|
-0.121000
|
3.52e-02
|
3.17e-01
|
7.70e-01
|
Toll Like Receptor 7/8 (TLR7/8) Cascade
|
102
|
8.94e-02
|
1.96e-01
|
0.12600
|
-0.056300
|
-1.12e-01
|
3.26e-01
|
5.03e-02
|
Signaling by FLT3 fusion proteins
|
19
|
6.37e-01
|
7.53e-01
|
0.12500
|
0.088600
|
8.85e-02
|
5.04e-01
|
5.04e-01
|
Toll-like Receptor Cascades
|
157
|
2.67e-02
|
7.88e-02
|
0.12400
|
-0.104000
|
-6.81e-02
|
2.50e-02
|
1.41e-01
|
Sphingolipid de novo biosynthesis
|
36
|
4.35e-01
|
5.87e-01
|
0.12400
|
0.121000
|
2.75e-02
|
2.09e-01
|
7.75e-01
|
Cell Cycle, Mitotic
|
481
|
2.13e-05
|
1.40e-04
|
0.12400
|
0.008670
|
-1.24e-01
|
7.46e-01
|
3.66e-06
|
Interleukin-17 signaling
|
67
|
2.17e-01
|
3.70e-01
|
0.12400
|
-0.003830
|
-1.24e-01
|
9.57e-01
|
8.06e-02
|
Regulated Necrosis
|
51
|
3.11e-01
|
4.70e-01
|
0.12300
|
-0.030400
|
-1.20e-01
|
7.07e-01
|
1.39e-01
|
M Phase
|
344
|
4.72e-04
|
2.42e-03
|
0.12300
|
0.031200
|
-1.19e-01
|
3.22e-01
|
1.48e-04
|
Gap-filling DNA repair synthesis and ligation in TC-NER
|
64
|
2.38e-01
|
3.95e-01
|
0.12300
|
0.078300
|
-9.51e-02
|
2.79e-01
|
1.89e-01
|
Thromboxane signalling through TP receptor
|
19
|
6.48e-01
|
7.60e-01
|
0.12300
|
-0.121000
|
-2.36e-02
|
3.62e-01
|
8.59e-01
|
Nuclear Envelope Breakdown
|
53
|
3.03e-01
|
4.65e-01
|
0.12300
|
-0.113000
|
4.82e-02
|
1.54e-01
|
5.44e-01
|
Signaling by high-kinase activity BRAF mutants
|
31
|
4.97e-01
|
6.42e-01
|
0.12300
|
-0.119000
|
2.99e-02
|
2.50e-01
|
7.73e-01
|
FLT3 signaling in disease
|
27
|
5.44e-01
|
6.82e-01
|
0.12300
|
0.120000
|
-2.65e-02
|
2.80e-01
|
8.12e-01
|
TRAF6-mediated induction of TAK1 complex within TLR4 complex
|
16
|
6.95e-01
|
7.88e-01
|
0.12300
|
-0.101000
|
-6.97e-02
|
4.84e-01
|
6.29e-01
|
B-WICH complex positively regulates rRNA expression
|
37
|
4.34e-01
|
5.86e-01
|
0.12300
|
0.119000
|
2.93e-02
|
2.10e-01
|
7.58e-01
|
TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation
|
100
|
1.06e-01
|
2.22e-01
|
0.12200
|
-0.040400
|
-1.16e-01
|
4.86e-01
|
4.59e-02
|
Ion channel transport
|
133
|
5.08e-02
|
1.28e-01
|
0.12200
|
-0.104000
|
-6.37e-02
|
3.79e-02
|
2.05e-01
|
Defects in vitamin and cofactor metabolism
|
20
|
6.37e-01
|
7.53e-01
|
0.12200
|
0.106000
|
6.14e-02
|
4.13e-01
|
6.35e-01
|
Regulation of MECP2 expression and activity
|
29
|
5.26e-01
|
6.67e-01
|
0.12200
|
-0.108000
|
5.69e-02
|
3.14e-01
|
5.96e-01
|
Phase 0 - rapid depolarisation
|
23
|
6.00e-01
|
7.22e-01
|
0.12200
|
0.118000
|
-3.08e-02
|
3.27e-01
|
7.98e-01
|
IRF3-mediated induction of type I IFN
|
12
|
7.66e-01
|
8.41e-01
|
0.12200
|
-0.116000
|
3.71e-02
|
4.86e-01
|
8.24e-01
|
Negative epigenetic regulation of rRNA expression
|
55
|
2.94e-01
|
4.57e-01
|
0.12200
|
0.121000
|
1.07e-02
|
1.20e-01
|
8.91e-01
|
Signaling by MET
|
75
|
1.90e-01
|
3.34e-01
|
0.12200
|
-0.039800
|
-1.15e-01
|
5.52e-01
|
8.57e-02
|
Regulation of insulin secretion
|
59
|
2.71e-01
|
4.31e-01
|
0.12100
|
-0.032200
|
-1.17e-01
|
6.69e-01
|
1.20e-01
|
Glutamate and glutamine metabolism
|
11
|
7.83e-01
|
8.55e-01
|
0.12100
|
-0.031200
|
-1.17e-01
|
8.58e-01
|
5.01e-01
|
Sphingolipid metabolism
|
72
|
2.02e-01
|
3.50e-01
|
0.12100
|
-0.094500
|
-7.61e-02
|
1.66e-01
|
2.64e-01
|
GPCR downstream signalling
|
361
|
3.95e-04
|
2.07e-03
|
0.12100
|
-0.104000
|
-6.19e-02
|
7.02e-04
|
4.38e-02
|
Glucagon signaling in metabolic regulation
|
25
|
5.77e-01
|
7.06e-01
|
0.12100
|
-0.078700
|
-9.15e-02
|
4.96e-01
|
4.28e-01
|
p75 NTR receptor-mediated signalling
|
91
|
1.38e-01
|
2.65e-01
|
0.12100
|
-0.114000
|
-3.95e-02
|
6.06e-02
|
5.15e-01
|
ALK mutants bind TKIs
|
11
|
7.89e-01
|
8.60e-01
|
0.12000
|
0.055100
|
-1.07e-01
|
7.52e-01
|
5.39e-01
|
Insulin receptor signalling cascade
|
40
|
4.24e-01
|
5.75e-01
|
0.12000
|
0.031400
|
-1.16e-01
|
7.31e-01
|
2.05e-01
|
Resolution of Sister Chromatid Cohesion
|
112
|
9.42e-02
|
2.03e-01
|
0.11900
|
0.065000
|
-1.00e-01
|
2.35e-01
|
6.71e-02
|
Circadian Clock
|
66
|
2.53e-01
|
4.13e-01
|
0.11800
|
0.044200
|
-1.10e-01
|
5.35e-01
|
1.23e-01
|
Negative regulation of MET activity
|
20
|
6.57e-01
|
7.67e-01
|
0.11800
|
-0.114000
|
-2.97e-02
|
3.76e-01
|
8.18e-01
|
Resolution of D-Loop Structures
|
33
|
5.05e-01
|
6.48e-01
|
0.11800
|
-0.053800
|
1.05e-01
|
5.93e-01
|
2.96e-01
|
Transcriptional Regulation by E2F6
|
34
|
4.91e-01
|
6.39e-01
|
0.11800
|
0.108000
|
4.62e-02
|
2.74e-01
|
6.41e-01
|
CDC42 GTPase cycle
|
146
|
5.11e-02
|
1.29e-01
|
0.11800
|
-0.097000
|
6.64e-02
|
4.32e-02
|
1.67e-01
|
Signaling by VEGF
|
105
|
1.17e-01
|
2.40e-01
|
0.11700
|
-0.117000
|
-7.53e-03
|
3.87e-02
|
8.94e-01
|
Ovarian tumor domain proteases
|
35
|
4.86e-01
|
6.33e-01
|
0.11700
|
-0.053500
|
-1.04e-01
|
5.84e-01
|
2.87e-01
|
Antigen processing: Ubiquitination & Proteasome degradation
|
282
|
3.34e-03
|
1.36e-02
|
0.11700
|
-0.021700
|
-1.15e-01
|
5.32e-01
|
9.23e-04
|
Nucleotide catabolism
|
24
|
6.15e-01
|
7.33e-01
|
0.11600
|
-0.075900
|
-8.75e-02
|
5.20e-01
|
4.58e-01
|
Cell death signalling via NRAGE, NRIF and NADE
|
73
|
2.32e-01
|
3.89e-01
|
0.11600
|
-0.116000
|
6.16e-04
|
8.73e-02
|
9.93e-01
|
Ca2+ pathway
|
54
|
3.38e-01
|
4.95e-01
|
0.11500
|
0.105000
|
4.89e-02
|
1.84e-01
|
5.34e-01
|
Opioid Signalling
|
78
|
2.13e-01
|
3.65e-01
|
0.11500
|
-0.081600
|
-8.05e-02
|
2.13e-01
|
2.19e-01
|
Deubiquitination
|
226
|
1.28e-02
|
4.22e-02
|
0.11400
|
0.004910
|
-1.14e-01
|
8.99e-01
|
3.16e-03
|
Amine ligand-binding receptors
|
11
|
8.08e-01
|
8.74e-01
|
0.11400
|
0.114000
|
-1.43e-04
|
5.13e-01
|
9.99e-01
|
SUMOylation of intracellular receptors
|
27
|
5.91e-01
|
7.16e-01
|
0.11400
|
0.044800
|
1.04e-01
|
6.87e-01
|
3.48e-01
|
G beta:gamma signalling through BTK
|
13
|
7.80e-01
|
8.53e-01
|
0.11300
|
-0.064600
|
9.33e-02
|
6.87e-01
|
5.60e-01
|
HCMV Late Events
|
59
|
3.21e-01
|
4.75e-01
|
0.11300
|
-0.010800
|
-1.13e-01
|
8.86e-01
|
1.34e-01
|
Signaling by RAF1 mutants
|
36
|
5.01e-01
|
6.46e-01
|
0.11300
|
-0.113000
|
4.71e-05
|
2.40e-01
|
1.00e+00
|
TP53 Regulates Metabolic Genes
|
80
|
2.20e-01
|
3.74e-01
|
0.11300
|
0.066000
|
-9.17e-02
|
3.07e-01
|
1.56e-01
|
RNA Polymerase III Transcription Initiation From Type 2 Promoter
|
27
|
5.99e-01
|
7.22e-01
|
0.11300
|
0.009510
|
-1.12e-01
|
9.32e-01
|
3.13e-01
|
Condensation of Prophase Chromosomes
|
19
|
6.96e-01
|
7.89e-01
|
0.11200
|
-0.041100
|
-1.05e-01
|
7.56e-01
|
4.30e-01
|
Constitutive Signaling by Aberrant PI3K in Cancer
|
56
|
3.45e-01
|
5.00e-01
|
0.11200
|
-0.069500
|
-8.82e-02
|
3.68e-01
|
2.54e-01
|
Nucleotide Excision Repair
|
110
|
1.30e-01
|
2.54e-01
|
0.11200
|
0.047400
|
-1.01e-01
|
3.91e-01
|
6.64e-02
|
GPCR ligand binding
|
197
|
2.54e-02
|
7.54e-02
|
0.11200
|
-0.038600
|
-1.05e-01
|
3.51e-01
|
1.12e-02
|
Glutathione conjugation
|
29
|
5.84e-01
|
7.11e-01
|
0.11200
|
0.068800
|
-8.81e-02
|
5.22e-01
|
4.12e-01
|
TBC/RABGAPs
|
44
|
4.39e-01
|
5.91e-01
|
0.11200
|
-0.109000
|
-2.49e-02
|
2.12e-01
|
7.75e-01
|
Signal transduction by L1
|
21
|
6.75e-01
|
7.77e-01
|
0.11100
|
-0.050400
|
-9.93e-02
|
6.89e-01
|
4.31e-01
|
RNA Polymerase I Promoter Clearance
|
56
|
3.58e-01
|
5.12e-01
|
0.11100
|
0.111000
|
-8.44e-03
|
1.53e-01
|
9.13e-01
|
RNA Polymerase I Transcription
|
56
|
3.58e-01
|
5.12e-01
|
0.11100
|
0.111000
|
-8.44e-03
|
1.53e-01
|
9.13e-01
|
Cell Cycle
|
591
|
2.99e-05
|
1.89e-04
|
0.11100
|
0.015700
|
-1.09e-01
|
5.17e-01
|
6.06e-06
|
SUMOylation of DNA methylation proteins
|
16
|
7.47e-01
|
8.27e-01
|
0.11000
|
0.015300
|
-1.09e-01
|
9.15e-01
|
4.49e-01
|
Reproduction
|
67
|
3.09e-01
|
4.70e-01
|
0.10900
|
0.102000
|
-3.72e-02
|
1.49e-01
|
5.99e-01
|
Presynaptic phase of homologous DNA pairing and strand exchange
|
38
|
5.11e-01
|
6.55e-01
|
0.10800
|
0.098100
|
4.57e-02
|
2.95e-01
|
6.26e-01
|
NOTCH3 Activation and Transmission of Signal to the Nucleus
|
25
|
6.47e-01
|
7.60e-01
|
0.10800
|
0.039700
|
-1.01e-01
|
7.31e-01
|
3.84e-01
|
RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function
|
39
|
5.08e-01
|
6.51e-01
|
0.10800
|
0.097000
|
-4.79e-02
|
2.95e-01
|
6.05e-01
|
RHO GTPases activate KTN1
|
10
|
8.42e-01
|
8.94e-01
|
0.10800
|
-0.087300
|
6.29e-02
|
6.33e-01
|
7.30e-01
|
RHOQ GTPase cycle
|
57
|
3.77e-01
|
5.31e-01
|
0.10700
|
-0.051900
|
9.40e-02
|
4.98e-01
|
2.20e-01
|
Myogenesis
|
21
|
6.99e-01
|
7.91e-01
|
0.10700
|
0.094200
|
-5.09e-02
|
4.55e-01
|
6.86e-01
|
Regulation of signaling by CBL
|
22
|
6.86e-01
|
7.81e-01
|
0.10700
|
-0.107000
|
-2.81e-03
|
3.85e-01
|
9.82e-01
|
Extension of Telomeres
|
49
|
4.40e-01
|
5.92e-01
|
0.10600
|
0.044700
|
-9.63e-02
|
5.88e-01
|
2.44e-01
|
Signaling by GPCR
|
401
|
1.27e-03
|
5.91e-03
|
0.10600
|
-0.083300
|
-6.58e-02
|
4.33e-03
|
2.42e-02
|
Regulated proteolysis of p75NTR
|
11
|
8.30e-01
|
8.89e-01
|
0.10600
|
-0.098700
|
-3.89e-02
|
5.71e-01
|
8.23e-01
|
Toll Like Receptor 9 (TLR9) Cascade
|
105
|
1.70e-01
|
3.11e-01
|
0.10600
|
-0.050400
|
-9.33e-02
|
3.73e-01
|
9.88e-02
|
Activation of G protein gated Potassium channels
|
19
|
7.31e-01
|
8.17e-01
|
0.10500
|
0.065400
|
-8.28e-02
|
6.22e-01
|
5.32e-01
|
G protein gated Potassium channels
|
19
|
7.31e-01
|
8.17e-01
|
0.10500
|
0.065400
|
-8.28e-02
|
6.22e-01
|
5.32e-01
|
Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits
|
19
|
7.31e-01
|
8.17e-01
|
0.10500
|
0.065400
|
-8.28e-02
|
6.22e-01
|
5.32e-01
|
mRNA Splicing
|
210
|
3.32e-02
|
9.25e-02
|
0.10500
|
0.097400
|
-3.91e-02
|
1.51e-02
|
3.29e-01
|
O-glycosylation of TSR domain-containing proteins
|
35
|
5.63e-01
|
6.96e-01
|
0.10500
|
-0.104000
|
1.11e-02
|
2.86e-01
|
9.09e-01
|
ESR-mediated signaling
|
152
|
8.61e-02
|
1.91e-01
|
0.10500
|
0.092300
|
-4.91e-02
|
4.97e-02
|
2.97e-01
|
Cilium Assembly
|
186
|
4.90e-02
|
1.25e-01
|
0.10400
|
0.102000
|
2.41e-02
|
1.71e-02
|
5.72e-01
|
Synthesis of glycosylphosphatidylinositol (GPI)
|
18
|
7.47e-01
|
8.27e-01
|
0.10400
|
-0.028100
|
1.00e-01
|
8.37e-01
|
4.61e-01
|
Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA
|
17
|
7.60e-01
|
8.37e-01
|
0.10400
|
-0.103000
|
1.75e-02
|
4.64e-01
|
9.01e-01
|
Recruitment of NuMA to mitotic centrosomes
|
87
|
2.49e-01
|
4.10e-01
|
0.10400
|
0.074200
|
-7.28e-02
|
2.32e-01
|
2.41e-01
|
EPH-Ephrin signaling
|
82
|
2.67e-01
|
4.29e-01
|
0.10400
|
-0.101000
|
-2.12e-02
|
1.13e-01
|
7.40e-01
|
Early SARS-CoV-2 Infection Events
|
33
|
5.87e-01
|
7.13e-01
|
0.10300
|
-0.053600
|
-8.84e-02
|
5.94e-01
|
3.80e-01
|
CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling
|
24
|
6.84e-01
|
7.81e-01
|
0.10300
|
0.022100
|
-1.01e-01
|
8.51e-01
|
3.94e-01
|
G-protein activation
|
18
|
7.55e-01
|
8.33e-01
|
0.10300
|
-0.095600
|
3.70e-02
|
4.83e-01
|
7.86e-01
|
Transcription-Coupled Nucleotide Excision Repair (TC-NER)
|
78
|
2.98e-01
|
4.60e-01
|
0.10200
|
0.052900
|
-8.76e-02
|
4.19e-01
|
1.81e-01
|
MAPK3 (ERK1) activation
|
10
|
8.55e-01
|
9.02e-01
|
0.10200
|
0.004770
|
1.02e-01
|
9.79e-01
|
5.77e-01
|
mRNA Splicing - Major Pathway
|
202
|
4.57e-02
|
1.18e-01
|
0.10200
|
0.088200
|
-5.11e-02
|
3.10e-02
|
2.11e-01
|
FOXO-mediated transcription
|
57
|
4.19e-01
|
5.72e-01
|
0.10100
|
0.096300
|
-3.12e-02
|
2.09e-01
|
6.84e-01
|
Transcriptional activation of mitochondrial biogenesis
|
49
|
4.71e-01
|
6.20e-01
|
0.10100
|
-0.100000
|
-1.35e-02
|
2.25e-01
|
8.70e-01
|
Resolution of Abasic Sites (AP sites)
|
38
|
5.59e-01
|
6.93e-01
|
0.10100
|
-0.052800
|
-8.58e-02
|
5.73e-01
|
3.60e-01
|
Polymerase switching on the C-strand of the telomere
|
26
|
6.73e-01
|
7.76e-01
|
0.10000
|
0.089500
|
4.56e-02
|
4.30e-01
|
6.88e-01
|
Diseases of signal transduction by growth factor receptors and second messengers
|
390
|
3.27e-03
|
1.34e-02
|
0.10000
|
-0.001300
|
-1.00e-01
|
9.65e-01
|
7.18e-04
|
SLC transporter disorders
|
70
|
3.54e-01
|
5.09e-01
|
0.09990
|
-0.094800
|
3.16e-02
|
1.70e-01
|
6.48e-01
|
SUMOylation of DNA damage response and repair proteins
|
77
|
3.16e-01
|
4.73e-01
|
0.09990
|
0.031000
|
9.50e-02
|
6.39e-01
|
1.50e-01
|
mRNA decay by 3’ to 5’ exoribonuclease
|
13
|
8.24e-01
|
8.86e-01
|
0.09980
|
0.095600
|
-2.87e-02
|
5.51e-01
|
8.58e-01
|
Signaling by ERBB2 ECD mutants
|
16
|
7.89e-01
|
8.60e-01
|
0.09950
|
-0.000825
|
9.95e-02
|
9.95e-01
|
4.91e-01
|
Synthesis of very long-chain fatty acyl-CoAs
|
18
|
7.66e-01
|
8.41e-01
|
0.09950
|
-0.002640
|
-9.94e-02
|
9.85e-01
|
4.65e-01
|
HCMV Early Events
|
76
|
3.30e-01
|
4.85e-01
|
0.09920
|
0.045800
|
-8.80e-02
|
4.90e-01
|
1.85e-01
|
VEGFA-VEGFR2 Pathway
|
96
|
2.47e-01
|
4.07e-01
|
0.09880
|
-0.098700
|
-5.30e-03
|
9.51e-02
|
9.29e-01
|
Synthesis of PIPs at the plasma membrane
|
50
|
4.83e-01
|
6.29e-01
|
0.09870
|
0.007030
|
9.84e-02
|
9.31e-01
|
2.29e-01
|
Signaling by NTRK2 (TRKB)
|
22
|
7.31e-01
|
8.17e-01
|
0.09800
|
-0.083300
|
5.16e-02
|
4.99e-01
|
6.75e-01
|
Metabolism of vitamins and cofactors
|
156
|
1.08e-01
|
2.26e-01
|
0.09790
|
-0.009410
|
-9.75e-02
|
8.39e-01
|
3.58e-02
|
Resolution of D-loop Structures through Holliday Junction Intermediates
|
32
|
6.34e-01
|
7.50e-01
|
0.09770
|
-0.028700
|
9.34e-02
|
7.79e-01
|
3.61e-01
|
Diseases of DNA repair
|
48
|
5.04e-01
|
6.48e-01
|
0.09740
|
0.092400
|
3.09e-02
|
2.68e-01
|
7.11e-01
|
Signaling by BRAF and RAF1 fusions
|
58
|
4.41e-01
|
5.93e-01
|
0.09730
|
-0.095600
|
1.81e-02
|
2.08e-01
|
8.12e-01
|
eNOS activation
|
11
|
8.55e-01
|
9.02e-01
|
0.09700
|
0.032900
|
9.13e-02
|
8.50e-01
|
6.00e-01
|
Activation of the pre-replicative complex
|
29
|
6.67e-01
|
7.73e-01
|
0.09700
|
0.080400
|
-5.43e-02
|
4.54e-01
|
6.13e-01
|
RHOD GTPase cycle
|
50
|
4.95e-01
|
6.41e-01
|
0.09660
|
0.080500
|
5.33e-02
|
3.25e-01
|
5.14e-01
|
Activation of gene expression by SREBF (SREBP)
|
42
|
5.59e-01
|
6.93e-01
|
0.09650
|
0.045500
|
-8.51e-02
|
6.10e-01
|
3.40e-01
|
TP53 Regulates Transcription of Cell Cycle Genes
|
44
|
5.39e-01
|
6.81e-01
|
0.09650
|
-0.048400
|
-8.34e-02
|
5.78e-01
|
3.38e-01
|
Signal Transduction
|
2031
|
1.74e-11
|
4.26e-10
|
0.09610
|
-0.013800
|
-9.51e-02
|
3.14e-01
|
3.47e-12
|
WNT ligand biogenesis and trafficking
|
16
|
8.03e-01
|
8.72e-01
|
0.09610
|
0.085400
|
-4.39e-02
|
5.54e-01
|
7.61e-01
|
PI3K events in ERBB2 signaling
|
14
|
8.26e-01
|
8.87e-01
|
0.09600
|
-0.061900
|
7.33e-02
|
6.88e-01
|
6.35e-01
|
RHO GTPase Effectors
|
244
|
3.73e-02
|
1.01e-01
|
0.09570
|
0.024200
|
-9.26e-02
|
5.16e-01
|
1.29e-02
|
HuR (ELAVL1) binds and stabilizes mRNA
|
10
|
8.71e-01
|
9.11e-01
|
0.09560
|
0.021000
|
9.33e-02
|
9.08e-01
|
6.10e-01
|
Homologous DNA Pairing and Strand Exchange
|
41
|
5.71e-01
|
7.02e-01
|
0.09510
|
0.060700
|
7.32e-02
|
5.02e-01
|
4.17e-01
|
PKA activation
|
16
|
8.07e-01
|
8.74e-01
|
0.09410
|
-0.046000
|
-8.22e-02
|
7.50e-01
|
5.69e-01
|
Antiviral mechanism by IFN-stimulated genes
|
79
|
3.57e-01
|
5.11e-01
|
0.09390
|
-0.063900
|
6.88e-02
|
3.26e-01
|
2.91e-01
|
Voltage gated Potassium channels
|
15
|
8.21e-01
|
8.85e-01
|
0.09390
|
-0.037400
|
8.61e-02
|
8.02e-01
|
5.64e-01
|
G alpha (q) signalling events
|
129
|
1.85e-01
|
3.29e-01
|
0.09390
|
-0.092600
|
1.54e-02
|
6.96e-02
|
7.62e-01
|
Regulation of TP53 Activity through Phosphorylation
|
86
|
3.23e-01
|
4.78e-01
|
0.09390
|
0.002290
|
-9.38e-02
|
9.71e-01
|
1.33e-01
|
Termination of O-glycan biosynthesis
|
14
|
8.32e-01
|
8.90e-01
|
0.09360
|
0.000839
|
-9.36e-02
|
9.96e-01
|
5.44e-01
|
Cellular response to heat stress
|
96
|
2.89e-01
|
4.52e-01
|
0.09360
|
0.060800
|
-7.11e-02
|
3.04e-01
|
2.29e-01
|
Class B/2 (Secretin family receptors)
|
49
|
5.31e-01
|
6.72e-01
|
0.09330
|
0.059600
|
-7.18e-02
|
4.70e-01
|
3.85e-01
|
Global Genome Nucleotide Excision Repair (GG-NER)
|
84
|
3.40e-01
|
4.97e-01
|
0.09320
|
0.051700
|
-7.75e-02
|
4.13e-01
|
2.20e-01
|
Aflatoxin activation and detoxification
|
11
|
8.68e-01
|
9.08e-01
|
0.09280
|
0.012200
|
-9.20e-02
|
9.44e-01
|
5.97e-01
|
Cell-cell junction organization
|
63
|
4.49e-01
|
5.97e-01
|
0.09270
|
0.053700
|
-7.55e-02
|
4.61e-01
|
3.00e-01
|
Processing of DNA double-strand break ends
|
60
|
4.67e-01
|
6.16e-01
|
0.09250
|
0.039400
|
-8.37e-02
|
5.97e-01
|
2.63e-01
|
Defective homologous recombination repair (HRR) due to BRCA2 loss of function
|
39
|
6.04e-01
|
7.26e-01
|
0.09250
|
0.069300
|
6.12e-02
|
4.54e-01
|
5.09e-01
|
Diseases of DNA Double-Strand Break Repair
|
39
|
6.04e-01
|
7.26e-01
|
0.09250
|
0.069300
|
6.12e-02
|
4.54e-01
|
5.09e-01
|
Transmission across Chemical Synapses
|
187
|
9.82e-02
|
2.09e-01
|
0.09180
|
0.045300
|
-7.99e-02
|
2.86e-01
|
5.99e-02
|
Adenylate cyclase inhibitory pathway
|
12
|
8.59e-01
|
9.04e-01
|
0.09180
|
0.091700
|
2.47e-03
|
5.82e-01
|
9.88e-01
|
Activation of HOX genes during differentiation
|
65
|
4.45e-01
|
5.94e-01
|
0.09170
|
0.073800
|
-5.45e-02
|
3.04e-01
|
4.48e-01
|
Activation of anterior HOX genes in hindbrain development during early embryogenesis
|
65
|
4.45e-01
|
5.94e-01
|
0.09170
|
0.073800
|
-5.45e-02
|
3.04e-01
|
4.48e-01
|
RNA Polymerase III Transcription Initiation
|
36
|
6.40e-01
|
7.54e-01
|
0.09140
|
0.043700
|
-8.03e-02
|
6.50e-01
|
4.05e-01
|
Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer
|
50
|
5.39e-01
|
6.81e-01
|
0.09130
|
0.055900
|
-7.21e-02
|
4.94e-01
|
3.78e-01
|
Oncogenic MAPK signaling
|
74
|
4.00e-01
|
5.55e-01
|
0.09120
|
-0.088100
|
2.37e-02
|
1.90e-01
|
7.25e-01
|
Regulation of innate immune responses to cytosolic DNA
|
14
|
8.40e-01
|
8.94e-01
|
0.09120
|
0.008950
|
-9.08e-02
|
9.54e-01
|
5.56e-01
|
Transcriptional Regulation by VENTX
|
39
|
6.16e-01
|
7.34e-01
|
0.09110
|
-0.002450
|
-9.10e-02
|
9.79e-01
|
3.25e-01
|
Neurotransmitter receptors and postsynaptic signal transmission
|
141
|
1.80e-01
|
3.24e-01
|
0.09080
|
0.038400
|
-8.23e-02
|
4.32e-01
|
9.21e-02
|
Activation of GABAB receptors
|
31
|
6.85e-01
|
7.81e-01
|
0.09060
|
0.075700
|
-4.98e-02
|
4.66e-01
|
6.31e-01
|
GABA B receptor activation
|
31
|
6.85e-01
|
7.81e-01
|
0.09060
|
0.075700
|
-4.98e-02
|
4.66e-01
|
6.31e-01
|
FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes
|
24
|
7.47e-01
|
8.27e-01
|
0.09020
|
0.089800
|
-8.33e-03
|
4.46e-01
|
9.44e-01
|
tRNA modification in the nucleus and cytosol
|
43
|
5.95e-01
|
7.18e-01
|
0.08990
|
0.089500
|
-8.17e-03
|
3.10e-01
|
9.26e-01
|
Anchoring of the basal body to the plasma membrane
|
95
|
3.18e-01
|
4.74e-01
|
0.08970
|
0.083600
|
3.26e-02
|
1.59e-01
|
5.83e-01
|
Phase II - Conjugation of compounds
|
68
|
4.45e-01
|
5.94e-01
|
0.08970
|
0.053200
|
-7.22e-02
|
4.48e-01
|
3.04e-01
|
RAC1 GTPase cycle
|
173
|
1.30e-01
|
2.54e-01
|
0.08950
|
-0.049300
|
7.46e-02
|
2.64e-01
|
9.07e-02
|
Dual incision in TC-NER
|
65
|
4.62e-01
|
6.13e-01
|
0.08940
|
0.079800
|
-4.04e-02
|
2.66e-01
|
5.73e-01
|
Telomere C-strand (Lagging Strand) Synthesis
|
34
|
6.67e-01
|
7.73e-01
|
0.08930
|
0.086000
|
-2.42e-02
|
3.86e-01
|
8.07e-01
|
RND2 GTPase cycle
|
36
|
6.53e-01
|
7.65e-01
|
0.08890
|
0.007730
|
8.85e-02
|
9.36e-01
|
3.58e-01
|
PKA-mediated phosphorylation of CREB
|
18
|
8.09e-01
|
8.74e-01
|
0.08880
|
-0.088300
|
9.19e-03
|
5.17e-01
|
9.46e-01
|
Peroxisomal protein import
|
57
|
5.18e-01
|
6.61e-01
|
0.08820
|
-0.043500
|
7.67e-02
|
5.70e-01
|
3.17e-01
|
RNA polymerase II transcribes snRNA genes
|
71
|
4.43e-01
|
5.94e-01
|
0.08800
|
0.077600
|
-4.15e-02
|
2.59e-01
|
5.46e-01
|
Lagging Strand Synthesis
|
20
|
7.97e-01
|
8.67e-01
|
0.08700
|
-0.000587
|
8.70e-02
|
9.96e-01
|
5.01e-01
|
Defective B3GALTL causes PpS
|
34
|
6.83e-01
|
7.81e-01
|
0.08670
|
-0.082900
|
2.56e-02
|
4.03e-01
|
7.96e-01
|
Activation of RAC1
|
11
|
8.84e-01
|
9.19e-01
|
0.08670
|
-0.046300
|
7.33e-02
|
7.90e-01
|
6.74e-01
|
Energy dependent regulation of mTOR by LKB1-AMPK
|
28
|
7.28e-01
|
8.17e-01
|
0.08670
|
0.042100
|
7.57e-02
|
7.00e-01
|
4.88e-01
|
SUMOylation of transcription factors
|
17
|
8.27e-01
|
8.87e-01
|
0.08660
|
-0.083500
|
2.31e-02
|
5.51e-01
|
8.69e-01
|
NCAM signaling for neurite out-growth
|
52
|
5.58e-01
|
6.93e-01
|
0.08620
|
-0.051400
|
-6.92e-02
|
5.22e-01
|
3.88e-01
|
SARS-CoV-2-host interactions
|
176
|
1.48e-01
|
2.80e-01
|
0.08590
|
0.036100
|
-7.79e-02
|
4.09e-01
|
7.49e-02
|
Translocation of SLC2A4 (GLUT4) to the plasma membrane
|
63
|
5.00e-01
|
6.45e-01
|
0.08580
|
0.085800
|
-2.33e-03
|
2.39e-01
|
9.74e-01
|
Cargo trafficking to the periciliary membrane
|
45
|
6.12e-01
|
7.33e-01
|
0.08520
|
0.080800
|
2.69e-02
|
3.49e-01
|
7.55e-01
|
Sensory processing of sound by inner hair cells of the cochlea
|
49
|
5.92e-01
|
7.16e-01
|
0.08500
|
0.070500
|
-4.74e-02
|
3.93e-01
|
5.66e-01
|
Activation of SMO
|
16
|
8.43e-01
|
8.94e-01
|
0.08470
|
0.029300
|
-7.95e-02
|
8.39e-01
|
5.82e-01
|
Sensory processing of sound
|
52
|
5.74e-01
|
7.04e-01
|
0.08460
|
0.083000
|
-1.65e-02
|
3.01e-01
|
8.37e-01
|
BMAL1:CLOCK,NPAS2 activates circadian gene expression
|
25
|
7.67e-01
|
8.41e-01
|
0.08440
|
0.022000
|
-8.14e-02
|
8.49e-01
|
4.81e-01
|
Frs2-mediated activation
|
12
|
8.81e-01
|
9.18e-01
|
0.08430
|
-0.074900
|
3.87e-02
|
6.53e-01
|
8.17e-01
|
RHOG GTPase cycle
|
71
|
4.73e-01
|
6.20e-01
|
0.08430
|
0.024600
|
-8.06e-02
|
7.20e-01
|
2.40e-01
|
HDACs deacetylate histones
|
36
|
6.83e-01
|
7.81e-01
|
0.08420
|
0.006180
|
-8.40e-02
|
9.49e-01
|
3.83e-01
|
Pre-NOTCH Expression and Processing
|
54
|
5.66e-01
|
6.98e-01
|
0.08360
|
-0.044600
|
-7.07e-02
|
5.71e-01
|
3.69e-01
|
Signaling by PDGFR in disease
|
20
|
8.11e-01
|
8.76e-01
|
0.08350
|
-0.082500
|
-1.28e-02
|
5.23e-01
|
9.21e-01
|
Fanconi Anemia Pathway
|
35
|
6.97e-01
|
7.90e-01
|
0.08330
|
-0.072200
|
4.15e-02
|
4.60e-01
|
6.71e-01
|
Paradoxical activation of RAF signaling by kinase inactive BRAF
|
40
|
6.63e-01
|
7.71e-01
|
0.08290
|
-0.082400
|
9.44e-03
|
3.68e-01
|
9.18e-01
|
Signaling by RAS mutants
|
40
|
6.63e-01
|
7.71e-01
|
0.08290
|
-0.082400
|
9.44e-03
|
3.68e-01
|
9.18e-01
|
Signaling by moderate kinase activity BRAF mutants
|
40
|
6.63e-01
|
7.71e-01
|
0.08290
|
-0.082400
|
9.44e-03
|
3.68e-01
|
9.18e-01
|
Signaling downstream of RAS mutants
|
40
|
6.63e-01
|
7.71e-01
|
0.08290
|
-0.082400
|
9.44e-03
|
3.68e-01
|
9.18e-01
|
SUMOylation of chromatin organization proteins
|
57
|
5.60e-01
|
6.93e-01
|
0.08280
|
-0.079100
|
2.44e-02
|
3.02e-01
|
7.50e-01
|
Positive epigenetic regulation of rRNA expression
|
52
|
5.90e-01
|
7.16e-01
|
0.08250
|
0.080800
|
-1.68e-02
|
3.14e-01
|
8.34e-01
|
DNA Damage Bypass
|
46
|
6.25e-01
|
7.41e-01
|
0.08250
|
0.078100
|
2.66e-02
|
3.60e-01
|
7.55e-01
|
DNA strand elongation
|
31
|
7.36e-01
|
8.21e-01
|
0.08120
|
0.005000
|
-8.11e-02
|
9.62e-01
|
4.35e-01
|
Nephrin family interactions
|
18
|
8.41e-01
|
8.94e-01
|
0.08030
|
0.079500
|
-1.15e-02
|
5.59e-01
|
9.33e-01
|
Signaling by ERBB2 in Cancer
|
24
|
7.94e-01
|
8.65e-01
|
0.08000
|
0.016000
|
7.84e-02
|
8.92e-01
|
5.06e-01
|
Mitotic Prophase
|
88
|
4.34e-01
|
5.86e-01
|
0.07930
|
-0.056200
|
-5.60e-02
|
3.63e-01
|
3.64e-01
|
Semaphorin interactions
|
62
|
5.62e-01
|
6.95e-01
|
0.07850
|
-0.056900
|
-5.42e-02
|
4.39e-01
|
4.61e-01
|
Interleukin-37 signaling
|
20
|
8.33e-01
|
8.90e-01
|
0.07850
|
-0.044500
|
6.47e-02
|
7.31e-01
|
6.16e-01
|
Processing of Capped Intronless Pre-mRNA
|
29
|
7.66e-01
|
8.41e-01
|
0.07850
|
-0.077000
|
1.50e-02
|
4.73e-01
|
8.88e-01
|
Prostacyclin signalling through prostacyclin receptor
|
14
|
8.78e-01
|
9.16e-01
|
0.07830
|
-0.047600
|
-6.22e-02
|
7.58e-01
|
6.87e-01
|
Regulation of PLK1 Activity at G2/M Transition
|
85
|
4.65e-01
|
6.15e-01
|
0.07790
|
0.072300
|
-2.89e-02
|
2.49e-01
|
6.45e-01
|
ISG15 antiviral mechanism
|
71
|
5.30e-01
|
6.71e-01
|
0.07780
|
-0.059900
|
4.96e-02
|
3.83e-01
|
4.70e-01
|
ADP signalling through P2Y purinoceptor 12
|
16
|
8.66e-01
|
9.08e-01
|
0.07710
|
0.070800
|
3.05e-02
|
6.24e-01
|
8.33e-01
|
G alpha (s) signalling events
|
83
|
4.77e-01
|
6.25e-01
|
0.07700
|
-0.061800
|
-4.60e-02
|
3.31e-01
|
4.70e-01
|
Epigenetic regulation of gene expression
|
133
|
3.09e-01
|
4.70e-01
|
0.07690
|
0.009900
|
7.63e-02
|
8.44e-01
|
1.29e-01
|
Regulation of beta-cell development
|
19
|
8.48e-01
|
8.97e-01
|
0.07630
|
-0.062600
|
4.36e-02
|
6.37e-01
|
7.42e-01
|
RHOC GTPase cycle
|
70
|
5.44e-01
|
6.82e-01
|
0.07620
|
0.008740
|
7.57e-02
|
8.99e-01
|
2.74e-01
|
Deadenylation of mRNA
|
22
|
8.27e-01
|
8.87e-01
|
0.07610
|
-0.009570
|
7.55e-02
|
9.38e-01
|
5.40e-01
|
Cell-extracellular matrix interactions
|
18
|
8.55e-01
|
9.02e-01
|
0.07590
|
-0.048100
|
-5.86e-02
|
7.24e-01
|
6.67e-01
|
IKK complex recruitment mediated by RIP1
|
23
|
8.22e-01
|
8.85e-01
|
0.07560
|
0.030400
|
-6.93e-02
|
8.01e-01
|
5.65e-01
|
NOTCH1 Intracellular Domain Regulates Transcription
|
47
|
6.70e-01
|
7.75e-01
|
0.07560
|
0.073300
|
-1.85e-02
|
3.85e-01
|
8.26e-01
|
Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants
|
57
|
6.15e-01
|
7.33e-01
|
0.07520
|
0.059700
|
4.57e-02
|
4.35e-01
|
5.51e-01
|
Constitutive Signaling by NOTCH1 PEST Domain Mutants
|
57
|
6.15e-01
|
7.33e-01
|
0.07520
|
0.059700
|
4.57e-02
|
4.35e-01
|
5.51e-01
|
Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer
|
57
|
6.15e-01
|
7.33e-01
|
0.07520
|
0.059700
|
4.57e-02
|
4.35e-01
|
5.51e-01
|
Signaling by NOTCH1 PEST Domain Mutants in Cancer
|
57
|
6.15e-01
|
7.33e-01
|
0.07520
|
0.059700
|
4.57e-02
|
4.35e-01
|
5.51e-01
|
Signaling by NOTCH1 in Cancer
|
57
|
6.15e-01
|
7.33e-01
|
0.07520
|
0.059700
|
4.57e-02
|
4.35e-01
|
5.51e-01
|
Viral Messenger RNA Synthesis
|
44
|
6.89e-01
|
7.84e-01
|
0.07520
|
-0.074300
|
-1.15e-02
|
3.94e-01
|
8.95e-01
|
RHOB GTPase cycle
|
66
|
5.71e-01
|
7.02e-01
|
0.07510
|
0.043900
|
6.09e-02
|
5.37e-01
|
3.92e-01
|
Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template
|
37
|
7.37e-01
|
8.21e-01
|
0.07460
|
0.056800
|
-4.84e-02
|
5.50e-01
|
6.10e-01
|
Neuronal System
|
260
|
1.20e-01
|
2.41e-01
|
0.07440
|
0.010200
|
-7.37e-02
|
7.77e-01
|
4.10e-02
|
FLT3 Signaling
|
36
|
7.40e-01
|
8.22e-01
|
0.07440
|
-0.044600
|
-5.95e-02
|
6.43e-01
|
5.37e-01
|
RNA Polymerase III Abortive And Retractive Initiation
|
41
|
7.19e-01
|
8.09e-01
|
0.07360
|
0.065900
|
-3.28e-02
|
4.65e-01
|
7.16e-01
|
RNA Polymerase III Transcription
|
41
|
7.19e-01
|
8.09e-01
|
0.07360
|
0.065900
|
-3.28e-02
|
4.65e-01
|
7.16e-01
|
Cell junction organization
|
88
|
4.94e-01
|
6.41e-01
|
0.07360
|
0.047800
|
-5.59e-02
|
4.38e-01
|
3.65e-01
|
Signaling by Non-Receptor Tyrosine Kinases
|
51
|
6.69e-01
|
7.74e-01
|
0.07280
|
0.028000
|
-6.72e-02
|
7.29e-01
|
4.06e-01
|
Signaling by PTK6
|
51
|
6.69e-01
|
7.74e-01
|
0.07280
|
0.028000
|
-6.72e-02
|
7.29e-01
|
4.06e-01
|
Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants
|
19
|
8.62e-01
|
9.04e-01
|
0.07260
|
0.053800
|
-4.89e-02
|
6.85e-01
|
7.12e-01
|
Signaling by Ligand-Responsive EGFR Variants in Cancer
|
19
|
8.62e-01
|
9.04e-01
|
0.07260
|
0.053800
|
-4.89e-02
|
6.85e-01
|
7.12e-01
|
Removal of the Flap Intermediate
|
14
|
8.95e-01
|
9.28e-01
|
0.07260
|
0.005520
|
7.24e-02
|
9.72e-01
|
6.39e-01
|
Arachidonic acid metabolism
|
36
|
7.56e-01
|
8.34e-01
|
0.07230
|
-0.067200
|
2.65e-02
|
4.85e-01
|
7.83e-01
|
Visual phototransduction
|
58
|
6.39e-01
|
7.53e-01
|
0.07210
|
0.068600
|
-2.23e-02
|
3.66e-01
|
7.70e-01
|
Nonhomologous End-Joining (NHEJ)
|
34
|
7.68e-01
|
8.41e-01
|
0.07210
|
-0.005130
|
7.19e-02
|
9.59e-01
|
4.68e-01
|
Metabolism of non-coding RNA
|
53
|
6.67e-01
|
7.73e-01
|
0.07140
|
0.011000
|
7.05e-02
|
8.90e-01
|
3.75e-01
|
snRNP Assembly
|
53
|
6.67e-01
|
7.73e-01
|
0.07140
|
0.011000
|
7.05e-02
|
8.90e-01
|
3.75e-01
|
HATs acetylate histones
|
82
|
5.37e-01
|
6.78e-01
|
0.07130
|
0.071300
|
1.31e-03
|
2.65e-01
|
9.84e-01
|
Signaling by FGFR1 in disease
|
32
|
7.83e-01
|
8.55e-01
|
0.07130
|
0.069100
|
1.75e-02
|
4.99e-01
|
8.64e-01
|
Platelet homeostasis
|
69
|
5.95e-01
|
7.18e-01
|
0.07090
|
-0.008410
|
-7.04e-02
|
9.04e-01
|
3.12e-01
|
ADORA2B mediated anti-inflammatory cytokines production
|
35
|
7.68e-01
|
8.41e-01
|
0.07070
|
-0.047700
|
-5.22e-02
|
6.26e-01
|
5.93e-01
|
Vasopressin regulates renal water homeostasis via Aquaporins
|
33
|
7.81e-01
|
8.54e-01
|
0.07070
|
0.070600
|
2.06e-03
|
4.83e-01
|
9.84e-01
|
E2F mediated regulation of DNA replication
|
21
|
8.59e-01
|
9.04e-01
|
0.06960
|
-0.009280
|
6.89e-02
|
9.41e-01
|
5.85e-01
|
Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex
|
12
|
9.18e-01
|
9.45e-01
|
0.06930
|
0.063200
|
-2.86e-02
|
7.05e-01
|
8.64e-01
|
Triglyceride catabolism
|
16
|
8.93e-01
|
9.26e-01
|
0.06840
|
-0.051700
|
-4.47e-02
|
7.20e-01
|
7.57e-01
|
FGFR1 mutant receptor activation
|
25
|
8.41e-01
|
8.94e-01
|
0.06830
|
0.023500
|
-6.41e-02
|
8.39e-01
|
5.79e-01
|
Mitochondrial calcium ion transport
|
21
|
8.68e-01
|
9.08e-01
|
0.06740
|
0.059000
|
-3.26e-02
|
6.40e-01
|
7.96e-01
|
Regulation of HSF1-mediated heat shock response
|
78
|
5.92e-01
|
7.16e-01
|
0.06740
|
0.047100
|
-4.82e-02
|
4.73e-01
|
4.62e-01
|
Rab regulation of trafficking
|
118
|
4.64e-01
|
6.13e-01
|
0.06600
|
-0.064900
|
-1.21e-02
|
2.24e-01
|
8.21e-01
|
RHO GTPases Activate WASPs and WAVEs
|
35
|
7.95e-01
|
8.65e-01
|
0.06600
|
-0.060500
|
-2.64e-02
|
5.36e-01
|
7.87e-01
|
RNA Polymerase I Transcription Initiation
|
47
|
7.38e-01
|
8.21e-01
|
0.06580
|
0.065800
|
-2.07e-03
|
4.35e-01
|
9.80e-01
|
Aquaporin-mediated transport
|
35
|
7.99e-01
|
8.68e-01
|
0.06570
|
0.062200
|
-2.12e-02
|
5.24e-01
|
8.28e-01
|
Organelle biogenesis and maintenance
|
271
|
1.81e-01
|
3.24e-01
|
0.06560
|
0.061300
|
-2.34e-02
|
8.30e-02
|
5.08e-01
|
Impaired BRCA2 binding to RAD51
|
33
|
8.09e-01
|
8.74e-01
|
0.06530
|
0.042700
|
4.94e-02
|
6.71e-01
|
6.24e-01
|
Regulation of lipid metabolism by PPARalpha
|
106
|
5.16e-01
|
6.59e-01
|
0.06500
|
-0.047000
|
4.49e-02
|
4.03e-01
|
4.25e-01
|
Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal
|
87
|
5.80e-01
|
7.08e-01
|
0.06490
|
0.018400
|
-6.23e-02
|
7.67e-01
|
3.16e-01
|
Amplification of signal from the kinetochores
|
87
|
5.80e-01
|
7.08e-01
|
0.06490
|
0.018400
|
-6.23e-02
|
7.67e-01
|
3.16e-01
|
Signaling by EGFR in Cancer
|
22
|
8.70e-01
|
9.09e-01
|
0.06480
|
-0.058700
|
-2.76e-02
|
6.34e-01
|
8.23e-01
|
VEGFR2 mediated vascular permeability
|
27
|
8.45e-01
|
8.96e-01
|
0.06470
|
-0.058300
|
2.80e-02
|
6.00e-01
|
8.01e-01
|
Signaling by ERBB4
|
51
|
7.28e-01
|
8.17e-01
|
0.06450
|
-0.064400
|
-2.80e-03
|
4.26e-01
|
9.72e-01
|
SUMOylation of transcription cofactors
|
44
|
7.62e-01
|
8.39e-01
|
0.06420
|
-0.000832
|
-6.42e-02
|
9.92e-01
|
4.61e-01
|
PCNA-Dependent Long Patch Base Excision Repair
|
21
|
8.78e-01
|
9.16e-01
|
0.06420
|
-0.018100
|
-6.16e-02
|
8.86e-01
|
6.25e-01
|
Metabolism of water-soluble vitamins and cofactors
|
108
|
5.20e-01
|
6.62e-01
|
0.06350
|
-0.035100
|
-5.29e-02
|
5.29e-01
|
3.42e-01
|
rRNA processing in the mitochondrion
|
10
|
9.42e-01
|
9.61e-01
|
0.06340
|
0.032600
|
-5.44e-02
|
8.59e-01
|
7.66e-01
|
DNA Repair
|
280
|
1.91e-01
|
3.37e-01
|
0.06330
|
0.005060
|
-6.31e-02
|
8.84e-01
|
6.97e-02
|
Potassium Channels
|
50
|
7.46e-01
|
8.27e-01
|
0.06280
|
0.015900
|
-6.07e-02
|
8.46e-01
|
4.58e-01
|
Glucagon-like Peptide-1 (GLP1) regulates insulin secretion
|
30
|
8.39e-01
|
8.94e-01
|
0.06260
|
0.014500
|
-6.10e-02
|
8.91e-01
|
5.63e-01
|
Metabolism of lipids
|
598
|
3.66e-02
|
1.00e-01
|
0.06190
|
-0.061500
|
6.87e-03
|
1.05e-02
|
7.75e-01
|
Signaling by Retinoic Acid
|
35
|
8.19e-01
|
8.83e-01
|
0.06170
|
-0.061300
|
6.67e-03
|
5.30e-01
|
9.46e-01
|
SARS-CoV-2 targets host intracellular signalling and regulatory pathways
|
12
|
9.33e-01
|
9.55e-01
|
0.06170
|
0.055400
|
2.71e-02
|
7.40e-01
|
8.71e-01
|
Mitotic Spindle Checkpoint
|
104
|
5.57e-01
|
6.92e-01
|
0.06170
|
0.031400
|
-5.31e-02
|
5.81e-01
|
3.50e-01
|
Gene Silencing by RNA
|
78
|
6.54e-01
|
7.65e-01
|
0.06010
|
0.045500
|
3.93e-02
|
4.88e-01
|
5.49e-01
|
Transcriptional regulation of white adipocyte differentiation
|
80
|
6.48e-01
|
7.60e-01
|
0.06000
|
-0.033400
|
-4.99e-02
|
6.05e-01
|
4.41e-01
|
Activation of kainate receptors upon glutamate binding
|
23
|
8.84e-01
|
9.19e-01
|
0.06000
|
0.038400
|
-4.62e-02
|
7.50e-01
|
7.02e-01
|
tRNA processing in the nucleus
|
59
|
7.30e-01
|
8.17e-01
|
0.06000
|
-0.037300
|
4.70e-02
|
6.21e-01
|
5.32e-01
|
Estrogen-dependent nuclear events downstream of ESR-membrane signaling
|
21
|
8.93e-01
|
9.26e-01
|
0.05990
|
-0.056200
|
-2.06e-02
|
6.56e-01
|
8.70e-01
|
HDR through Single Strand Annealing (SSA)
|
35
|
8.32e-01
|
8.90e-01
|
0.05940
|
-0.024200
|
5.42e-02
|
8.04e-01
|
5.79e-01
|
Cytochrome P450 - arranged by substrate type
|
32
|
8.48e-01
|
8.97e-01
|
0.05890
|
-0.045000
|
3.80e-02
|
6.59e-01
|
7.10e-01
|
MAP2K and MAPK activation
|
35
|
8.36e-01
|
8.93e-01
|
0.05870
|
-0.050700
|
2.97e-02
|
6.04e-01
|
7.61e-01
|
Netrin-1 signaling
|
41
|
8.08e-01
|
8.74e-01
|
0.05870
|
0.036100
|
4.63e-02
|
6.89e-01
|
6.08e-01
|
RHOA GTPase cycle
|
143
|
4.82e-01
|
6.29e-01
|
0.05870
|
-0.057300
|
1.28e-02
|
2.37e-01
|
7.92e-01
|
RNA Polymerase II Transcription Termination
|
66
|
7.16e-01
|
8.07e-01
|
0.05850
|
-0.042500
|
4.02e-02
|
5.50e-01
|
5.72e-01
|
PPARA activates gene expression
|
104
|
6.00e-01
|
7.22e-01
|
0.05760
|
-0.040400
|
4.11e-02
|
4.77e-01
|
4.69e-01
|
ERK/MAPK targets
|
22
|
8.97e-01
|
9.30e-01
|
0.05760
|
0.031700
|
-4.81e-02
|
7.97e-01
|
6.96e-01
|
Resolution of AP sites via the multiple-nucleotide patch replacement pathway
|
25
|
8.84e-01
|
9.19e-01
|
0.05720
|
-0.025100
|
-5.14e-02
|
8.28e-01
|
6.56e-01
|
Signaling by ERBB2 TMD/JMD mutants
|
20
|
9.09e-01
|
9.40e-01
|
0.05650
|
-0.056400
|
-3.43e-03
|
6.63e-01
|
9.79e-01
|
RAC2 GTPase cycle
|
85
|
6.75e-01
|
7.77e-01
|
0.05590
|
-0.045800
|
3.19e-02
|
4.65e-01
|
6.11e-01
|
Glucagon-type ligand receptors
|
16
|
9.28e-01
|
9.52e-01
|
0.05580
|
0.015900
|
-5.35e-02
|
9.12e-01
|
7.11e-01
|
Pre-NOTCH Transcription and Translation
|
38
|
8.39e-01
|
8.94e-01
|
0.05540
|
0.046900
|
2.94e-02
|
6.17e-01
|
7.54e-01
|
Loss of Nlp from mitotic centrosomes
|
67
|
7.40e-01
|
8.22e-01
|
0.05480
|
0.053200
|
1.30e-02
|
4.52e-01
|
8.54e-01
|
Loss of proteins required for interphase microtubule organization from the centrosome
|
67
|
7.40e-01
|
8.22e-01
|
0.05480
|
0.053200
|
1.30e-02
|
4.52e-01
|
8.54e-01
|
GABA receptor activation
|
39
|
8.40e-01
|
8.94e-01
|
0.05470
|
0.053500
|
-1.17e-02
|
5.63e-01
|
9.00e-01
|
Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA
|
17
|
9.27e-01
|
9.51e-01
|
0.05470
|
-0.006710
|
5.42e-02
|
9.62e-01
|
6.99e-01
|
Metabolism of porphyrins
|
21
|
9.11e-01
|
9.42e-01
|
0.05460
|
0.026600
|
-4.77e-02
|
8.33e-01
|
7.05e-01
|
Mitotic Prometaphase
|
188
|
4.44e-01
|
5.94e-01
|
0.05420
|
0.041100
|
-3.53e-02
|
3.32e-01
|
4.05e-01
|
Nuclear Receptor transcription pathway
|
39
|
8.44e-01
|
8.96e-01
|
0.05400
|
0.051200
|
-1.71e-02
|
5.80e-01
|
8.53e-01
|
Regulation of Expression and Function of Type II Classical Cadherins
|
29
|
8.82e-01
|
9.18e-01
|
0.05400
|
0.015100
|
-5.18e-02
|
8.88e-01
|
6.29e-01
|
Regulation of Homotypic Cell-Cell Adhesion
|
29
|
8.82e-01
|
9.18e-01
|
0.05400
|
0.015100
|
-5.18e-02
|
8.88e-01
|
6.29e-01
|
SUMOylation of RNA binding proteins
|
47
|
8.17e-01
|
8.81e-01
|
0.05380
|
-0.051500
|
1.53e-02
|
5.41e-01
|
8.56e-01
|
Metabolism of steroids
|
120
|
6.06e-01
|
7.27e-01
|
0.05310
|
0.014800
|
-5.10e-02
|
7.79e-01
|
3.35e-01
|
Extra-nuclear estrogen signaling
|
66
|
7.59e-01
|
8.36e-01
|
0.05290
|
-0.001050
|
-5.29e-02
|
9.88e-01
|
4.58e-01
|
HDR through Homologous Recombination (HRR)
|
65
|
7.68e-01
|
8.41e-01
|
0.05210
|
-0.002280
|
5.21e-02
|
9.75e-01
|
4.68e-01
|
Processive synthesis on the lagging strand
|
15
|
9.42e-01
|
9.61e-01
|
0.05180
|
-0.020300
|
4.77e-02
|
8.92e-01
|
7.49e-01
|
SUMO E3 ligases SUMOylate target proteins
|
162
|
5.41e-01
|
6.81e-01
|
0.05070
|
-0.041300
|
2.95e-02
|
3.65e-01
|
5.17e-01
|
Centrosome maturation
|
79
|
7.49e-01
|
8.28e-01
|
0.04960
|
0.049500
|
-1.35e-03
|
4.47e-01
|
9.83e-01
|
Recruitment of mitotic centrosome proteins and complexes
|
79
|
7.49e-01
|
8.28e-01
|
0.04960
|
0.049500
|
-1.35e-03
|
4.47e-01
|
9.83e-01
|
Tie2 Signaling
|
15
|
9.47e-01
|
9.64e-01
|
0.04890
|
-0.035500
|
-3.36e-02
|
8.12e-01
|
8.22e-01
|
Signaling by ERBB2 KD Mutants
|
23
|
9.22e-01
|
9.47e-01
|
0.04870
|
0.001180
|
4.87e-02
|
9.92e-01
|
6.86e-01
|
HDR through MMEJ (alt-NHEJ)
|
12
|
9.60e-01
|
9.71e-01
|
0.04790
|
-0.016300
|
4.50e-02
|
9.22e-01
|
7.87e-01
|
DNA Double-Strand Break Repair
|
129
|
6.44e-01
|
7.58e-01
|
0.04770
|
-0.028600
|
-3.81e-02
|
5.75e-01
|
4.55e-01
|
Signaling by ERBB2
|
47
|
8.56e-01
|
9.02e-01
|
0.04720
|
0.017200
|
-4.39e-02
|
8.39e-01
|
6.03e-01
|
Transcriptional Regulation by MECP2
|
48
|
8.55e-01
|
9.02e-01
|
0.04690
|
0.029400
|
-3.65e-02
|
7.24e-01
|
6.62e-01
|
Synthesis of Prostaglandins (PG) and Thromboxanes (TX)
|
14
|
9.56e-01
|
9.68e-01
|
0.04630
|
-0.011400
|
-4.49e-02
|
9.41e-01
|
7.71e-01
|
Processing of Capped Intron-Containing Pre-mRNA
|
278
|
4.14e-01
|
5.67e-01
|
0.04630
|
0.044600
|
1.24e-02
|
2.02e-01
|
7.23e-01
|
Endogenous sterols
|
20
|
9.37e-01
|
9.58e-01
|
0.04630
|
-0.038000
|
-2.64e-02
|
7.69e-01
|
8.38e-01
|
Tight junction interactions
|
17
|
9.48e-01
|
9.65e-01
|
0.04550
|
0.040300
|
2.11e-02
|
7.74e-01
|
8.80e-01
|
Activation of ATR in response to replication stress
|
31
|
9.12e-01
|
9.42e-01
|
0.04460
|
0.008570
|
-4.37e-02
|
9.34e-01
|
6.73e-01
|
Cell-Cell communication
|
116
|
7.20e-01
|
8.10e-01
|
0.04380
|
0.033000
|
-2.89e-02
|
5.40e-01
|
5.91e-01
|
Inactivation of APC/C via direct inhibition of the APC/C complex
|
21
|
9.44e-01
|
9.62e-01
|
0.04270
|
0.006070
|
-4.23e-02
|
9.62e-01
|
7.37e-01
|
Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components
|
21
|
9.44e-01
|
9.62e-01
|
0.04270
|
0.006070
|
-4.23e-02
|
9.62e-01
|
7.37e-01
|
RHOJ GTPase cycle
|
53
|
8.67e-01
|
9.08e-01
|
0.04260
|
-0.014400
|
4.01e-02
|
8.56e-01
|
6.14e-01
|
Termination of translesion DNA synthesis
|
31
|
9.20e-01
|
9.46e-01
|
0.04230
|
0.041900
|
6.41e-03
|
6.87e-01
|
9.51e-01
|
Phase I - Functionalization of compounds
|
65
|
8.42e-01
|
8.94e-01
|
0.04200
|
0.020400
|
3.67e-02
|
7.76e-01
|
6.09e-01
|
Postmitotic nuclear pore complex (NPC) reformation
|
27
|
9.31e-01
|
9.53e-01
|
0.04180
|
-0.032700
|
-2.60e-02
|
7.69e-01
|
8.15e-01
|
Glycogen breakdown (glycogenolysis)
|
13
|
9.67e-01
|
9.76e-01
|
0.04130
|
0.009750
|
-4.01e-02
|
9.51e-01
|
8.02e-01
|
Prolonged ERK activation events
|
14
|
9.68e-01
|
9.76e-01
|
0.03950
|
0.001880
|
3.95e-02
|
9.90e-01
|
7.98e-01
|
RHOF GTPase cycle
|
39
|
9.16e-01
|
9.44e-01
|
0.03900
|
-0.034200
|
1.89e-02
|
7.12e-01
|
8.38e-01
|
Signaling by NOTCH1
|
72
|
8.48e-01
|
8.97e-01
|
0.03900
|
0.026300
|
2.88e-02
|
7.00e-01
|
6.73e-01
|
Homology Directed Repair
|
100
|
8.06e-01
|
8.74e-01
|
0.03790
|
-0.016400
|
-3.42e-02
|
7.77e-01
|
5.55e-01
|
NOTCH3 Intracellular Domain Regulates Transcription
|
22
|
9.54e-01
|
9.68e-01
|
0.03780
|
-0.025200
|
2.82e-02
|
8.38e-01
|
8.19e-01
|
Glyoxylate metabolism and glycine degradation
|
23
|
9.54e-01
|
9.68e-01
|
0.03730
|
0.030200
|
-2.18e-02
|
8.02e-01
|
8.56e-01
|
Inositol phosphate metabolism
|
42
|
9.18e-01
|
9.45e-01
|
0.03670
|
-0.033000
|
-1.61e-02
|
7.12e-01
|
8.57e-01
|
Signaling by NOTCH2
|
31
|
9.40e-01
|
9.60e-01
|
0.03650
|
-0.000942
|
-3.65e-02
|
9.93e-01
|
7.25e-01
|
Regulation of CDH11 Expression and Function
|
27
|
9.49e-01
|
9.65e-01
|
0.03600
|
-0.035800
|
-3.97e-03
|
7.48e-01
|
9.72e-01
|
Synthesis of IP3 and IP4 in the cytosol
|
22
|
9.58e-01
|
9.70e-01
|
0.03590
|
0.029200
|
2.09e-02
|
8.13e-01
|
8.66e-01
|
SUMOylation
|
168
|
7.31e-01
|
8.17e-01
|
0.03560
|
-0.029400
|
2.01e-02
|
5.12e-01
|
6.54e-01
|
RHO GTPase cycle
|
418
|
4.73e-01
|
6.20e-01
|
0.03520
|
-0.019900
|
2.90e-02
|
4.87e-01
|
3.11e-01
|
G2/M DNA damage checkpoint
|
57
|
9.02e-01
|
9.34e-01
|
0.03490
|
0.032100
|
-1.37e-02
|
6.75e-01
|
8.58e-01
|
Deadenylation-dependent mRNA decay
|
50
|
9.16e-01
|
9.44e-01
|
0.03430
|
0.010100
|
-3.28e-02
|
9.01e-01
|
6.88e-01
|
RAB GEFs exchange GTP for GDP on RABs
|
86
|
8.59e-01
|
9.04e-01
|
0.03430
|
-0.029400
|
-1.75e-02
|
6.37e-01
|
7.79e-01
|
Transcriptional regulation by small RNAs
|
53
|
9.18e-01
|
9.45e-01
|
0.03290
|
0.026200
|
-2.00e-02
|
7.42e-01
|
8.01e-01
|
Biological oxidations
|
137
|
8.04e-01
|
8.73e-01
|
0.03280
|
0.020100
|
-2.60e-02
|
6.85e-01
|
6.00e-01
|
Constitutive Signaling by Overexpressed ERBB2
|
11
|
9.82e-01
|
9.87e-01
|
0.03280
|
0.024400
|
2.19e-02
|
8.88e-01
|
9.00e-01
|
Signaling by NOTCH3
|
46
|
9.30e-01
|
9.53e-01
|
0.03260
|
0.017700
|
-2.74e-02
|
8.35e-01
|
7.48e-01
|
Generic Transcription Pathway
|
1079
|
2.01e-01
|
3.49e-01
|
0.03240
|
0.028000
|
1.64e-02
|
1.24e-01
|
3.67e-01
|
Signaling by Rho GTPases
|
598
|
4.37e-01
|
5.89e-01
|
0.03090
|
0.002170
|
-3.09e-02
|
9.28e-01
|
1.99e-01
|
RNA Polymerase II Transcription
|
1197
|
2.02e-01
|
3.50e-01
|
0.03090
|
0.027400
|
1.43e-02
|
1.14e-01
|
4.10e-01
|
tRNA processing
|
109
|
8.62e-01
|
9.04e-01
|
0.03020
|
0.021700
|
2.09e-02
|
6.96e-01
|
7.06e-01
|
Signaling by Rho GTPases, Miro GTPases and RHOBTB3
|
613
|
4.57e-01
|
6.06e-01
|
0.02970
|
-0.000624
|
-2.97e-02
|
9.79e-01
|
2.11e-01
|
AURKA Activation by TPX2
|
70
|
9.13e-01
|
9.43e-01
|
0.02940
|
0.028600
|
6.70e-03
|
6.79e-01
|
9.23e-01
|
Gene expression (Transcription)
|
1356
|
1.99e-01
|
3.46e-01
|
0.02930
|
0.019700
|
2.17e-02
|
2.29e-01
|
1.85e-01
|
Dual Incision in GG-NER
|
41
|
9.55e-01
|
9.68e-01
|
0.02740
|
0.024800
|
1.16e-02
|
7.83e-01
|
8.98e-01
|
Phosphorylation of the APC/C
|
20
|
9.78e-01
|
9.85e-01
|
0.02720
|
-0.013000
|
-2.40e-02
|
9.20e-01
|
8.53e-01
|
Signaling by Nuclear Receptors
|
212
|
8.30e-01
|
8.89e-01
|
0.02450
|
0.007070
|
-2.34e-02
|
8.59e-01
|
5.57e-01
|
Aberrant regulation of mitotic exit in cancer due to RB1 defects
|
20
|
9.82e-01
|
9.87e-01
|
0.02440
|
0.014700
|
1.95e-02
|
9.09e-01
|
8.80e-01
|
Class I peroxisomal membrane protein import
|
19
|
9.84e-01
|
9.88e-01
|
0.02400
|
0.011200
|
-2.12e-02
|
9.33e-01
|
8.73e-01
|
RAC3 GTPase cycle
|
87
|
9.31e-01
|
9.53e-01
|
0.02350
|
-0.022700
|
-5.79e-03
|
7.14e-01
|
9.26e-01
|
Nicotinate metabolism
|
27
|
9.80e-01
|
9.86e-01
|
0.02240
|
-0.022300
|
1.87e-03
|
8.41e-01
|
9.87e-01
|
RHOH GTPase cycle
|
32
|
9.77e-01
|
9.85e-01
|
0.02180
|
0.006750
|
2.07e-02
|
9.47e-01
|
8.39e-01
|
p130Cas linkage to MAPK signaling for integrins
|
12
|
9.94e-01
|
9.96e-01
|
0.01830
|
-0.011100
|
-1.46e-02
|
9.47e-01
|
9.30e-01
|
Activated NOTCH1 Transmits Signal to the Nucleus
|
30
|
9.88e-01
|
9.92e-01
|
0.01600
|
0.007110
|
1.44e-02
|
9.46e-01
|
8.92e-01
|
HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA)
|
94
|
9.65e-01
|
9.75e-01
|
0.01600
|
-0.009090
|
-1.31e-02
|
8.79e-01
|
8.26e-01
|
Fatty acid metabolism
|
140
|
9.55e-01
|
9.68e-01
|
0.01490
|
-0.004020
|
1.44e-02
|
9.35e-01
|
7.69e-01
|
Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase
|
20
|
9.95e-01
|
9.97e-01
|
0.01280
|
0.012500
|
-2.57e-03
|
9.23e-01
|
9.84e-01
|
MTOR signalling
|
40
|
9.91e-01
|
9.94e-01
|
0.01230
|
-0.008440
|
-8.99e-03
|
9.26e-01
|
9.22e-01
|
Chromatin modifying enzymes
|
203
|
9.67e-01
|
9.76e-01
|
0.01050
|
-0.002860
|
-1.01e-02
|
9.44e-01
|
8.04e-01
|
Chromatin organization
|
203
|
9.67e-01
|
9.76e-01
|
0.01050
|
-0.002860
|
-1.01e-02
|
9.44e-01
|
8.04e-01
|
Nicotinamide salvaging
|
16
|
9.99e-01
|
9.99e-01
|
0.00777
|
0.001940
|
7.52e-03
|
9.89e-01
|
9.58e-01
|
Phase 2 - plateau phase
|
10
|
9.99e-01
|
9.99e-01
|
0.00740
|
0.007160
|
1.86e-03
|
9.69e-01
|
9.92e-01
|