ALPHA LINOLENIC OMEGA3 AND LINOLEIC OMEGA6 ACID METABOLISM
|
12
|
9.58e-04
|
8.23e-03
|
0.78400
|
6.08e-01
|
0.494000
|
2.65e-04
|
3.03e-03
|
FORMATION OF TUBULIN FOLDING INTERMEDIATES BY CCT TRIC
|
19
|
2.43e-07
|
9.85e-06
|
0.77600
|
7.07e-01
|
0.320000
|
9.37e-08
|
1.56e-02
|
PURINE RIBONUCLEOSIDE MONOPHOSPHATE BIOSYNTHESIS
|
12
|
2.27e-03
|
1.50e-02
|
0.74100
|
5.59e-01
|
0.486000
|
7.92e-04
|
3.59e-03
|
RHOBTB3 ATPASE CYCLE
|
10
|
7.24e-03
|
3.34e-02
|
0.72900
|
5.53e-01
|
0.475000
|
2.45e-03
|
9.33e-03
|
CITRIC ACID CYCLE TCA CYCLE
|
22
|
2.54e-05
|
4.81e-04
|
0.72800
|
5.19e-01
|
0.511000
|
2.50e-05
|
3.39e-05
|
BBSOME MEDIATED CARGO TARGETING TO CILIUM
|
23
|
2.82e-05
|
5.27e-04
|
0.70000
|
5.34e-01
|
0.452000
|
9.32e-06
|
1.73e-04
|
OLFACTORY SIGNALING PATHWAY
|
37
|
1.32e-07
|
5.97e-06
|
0.68600
|
-4.72e-01
|
-0.498000
|
6.88e-07
|
1.55e-07
|
CALNEXIN CALRETICULIN CYCLE
|
26
|
3.26e-05
|
5.90e-04
|
0.66100
|
4.55e-01
|
0.479000
|
5.90e-05
|
2.32e-05
|
GOLGI CISTERNAE PERICENTRIOLAR STACK REORGANIZATION
|
12
|
2.16e-03
|
1.46e-02
|
0.64600
|
5.75e-01
|
0.295000
|
5.68e-04
|
7.70e-02
|
NUCLEOBASE BIOSYNTHESIS
|
15
|
2.74e-03
|
1.72e-02
|
0.63600
|
5.07e-01
|
0.384000
|
6.70e-04
|
9.94e-03
|
RETROGRADE NEUROTROPHIN SIGNALLING
|
13
|
1.03e-02
|
4.43e-02
|
0.62200
|
4.52e-01
|
0.427000
|
4.77e-03
|
7.74e-03
|
N GLYCAN TRIMMING IN THE ER AND CALNEXIN CALRETICULIN CYCLE
|
35
|
1.30e-05
|
2.89e-04
|
0.59500
|
4.20e-01
|
0.422000
|
1.74e-05
|
1.53e-05
|
BRANCHED CHAIN AMINO ACID CATABOLISM
|
21
|
8.17e-04
|
7.40e-03
|
0.59200
|
3.59e-01
|
0.470000
|
4.42e-03
|
1.91e-04
|
ER QUALITY CONTROL COMPARTMENT ERQC
|
21
|
7.29e-04
|
6.86e-03
|
0.59000
|
3.49e-01
|
0.476000
|
5.66e-03
|
1.57e-04
|
SYNTHESIS OF VERY LONG CHAIN FATTY ACYL COAS
|
20
|
2.07e-03
|
1.42e-02
|
0.58200
|
3.97e-01
|
0.426000
|
2.11e-03
|
9.74e-04
|
LDL CLEARANCE
|
16
|
7.82e-03
|
3.51e-02
|
0.57000
|
4.37e-01
|
0.365000
|
2.47e-03
|
1.15e-02
|
COPI INDEPENDENT GOLGI TO ER RETROGRADE TRAFFIC
|
44
|
8.88e-08
|
4.54e-06
|
0.56700
|
4.93e-01
|
0.280000
|
1.48e-08
|
1.31e-03
|
GLYCOSPHINGOLIPID METABOLISM
|
38
|
1.57e-05
|
3.24e-04
|
0.56600
|
4.07e-01
|
0.394000
|
1.44e-05
|
2.58e-05
|
RECEPTOR MEDIATED MITOPHAGY
|
11
|
4.28e-02
|
1.26e-01
|
0.55400
|
4.24e-01
|
0.357000
|
1.49e-02
|
4.03e-02
|
SYNTHESIS OF PYROPHOSPHATES IN THE CYTOSOL
|
10
|
6.23e-02
|
1.61e-01
|
0.54800
|
4.14e-01
|
0.359000
|
2.35e-02
|
4.91e-02
|
ASPARTATE AND ASPARAGINE METABOLISM
|
10
|
4.39e-02
|
1.29e-01
|
0.54800
|
3.02e-01
|
0.457000
|
9.79e-02
|
1.24e-02
|
TRANSPORT OF CONNEXONS TO THE PLASMA MEMBRANE
|
13
|
2.65e-04
|
3.24e-03
|
0.53900
|
5.35e-01
|
0.068800
|
8.36e-04
|
6.68e-01
|
TRANSLATION OF REPLICASE AND ASSEMBLY OF THE REPLICATION TRANSCRIPTION COMPLEX
|
12
|
3.82e-02
|
1.17e-01
|
0.53700
|
4.17e-01
|
0.339000
|
1.24e-02
|
4.20e-02
|
KERATAN SULFATE BIOSYNTHESIS
|
24
|
5.54e-05
|
9.32e-04
|
0.53600
|
4.96e-01
|
0.201000
|
2.55e-05
|
8.80e-02
|
INHIBITION OF REPLICATION INITIATION OF DAMAGED DNA BY RB1 E2F1
|
13
|
1.51e-02
|
5.76e-02
|
0.53300
|
2.67e-01
|
0.462000
|
9.62e-02
|
3.95e-03
|
THE ROLE OF NEF IN HIV 1 REPLICATION AND DISEASE PATHOGENESIS
|
27
|
7.41e-04
|
6.92e-03
|
0.52900
|
3.27e-01
|
0.416000
|
3.27e-03
|
1.85e-04
|
WNT LIGAND BIOGENESIS AND TRAFFICKING
|
21
|
4.71e-03
|
2.46e-02
|
0.52500
|
3.97e-01
|
0.343000
|
1.62e-03
|
6.46e-03
|
GLYCOGEN SYNTHESIS
|
14
|
1.42e-02
|
5.55e-02
|
0.52200
|
4.49e-01
|
0.266000
|
3.63e-03
|
8.49e-02
|
GLYCOGEN STORAGE DISEASES
|
12
|
2.09e-02
|
7.39e-02
|
0.50700
|
4.54e-01
|
0.225000
|
6.45e-03
|
1.77e-01
|
CARGO TRAFFICKING TO THE PERICILIARY MEMBRANE
|
49
|
1.08e-05
|
2.51e-04
|
0.50600
|
3.70e-01
|
0.345000
|
7.34e-06
|
2.87e-05
|
INSULIN PROCESSING
|
24
|
3.92e-03
|
2.18e-02
|
0.50400
|
3.47e-01
|
0.366000
|
3.26e-03
|
1.94e-03
|
SYNTHESIS OF PIPS AT THE LATE ENDOSOME MEMBRANE
|
11
|
2.17e-03
|
1.46e-02
|
0.50200
|
5.86e-02
|
0.498000
|
7.36e-01
|
4.20e-03
|
GLYCOGEN METABOLISM
|
25
|
1.68e-03
|
1.26e-02
|
0.49900
|
4.13e-01
|
0.280000
|
3.54e-04
|
1.52e-02
|
FATTY ACYL COA BIOSYNTHESIS
|
32
|
7.26e-04
|
6.86e-03
|
0.49800
|
3.43e-01
|
0.362000
|
7.81e-04
|
4.00e-04
|
COOPERATION OF PREFOLDIN AND TRIC CCT IN ACTIN AND TUBULIN FOLDING
|
26
|
1.99e-05
|
3.98e-04
|
0.49800
|
4.77e-01
|
0.142000
|
2.52e-05
|
2.12e-01
|
KERATAN SULFATE KERATIN METABOLISM
|
30
|
3.75e-05
|
6.68e-04
|
0.49800
|
4.57e-01
|
0.197000
|
1.46e-05
|
6.20e-02
|
SPHINGOLIPID METABOLISM
|
80
|
6.31e-09
|
4.13e-07
|
0.49500
|
3.01e-01
|
0.393000
|
3.32e-06
|
1.22e-09
|
CD28 DEPENDENT VAV1 PATHWAY
|
11
|
5.59e-02
|
1.50e-01
|
0.49000
|
4.18e-01
|
0.257000
|
1.64e-02
|
1.40e-01
|
IRE1ALPHA ACTIVATES CHAPERONES
|
50
|
1.14e-05
|
2.58e-04
|
0.48900
|
3.84e-01
|
0.304000
|
2.69e-06
|
2.05e-04
|
CTLA4 INHIBITORY SIGNALING
|
20
|
1.16e-02
|
4.80e-02
|
0.48700
|
3.10e-01
|
0.376000
|
1.65e-02
|
3.59e-03
|
SYNTHESIS OF PIPS AT THE GOLGI MEMBRANE
|
15
|
2.79e-02
|
9.24e-02
|
0.48700
|
2.81e-01
|
0.398000
|
5.98e-02
|
7.60e-03
|
SCAVENGING OF HEME FROM PLASMA
|
11
|
4.81e-02
|
1.35e-01
|
0.48500
|
-2.34e-01
|
-0.425000
|
1.79e-01
|
1.46e-02
|
WNT5A DEPENDENT INTERNALIZATION OF FZD2 FZD5 AND ROR2
|
13
|
3.43e-02
|
1.09e-01
|
0.48200
|
4.15e-01
|
0.246000
|
9.62e-03
|
1.25e-01
|
MET ACTIVATES RAP1 AND RAC1
|
10
|
2.86e-02
|
9.42e-02
|
0.48000
|
1.59e-01
|
0.453000
|
3.83e-01
|
1.32e-02
|
INSERTION OF TAIL ANCHORED PROTEINS INTO THE ENDOPLASMIC RETICULUM MEMBRANE
|
22
|
4.26e-03
|
2.30e-02
|
0.47900
|
4.07e-01
|
0.254000
|
9.60e-04
|
3.92e-02
|
ADENYLATE CYCLASE INHIBITORY PATHWAY
|
13
|
5.90e-02
|
1.55e-01
|
0.47900
|
3.00e-01
|
0.374000
|
6.11e-02
|
1.96e-02
|
SUPPRESSION OF PHAGOSOMAL MATURATION
|
12
|
6.15e-02
|
1.60e-01
|
0.47800
|
3.93e-01
|
0.271000
|
1.83e-02
|
1.04e-01
|
PYRUVATE METABOLISM AND CITRIC ACID TCA CYCLE
|
51
|
2.90e-05
|
5.33e-04
|
0.47500
|
3.28e-01
|
0.344000
|
5.12e-05
|
2.16e-05
|
HSP90 CHAPERONE CYCLE FOR STEROID HORMONE RECEPTORS SHR
|
48
|
5.18e-10
|
5.08e-08
|
0.47300
|
4.65e-01
|
0.087300
|
2.45e-08
|
2.95e-01
|
POSTMITOTIC NUCLEAR PORE COMPLEX NPC REFORMATION
|
26
|
1.41e-03
|
1.13e-02
|
0.47300
|
2.38e-01
|
0.409000
|
3.57e-02
|
3.08e-04
|
SYNTHESIS OF PIPS AT THE EARLY ENDOSOME MEMBRANE
|
16
|
1.42e-04
|
1.91e-03
|
0.47000
|
1.42e-02
|
0.470000
|
9.22e-01
|
1.14e-03
|
CYTOSOLIC TRNA AMINOACYLATION
|
24
|
2.35e-03
|
1.53e-02
|
0.46900
|
4.08e-01
|
0.232000
|
5.42e-04
|
4.88e-02
|
PURINE SALVAGE
|
12
|
3.40e-02
|
1.08e-01
|
0.46600
|
4.22e-01
|
0.198000
|
1.14e-02
|
2.34e-01
|
SEALING OF THE NUCLEAR ENVELOPE NE BY ESCRT III
|
23
|
3.85e-04
|
4.27e-03
|
0.46300
|
4.39e-01
|
0.144000
|
2.64e-04
|
2.31e-01
|
HYALURONAN UPTAKE AND DEGRADATION
|
11
|
1.20e-01
|
2.59e-01
|
0.46000
|
3.36e-01
|
0.314000
|
5.34e-02
|
7.17e-02
|
RAP1 SIGNALLING
|
15
|
5.50e-02
|
1.49e-01
|
0.46000
|
3.10e-01
|
0.340000
|
3.79e-02
|
2.26e-02
|
GLYCOGEN BREAKDOWN GLYCOGENOLYSIS
|
14
|
3.81e-02
|
1.17e-01
|
0.45800
|
3.94e-01
|
0.235000
|
1.08e-02
|
1.28e-01
|
GAP JUNCTION ASSEMBLY
|
21
|
6.03e-05
|
9.72e-04
|
0.45700
|
4.54e-01
|
0.053500
|
3.14e-04
|
6.71e-01
|
GLUTAMATE AND GLUTAMINE METABOLISM
|
13
|
8.54e-02
|
2.04e-01
|
0.45700
|
3.21e-01
|
0.325000
|
4.53e-02
|
4.24e-02
|
DEFECTS OF CONTACT ACTIVATION SYSTEM CAS AND KALLIKREIN KININ SYSTEM KKS
|
11
|
7.84e-02
|
1.92e-01
|
0.45600
|
-2.33e-01
|
-0.392000
|
1.81e-01
|
2.44e-02
|
NUCLEOTIDE LIKE PURINERGIC RECEPTORS
|
13
|
8.10e-02
|
1.96e-01
|
0.45600
|
2.94e-01
|
0.348000
|
6.65e-02
|
2.98e-02
|
ENDOSOMAL VACUOLAR PATHWAY
|
10
|
2.26e-03
|
1.50e-02
|
0.45500
|
-4.53e-01
|
0.045300
|
1.32e-02
|
8.04e-01
|
SYNTHESIS OF GLYCOSYLPHOSPHATIDYLINOSITOL GPI
|
18
|
1.43e-02
|
5.55e-02
|
0.45200
|
2.21e-01
|
0.394000
|
1.05e-01
|
3.80e-03
|
PEROXISOMAL LIPID METABOLISM
|
27
|
6.81e-03
|
3.17e-02
|
0.45100
|
3.13e-01
|
0.325000
|
4.92e-03
|
3.45e-03
|
RESPONSE OF MTB TO PHAGOCYTOSIS
|
21
|
1.33e-02
|
5.32e-02
|
0.44800
|
3.70e-01
|
0.252000
|
3.31e-03
|
4.53e-02
|
FERTILIZATION
|
13
|
4.20e-02
|
1.25e-01
|
0.44700
|
-2.06e-01
|
-0.397000
|
1.99e-01
|
1.32e-02
|
RHO GTPASES ACTIVATE IQGAPS
|
23
|
3.97e-04
|
4.29e-03
|
0.44400
|
4.28e-01
|
0.120000
|
3.81e-04
|
3.20e-01
|
COPI MEDIATED ANTEROGRADE TRANSPORT
|
91
|
4.50e-09
|
3.12e-07
|
0.44400
|
3.76e-01
|
0.236000
|
5.76e-10
|
9.92e-05
|
ACTIVATED NTRK2 SIGNALS THROUGH FRS2 AND FRS3
|
10
|
1.34e-01
|
2.79e-01
|
0.44200
|
3.66e-01
|
0.248000
|
4.51e-02
|
1.74e-01
|
PTK6 REGULATES RHO GTPASES RAS GTPASE AND MAP KINASES
|
13
|
9.64e-02
|
2.21e-01
|
0.44200
|
2.91e-01
|
0.332000
|
6.91e-02
|
3.81e-02
|
SPHINGOLIPID DE NOVO BIOSYNTHESIS
|
42
|
5.31e-05
|
9.05e-04
|
0.44000
|
2.04e-01
|
0.390000
|
2.24e-02
|
1.22e-05
|
RAF ACTIVATION
|
34
|
2.66e-03
|
1.67e-02
|
0.43900
|
3.11e-01
|
0.309000
|
1.69e-03
|
1.81e-03
|
VLDLR INTERNALISATION AND DEGRADATION
|
12
|
1.05e-01
|
2.34e-01
|
0.43800
|
3.52e-01
|
0.262000
|
3.49e-02
|
1.16e-01
|
PROLONGED ERK ACTIVATION EVENTS
|
13
|
4.67e-02
|
1.34e-01
|
0.43800
|
1.99e-01
|
0.390000
|
2.13e-01
|
1.49e-02
|
CHK1 CHK2 CDS1 MEDIATED INACTIVATION OF CYCLIN B CDK1 COMPLEX
|
10
|
3.97e-03
|
2.18e-02
|
0.43700
|
4.36e-01
|
-0.036400
|
1.70e-02
|
8.42e-01
|
REGULATION OF TP53 ACTIVITY THROUGH ASSOCIATION WITH CO FACTORS
|
14
|
1.79e-02
|
6.62e-02
|
0.43300
|
4.08e-01
|
0.146000
|
8.18e-03
|
3.44e-01
|
NUCLEAR ENVELOPE NE REASSEMBLY
|
64
|
1.36e-05
|
2.92e-04
|
0.43200
|
3.34e-01
|
0.274000
|
3.78e-06
|
1.54e-04
|
ACETYLCHOLINE BINDING AND DOWNSTREAM EVENTS
|
10
|
5.68e-02
|
1.51e-01
|
0.43200
|
1.44e-01
|
0.407000
|
4.31e-01
|
2.58e-02
|
HIGHLY CALCIUM PERMEABLE POSTSYNAPTIC NICOTINIC ACETYLCHOLINE RECEPTORS
|
10
|
5.68e-02
|
1.51e-01
|
0.43200
|
1.44e-01
|
0.407000
|
4.31e-01
|
2.58e-02
|
PLATELET SENSITIZATION BY LDL
|
15
|
4.73e-02
|
1.34e-01
|
0.43000
|
2.23e-01
|
0.368000
|
1.34e-01
|
1.37e-02
|
CAMK IV MEDIATED PHOSPHORYLATION OF CREB
|
10
|
6.40e-03
|
3.05e-02
|
0.43000
|
-1.55e-02
|
0.430000
|
9.32e-01
|
1.86e-02
|
KILLING MECHANISMS
|
11
|
1.27e-01
|
2.71e-01
|
0.42800
|
-3.53e-01
|
-0.241000
|
4.25e-02
|
1.67e-01
|
VEGFR2 MEDIATED VASCULAR PERMEABILITY
|
27
|
1.16e-02
|
4.80e-02
|
0.42600
|
2.92e-01
|
0.310000
|
8.69e-03
|
5.28e-03
|
RECYCLING PATHWAY OF L1
|
40
|
1.39e-04
|
1.88e-03
|
0.42500
|
3.79e-01
|
0.194000
|
3.41e-05
|
3.39e-02
|
EPHRIN SIGNALING
|
19
|
4.42e-02
|
1.29e-01
|
0.42500
|
2.99e-01
|
0.303000
|
2.41e-02
|
2.24e-02
|
ADVANCED GLYCOSYLATION ENDPRODUCT RECEPTOR SIGNALING
|
11
|
1.93e-02
|
6.92e-02
|
0.42500
|
4.18e-01
|
0.079000
|
1.65e-02
|
6.50e-01
|
MRNA DECAY BY 5 TO 3 EXORIBONUCLEASE
|
15
|
8.41e-02
|
2.02e-01
|
0.42500
|
-3.14e-01
|
-0.285000
|
3.50e-02
|
5.57e-02
|
CS DS DEGRADATION
|
14
|
3.54e-02
|
1.12e-01
|
0.42400
|
3.86e-01
|
0.175000
|
1.24e-02
|
2.56e-01
|
KSRP KHSRP BINDS AND DESTABILIZES MRNA
|
16
|
7.60e-02
|
1.89e-01
|
0.42100
|
-3.05e-01
|
-0.290000
|
3.48e-02
|
4.45e-02
|
ATF6 ATF6 ALPHA ACTIVATES CHAPERONE GENES
|
10
|
1.50e-01
|
2.99e-01
|
0.42000
|
3.56e-01
|
0.224000
|
5.14e-02
|
2.20e-01
|
TRANSCRIPTION OF E2F TARGETS UNDER NEGATIVE CONTROL BY DREAM COMPLEX
|
18
|
4.72e-02
|
1.34e-01
|
0.42000
|
2.56e-01
|
0.332000
|
5.97e-02
|
1.47e-02
|
RUNX1 REGULATES GENES INVOLVED IN MEGAKARYOCYTE DIFFERENTIATION AND PLATELET FUNCTION
|
53
|
1.77e-04
|
2.29e-03
|
0.41900
|
-2.70e-01
|
-0.320000
|
6.80e-04
|
5.56e-05
|
N GLYCAN ANTENNAE ELONGATION IN THE MEDIAL TRANS GOLGI
|
24
|
9.91e-03
|
4.27e-02
|
0.41700
|
3.57e-01
|
0.216000
|
2.43e-03
|
6.75e-02
|
N GLYCAN ANTENNAE ELONGATION
|
15
|
1.42e-03
|
1.13e-02
|
0.41700
|
4.17e-01
|
0.011100
|
5.20e-03
|
9.41e-01
|
SPRY REGULATION OF FGF SIGNALING
|
16
|
7.41e-02
|
1.86e-01
|
0.41600
|
3.22e-01
|
0.264000
|
2.60e-02
|
6.76e-02
|
TRANSCRIPTION OF E2F TARGETS UNDER NEGATIVE CONTROL BY P107 RBL1 AND P130 RBL2 IN COMPLEX WITH HDAC1
|
15
|
8.62e-02
|
2.05e-01
|
0.41600
|
2.62e-01
|
0.323000
|
7.92e-02
|
3.02e-02
|
DERMATAN SULFATE BIOSYNTHESIS
|
11
|
1.57e-01
|
3.07e-01
|
0.41600
|
3.32e-01
|
0.250000
|
5.65e-02
|
1.51e-01
|
MATURATION OF SARS COV 2 SPIKE PROTEIN
|
29
|
7.56e-03
|
3.44e-02
|
0.41400
|
3.33e-01
|
0.247000
|
1.90e-03
|
2.15e-02
|
REGULATION OF PYRUVATE DEHYDROGENASE PDH COMPLEX
|
15
|
5.65e-02
|
1.51e-01
|
0.41300
|
2.09e-01
|
0.356000
|
1.60e-01
|
1.69e-02
|
ASSOCIATION OF TRIC CCT WITH TARGET PROTEINS DURING BIOSYNTHESIS
|
38
|
1.15e-03
|
9.58e-03
|
0.41300
|
3.45e-01
|
0.227000
|
2.34e-04
|
1.55e-02
|
COHESIN LOADING ONTO CHROMATIN
|
10
|
1.69e-03
|
1.26e-02
|
0.41100
|
-1.53e-01
|
0.381000
|
4.01e-01
|
3.71e-02
|
INTRA GOLGI TRAFFIC
|
43
|
3.03e-04
|
3.54e-03
|
0.40900
|
2.06e-01
|
0.353000
|
1.95e-02
|
6.11e-05
|
GOLGI TO ER RETROGRADE TRANSPORT
|
119
|
4.79e-10
|
5.08e-08
|
0.40800
|
3.47e-01
|
0.214000
|
5.98e-11
|
5.46e-05
|
CARNITINE METABOLISM
|
14
|
1.63e-03
|
1.24e-02
|
0.40800
|
-1.76e-02
|
0.408000
|
9.09e-01
|
8.27e-03
|
INFECTION WITH MYCOBACTERIUM TUBERCULOSIS
|
24
|
1.87e-02
|
6.79e-02
|
0.40700
|
3.32e-01
|
0.237000
|
4.93e-03
|
4.47e-02
|
BETA OXIDATION OF VERY LONG CHAIN FATTY ACIDS
|
11
|
8.42e-02
|
2.02e-01
|
0.40200
|
3.71e-01
|
0.156000
|
3.33e-02
|
3.70e-01
|
GAMMA CARBOXYLATION HYPUSINE FORMATION AND ARYLSULFATASE ACTIVATION
|
30
|
1.16e-02
|
4.80e-02
|
0.40200
|
3.02e-01
|
0.266000
|
4.25e-03
|
1.18e-02
|
ACYL CHAIN REMODELLING OF PG
|
10
|
1.67e-01
|
3.19e-01
|
0.40200
|
2.06e-01
|
0.345000
|
2.59e-01
|
5.92e-02
|
DEPOLYMERISATION OF THE NUCLEAR LAMINA
|
13
|
1.51e-01
|
3.00e-01
|
0.39800
|
2.65e-01
|
0.297000
|
9.80e-02
|
6.40e-02
|
RHOF GTPASE CYCLE
|
41
|
3.97e-04
|
4.29e-03
|
0.39800
|
1.85e-01
|
0.352000
|
4.09e-02
|
9.53e-05
|
ERKS ARE INACTIVATED
|
13
|
1.50e-01
|
2.99e-01
|
0.39700
|
2.59e-01
|
0.301000
|
1.06e-01
|
6.03e-02
|
APOPTOSIS INDUCED DNA FRAGMENTATION
|
10
|
2.32e-01
|
4.01e-01
|
0.39400
|
-3.05e-01
|
-0.249000
|
9.46e-02
|
1.72e-01
|
LYSOSOME VESICLE BIOGENESIS
|
33
|
6.37e-03
|
3.05e-02
|
0.39200
|
3.19e-01
|
0.228000
|
1.53e-03
|
2.36e-02
|
O LINKED GLYCOSYLATION OF MUCINS
|
40
|
3.18e-03
|
1.89e-02
|
0.39100
|
2.48e-01
|
0.303000
|
6.63e-03
|
9.28e-04
|
KERATAN SULFATE DEGRADATION
|
11
|
4.24e-02
|
1.26e-01
|
0.39100
|
3.82e-01
|
0.086100
|
2.84e-02
|
6.21e-01
|
TRANSPORT TO THE GOLGI AND SUBSEQUENT MODIFICATION
|
171
|
4.57e-12
|
8.96e-10
|
0.39100
|
3.20e-01
|
0.226000
|
5.66e-13
|
3.66e-07
|
ACTIVATION OF THE TFAP2 AP 2 FAMILY OF TRANSCRIPTION FACTORS
|
10
|
1.68e-01
|
3.21e-01
|
0.39100
|
-1.90e-01
|
-0.342000
|
2.99e-01
|
6.11e-02
|
CA DEPENDENT EVENTS
|
36
|
1.95e-03
|
1.37e-02
|
0.39000
|
1.94e-01
|
0.338000
|
4.38e-02
|
4.41e-04
|
ACTIVATION OF AMPK DOWNSTREAM OF NMDARS
|
20
|
3.93e-03
|
2.18e-02
|
0.39000
|
3.79e-01
|
0.092900
|
3.35e-03
|
4.72e-01
|
RHOV GTPASE CYCLE
|
33
|
3.57e-04
|
4.04e-03
|
0.39000
|
1.24e-01
|
0.370000
|
2.19e-01
|
2.37e-04
|
SIGNALING BY CTNNB1 PHOSPHO SITE MUTANTS
|
15
|
9.08e-02
|
2.13e-01
|
0.38600
|
2.06e-01
|
0.327000
|
1.67e-01
|
2.85e-02
|
NCAM1 INTERACTIONS
|
42
|
1.09e-03
|
9.16e-03
|
0.38400
|
-1.99e-01
|
-0.329000
|
2.58e-02
|
2.27e-04
|
TRNA AMINOACYLATION
|
42
|
2.38e-03
|
1.53e-02
|
0.38400
|
3.08e-01
|
0.230000
|
5.63e-04
|
1.00e-02
|
ER TO GOLGI ANTEROGRADE TRANSPORT
|
142
|
9.44e-10
|
7.72e-08
|
0.38100
|
3.13e-01
|
0.217000
|
1.22e-10
|
8.15e-06
|
GLUCONEOGENESIS
|
27
|
8.54e-03
|
3.79e-02
|
0.38000
|
3.38e-01
|
0.174000
|
2.38e-03
|
1.17e-01
|
POST CHAPERONIN TUBULIN FOLDING PATHWAY
|
17
|
6.64e-04
|
6.41e-03
|
0.38000
|
3.78e-01
|
-0.041800
|
6.99e-03
|
7.65e-01
|
NEF MEDIATES DOWN MODULATION OF CELL SURFACE RECEPTORS BY RECRUITING THEM TO CLATHRIN ADAPTERS
|
21
|
5.96e-02
|
1.57e-01
|
0.37800
|
2.39e-01
|
0.293000
|
5.79e-02
|
2.03e-02
|
PROCESSIVE SYNTHESIS ON THE LAGGING STRAND
|
15
|
1.05e-02
|
4.47e-02
|
0.37700
|
5.30e-02
|
0.374000
|
7.23e-01
|
1.22e-02
|
ACYL CHAIN REMODELLING OF PE
|
17
|
1.11e-01
|
2.43e-01
|
0.37700
|
2.77e-01
|
0.255000
|
4.78e-02
|
6.88e-02
|
SYNTHESIS OF ACTIVE UBIQUITIN ROLES OF E1 AND E2 ENZYMES
|
29
|
3.53e-03
|
2.03e-02
|
0.37700
|
3.46e-01
|
0.149000
|
1.26e-03
|
1.66e-01
|
LYSINE CATABOLISM
|
11
|
2.42e-01
|
4.12e-01
|
0.37700
|
2.72e-01
|
0.261000
|
1.18e-01
|
1.35e-01
|
SULFUR AMINO ACID METABOLISM
|
23
|
1.51e-02
|
5.76e-02
|
0.37600
|
3.40e-01
|
0.162000
|
4.79e-03
|
1.79e-01
|
NA CL DEPENDENT NEUROTRANSMITTER TRANSPORTERS
|
13
|
1.92e-01
|
3.54e-01
|
0.37400
|
2.61e-01
|
0.268000
|
1.03e-01
|
9.45e-02
|
PEROXISOMAL PROTEIN IMPORT
|
59
|
4.36e-04
|
4.54e-03
|
0.37200
|
2.91e-01
|
0.232000
|
1.13e-04
|
2.03e-03
|
INITIATION OF NUCLEAR ENVELOPE NE REFORMATION
|
17
|
7.85e-02
|
1.92e-01
|
0.37200
|
3.16e-01
|
0.197000
|
2.42e-02
|
1.60e-01
|
GAP JUNCTION TRAFFICKING AND REGULATION
|
33
|
8.47e-04
|
7.55e-03
|
0.37200
|
3.51e-01
|
0.122000
|
4.84e-04
|
2.26e-01
|
ASPARAGINE N LINKED GLYCOSYLATION
|
285
|
9.08e-17
|
2.67e-14
|
0.37100
|
2.92e-01
|
0.229000
|
2.62e-17
|
2.83e-11
|
TP53 REGULATES TRANSCRIPTION OF CASPASE ACTIVATORS AND CASPASES
|
11
|
2.47e-01
|
4.19e-01
|
0.36900
|
-2.39e-01
|
-0.282000
|
1.70e-01
|
1.06e-01
|
RETROGRADE TRANSPORT AT THE TRANS GOLGI NETWORK
|
48
|
1.03e-03
|
8.68e-03
|
0.36900
|
2.01e-01
|
0.310000
|
1.60e-02
|
2.07e-04
|
G PROTEIN MEDIATED EVENTS
|
52
|
8.83e-05
|
1.30e-03
|
0.36700
|
1.51e-01
|
0.335000
|
5.95e-02
|
2.95e-05
|
ACTIVATION OF BAD AND TRANSLOCATION TO MITOCHONDRIA
|
15
|
4.15e-02
|
1.24e-01
|
0.36600
|
3.47e-01
|
0.117000
|
1.99e-02
|
4.34e-01
|
E2F MEDIATED REGULATION OF DNA REPLICATION
|
19
|
6.07e-02
|
1.59e-01
|
0.36600
|
1.90e-01
|
0.313000
|
1.52e-01
|
1.81e-02
|
INTERFERON ALPHA BETA SIGNALING
|
53
|
2.21e-07
|
9.30e-06
|
0.36600
|
-3.63e-01
|
-0.047900
|
4.98e-06
|
5.47e-01
|
DARPP 32 EVENTS
|
23
|
4.56e-02
|
1.32e-01
|
0.36600
|
2.99e-01
|
0.211000
|
1.32e-02
|
8.01e-02
|
ABC TRANSPORTERS IN LIPID HOMEOSTASIS
|
14
|
3.93e-02
|
1.19e-01
|
0.36400
|
9.62e-02
|
0.351000
|
5.33e-01
|
2.28e-02
|
ACTIVATION OF RAC1
|
13
|
2.09e-01
|
3.70e-01
|
0.36400
|
2.56e-01
|
0.259000
|
1.10e-01
|
1.06e-01
|
DNA METHYLATION
|
23
|
1.82e-02
|
6.68e-02
|
0.36300
|
-1.51e-01
|
-0.330000
|
2.09e-01
|
6.10e-03
|
REGULATION OF IFNG SIGNALING
|
13
|
2.03e-01
|
3.64e-01
|
0.36300
|
2.34e-01
|
0.277000
|
1.44e-01
|
8.34e-02
|
SYNTHESIS SECRETION AND DEACYLATION OF GHRELIN
|
13
|
2.08e-01
|
3.70e-01
|
0.36200
|
2.72e-01
|
0.240000
|
8.98e-02
|
1.35e-01
|
RHO GTPASES ACTIVATE WASPS AND WAVES
|
36
|
1.40e-02
|
5.53e-02
|
0.36200
|
2.53e-01
|
0.259000
|
8.70e-03
|
7.25e-03
|
CREB1 PHOSPHORYLATION THROUGH THE ACTIVATION OF ADENYLATE CYCLASE
|
11
|
2.39e-01
|
4.10e-01
|
0.36100
|
2.94e-01
|
0.209000
|
9.16e-02
|
2.30e-01
|
MHC CLASS II ANTIGEN PRESENTATION
|
102
|
3.45e-07
|
1.36e-05
|
0.36000
|
3.11e-01
|
0.181000
|
5.60e-08
|
1.61e-03
|
INSULIN RECEPTOR RECYCLING
|
20
|
3.54e-02
|
1.12e-01
|
0.36000
|
3.25e-01
|
0.154000
|
1.19e-02
|
2.33e-01
|
DISASSEMBLY OF THE DESTRUCTION COMPLEX AND RECRUITMENT OF AXIN TO THE MEMBRANE
|
26
|
3.74e-02
|
1.15e-01
|
0.35800
|
2.12e-01
|
0.289000
|
6.20e-02
|
1.08e-02
|
TP53 REGULATES TRANSCRIPTION OF GENES INVOLVED IN G2 CELL CYCLE ARREST
|
15
|
1.57e-01
|
3.07e-01
|
0.35800
|
2.84e-01
|
0.218000
|
5.73e-02
|
1.44e-01
|
SYNTHESIS OF PA
|
29
|
2.94e-02
|
9.63e-02
|
0.35700
|
2.21e-01
|
0.281000
|
3.93e-02
|
8.94e-03
|
REGULATION OF TP53 EXPRESSION AND DEGRADATION
|
34
|
1.72e-02
|
6.39e-02
|
0.35700
|
2.26e-01
|
0.276000
|
2.27e-02
|
5.35e-03
|
TRANSCRIPTIONAL REGULATION OF PLURIPOTENT STEM CELLS
|
18
|
1.14e-01
|
2.48e-01
|
0.35600
|
2.20e-01
|
0.280000
|
1.06e-01
|
3.99e-02
|
SIGNALING BY HIPPO
|
20
|
4.22e-02
|
1.25e-01
|
0.35500
|
1.57e-01
|
0.318000
|
2.24e-01
|
1.38e-02
|
PKA MEDIATED PHOSPHORYLATION OF CREB
|
19
|
9.57e-02
|
2.21e-01
|
0.35500
|
2.85e-01
|
0.211000
|
3.14e-02
|
1.12e-01
|
COPI DEPENDENT GOLGI TO ER RETROGRADE TRAFFIC
|
86
|
2.88e-06
|
8.47e-05
|
0.35400
|
3.12e-01
|
0.168000
|
5.81e-07
|
6.95e-03
|
PROTEIN METHYLATION
|
17
|
7.77e-02
|
1.91e-01
|
0.35400
|
3.13e-01
|
0.165000
|
2.57e-02
|
2.38e-01
|
CYTOSOLIC SULFONATION OF SMALL MOLECULES
|
15
|
6.72e-02
|
1.70e-01
|
0.35300
|
1.30e-01
|
0.328000
|
3.82e-01
|
2.76e-02
|
BETA CATENIN PHOSPHORYLATION CASCADE
|
16
|
1.36e-01
|
2.82e-01
|
0.35300
|
2.05e-01
|
0.287000
|
1.55e-01
|
4.66e-02
|
CHONDROITIN SULFATE BIOSYNTHESIS
|
18
|
1.32e-01
|
2.76e-01
|
0.35200
|
2.52e-01
|
0.246000
|
6.42e-02
|
7.10e-02
|
RHOU GTPASE CYCLE
|
34
|
3.12e-04
|
3.59e-03
|
0.35100
|
7.15e-02
|
0.344000
|
4.71e-01
|
5.25e-04
|
CREB1 PHOSPHORYLATION THROUGH NMDA RECEPTOR MEDIATED ACTIVATION OF RAS SIGNALING
|
28
|
4.50e-02
|
1.31e-01
|
0.35000
|
2.45e-01
|
0.250000
|
2.51e-02
|
2.23e-02
|
CD28 CO STIMULATION
|
31
|
1.99e-02
|
7.08e-02
|
0.34900
|
1.94e-01
|
0.290000
|
6.20e-02
|
5.14e-03
|
INTRA GOLGI AND RETROGRADE GOLGI TO ER TRAFFIC
|
185
|
9.83e-10
|
7.72e-08
|
0.34900
|
2.66e-01
|
0.226000
|
4.81e-10
|
1.10e-07
|
GAP JUNCTION DEGRADATION
|
11
|
2.84e-01
|
4.57e-01
|
0.34900
|
2.70e-01
|
0.221000
|
1.21e-01
|
2.05e-01
|
ACTIVATED PKN1 STIMULATES TRANSCRIPTION OF AR ANDROGEN RECEPTOR REGULATED GENES KLK2 AND KLK3
|
24
|
2.76e-02
|
9.19e-02
|
0.34800
|
-1.57e-01
|
-0.310000
|
1.82e-01
|
8.50e-03
|
MITOCHONDRIAL TRNA AMINOACYLATION
|
21
|
8.81e-02
|
2.07e-01
|
0.34800
|
2.14e-01
|
0.274000
|
8.95e-02
|
2.98e-02
|
NEGATIVE REGULATION OF MET ACTIVITY
|
20
|
7.69e-02
|
1.90e-01
|
0.34600
|
1.85e-01
|
0.293000
|
1.53e-01
|
2.35e-02
|
G1 S SPECIFIC TRANSCRIPTION
|
26
|
5.64e-02
|
1.51e-01
|
0.34600
|
2.62e-01
|
0.226000
|
2.08e-02
|
4.65e-02
|
TELOMERE C STRAND SYNTHESIS INITIATION
|
13
|
2.46e-01
|
4.18e-01
|
0.34500
|
2.46e-01
|
0.241000
|
1.24e-01
|
1.32e-01
|
DISEASES ASSOCIATED WITH GLYCOSAMINOGLYCAN METABOLISM
|
39
|
1.36e-03
|
1.11e-02
|
0.34500
|
3.20e-01
|
0.129000
|
5.54e-04
|
1.64e-01
|
AUTOPHAGY
|
138
|
8.71e-08
|
4.54e-06
|
0.34400
|
2.80e-01
|
0.199000
|
1.30e-08
|
5.68e-05
|
IRON UPTAKE AND TRANSPORT
|
51
|
2.12e-03
|
1.45e-02
|
0.34200
|
2.84e-01
|
0.191000
|
4.53e-04
|
1.82e-02
|
DEFECTS IN COBALAMIN B12 METABOLISM
|
13
|
1.93e-01
|
3.55e-01
|
0.34200
|
1.81e-01
|
0.290000
|
2.58e-01
|
6.98e-02
|
COBALAMIN CBL VITAMIN B12 TRANSPORT AND METABOLISM
|
14
|
1.70e-01
|
3.22e-01
|
0.34200
|
1.81e-01
|
0.291000
|
2.42e-01
|
5.98e-02
|
COLLAGEN CHAIN TRIMERIZATION
|
41
|
4.91e-03
|
2.53e-02
|
0.34200
|
-1.75e-01
|
-0.294000
|
5.29e-02
|
1.15e-03
|
CARGO CONCENTRATION IN THE ER
|
31
|
1.58e-02
|
5.93e-02
|
0.34100
|
2.97e-01
|
0.168000
|
4.20e-03
|
1.06e-01
|
ATF6 ATF6 ALPHA ACTIVATES CHAPERONES
|
12
|
2.78e-01
|
4.50e-01
|
0.34100
|
2.27e-01
|
0.254000
|
1.73e-01
|
1.27e-01
|
UPTAKE AND FUNCTION OF ANTHRAX TOXINS
|
11
|
3.12e-01
|
4.84e-01
|
0.33900
|
2.54e-01
|
0.225000
|
1.45e-01
|
1.96e-01
|
ACTIVATION OF SMO
|
16
|
6.62e-02
|
1.69e-01
|
0.33900
|
1.20e-01
|
0.317000
|
4.05e-01
|
2.83e-02
|
SYNTHESIS OF IP3 AND IP4 IN THE CYTOSOL
|
25
|
1.14e-02
|
4.79e-02
|
0.33900
|
1.10e-01
|
0.320000
|
3.41e-01
|
5.58e-03
|
BUDDING AND MATURATION OF HIV VIRION
|
27
|
5.29e-02
|
1.45e-01
|
0.33800
|
2.65e-01
|
0.210000
|
1.71e-02
|
5.91e-02
|
AGGREPHAGY
|
34
|
1.11e-04
|
1.57e-03
|
0.33600
|
3.35e-01
|
0.022500
|
7.27e-04
|
8.20e-01
|
GASTRIN CREB SIGNALLING PATHWAY VIA PKC AND MAPK
|
16
|
1.75e-01
|
3.28e-01
|
0.33500
|
2.67e-01
|
0.202000
|
6.42e-02
|
1.62e-01
|
GLUTATHIONE SYNTHESIS AND RECYCLING
|
11
|
3.26e-01
|
4.98e-01
|
0.33500
|
2.29e-01
|
0.244000
|
1.88e-01
|
1.62e-01
|
INOSITOL PHOSPHATE METABOLISM
|
46
|
1.90e-03
|
1.35e-02
|
0.33400
|
1.54e-01
|
0.297000
|
7.14e-02
|
4.90e-04
|
GLYCOSAMINOGLYCAN METABOLISM
|
113
|
8.28e-06
|
2.03e-04
|
0.33400
|
2.55e-01
|
0.216000
|
2.77e-06
|
7.39e-05
|
INTRAFLAGELLAR TRANSPORT
|
52
|
2.97e-06
|
8.52e-05
|
0.33400
|
3.32e-01
|
0.041000
|
3.48e-05
|
6.09e-01
|
FGFR2 LIGAND BINDING AND ACTIVATION
|
12
|
2.87e-01
|
4.61e-01
|
0.33400
|
-2.55e-01
|
-0.216000
|
1.26e-01
|
1.95e-01
|
EUKARYOTIC TRANSLATION ELONGATION
|
87
|
1.09e-05
|
2.51e-04
|
0.33400
|
-1.59e-01
|
-0.293000
|
1.06e-02
|
2.25e-06
|
TRANS GOLGI NETWORK VESICLE BUDDING
|
70
|
6.23e-04
|
6.12e-03
|
0.33300
|
2.06e-01
|
0.262000
|
2.93e-03
|
1.55e-04
|
AMINE LIGAND BINDING RECEPTORS
|
29
|
4.62e-02
|
1.33e-01
|
0.33300
|
2.04e-01
|
0.262000
|
5.69e-02
|
1.44e-02
|
COPII MEDIATED VESICLE TRANSPORT
|
66
|
7.79e-04
|
7.11e-03
|
0.33200
|
2.68e-01
|
0.197000
|
1.69e-04
|
5.72e-03
|
SELECTIVE AUTOPHAGY
|
71
|
5.73e-05
|
9.36e-04
|
0.33200
|
2.97e-01
|
0.147000
|
1.49e-05
|
3.17e-02
|
RESPONSE OF EIF2AK4 GCN2 TO AMINO ACID DEFICIENCY
|
95
|
1.31e-06
|
4.04e-05
|
0.33100
|
-1.40e-01
|
-0.300000
|
1.86e-02
|
4.29e-07
|
RNA POLYMERASE III TRANSCRIPTION TERMINATION
|
23
|
2.58e-02
|
8.72e-02
|
0.32900
|
-1.19e-01
|
-0.307000
|
3.25e-01
|
1.07e-02
|
PENTOSE PHOSPHATE PATHWAY
|
13
|
2.57e-01
|
4.31e-01
|
0.32900
|
2.61e-01
|
0.200000
|
1.03e-01
|
2.12e-01
|
COMPLEX I BIOGENESIS
|
56
|
1.54e-03
|
1.21e-02
|
0.32800
|
-1.75e-01
|
-0.278000
|
2.37e-02
|
3.22e-04
|
G0 AND EARLY G1
|
25
|
8.81e-02
|
2.07e-01
|
0.32700
|
2.37e-01
|
0.226000
|
4.06e-02
|
5.07e-02
|
SYNTHESIS OF BILE ACIDS AND BILE SALTS VIA 7ALPHA HYDROXYCHOLESTEROL
|
14
|
2.38e-01
|
4.09e-01
|
0.32600
|
1.99e-01
|
0.259000
|
1.98e-01
|
9.39e-02
|
BIOTIN TRANSPORT AND METABOLISM
|
11
|
1.42e-02
|
5.55e-02
|
0.32600
|
-1.05e-01
|
0.309000
|
5.48e-01
|
7.63e-02
|
TERMINATION OF O GLYCAN BIOSYNTHESIS
|
10
|
3.00e-01
|
4.73e-01
|
0.32600
|
1.63e-01
|
0.282000
|
3.73e-01
|
1.23e-01
|
FORMATION OF APOPTOSOME
|
10
|
3.55e-01
|
5.22e-01
|
0.32400
|
2.62e-01
|
0.190000
|
1.52e-01
|
2.97e-01
|
RAB GERANYLGERANYLATION
|
57
|
1.72e-03
|
1.26e-02
|
0.32300
|
2.73e-01
|
0.173000
|
3.60e-04
|
2.43e-02
|
DISEASES OF DNA REPAIR
|
11
|
3.28e-01
|
5.00e-01
|
0.32300
|
1.95e-01
|
0.257000
|
2.62e-01
|
1.39e-01
|
HSF1 ACTIVATION
|
25
|
5.05e-04
|
5.11e-03
|
0.32300
|
3.22e-01
|
-0.029200
|
5.38e-03
|
8.00e-01
|
VXPX CARGO TARGETING TO CILIUM
|
19
|
1.41e-01
|
2.89e-01
|
0.32300
|
1.89e-01
|
0.261000
|
1.53e-01
|
4.89e-02
|
DAG AND IP3 SIGNALING
|
40
|
5.95e-03
|
2.89e-02
|
0.32200
|
1.45e-01
|
0.287000
|
1.13e-01
|
1.67e-03
|
CONDENSATION OF PROPHASE CHROMOSOMES
|
30
|
1.07e-02
|
4.54e-02
|
0.32100
|
-1.15e-01
|
-0.300000
|
2.75e-01
|
4.50e-03
|
DISEASES ASSOCIATED WITH N GLYCOSYLATION OF PROTEINS
|
17
|
2.02e-01
|
3.63e-01
|
0.32100
|
2.16e-01
|
0.237000
|
1.23e-01
|
9.03e-02
|
MTOR SIGNALLING
|
40
|
2.08e-02
|
7.36e-02
|
0.32100
|
2.02e-01
|
0.249000
|
2.69e-02
|
6.47e-03
|
GABA RECEPTOR ACTIVATION
|
55
|
5.68e-03
|
2.81e-02
|
0.32100
|
2.38e-01
|
0.215000
|
2.24e-03
|
5.93e-03
|
MATURATION OF NUCLEOPROTEIN
|
10
|
1.18e-01
|
2.56e-01
|
0.32000
|
-3.16e-01
|
-0.050100
|
8.32e-02
|
7.84e-01
|
PLATELET ADHESION TO EXPOSED COLLAGEN
|
13
|
2.95e-01
|
4.67e-01
|
0.32000
|
-2.38e-01
|
-0.214000
|
1.38e-01
|
1.81e-01
|
PARASITE INFECTION
|
54
|
1.71e-03
|
1.26e-02
|
0.32000
|
1.56e-01
|
0.279000
|
4.72e-02
|
3.95e-04
|
REGULATION OF MECP2 EXPRESSION AND ACTIVITY
|
29
|
2.58e-02
|
8.72e-02
|
0.32000
|
-2.85e-01
|
-0.144000
|
7.90e-03
|
1.78e-01
|
ADENYLATE CYCLASE ACTIVATING PATHWAY
|
10
|
3.67e-01
|
5.33e-01
|
0.31900
|
1.88e-01
|
0.257000
|
3.03e-01
|
1.59e-01
|
G ALPHA Z SIGNALLING EVENTS
|
44
|
8.58e-03
|
3.80e-02
|
0.31800
|
2.69e-01
|
0.169000
|
2.04e-03
|
5.22e-02
|
SIGNALING BY HEDGEHOG
|
141
|
3.92e-07
|
1.49e-05
|
0.31700
|
2.65e-01
|
0.174000
|
5.58e-08
|
3.59e-04
|
ACTIVATION OF NMDA RECEPTORS AND POSTSYNAPTIC EVENTS
|
84
|
3.90e-04
|
4.29e-03
|
0.31600
|
2.00e-01
|
0.244000
|
1.54e-03
|
1.09e-04
|
BINDING AND UPTAKE OF LIGANDS BY SCAVENGER RECEPTORS
|
34
|
1.93e-03
|
1.37e-02
|
0.31500
|
-7.19e-02
|
-0.307000
|
4.68e-01
|
1.96e-03
|
PYRUVATE METABOLISM
|
27
|
8.89e-02
|
2.09e-01
|
0.31400
|
2.15e-01
|
0.229000
|
5.33e-02
|
3.97e-02
|
TRANSLOCATION OF SLC2A4 GLUT4 TO THE PLASMA MEMBRANE
|
63
|
1.59e-03
|
1.23e-02
|
0.31400
|
2.62e-01
|
0.173000
|
3.31e-04
|
1.76e-02
|
SIGNAL AMPLIFICATION
|
31
|
3.58e-02
|
1.12e-01
|
0.31300
|
2.67e-01
|
0.164000
|
9.97e-03
|
1.15e-01
|
PKA ACTIVATION IN GLUCAGON SIGNALLING
|
16
|
1.98e-01
|
3.61e-01
|
0.31300
|
2.60e-01
|
0.175000
|
7.18e-02
|
2.26e-01
|
PROCESSING AND ACTIVATION OF SUMO
|
10
|
3.80e-01
|
5.43e-01
|
0.31300
|
2.53e-01
|
0.184000
|
1.66e-01
|
3.14e-01
|
PLASMA LIPOPROTEIN CLEARANCE
|
28
|
8.17e-02
|
1.97e-01
|
0.31300
|
2.32e-01
|
0.210000
|
3.39e-02
|
5.44e-02
|
REGULATION OF INSULIN LIKE GROWTH FACTOR IGF TRANSPORT AND UPTAKE BY INSULIN LIKE GROWTH FACTOR BINDING PROTEINS IGFBPS
|
91
|
2.03e-04
|
2.57e-03
|
0.31200
|
2.47e-01
|
0.190000
|
4.60e-05
|
1.72e-03
|
AMINO ACID TRANSPORT ACROSS THE PLASMA MEMBRANE
|
25
|
5.72e-02
|
1.51e-01
|
0.31200
|
1.49e-01
|
0.274000
|
1.96e-01
|
1.78e-02
|
RAB GEFS EXCHANGE GTP FOR GDP ON RABS
|
88
|
3.03e-04
|
3.54e-03
|
0.31200
|
1.93e-01
|
0.244000
|
1.71e-03
|
7.57e-05
|
METABOLISM OF CARBOHYDRATES
|
260
|
8.26e-11
|
1.08e-08
|
0.31100
|
2.38e-01
|
0.200000
|
3.75e-11
|
2.78e-08
|
PRESYNAPTIC DEPOLARIZATION AND CALCIUM CHANNEL OPENING
|
11
|
1.67e-01
|
3.19e-01
|
0.31100
|
-2.98e-01
|
-0.087600
|
8.71e-02
|
6.15e-01
|
SYNTHESIS OF PE
|
13
|
2.96e-01
|
4.68e-01
|
0.31000
|
1.87e-01
|
0.248000
|
2.44e-01
|
1.22e-01
|
NEGATIVE REGULATION OF FGFR3 SIGNALING
|
24
|
1.23e-01
|
2.65e-01
|
0.31000
|
2.23e-01
|
0.215000
|
5.83e-02
|
6.84e-02
|
GLYCEROPHOSPHOLIPID BIOSYNTHESIS
|
108
|
7.47e-05
|
1.14e-03
|
0.30900
|
2.03e-01
|
0.234000
|
2.72e-04
|
2.77e-05
|
ENERGY DEPENDENT REGULATION OF MTOR BY LKB1 AMPK
|
28
|
7.90e-02
|
1.92e-01
|
0.30900
|
1.93e-01
|
0.242000
|
7.69e-02
|
2.70e-02
|
GOLGI ASSOCIATED VESICLE BIOGENESIS
|
55
|
3.54e-03
|
2.03e-02
|
0.30900
|
1.64e-01
|
0.262000
|
3.55e-02
|
7.87e-04
|
PI METABOLISM
|
79
|
4.37e-05
|
7.68e-04
|
0.30800
|
1.25e-01
|
0.281000
|
5.40e-02
|
1.53e-05
|
PKMTS METHYLATE HISTONE LYSINES
|
51
|
2.98e-03
|
1.80e-02
|
0.30800
|
-2.72e-01
|
-0.143000
|
7.66e-04
|
7.64e-02
|
HSF1 DEPENDENT TRANSACTIVATION
|
33
|
9.26e-04
|
8.01e-03
|
0.30700
|
3.06e-01
|
0.033100
|
2.39e-03
|
7.42e-01
|
LISTERIA MONOCYTOGENES ENTRY INTO HOST CELLS
|
20
|
1.49e-01
|
2.99e-01
|
0.30700
|
1.76e-01
|
0.251000
|
1.72e-01
|
5.16e-02
|
ASSEMBLY AND CELL SURFACE PRESENTATION OF NMDA RECEPTORS
|
36
|
4.74e-02
|
1.34e-01
|
0.30600
|
2.19e-01
|
0.214000
|
2.33e-02
|
2.66e-02
|
MTORC1 MEDIATED SIGNALLING
|
24
|
1.30e-01
|
2.73e-01
|
0.30600
|
2.09e-01
|
0.223000
|
7.65e-02
|
5.86e-02
|
ACTIVATION OF THE AP 1 FAMILY OF TRANSCRIPTION FACTORS
|
10
|
4.09e-01
|
5.72e-01
|
0.30600
|
2.41e-01
|
0.188000
|
1.87e-01
|
3.03e-01
|
PHOSPHOLIPID METABOLISM
|
186
|
1.97e-08
|
1.16e-06
|
0.30500
|
1.70e-01
|
0.253000
|
6.54e-05
|
2.60e-09
|
GLUTAMATE NEUROTRANSMITTER RELEASE CYCLE
|
23
|
7.75e-02
|
1.91e-01
|
0.30400
|
1.42e-01
|
0.269000
|
2.37e-01
|
2.56e-02
|
CARBOXYTERMINAL POST TRANSLATIONAL MODIFICATIONS OF TUBULIN
|
36
|
5.13e-03
|
2.60e-02
|
0.30400
|
2.88e-01
|
0.096400
|
2.75e-03
|
3.17e-01
|
MEMBRANE TRAFFICKING
|
581
|
1.19e-21
|
7.01e-19
|
0.30400
|
1.98e-01
|
0.230000
|
3.56e-16
|
3.13e-21
|
WNT5A DEPENDENT INTERNALIZATION OF FZD4
|
15
|
2.40e-01
|
4.11e-01
|
0.30200
|
2.52e-01
|
0.167000
|
9.12e-02
|
2.62e-01
|
COOPERATION OF PDCL PHLP1 AND TRIC CCT IN G PROTEIN BETA FOLDING
|
36
|
8.83e-03
|
3.88e-02
|
0.30200
|
2.81e-01
|
0.111000
|
3.55e-03
|
2.47e-01
|
PRE NOTCH PROCESSING IN GOLGI
|
18
|
1.69e-01
|
3.21e-01
|
0.30200
|
1.59e-01
|
0.257000
|
2.42e-01
|
5.95e-02
|
ENDOSOMAL SORTING COMPLEX REQUIRED FOR TRANSPORT ESCRT
|
30
|
8.10e-02
|
1.96e-01
|
0.30200
|
2.26e-01
|
0.200000
|
3.22e-02
|
5.75e-02
|
ADP SIGNALLING THROUGH P2Y PURINOCEPTOR 12
|
20
|
4.73e-02
|
1.34e-01
|
0.30200
|
2.89e-01
|
0.086200
|
2.52e-02
|
5.05e-01
|
SYNTHESIS OF BILE ACIDS AND BILE SALTS
|
23
|
1.34e-01
|
2.79e-01
|
0.30100
|
1.84e-01
|
0.239000
|
1.27e-01
|
4.77e-02
|
SARS COV 2 INFECTION
|
65
|
4.85e-03
|
2.53e-02
|
0.30100
|
2.15e-01
|
0.211000
|
2.78e-03
|
3.27e-03
|
TBC RABGAPS
|
43
|
2.48e-02
|
8.48e-02
|
0.30100
|
1.87e-01
|
0.236000
|
3.42e-02
|
7.49e-03
|
PRC2 METHYLATES HISTONES AND DNA
|
32
|
4.58e-02
|
1.33e-01
|
0.30000
|
-1.61e-01
|
-0.254000
|
1.15e-01
|
1.30e-02
|
SEROTONIN RECEPTORS
|
10
|
3.58e-01
|
5.26e-01
|
0.29900
|
2.60e-01
|
0.148000
|
1.54e-01
|
4.18e-01
|
ELEVATION OF CYTOSOLIC CA2 LEVELS
|
14
|
4.11e-02
|
1.24e-01
|
0.29800
|
3.80e-03
|
0.298000
|
9.80e-01
|
5.33e-02
|
REGULATION OF KIT SIGNALING
|
16
|
2.68e-01
|
4.40e-01
|
0.29800
|
1.95e-01
|
0.226000
|
1.77e-01
|
1.18e-01
|
CLATHRIN MEDIATED ENDOCYTOSIS
|
133
|
1.77e-05
|
3.60e-04
|
0.29800
|
1.93e-01
|
0.228000
|
1.27e-04
|
5.85e-06
|
CHONDROITIN SULFATE DERMATAN SULFATE METABOLISM
|
48
|
1.92e-02
|
6.89e-02
|
0.29800
|
2.27e-01
|
0.193000
|
6.46e-03
|
2.10e-02
|
CLASS I PEROXISOMAL MEMBRANE PROTEIN IMPORT
|
20
|
1.96e-01
|
3.59e-01
|
0.29700
|
1.94e-01
|
0.225000
|
1.33e-01
|
8.18e-02
|
INTEGRATION OF ENERGY METABOLISM
|
100
|
2.94e-04
|
3.50e-03
|
0.29700
|
2.25e-01
|
0.193000
|
9.88e-05
|
8.57e-04
|
NUCLEAR PORE COMPLEX NPC DISASSEMBLY
|
32
|
4.32e-04
|
4.54e-03
|
0.29600
|
-1.32e-02
|
0.296000
|
8.97e-01
|
3.75e-03
|
VEGFR2 MEDIATED CELL PROLIFERATION
|
19
|
2.19e-01
|
3.85e-01
|
0.29600
|
2.15e-01
|
0.204000
|
1.04e-01
|
1.25e-01
|
INTERFERON GAMMA SIGNALING
|
73
|
1.04e-06
|
3.41e-05
|
0.29600
|
-2.94e-01
|
-0.039500
|
1.46e-05
|
5.60e-01
|
LOSS OF FUNCTION OF MECP2 IN RETT SYNDROME
|
13
|
2.89e-01
|
4.63e-01
|
0.29600
|
-2.52e-01
|
-0.155000
|
1.16e-01
|
3.33e-01
|
NUCLEOTIDE SALVAGE
|
21
|
1.09e-01
|
2.41e-01
|
0.29600
|
2.62e-01
|
0.138000
|
3.78e-02
|
2.74e-01
|
RESOLUTION OF SISTER CHROMATID COHESION
|
102
|
2.13e-04
|
2.64e-03
|
0.29600
|
1.84e-01
|
0.232000
|
1.36e-03
|
5.26e-05
|
UNFOLDED PROTEIN RESPONSE UPR
|
85
|
8.55e-04
|
7.56e-03
|
0.29500
|
2.32e-01
|
0.182000
|
2.14e-04
|
3.66e-03
|
O GLYCOSYLATION OF TSR DOMAIN CONTAINING PROTEINS
|
35
|
5.11e-02
|
1.41e-01
|
0.29500
|
-2.36e-01
|
-0.176000
|
1.55e-02
|
7.12e-02
|
RHOG GTPASE CYCLE
|
74
|
5.67e-05
|
9.36e-04
|
0.29500
|
9.94e-02
|
0.277000
|
1.39e-01
|
3.73e-05
|
HDACS DEACETYLATE HISTONES
|
49
|
2.14e-02
|
7.54e-02
|
0.29400
|
-2.07e-01
|
-0.210000
|
1.24e-02
|
1.11e-02
|
TRANSFERRIN ENDOCYTOSIS AND RECYCLING
|
26
|
7.54e-02
|
1.88e-01
|
0.29400
|
2.56e-01
|
0.144000
|
2.39e-02
|
2.03e-01
|
DEFECTIVE CFTR CAUSES CYSTIC FIBROSIS
|
58
|
3.14e-04
|
3.59e-03
|
0.29400
|
2.80e-01
|
0.089900
|
2.31e-04
|
2.36e-01
|
RESOLUTION OF D LOOP STRUCTURES THROUGH SYNTHESIS DEPENDENT STRAND ANNEALING SDSA
|
25
|
9.31e-03
|
4.06e-02
|
0.29200
|
-2.89e-01
|
-0.035000
|
1.22e-02
|
7.62e-01
|
HDMS DEMETHYLATE HISTONES
|
30
|
4.31e-03
|
2.32e-02
|
0.29100
|
-2.88e-01
|
-0.039900
|
6.28e-03
|
7.05e-01
|
RHOBTB2 GTPASE CYCLE
|
23
|
1.27e-01
|
2.71e-01
|
0.29100
|
2.45e-01
|
0.157000
|
4.23e-02
|
1.91e-01
|
UPTAKE AND ACTIONS OF BACTERIAL TOXINS
|
28
|
5.58e-02
|
1.50e-01
|
0.29000
|
2.58e-01
|
0.132000
|
1.82e-02
|
2.27e-01
|
MAPK TARGETS NUCLEAR EVENTS MEDIATED BY MAP KINASES
|
31
|
3.81e-02
|
1.17e-01
|
0.29000
|
1.28e-01
|
0.260000
|
2.17e-01
|
1.23e-02
|
RHOJ GTPASE CYCLE
|
54
|
7.57e-04
|
7.01e-03
|
0.28900
|
9.11e-02
|
0.275000
|
2.47e-01
|
4.79e-04
|
DEFECTS IN VITAMIN AND COFACTOR METABOLISM
|
21
|
3.91e-02
|
1.19e-01
|
0.28900
|
6.67e-02
|
0.282000
|
5.97e-01
|
2.55e-02
|
REGULATION OF HSF1 MEDIATED HEAT SHOCK RESPONSE
|
75
|
3.40e-03
|
1.99e-02
|
0.28800
|
1.91e-01
|
0.215000
|
4.20e-03
|
1.30e-03
|
DEADENYLATION OF MRNA
|
25
|
1.01e-01
|
2.29e-01
|
0.28800
|
1.48e-01
|
0.247000
|
2.01e-01
|
3.28e-02
|
TP53 REGULATES TRANSCRIPTION OF SEVERAL ADDITIONAL CELL DEATH GENES WHOSE SPECIFIC ROLES IN P53 DEPENDENT APOPTOSIS REMAIN UNCERTAIN
|
12
|
3.54e-01
|
5.22e-01
|
0.28700
|
2.40e-01
|
0.158000
|
1.50e-01
|
3.44e-01
|
RHOB GTPASE CYCLE
|
67
|
1.14e-06
|
3.62e-05
|
0.28700
|
1.06e-02
|
0.287000
|
8.81e-01
|
4.84e-05
|
MITOPHAGY
|
29
|
6.23e-02
|
1.61e-01
|
0.28700
|
2.51e-01
|
0.140000
|
1.94e-02
|
1.92e-01
|
FCGAMMA RECEPTOR FCGR DEPENDENT PHAGOCYTOSIS
|
81
|
8.87e-04
|
7.73e-03
|
0.28600
|
1.55e-01
|
0.241000
|
1.60e-02
|
1.78e-04
|
BUTYRATE RESPONSE FACTOR 1 BRF1 BINDS AND DESTABILIZES MRNA
|
16
|
3.05e-01
|
4.77e-01
|
0.28600
|
-2.01e-01
|
-0.203000
|
1.64e-01
|
1.59e-01
|
PROTEIN LOCALIZATION
|
158
|
1.03e-06
|
3.41e-05
|
0.28500
|
2.42e-01
|
0.151000
|
1.54e-07
|
1.09e-03
|
NEUROTRANSMITTER RECEPTORS AND POSTSYNAPTIC SIGNAL TRANSMISSION
|
182
|
1.64e-06
|
4.95e-05
|
0.28500
|
1.94e-01
|
0.209000
|
6.70e-06
|
1.24e-06
|
FATTY ACID METABOLISM
|
146
|
2.27e-05
|
4.46e-04
|
0.28400
|
1.92e-01
|
0.209000
|
6.07e-05
|
1.30e-05
|
PROLACTIN RECEPTOR SIGNALING
|
11
|
3.77e-01
|
5.42e-01
|
0.28400
|
2.43e-01
|
0.148000
|
1.63e-01
|
3.97e-01
|
HS GAG BIOSYNTHESIS
|
30
|
1.09e-01
|
2.41e-01
|
0.28400
|
2.11e-01
|
0.190000
|
4.56e-02
|
7.18e-02
|
NEUROTOXICITY OF CLOSTRIDIUM TOXINS
|
10
|
3.30e-01
|
5.03e-01
|
0.28400
|
2.61e-01
|
0.111000
|
1.53e-01
|
5.42e-01
|
B WICH COMPLEX POSITIVELY REGULATES RRNA EXPRESSION
|
50
|
2.59e-02
|
8.72e-02
|
0.28300
|
-1.90e-01
|
-0.209000
|
1.99e-02
|
1.05e-02
|
FCGR3A MEDIATED IL10 SYNTHESIS
|
32
|
9.28e-02
|
2.17e-01
|
0.28300
|
1.83e-01
|
0.216000
|
7.32e-02
|
3.48e-02
|
CHOLESTEROL BIOSYNTHESIS
|
24
|
4.22e-02
|
1.25e-01
|
0.28300
|
2.70e-01
|
0.083200
|
2.19e-02
|
4.80e-01
|
REGULATION OF FOXO TRANSCRIPTIONAL ACTIVITY BY ACETYLATION
|
10
|
3.78e-01
|
5.42e-01
|
0.28200
|
-2.51e-01
|
-0.129000
|
1.70e-01
|
4.82e-01
|
GABA B RECEPTOR ACTIVATION
|
40
|
5.63e-02
|
1.51e-01
|
0.28200
|
2.03e-01
|
0.195000
|
2.61e-02
|
3.31e-02
|
SIALIC ACID METABOLISM
|
32
|
9.59e-02
|
2.21e-01
|
0.28100
|
2.14e-01
|
0.183000
|
3.64e-02
|
7.39e-02
|
THE PHOTOTRANSDUCTION CASCADE
|
22
|
4.14e-02
|
1.24e-01
|
0.28100
|
-6.55e-02
|
-0.273000
|
5.95e-01
|
2.66e-02
|
REGULATION OF RUNX1 EXPRESSION AND ACTIVITY
|
17
|
2.76e-01
|
4.50e-01
|
0.28100
|
-2.22e-01
|
-0.172000
|
1.13e-01
|
2.19e-01
|
TRISTETRAPROLIN TTP ZFP36 BINDS AND DESTABILIZES MRNA
|
16
|
2.80e-01
|
4.53e-01
|
0.27900
|
-2.30e-01
|
-0.158000
|
1.11e-01
|
2.73e-01
|
OPIOID SIGNALLING
|
87
|
1.18e-03
|
9.75e-03
|
0.27900
|
1.62e-01
|
0.227000
|
8.94e-03
|
2.51e-04
|
INTRINSIC PATHWAY OF FIBRIN CLOT FORMATION
|
15
|
2.12e-01
|
3.76e-01
|
0.27900
|
-1.15e-01
|
-0.254000
|
4.40e-01
|
8.86e-02
|
NONSENSE MEDIATED DECAY NMD
|
109
|
7.03e-05
|
1.12e-03
|
0.27800
|
-1.38e-01
|
-0.241000
|
1.28e-02
|
1.37e-05
|
CLEC7A DECTIN 1 INDUCES NFAT ACTIVATION
|
11
|
4.55e-01
|
6.20e-01
|
0.27700
|
1.79e-01
|
0.212000
|
3.04e-01
|
2.24e-01
|
RESOLUTION OF D LOOP STRUCTURES
|
31
|
1.17e-02
|
4.80e-02
|
0.27700
|
-2.70e-01
|
-0.061600
|
9.23e-03
|
5.53e-01
|
HEDGEHOG OFF STATE
|
106
|
5.66e-06
|
1.46e-04
|
0.27700
|
2.59e-01
|
0.096600
|
3.99e-06
|
8.60e-02
|
BLOOD GROUP SYSTEMS BIOSYNTHESIS
|
15
|
3.28e-01
|
5.00e-01
|
0.27600
|
1.65e-01
|
0.221000
|
2.67e-01
|
1.38e-01
|
NEPHRIN FAMILY INTERACTIONS
|
23
|
5.58e-02
|
1.50e-01
|
0.27600
|
8.14e-02
|
0.264000
|
4.99e-01
|
2.86e-02
|
FOXO MEDIATED TRANSCRIPTION OF CELL CYCLE GENES
|
15
|
1.37e-01
|
2.82e-01
|
0.27600
|
7.26e-02
|
0.266000
|
6.26e-01
|
7.45e-02
|
NUCLEAR IMPORT OF REV PROTEIN
|
32
|
1.99e-03
|
1.39e-02
|
0.27500
|
2.58e-03
|
0.275000
|
9.80e-01
|
7.13e-03
|
SYNTHESIS OF PIPS AT THE PLASMA MEMBRANE
|
52
|
4.91e-03
|
2.53e-02
|
0.27400
|
1.10e-01
|
0.252000
|
1.71e-01
|
1.71e-03
|
TIGHT JUNCTION INTERACTIONS
|
16
|
3.11e-01
|
4.83e-01
|
0.27400
|
1.66e-01
|
0.219000
|
2.51e-01
|
1.30e-01
|
VESICLE MEDIATED TRANSPORT
|
613
|
1.95e-18
|
7.66e-16
|
0.27400
|
1.85e-01
|
0.202000
|
5.38e-15
|
1.57e-17
|
LAMININ INTERACTIONS
|
29
|
3.31e-02
|
1.06e-01
|
0.27400
|
-2.59e-01
|
-0.088400
|
1.57e-02
|
4.10e-01
|
RAC2 GTPASE CYCLE
|
87
|
8.72e-05
|
1.30e-03
|
0.27300
|
1.00e-01
|
0.254000
|
1.07e-01
|
4.24e-05
|
SYNTHESIS OF PC
|
26
|
1.69e-01
|
3.22e-01
|
0.27200
|
2.05e-01
|
0.180000
|
7.09e-02
|
1.13e-01
|
UNWINDING OF DNA
|
12
|
3.69e-01
|
5.35e-01
|
0.27200
|
1.38e-01
|
0.235000
|
4.09e-01
|
1.59e-01
|
CD28 DEPENDENT PI3K AKT SIGNALING
|
21
|
1.50e-01
|
2.99e-01
|
0.27200
|
1.24e-01
|
0.242000
|
3.23e-01
|
5.52e-02
|
INTEGRIN CELL SURFACE INTERACTIONS
|
75
|
6.08e-03
|
2.92e-02
|
0.27100
|
-2.06e-01
|
-0.177000
|
2.05e-03
|
8.16e-03
|
TETRAHYDROBIOPTERIN BH4 SYNTHESIS RECYCLING SALVAGE AND REGULATION
|
10
|
5.34e-02
|
1.46e-01
|
0.27100
|
1.23e-01
|
-0.241000
|
4.99e-01
|
1.86e-01
|
DEGRADATION OF CYSTEINE AND HOMOCYSTEINE
|
13
|
1.46e-01
|
2.95e-01
|
0.27100
|
2.67e-01
|
0.048100
|
9.60e-02
|
7.64e-01
|
PEPTIDE HORMONE METABOLISM
|
60
|
1.84e-02
|
6.73e-02
|
0.27000
|
1.99e-01
|
0.183000
|
7.79e-03
|
1.40e-02
|
SCAVENGING BY CLASS A RECEPTORS
|
14
|
2.29e-02
|
7.96e-02
|
0.27000
|
9.28e-02
|
-0.253000
|
5.48e-01
|
1.01e-01
|
INTERACTIONS OF REV WITH HOST CELLULAR PROTEINS
|
35
|
3.87e-03
|
2.18e-02
|
0.27000
|
3.41e-02
|
0.268000
|
7.27e-01
|
6.13e-03
|
RAB REGULATION OF TRAFFICKING
|
119
|
1.58e-04
|
2.09e-03
|
0.27000
|
1.53e-01
|
0.222000
|
3.89e-03
|
2.93e-05
|
METABOLISM OF NUCLEOTIDES
|
92
|
9.72e-04
|
8.29e-03
|
0.26900
|
2.25e-01
|
0.148000
|
1.96e-04
|
1.39e-02
|
ATTENUATION PHASE
|
23
|
1.41e-03
|
1.13e-02
|
0.26900
|
2.43e-01
|
-0.117000
|
4.40e-02
|
3.31e-01
|
PIWI INTERACTING RNA PIRNA BIOGENESIS
|
19
|
2.56e-01
|
4.29e-01
|
0.26900
|
-1.59e-01
|
-0.218000
|
2.31e-01
|
1.01e-01
|
TRANSMISSION ACROSS CHEMICAL SYNAPSES
|
243
|
1.01e-07
|
4.76e-06
|
0.26900
|
1.74e-01
|
0.205000
|
3.13e-06
|
3.94e-08
|
FORMATION OF THE CORNIFIED ENVELOPE
|
31
|
1.12e-04
|
1.57e-03
|
0.26900
|
1.33e-01
|
-0.233000
|
1.99e-01
|
2.47e-02
|
THE ROLE OF GTSE1 IN G2 M PROGRESSION AFTER G2 CHECKPOINT
|
66
|
9.26e-07
|
3.20e-05
|
0.26900
|
2.67e-01
|
-0.025300
|
1.73e-04
|
7.22e-01
|
REGULATION OF LOCALIZATION OF FOXO TRANSCRIPTION FACTORS
|
12
|
3.42e-01
|
5.12e-01
|
0.26800
|
2.40e-01
|
0.120000
|
1.51e-01
|
4.70e-01
|
SEMA3A PLEXIN REPULSION SIGNALING BY INHIBITING INTEGRIN ADHESION
|
14
|
7.28e-02
|
1.83e-01
|
0.26800
|
1.31e-04
|
0.268000
|
9.99e-01
|
8.25e-02
|
CELLULAR RESPONSE TO HEAT STRESS
|
94
|
2.17e-03
|
1.46e-02
|
0.26800
|
1.97e-01
|
0.181000
|
9.47e-04
|
2.43e-03
|
HEPARAN SULFATE HEPARIN HS GAG METABOLISM
|
52
|
2.35e-02
|
8.10e-02
|
0.26800
|
2.19e-01
|
0.153000
|
6.26e-03
|
5.57e-02
|
SIRT1 NEGATIVELY REGULATES RRNA EXPRESSION
|
27
|
9.32e-02
|
2.17e-01
|
0.26700
|
-1.22e-01
|
-0.238000
|
2.74e-01
|
3.22e-02
|
DEFECTIVE B4GALT7 CAUSES EDS PROGEROID TYPE
|
20
|
8.43e-02
|
2.02e-01
|
0.26700
|
2.58e-01
|
0.071400
|
4.62e-02
|
5.81e-01
|
ROS AND RNS PRODUCTION IN PHAGOCYTES
|
28
|
1.14e-02
|
4.79e-02
|
0.26600
|
2.65e-01
|
0.027900
|
1.53e-02
|
7.98e-01
|
SARS COV 1 INFECTION
|
48
|
4.28e-02
|
1.26e-01
|
0.26600
|
1.73e-01
|
0.202000
|
3.84e-02
|
1.53e-02
|
EPHB MEDIATED FORWARD SIGNALING
|
42
|
6.48e-02
|
1.66e-01
|
0.26600
|
1.75e-01
|
0.200000
|
4.92e-02
|
2.49e-02
|
SIGNALING BY WNT IN CANCER
|
31
|
6.41e-02
|
1.65e-01
|
0.26600
|
1.18e-01
|
0.238000
|
2.54e-01
|
2.17e-02
|
CELLULAR HEXOSE TRANSPORT
|
12
|
1.59e-01
|
3.09e-01
|
0.26600
|
3.46e-02
|
0.264000
|
8.36e-01
|
1.14e-01
|
MITOCHONDRIAL IRON SULFUR CLUSTER BIOGENESIS
|
13
|
2.78e-01
|
4.50e-01
|
0.26600
|
-1.03e-01
|
-0.245000
|
5.20e-01
|
1.26e-01
|
PROTEIN UBIQUITINATION
|
70
|
7.75e-03
|
3.51e-02
|
0.26500
|
2.14e-01
|
0.156000
|
1.92e-03
|
2.37e-02
|
MITOTIC TELOPHASE CYTOKINESIS
|
13
|
2.80e-02
|
9.27e-02
|
0.26500
|
-1.13e-01
|
0.240000
|
4.82e-01
|
1.34e-01
|
SIGNAL TRANSDUCTION BY L1
|
21
|
2.25e-01
|
3.91e-01
|
0.26500
|
2.17e-01
|
0.151000
|
8.46e-02
|
2.31e-01
|
MECP2 REGULATES NEURONAL RECEPTORS AND CHANNELS
|
18
|
3.00e-02
|
9.73e-02
|
0.26400
|
-1.42e-02
|
0.264000
|
9.17e-01
|
5.25e-02
|
NS1 MEDIATED EFFECTS ON HOST PATHWAYS
|
37
|
1.23e-04
|
1.69e-03
|
0.26400
|
-7.15e-02
|
0.254000
|
4.52e-01
|
7.44e-03
|
TRIGLYCERIDE CATABOLISM
|
14
|
3.06e-01
|
4.77e-01
|
0.26400
|
2.34e-01
|
0.122000
|
1.29e-01
|
4.29e-01
|
GLUCAGON SIGNALING IN METABOLIC REGULATION
|
30
|
2.95e-02
|
9.64e-02
|
0.26400
|
2.53e-01
|
0.074500
|
1.63e-02
|
4.80e-01
|
HEDGEHOG LIGAND BIOGENESIS
|
61
|
2.76e-03
|
1.72e-02
|
0.26400
|
2.43e-01
|
0.102000
|
1.03e-03
|
1.67e-01
|
CYCLIN A CDK2 ASSOCIATED EVENTS AT S PHASE ENTRY
|
84
|
1.38e-03
|
1.12e-02
|
0.26300
|
2.28e-01
|
0.132000
|
3.05e-04
|
3.71e-02
|
ERYTHROPOIETIN ACTIVATES RAS
|
13
|
4.35e-01
|
5.98e-01
|
0.26300
|
1.99e-01
|
0.172000
|
2.14e-01
|
2.83e-01
|
CLASS B 2 SECRETIN FAMILY RECEPTORS
|
72
|
6.07e-03
|
2.92e-02
|
0.26200
|
2.18e-01
|
0.145000
|
1.40e-03
|
3.36e-02
|
DCC MEDIATED ATTRACTIVE SIGNALING
|
14
|
9.68e-02
|
2.21e-01
|
0.26100
|
1.29e-02
|
0.261000
|
9.33e-01
|
9.07e-02
|
FCERI MEDIATED MAPK ACTIVATION
|
28
|
1.73e-01
|
3.27e-01
|
0.26100
|
1.74e-01
|
0.195000
|
1.10e-01
|
7.48e-02
|
EXTRA NUCLEAR ESTROGEN SIGNALING
|
68
|
4.95e-03
|
2.53e-02
|
0.26100
|
2.27e-01
|
0.129000
|
1.20e-03
|
6.59e-02
|
RNA POLYMERASE III CHAIN ELONGATION
|
18
|
6.14e-02
|
1.60e-01
|
0.26100
|
-2.50e-02
|
-0.260000
|
8.54e-01
|
5.67e-02
|
RMTS METHYLATE HISTONE ARGININES
|
46
|
3.10e-02
|
1.00e-01
|
0.26000
|
-1.33e-01
|
-0.224000
|
1.20e-01
|
8.60e-03
|
ERK MAPK TARGETS
|
22
|
4.76e-02
|
1.34e-01
|
0.26000
|
4.33e-02
|
0.256000
|
7.25e-01
|
3.74e-02
|
INTERLEUKIN 10 SIGNALING
|
19
|
2.69e-01
|
4.42e-01
|
0.25900
|
-2.15e-01
|
-0.145000
|
1.05e-01
|
2.74e-01
|
RESPIRATORY ELECTRON TRANSPORT
|
102
|
2.92e-04
|
3.50e-03
|
0.25900
|
-1.22e-01
|
-0.228000
|
3.39e-02
|
6.75e-05
|
METABOLISM OF POLYAMINES
|
57
|
2.24e-03
|
1.50e-02
|
0.25800
|
2.46e-01
|
0.079700
|
1.34e-03
|
2.98e-01
|
REGULATION OF GENE EXPRESSION BY HYPOXIA INDUCIBLE FACTOR
|
10
|
1.43e-01
|
2.91e-01
|
0.25800
|
-2.40e-02
|
0.257000
|
8.95e-01
|
1.59e-01
|
SLBP DEPENDENT PROCESSING OF REPLICATION DEPENDENT HISTONE PRE MRNAS
|
11
|
7.87e-02
|
1.92e-01
|
0.25800
|
6.80e-02
|
-0.249000
|
6.96e-01
|
1.53e-01
|
CHEMOKINE RECEPTORS BIND CHEMOKINES
|
17
|
2.33e-01
|
4.03e-01
|
0.25700
|
-2.33e-01
|
-0.110000
|
9.68e-02
|
4.33e-01
|
PHOSPHOLIPASE C MEDIATED CASCADE FGFR2
|
12
|
4.87e-01
|
6.47e-01
|
0.25700
|
-1.82e-01
|
-0.181000
|
2.74e-01
|
2.77e-01
|
TP53 REGULATES TRANSCRIPTION OF ADDITIONAL CELL CYCLE GENES WHOSE EXACT ROLE IN THE P53 PATHWAY REMAIN UNCERTAIN
|
20
|
1.67e-01
|
3.19e-01
|
0.25700
|
2.35e-01
|
0.103000
|
6.87e-02
|
4.27e-01
|
REGULATION OF INSULIN SECRETION
|
72
|
1.07e-02
|
4.55e-02
|
0.25600
|
2.03e-01
|
0.157000
|
2.96e-03
|
2.11e-02
|
PROTEIN FOLDING
|
90
|
1.33e-05
|
2.90e-04
|
0.25600
|
2.50e-01
|
0.053600
|
4.07e-05
|
3.80e-01
|
INTERACTION BETWEEN L1 AND ANKYRINS
|
27
|
5.71e-02
|
1.51e-01
|
0.25500
|
-2.43e-01
|
-0.077000
|
2.86e-02
|
4.89e-01
|
SIGNALLING TO ERKS
|
33
|
1.13e-01
|
2.48e-01
|
0.25400
|
1.43e-01
|
0.210000
|
1.55e-01
|
3.70e-02
|
THROMBIN SIGNALLING THROUGH PROTEINASE ACTIVATED RECEPTORS PARS
|
28
|
9.69e-02
|
2.21e-01
|
0.25400
|
2.30e-01
|
0.108000
|
3.56e-02
|
3.22e-01
|
NEGATIVE REGULATION OF FGFR4 SIGNALING
|
24
|
1.97e-01
|
3.61e-01
|
0.25400
|
2.13e-01
|
0.138000
|
7.15e-02
|
2.41e-01
|
MITOTIC METAPHASE AND ANAPHASE
|
207
|
5.72e-06
|
1.46e-04
|
0.25100
|
1.93e-01
|
0.161000
|
1.78e-06
|
6.75e-05
|
METABOLISM OF LIPIDS
|
616
|
1.65e-16
|
3.89e-14
|
0.25100
|
1.52e-01
|
0.200000
|
1.47e-10
|
3.16e-17
|
PLASMA LIPOPROTEIN ASSEMBLY REMODELING AND CLEARANCE
|
49
|
3.91e-02
|
1.19e-01
|
0.25000
|
1.36e-01
|
0.210000
|
1.00e-01
|
1.09e-02
|
AMINO ACIDS REGULATE MTORC1
|
51
|
5.38e-02
|
1.47e-01
|
0.25000
|
1.86e-01
|
0.167000
|
2.14e-02
|
3.91e-02
|
METABOLISM OF WATER SOLUBLE VITAMINS AND COFACTORS
|
101
|
5.08e-04
|
5.11e-03
|
0.24900
|
1.15e-01
|
0.221000
|
4.51e-02
|
1.23e-04
|
REGULATION OF HMOX1 EXPRESSION AND ACTIVITY
|
63
|
3.34e-03
|
1.97e-02
|
0.24900
|
2.32e-01
|
0.090200
|
1.43e-03
|
2.16e-01
|
VITAMIN B5 PANTOTHENATE METABOLISM
|
15
|
4.10e-01
|
5.73e-01
|
0.24900
|
1.53e-01
|
0.196000
|
3.04e-01
|
1.88e-01
|
GPVI MEDIATED ACTIVATION CASCADE
|
31
|
1.32e-01
|
2.76e-01
|
0.24700
|
1.32e-01
|
0.209000
|
2.02e-01
|
4.43e-02
|
RHOC GTPASE CYCLE
|
73
|
1.69e-04
|
2.21e-03
|
0.24700
|
4.80e-02
|
0.242000
|
4.79e-01
|
3.48e-04
|
METABOLISM OF ANGIOTENSINOGEN TO ANGIOTENSINS
|
10
|
4.15e-01
|
5.79e-01
|
0.24600
|
9.01e-02
|
0.229000
|
6.22e-01
|
2.10e-01
|
HEME BIOSYNTHESIS
|
13
|
3.32e-01
|
5.04e-01
|
0.24600
|
9.47e-02
|
0.227000
|
5.55e-01
|
1.56e-01
|
TRIGLYCERIDE BIOSYNTHESIS
|
10
|
1.37e-01
|
2.82e-01
|
0.24600
|
-5.03e-02
|
0.241000
|
7.83e-01
|
1.87e-01
|
SYNTHESIS OF PROSTAGLANDINS PG AND THROMBOXANES TX
|
12
|
3.48e-01
|
5.15e-01
|
0.24600
|
2.29e-01
|
0.089100
|
1.70e-01
|
5.93e-01
|
ACTIVATION OF IRF3 IRF7 MEDIATED BY TBK1 IKK EPSILON
|
16
|
2.62e-01
|
4.33e-01
|
0.24400
|
9.37e-02
|
0.226000
|
5.16e-01
|
1.18e-01
|
ABC TRANSPORTER DISORDERS
|
69
|
1.90e-03
|
1.35e-02
|
0.24400
|
2.30e-01
|
0.082300
|
9.63e-04
|
2.38e-01
|
RHO GTPASES ACTIVATE NADPH OXIDASES
|
20
|
3.13e-01
|
4.84e-01
|
0.24300
|
1.43e-01
|
0.196000
|
2.67e-01
|
1.29e-01
|
INTERACTIONS OF VPR WITH HOST CELLULAR PROTEINS
|
34
|
5.92e-03
|
2.89e-02
|
0.24300
|
3.19e-03
|
0.243000
|
9.74e-01
|
1.43e-02
|
CGMP EFFECTS
|
15
|
3.80e-01
|
5.43e-01
|
0.24200
|
-2.07e-01
|
-0.126000
|
1.65e-01
|
3.98e-01
|
KERATINIZATION
|
32
|
4.96e-04
|
5.07e-03
|
0.24200
|
1.19e-01
|
-0.211000
|
2.45e-01
|
3.89e-02
|
RND2 GTPASE CYCLE
|
39
|
6.98e-03
|
3.24e-02
|
0.24200
|
3.10e-02
|
0.240000
|
7.38e-01
|
9.48e-03
|
BILE ACID AND BILE SALT METABOLISM
|
26
|
1.56e-01
|
3.06e-01
|
0.24200
|
1.11e-01
|
0.215000
|
3.27e-01
|
5.77e-02
|
INTERLEUKIN 6 SIGNALING
|
10
|
5.61e-01
|
7.05e-01
|
0.24200
|
1.43e-01
|
0.195000
|
4.34e-01
|
2.85e-01
|
CARGO RECOGNITION FOR CLATHRIN MEDIATED ENDOCYTOSIS
|
93
|
7.56e-03
|
3.44e-02
|
0.24100
|
1.71e-01
|
0.170000
|
4.42e-03
|
4.60e-03
|
PLATELET ACTIVATION SIGNALING AND AGGREGATION
|
224
|
8.17e-06
|
2.03e-04
|
0.24100
|
1.63e-01
|
0.177000
|
2.57e-05
|
5.20e-06
|
JNK C JUN KINASES PHOSPHORYLATION AND ACTIVATION MEDIATED BY ACTIVATED HUMAN TAK1
|
22
|
3.13e-01
|
4.84e-01
|
0.24100
|
1.64e-01
|
0.176000
|
1.84e-01
|
1.52e-01
|
NUCLEOBASE CATABOLISM
|
31
|
1.86e-01
|
3.47e-01
|
0.24000
|
1.86e-01
|
0.153000
|
7.37e-02
|
1.41e-01
|
RHO GTPASES ACTIVATE FORMINS
|
119
|
1.90e-03
|
1.35e-02
|
0.24000
|
1.59e-01
|
0.180000
|
2.70e-03
|
7.20e-04
|
EXPORT OF VIRAL RIBONUCLEOPROTEINS FROM NUCLEUS
|
31
|
3.18e-03
|
1.89e-02
|
0.24000
|
-4.43e-02
|
0.236000
|
6.70e-01
|
2.30e-02
|
GLUCOSE METABOLISM
|
81
|
1.54e-02
|
5.83e-02
|
0.23900
|
1.69e-01
|
0.169000
|
8.65e-03
|
8.61e-03
|
RHOBTB1 GTPASE CYCLE
|
23
|
1.95e-01
|
3.58e-01
|
0.23800
|
1.06e-01
|
0.214000
|
3.78e-01
|
7.63e-02
|
TNFR1 INDUCED PROAPOPTOTIC SIGNALING
|
12
|
3.96e-01
|
5.61e-01
|
0.23800
|
9.56e-02
|
0.218000
|
5.66e-01
|
1.90e-01
|
REGULATION OF GLUCOKINASE BY GLUCOKINASE REGULATORY PROTEIN
|
29
|
4.64e-03
|
2.44e-02
|
0.23800
|
-4.72e-02
|
0.234000
|
6.60e-01
|
2.95e-02
|
SIGNALING BY NODAL
|
15
|
9.70e-02
|
2.21e-01
|
0.23800
|
-2.38e-01
|
0.010100
|
1.11e-01
|
9.46e-01
|
ESTROGEN DEPENDENT NUCLEAR EVENTS DOWNSTREAM OF ESR MEMBRANE SIGNALING
|
21
|
2.59e-01
|
4.32e-01
|
0.23800
|
1.18e-01
|
0.206000
|
3.48e-01
|
1.02e-01
|
GLUCAGON LIKE PEPTIDE 1 GLP1 REGULATES INSULIN SECRETION
|
39
|
6.82e-02
|
1.72e-01
|
0.23800
|
2.11e-01
|
0.109000
|
2.25e-02
|
2.39e-01
|
RHOQ GTPASE CYCLE
|
57
|
4.22e-04
|
4.48e-03
|
0.23800
|
1.29e-02
|
0.237000
|
8.66e-01
|
1.96e-03
|
RESPONSE TO ELEVATED PLATELET CYTOSOLIC CA2
|
107
|
4.12e-03
|
2.23e-02
|
0.23600
|
1.79e-01
|
0.154000
|
1.40e-03
|
5.96e-03
|
INHIBITION OF DNA RECOMBINATION AT TELOMERE
|
38
|
1.86e-02
|
6.79e-02
|
0.23600
|
-5.14e-02
|
-0.230000
|
5.83e-01
|
1.40e-02
|
BIOSYNTHESIS OF THE N GLYCAN PRECURSOR DOLICHOL LIPID LINKED OLIGOSACCHARIDE LLO AND TRANSFER TO A NASCENT PROTEIN
|
76
|
2.18e-02
|
7.61e-02
|
0.23600
|
1.71e-01
|
0.162000
|
9.95e-03
|
1.46e-02
|
EGFR DOWNREGULATION
|
28
|
2.42e-01
|
4.12e-01
|
0.23500
|
1.74e-01
|
0.159000
|
1.11e-01
|
1.46e-01
|
RECOGNITION AND ASSOCIATION OF DNA GLYCOSYLASE WITH SITE CONTAINING AN AFFECTED PURINE
|
25
|
3.63e-02
|
1.13e-01
|
0.23500
|
-1.42e-02
|
-0.235000
|
9.02e-01
|
4.23e-02
|
NEUTROPHIL DEGRANULATION
|
386
|
8.34e-10
|
7.55e-08
|
0.23500
|
1.92e-01
|
0.135000
|
1.12e-10
|
5.22e-06
|
MISCELLANEOUS TRANSPORT AND BINDING EVENTS
|
21
|
2.23e-01
|
3.89e-01
|
0.23400
|
9.96e-02
|
0.212000
|
4.29e-01
|
9.23e-02
|
RHOD GTPASE CYCLE
|
51
|
1.44e-02
|
5.60e-02
|
0.23400
|
8.00e-02
|
0.220000
|
3.23e-01
|
6.50e-03
|
HIV ELONGATION ARREST AND RECOVERY
|
32
|
8.78e-02
|
2.07e-01
|
0.23400
|
-9.07e-02
|
-0.216000
|
3.75e-01
|
3.48e-02
|
FORMATION OF ATP BY CHEMIOSMOTIC COUPLING
|
18
|
2.05e-01
|
3.66e-01
|
0.23400
|
-7.15e-02
|
-0.222000
|
5.99e-01
|
1.02e-01
|
NRAGE SIGNALS DEATH THROUGH JNK
|
54
|
1.04e-04
|
1.51e-03
|
0.23300
|
-3.58e-02
|
0.231000
|
6.49e-01
|
3.37e-03
|
A TETRASACCHARIDE LINKER SEQUENCE IS REQUIRED FOR GAG SYNTHESIS
|
26
|
9.84e-02
|
2.24e-01
|
0.23300
|
2.23e-01
|
0.069600
|
4.93e-02
|
5.39e-01
|
DISEASES ASSOCIATED WITH GLYCOSYLATION PRECURSOR BIOSYNTHESIS
|
18
|
3.42e-01
|
5.12e-01
|
0.23300
|
1.99e-01
|
0.122000
|
1.44e-01
|
3.72e-01
|
RAS ACTIVATION UPON CA2 INFLUX THROUGH NMDA RECEPTOR
|
20
|
3.69e-01
|
5.35e-01
|
0.23300
|
1.74e-01
|
0.155000
|
1.77e-01
|
2.32e-01
|
MITOTIC SPINDLE CHECKPOINT
|
97
|
3.25e-03
|
1.92e-02
|
0.23300
|
1.21e-01
|
0.199000
|
3.94e-02
|
7.26e-04
|
TRANSPORT OF THE SLBP DEPENDANT MATURE MRNA
|
34
|
3.15e-02
|
1.02e-01
|
0.23300
|
5.09e-02
|
0.227000
|
6.08e-01
|
2.20e-02
|
ROLE OF PHOSPHOLIPIDS IN PHAGOCYTOSIS
|
22
|
3.37e-01
|
5.10e-01
|
0.23200
|
1.54e-01
|
0.174000
|
2.13e-01
|
1.58e-01
|
REGULATION OF CHOLESTEROL BIOSYNTHESIS BY SREBP SREBF
|
56
|
4.72e-02
|
1.34e-01
|
0.23200
|
1.32e-01
|
0.191000
|
8.86e-02
|
1.36e-02
|
SUMOYLATION OF SUMOYLATION PROTEINS
|
33
|
6.07e-03
|
2.92e-02
|
0.23200
|
-1.91e-02
|
0.231000
|
8.49e-01
|
2.18e-02
|
PLATELET CALCIUM HOMEOSTASIS
|
26
|
5.74e-03
|
2.83e-02
|
0.23100
|
-7.98e-02
|
0.217000
|
4.81e-01
|
5.52e-02
|
CYCLIN A B1 B2 ASSOCIATED EVENTS DURING G2 M TRANSITION
|
22
|
3.15e-01
|
4.87e-01
|
0.23100
|
1.86e-01
|
0.138000
|
1.31e-01
|
2.63e-01
|
SUMOYLATION OF DNA REPLICATION PROTEINS
|
43
|
2.68e-02
|
8.97e-02
|
0.23100
|
7.37e-02
|
0.219000
|
4.03e-01
|
1.30e-02
|
GP1B IX V ACTIVATION SIGNALLING
|
11
|
5.81e-01
|
7.21e-01
|
0.23100
|
-1.50e-01
|
-0.175000
|
3.90e-01
|
3.14e-01
|
NITRIC OXIDE STIMULATES GUANYLATE CYCLASE
|
20
|
3.23e-01
|
4.95e-01
|
0.22900
|
-1.94e-01
|
-0.122000
|
1.33e-01
|
3.45e-01
|
GLYOXYLATE METABOLISM AND GLYCINE DEGRADATION
|
26
|
2.42e-01
|
4.12e-01
|
0.22900
|
1.27e-01
|
0.191000
|
2.63e-01
|
9.20e-02
|
MAP3K8 TPL2 DEPENDENT MAPK1 3 ACTIVATION
|
16
|
3.71e-01
|
5.36e-01
|
0.22900
|
1.09e-01
|
0.201000
|
4.50e-01
|
1.63e-01
|
INTERLEUKIN 17 SIGNALING
|
68
|
8.04e-03
|
3.60e-02
|
0.22900
|
9.13e-02
|
0.210000
|
1.93e-01
|
2.82e-03
|
NEDDYLATION
|
217
|
1.44e-05
|
3.03e-04
|
0.22900
|
1.85e-01
|
0.134000
|
2.56e-06
|
7.07e-04
|
TNF SIGNALING
|
43
|
1.20e-01
|
2.59e-01
|
0.22800
|
1.43e-01
|
0.178000
|
1.05e-01
|
4.35e-02
|
SIGNALING BY NTRKS
|
129
|
1.50e-03
|
1.18e-02
|
0.22800
|
1.37e-01
|
0.183000
|
7.39e-03
|
3.46e-04
|
METABOLISM OF COFACTORS
|
19
|
2.66e-02
|
8.93e-02
|
0.22800
|
7.66e-02
|
-0.214000
|
5.63e-01
|
1.06e-01
|
NEF MEDIATED DOWNREGULATION OF MHC CLASS I COMPLEX CELL SURFACE EXPRESSION
|
13
|
1.54e-01
|
3.04e-01
|
0.22800
|
-1.12e-02
|
0.227000
|
9.44e-01
|
1.56e-01
|
TRANSPORT OF INORGANIC CATIONS ANIONS AND AMINO ACIDS OLIGOPEPTIDES
|
83
|
2.73e-04
|
3.32e-03
|
0.22800
|
4.72e-02
|
0.223000
|
4.58e-01
|
4.58e-04
|
VASOPRESSIN REGULATES RENAL WATER HOMEOSTASIS VIA AQUAPORINS
|
37
|
9.65e-02
|
2.21e-01
|
0.22700
|
2.02e-01
|
0.103000
|
3.34e-02
|
2.76e-01
|
MUCOPOLYSACCHARIDOSES
|
11
|
5.98e-01
|
7.32e-01
|
0.22700
|
1.58e-01
|
0.162000
|
3.63e-01
|
3.51e-01
|
RHOA GTPASE CYCLE
|
141
|
5.47e-06
|
1.46e-04
|
0.22700
|
6.44e-02
|
0.217000
|
1.87e-01
|
8.35e-06
|
INLB MEDIATED ENTRY OF LISTERIA MONOCYTOGENES INTO HOST CELL
|
15
|
4.67e-01
|
6.29e-01
|
0.22700
|
1.34e-01
|
0.183000
|
3.70e-01
|
2.19e-01
|
REGULATION OF SIGNALING BY CBL
|
22
|
1.36e-01
|
2.82e-01
|
0.22700
|
5.80e-02
|
0.219000
|
6.38e-01
|
7.53e-02
|
SIGNALING BY FGFR3
|
34
|
1.99e-01
|
3.61e-01
|
0.22600
|
1.72e-01
|
0.147000
|
8.24e-02
|
1.38e-01
|
NEGATIVE REGULATION OF NMDA RECEPTOR MEDIATED NEURONAL TRANSMISSION
|
21
|
2.35e-01
|
4.05e-01
|
0.22600
|
9.20e-02
|
0.207000
|
4.66e-01
|
1.01e-01
|
POST TRANSLATIONAL PROTEIN MODIFICATION
|
1225
|
8.15e-24
|
9.59e-21
|
0.22600
|
1.64e-01
|
0.156000
|
7.90e-22
|
8.57e-20
|
NUCLEAR ENVELOPE BREAKDOWN
|
49
|
1.01e-02
|
4.34e-02
|
0.22600
|
5.23e-02
|
0.220000
|
5.27e-01
|
7.79e-03
|
NR1H3 NR1H2 REGULATE GENE EXPRESSION LINKED TO CHOLESTEROL TRANSPORT AND EFFLUX
|
32
|
1.26e-01
|
2.69e-01
|
0.22500
|
-2.03e-01
|
-0.097100
|
4.72e-02
|
3.42e-01
|
IMMUNOREGULATORY INTERACTIONS BETWEEN A LYMPHOID AND A NON LYMPHOID CELL
|
51
|
5.02e-02
|
1.39e-01
|
0.22500
|
-1.96e-01
|
-0.109000
|
1.52e-02
|
1.77e-01
|
PROCESSING OF SMDT1
|
16
|
3.33e-01
|
5.06e-01
|
0.22400
|
2.06e-01
|
0.089400
|
1.54e-01
|
5.36e-01
|
REGULATION OF PTEN STABILITY AND ACTIVITY
|
66
|
5.59e-03
|
2.79e-02
|
0.22400
|
2.12e-01
|
0.072300
|
2.88e-03
|
3.10e-01
|
SIGNALING BY RETINOIC ACID
|
33
|
2.00e-01
|
3.62e-01
|
0.22400
|
1.35e-01
|
0.179000
|
1.80e-01
|
7.54e-02
|
SIGNALING BY VEGF
|
103
|
5.29e-03
|
2.67e-02
|
0.22400
|
1.27e-01
|
0.185000
|
2.62e-02
|
1.22e-03
|
CASPASE ACTIVATION VIA DEPENDENCE RECEPTORS IN THE ABSENCE OF LIGAND
|
10
|
5.86e-01
|
7.22e-01
|
0.22300
|
1.19e-01
|
0.189000
|
5.13e-01
|
3.01e-01
|
SEPARATION OF SISTER CHROMATIDS
|
166
|
4.73e-04
|
4.89e-03
|
0.22300
|
1.71e-01
|
0.142000
|
1.40e-04
|
1.55e-03
|
PECAM1 INTERACTIONS
|
12
|
2.15e-01
|
3.78e-01
|
0.22300
|
1.63e-03
|
0.223000
|
9.92e-01
|
1.82e-01
|
BASE EXCISION REPAIR AP SITE FORMATION
|
32
|
1.02e-01
|
2.30e-01
|
0.22200
|
-8.20e-02
|
-0.207000
|
4.22e-01
|
4.29e-02
|
ANTIGEN PRESENTATION FOLDING ASSEMBLY AND PEPTIDE LOADING OF CLASS I MHC
|
24
|
7.62e-02
|
1.89e-01
|
0.22200
|
2.89e-02
|
0.221000
|
8.07e-01
|
6.15e-02
|
CROSS PRESENTATION OF SOLUBLE EXOGENOUS ANTIGENS ENDOSOMES
|
46
|
6.70e-03
|
3.14e-02
|
0.22200
|
2.21e-01
|
0.026200
|
9.65e-03
|
7.59e-01
|
TRAF3 DEPENDENT IRF ACTIVATION PATHWAY
|
13
|
1.32e-01
|
2.76e-01
|
0.22200
|
-2.19e-01
|
0.036900
|
1.72e-01
|
8.18e-01
|
SYNTHESIS OF SUBSTRATES IN N GLYCAN BIOSYTHESIS
|
62
|
5.59e-02
|
1.50e-01
|
0.22200
|
1.73e-01
|
0.138000
|
1.84e-02
|
5.94e-02
|
FOXO MEDIATED TRANSCRIPTION OF CELL DEATH GENES
|
15
|
2.40e-01
|
4.11e-01
|
0.22100
|
-2.17e-01
|
-0.044400
|
1.46e-01
|
7.66e-01
|
RESPONSE OF EIF2AK1 HRI TO HEME DEFICIENCY
|
15
|
8.66e-02
|
2.06e-01
|
0.22100
|
2.16e-01
|
-0.048300
|
1.48e-01
|
7.46e-01
|
ACYL CHAIN REMODELLING OF PC
|
17
|
4.56e-01
|
6.20e-01
|
0.22100
|
1.72e-01
|
0.140000
|
2.21e-01
|
3.19e-01
|
DISEASES OF CARBOHYDRATE METABOLISM
|
29
|
2.18e-01
|
3.84e-01
|
0.22100
|
1.87e-01
|
0.118000
|
8.12e-02
|
2.72e-01
|
P130CAS LINKAGE TO MAPK SIGNALING FOR INTEGRINS
|
12
|
1.30e-01
|
2.73e-01
|
0.22100
|
-5.92e-02
|
0.213000
|
7.23e-01
|
2.02e-01
|
INTEGRIN SIGNALING
|
24
|
1.99e-01
|
3.61e-01
|
0.22100
|
8.65e-02
|
0.203000
|
4.63e-01
|
8.48e-02
|
GABA SYNTHESIS RELEASE REUPTAKE AND DEGRADATION
|
18
|
4.08e-01
|
5.71e-01
|
0.22100
|
1.82e-01
|
0.125000
|
1.81e-01
|
3.60e-01
|
G ALPHA Q SIGNALLING EVENTS
|
153
|
6.05e-04
|
6.04e-03
|
0.22100
|
1.80e-01
|
0.127000
|
1.24e-04
|
6.54e-03
|
TRANSPORT OF MATURE MRNAS DERIVED FROM INTRONLESS TRANSCRIPTS
|
41
|
2.44e-02
|
8.37e-02
|
0.22100
|
4.94e-02
|
0.215000
|
5.85e-01
|
1.73e-02
|
DOWNSTREAM SIGNALING EVENTS OF B CELL RECEPTOR BCR
|
78
|
3.43e-03
|
1.99e-02
|
0.22000
|
2.07e-01
|
0.076000
|
1.61e-03
|
2.46e-01
|
NEGATIVE REGULATION OF MAPK PATHWAY
|
42
|
1.54e-01
|
3.04e-01
|
0.22000
|
1.66e-01
|
0.145000
|
6.34e-02
|
1.04e-01
|
RESPIRATORY ELECTRON TRANSPORT ATP SYNTHESIS BY CHEMIOSMOTIC COUPLING AND HEAT PRODUCTION BY UNCOUPLING PROTEINS
|
125
|
4.18e-04
|
4.47e-03
|
0.22000
|
-9.42e-02
|
-0.199000
|
6.92e-02
|
1.23e-04
|
SIGNALING BY NTRK2 TRKB
|
24
|
2.15e-01
|
3.78e-01
|
0.22000
|
9.05e-02
|
0.200000
|
4.43e-01
|
8.99e-02
|
HDR THROUGH HOMOLOGOUS RECOMBINATION HRR
|
64
|
6.67e-03
|
3.14e-02
|
0.21900
|
-2.09e-01
|
-0.066200
|
3.80e-03
|
3.60e-01
|
HYALURONAN METABOLISM
|
15
|
5.17e-01
|
6.72e-01
|
0.21900
|
1.48e-01
|
0.162000
|
3.20e-01
|
2.78e-01
|
COSTIMULATION BY THE CD28 FAMILY
|
50
|
6.70e-02
|
1.70e-01
|
0.21900
|
1.11e-01
|
0.189000
|
1.76e-01
|
2.06e-02
|
CELL EXTRACELLULAR MATRIX INTERACTIONS
|
18
|
4.57e-01
|
6.20e-01
|
0.21900
|
1.54e-01
|
0.156000
|
2.59e-01
|
2.53e-01
|
HOST INTERACTIONS OF HIV FACTORS
|
125
|
4.47e-03
|
2.37e-02
|
0.21900
|
1.58e-01
|
0.151000
|
2.24e-03
|
3.57e-03
|
HOMOLOGOUS DNA PAIRING AND STRAND EXCHANGE
|
41
|
1.42e-02
|
5.55e-02
|
0.21900
|
-2.17e-01
|
-0.028400
|
1.63e-02
|
7.53e-01
|
TICAM1 DEPENDENT ACTIVATION OF IRF3 IRF7
|
12
|
4.00e-01
|
5.64e-01
|
0.21800
|
6.75e-02
|
0.207000
|
6.86e-01
|
2.14e-01
|
TNF RECEPTOR SUPERFAMILY TNFSF MEMBERS MEDIATING NON CANONICAL NF KB PATHWAY
|
12
|
8.63e-02
|
2.05e-01
|
0.21800
|
-1.53e-01
|
0.155000
|
3.60e-01
|
3.52e-01
|
METABOLISM OF STEROIDS
|
116
|
6.53e-03
|
3.10e-02
|
0.21700
|
1.40e-01
|
0.165000
|
9.06e-03
|
2.15e-03
|
MYD88 INDEPENDENT TLR4 CASCADE
|
93
|
1.09e-02
|
4.61e-02
|
0.21700
|
1.20e-01
|
0.180000
|
4.61e-02
|
2.66e-03
|
TRANSLATION OF SARS COV 2 STRUCTURAL PROTEINS
|
44
|
1.54e-01
|
3.04e-01
|
0.21600
|
1.57e-01
|
0.149000
|
7.24e-02
|
8.65e-02
|
SIGNALING BY BMP
|
25
|
1.45e-01
|
2.94e-01
|
0.21600
|
6.35e-02
|
0.207000
|
5.82e-01
|
7.37e-02
|
HEDGEHOG ON STATE
|
82
|
1.88e-02
|
6.82e-02
|
0.21600
|
1.80e-01
|
0.119000
|
4.83e-03
|
6.29e-02
|
PI 3K CASCADE FGFR2
|
17
|
1.91e-01
|
3.53e-01
|
0.21600
|
-2.13e-01
|
-0.032800
|
1.28e-01
|
8.15e-01
|
STAT5 ACTIVATION DOWNSTREAM OF FLT3 ITD MUTANTS
|
10
|
3.79e-01
|
5.42e-01
|
0.21600
|
-2.13e-01
|
-0.033100
|
2.44e-01
|
8.56e-01
|
SLC TRANSPORTER DISORDERS
|
75
|
8.76e-04
|
7.70e-03
|
0.21600
|
3.73e-02
|
0.212000
|
5.77e-01
|
1.49e-03
|
REDUCTION OF CYTOSOLIC CA LEVELS
|
12
|
9.66e-02
|
2.21e-01
|
0.21500
|
-1.77e-01
|
0.122000
|
2.88e-01
|
4.63e-01
|
G ALPHA I SIGNALLING EVENTS
|
204
|
2.13e-04
|
2.64e-03
|
0.21500
|
1.54e-01
|
0.149000
|
1.47e-04
|
2.38e-04
|
REGULATION OF GLYCOLYSIS BY FRUCTOSE 2 6 BISPHOSPHATE METABOLISM
|
11
|
6.29e-01
|
7.52e-01
|
0.21400
|
1.60e-01
|
0.143000
|
3.59e-01
|
4.11e-01
|
RND1 GTPASE CYCLE
|
38
|
3.46e-02
|
1.10e-01
|
0.21400
|
4.36e-02
|
0.210000
|
6.42e-01
|
2.52e-02
|
FC EPSILON RECEPTOR FCERI SIGNALING
|
123
|
1.36e-03
|
1.11e-02
|
0.21400
|
1.88e-01
|
0.103000
|
3.19e-04
|
4.93e-02
|
FGFR2 MUTANT RECEPTOR ACTIVATION
|
27
|
2.91e-01
|
4.64e-01
|
0.21400
|
-1.25e-01
|
-0.174000
|
2.62e-01
|
1.18e-01
|
LATE ENDOSOMAL MICROAUTOPHAGY
|
31
|
1.66e-01
|
3.19e-01
|
0.21400
|
1.92e-01
|
0.094000
|
6.38e-02
|
3.65e-01
|
POSITIVE EPIGENETIC REGULATION OF RRNA EXPRESSION
|
65
|
6.52e-02
|
1.67e-01
|
0.21400
|
-1.41e-01
|
-0.161000
|
4.98e-02
|
2.50e-02
|
MEIOTIC RECOMBINATION
|
41
|
9.91e-02
|
2.25e-01
|
0.21300
|
-9.55e-02
|
-0.190000
|
2.90e-01
|
3.49e-02
|
NEUROTRANSMITTER RELEASE CYCLE
|
48
|
5.70e-02
|
1.51e-01
|
0.21300
|
8.87e-02
|
0.194000
|
2.88e-01
|
2.04e-02
|
BMAL1 CLOCK NPAS2 ACTIVATES CIRCADIAN GENE EXPRESSION
|
26
|
7.39e-03
|
3.40e-02
|
0.21200
|
-1.75e-01
|
0.120000
|
1.22e-01
|
2.91e-01
|
ACTIVATION OF BH3 ONLY PROTEINS
|
30
|
1.47e-01
|
2.97e-01
|
0.21200
|
1.97e-01
|
0.080300
|
6.25e-02
|
4.47e-01
|
SHC1 EVENTS IN EGFR SIGNALING
|
11
|
1.20e-01
|
2.59e-01
|
0.21200
|
1.55e-01
|
-0.145000
|
3.75e-01
|
4.06e-01
|
FCERI MEDIATED NF KB ACTIVATION
|
76
|
1.74e-03
|
1.27e-02
|
0.21100
|
2.06e-01
|
0.046400
|
1.90e-03
|
4.84e-01
|
SEMA3A PAK DEPENDENT AXON REPULSION
|
16
|
5.16e-01
|
6.72e-01
|
0.21100
|
1.37e-01
|
0.160000
|
3.41e-01
|
2.67e-01
|
KINESINS
|
47
|
3.58e-02
|
1.12e-01
|
0.21100
|
2.00e-01
|
0.065900
|
1.76e-02
|
4.35e-01
|
SIGNALING BY EGFR
|
47
|
1.40e-01
|
2.87e-01
|
0.21100
|
1.32e-01
|
0.164000
|
1.16e-01
|
5.20e-02
|
RAC3 GTPASE CYCLE
|
90
|
2.83e-03
|
1.75e-02
|
0.21100
|
7.50e-02
|
0.197000
|
2.19e-01
|
1.25e-03
|
SRP DEPENDENT COTRANSLATIONAL PROTEIN TARGETING TO MEMBRANE
|
106
|
1.81e-04
|
2.32e-03
|
0.21000
|
-4.82e-02
|
-0.205000
|
3.92e-01
|
2.74e-04
|
DOWNSTREAM SIGNAL TRANSDUCTION
|
29
|
1.67e-01
|
3.19e-01
|
0.20900
|
7.99e-02
|
0.194000
|
4.57e-01
|
7.12e-02
|
REGULATION OF GENE EXPRESSION IN LATE STAGE BRANCHING MORPHOGENESIS PANCREATIC BUD PRECURSOR CELLS
|
15
|
1.25e-01
|
2.68e-01
|
0.20900
|
-2.06e-01
|
0.034600
|
1.66e-01
|
8.16e-01
|
TRANSPORT OF VITAMINS NUCLEOSIDES AND RELATED MOLECULES
|
33
|
1.02e-01
|
2.30e-01
|
0.20900
|
6.56e-02
|
0.198000
|
5.14e-01
|
4.91e-02
|
NEURONAL SYSTEM
|
370
|
5.28e-07
|
1.88e-05
|
0.20800
|
1.37e-01
|
0.156000
|
6.01e-06
|
2.59e-07
|
ERCC6 CSB AND EHMT2 G9A POSITIVELY REGULATE RRNA EXPRESSION
|
35
|
1.04e-01
|
2.33e-01
|
0.20800
|
-7.25e-02
|
-0.195000
|
4.58e-01
|
4.60e-02
|
MITOTIC G1 PHASE AND G1 S TRANSITION
|
142
|
2.03e-03
|
1.41e-02
|
0.20700
|
1.71e-01
|
0.117000
|
4.35e-04
|
1.64e-02
|
TRIGLYCERIDE METABOLISM
|
24
|
3.46e-01
|
5.15e-01
|
0.20700
|
1.16e-01
|
0.172000
|
3.27e-01
|
1.45e-01
|
EPH EPHRIN SIGNALING
|
92
|
2.62e-02
|
8.80e-02
|
0.20700
|
1.58e-01
|
0.133000
|
8.91e-03
|
2.70e-02
|
G BETA GAMMA SIGNALLING THROUGH CDC42
|
19
|
1.39e-01
|
2.86e-01
|
0.20700
|
2.06e-01
|
0.010400
|
1.20e-01
|
9.38e-01
|
CASPASE ACTIVATION VIA DEATH RECEPTORS IN THE PRESENCE OF LIGAND
|
13
|
5.86e-01
|
7.22e-01
|
0.20600
|
-1.64e-01
|
-0.124000
|
3.06e-01
|
4.37e-01
|
SIGNALING BY SCF KIT
|
41
|
1.62e-01
|
3.14e-01
|
0.20600
|
1.12e-01
|
0.172000
|
2.13e-01
|
5.63e-02
|
CYTOCHROME C MEDIATED APOPTOTIC RESPONSE
|
12
|
6.32e-01
|
7.53e-01
|
0.20500
|
1.44e-01
|
0.146000
|
3.86e-01
|
3.81e-01
|
ABERRANT REGULATION OF MITOTIC EXIT IN CANCER DUE TO RB1 DEFECTS
|
19
|
4.76e-01
|
6.35e-01
|
0.20500
|
1.33e-01
|
0.156000
|
3.17e-01
|
2.38e-01
|
RND3 GTPASE CYCLE
|
38
|
9.88e-02
|
2.25e-01
|
0.20500
|
7.45e-02
|
0.191000
|
4.27e-01
|
4.19e-02
|
REGULATION OF TNFR1 SIGNALING
|
34
|
2.60e-01
|
4.33e-01
|
0.20400
|
1.26e-01
|
0.160000
|
2.03e-01
|
1.06e-01
|
INTERLEUKIN 37 SIGNALING
|
18
|
3.09e-01
|
4.81e-01
|
0.20400
|
6.58e-02
|
0.193000
|
6.29e-01
|
1.56e-01
|
METABOLISM OF PORPHYRINS
|
19
|
2.84e-01
|
4.57e-01
|
0.20400
|
6.36e-02
|
0.194000
|
6.31e-01
|
1.44e-01
|
REGULATION OF RAS BY GAPS
|
66
|
1.58e-02
|
5.93e-02
|
0.20300
|
1.91e-01
|
0.068900
|
7.18e-03
|
3.33e-01
|
FACTORS INVOLVED IN MEGAKARYOCYTE DEVELOPMENT AND PLATELET PRODUCTION
|
119
|
1.17e-02
|
4.80e-02
|
0.20300
|
1.39e-01
|
0.148000
|
8.99e-03
|
5.21e-03
|
PINK1 PRKN MEDIATED MITOPHAGY
|
22
|
2.50e-01
|
4.23e-01
|
0.20300
|
1.91e-01
|
0.067900
|
1.21e-01
|
5.81e-01
|
METABOLISM OF FAT SOLUBLE VITAMINS
|
32
|
2.01e-01
|
3.63e-01
|
0.20200
|
1.80e-01
|
0.092600
|
7.79e-02
|
3.65e-01
|
SHC MEDIATED CASCADE FGFR4
|
13
|
1.07e-01
|
2.39e-01
|
0.20200
|
1.15e-01
|
-0.167000
|
4.74e-01
|
2.98e-01
|
E3 UBIQUITIN LIGASES UBIQUITINATE TARGET PROTEINS
|
51
|
1.40e-01
|
2.88e-01
|
0.20200
|
1.57e-01
|
0.126000
|
5.19e-02
|
1.19e-01
|
RORA ACTIVATES GENE EXPRESSION
|
18
|
5.56e-02
|
1.50e-01
|
0.20100
|
-1.80e-01
|
0.089400
|
1.85e-01
|
5.11e-01
|
CONSTITUTIVE SIGNALING BY AKT1 E17K IN CANCER
|
26
|
3.87e-01
|
5.49e-01
|
0.20100
|
1.41e-01
|
0.143000
|
2.14e-01
|
2.08e-01
|
PROSTACYCLIN SIGNALLING THROUGH PROSTACYCLIN RECEPTOR
|
17
|
6.66e-02
|
1.70e-01
|
0.20100
|
1.80e-01
|
-0.089400
|
2.00e-01
|
5.23e-01
|
FORMATION OF THE BETA CATENIN TCF TRANSACTIVATING COMPLEX
|
49
|
2.31e-02
|
8.01e-02
|
0.20000
|
-4.13e-02
|
-0.196000
|
6.17e-01
|
1.76e-02
|
HDR THROUGH SINGLE STRAND ANNEALING SSA
|
37
|
5.98e-02
|
1.57e-01
|
0.20000
|
-1.96e-01
|
-0.042600
|
3.94e-02
|
6.54e-01
|
TRNA PROCESSING IN THE NUCLEUS
|
56
|
4.89e-02
|
1.37e-01
|
0.20000
|
8.08e-02
|
0.183000
|
2.96e-01
|
1.79e-02
|
CD209 DC SIGN SIGNALING
|
18
|
5.16e-01
|
6.72e-01
|
0.20000
|
1.31e-01
|
0.151000
|
3.35e-01
|
2.69e-01
|
GPCR LIGAND BINDING
|
268
|
3.26e-06
|
9.15e-05
|
0.20000
|
1.76e-01
|
0.093400
|
6.95e-07
|
8.56e-03
|
ABC FAMILY PROTEINS MEDIATED TRANSPORT
|
94
|
1.73e-02
|
6.40e-02
|
0.19900
|
1.70e-01
|
0.104000
|
4.43e-03
|
8.07e-02
|
DISORDERS OF TRANSMEMBRANE TRANSPORTERS
|
144
|
5.31e-03
|
2.67e-02
|
0.19900
|
1.30e-01
|
0.151000
|
7.08e-03
|
1.83e-03
|
ROLE OF LAT2 NTAL LAB ON CALCIUM MOBILIZATION
|
14
|
2.90e-01
|
4.64e-01
|
0.19900
|
2.19e-02
|
0.198000
|
8.87e-01
|
2.01e-01
|
MISMATCH REPAIR
|
15
|
2.08e-01
|
3.70e-01
|
0.19900
|
-2.63e-03
|
0.199000
|
9.86e-01
|
1.83e-01
|
SLC MEDIATED TRANSMEMBRANE TRANSPORT
|
191
|
7.29e-05
|
1.14e-03
|
0.19900
|
8.61e-02
|
0.179000
|
4.04e-02
|
2.06e-05
|
DEGRADATION OF GLI1 BY THE PROTEASOME
|
57
|
8.80e-03
|
3.88e-02
|
0.19900
|
1.96e-01
|
0.029200
|
1.04e-02
|
7.03e-01
|
LGI ADAM INTERACTIONS
|
14
|
1.66e-01
|
3.19e-01
|
0.19800
|
3.86e-02
|
-0.195000
|
8.03e-01
|
2.07e-01
|
DSCAM INTERACTIONS
|
11
|
2.06e-01
|
3.68e-01
|
0.19800
|
-1.87e-01
|
0.065300
|
2.83e-01
|
7.08e-01
|
NEGATIVE REGULATION OF THE PI3K AKT NETWORK
|
97
|
3.82e-03
|
2.16e-02
|
0.19800
|
7.02e-02
|
0.185000
|
2.32e-01
|
1.68e-03
|
HDR THROUGH MMEJ ALT NHEJ
|
10
|
2.22e-01
|
3.88e-01
|
0.19700
|
-8.04e-02
|
0.180000
|
6.60e-01
|
3.24e-01
|
NETRIN 1 SIGNALING
|
50
|
1.25e-02
|
5.04e-02
|
0.19600
|
1.92e-02
|
0.196000
|
8.15e-01
|
1.68e-02
|
THROMBOXANE SIGNALLING THROUGH TP RECEPTOR
|
23
|
9.35e-02
|
2.17e-01
|
0.19600
|
1.96e-01
|
-0.004560
|
1.04e-01
|
9.70e-01
|
METAL ION SLC TRANSPORTERS
|
25
|
2.53e-01
|
4.27e-01
|
0.19600
|
1.82e-01
|
0.072600
|
1.16e-01
|
5.30e-01
|
NEGATIVE REGULATION OF NOTCH4 SIGNALING
|
54
|
4.09e-03
|
2.23e-02
|
0.19500
|
1.95e-01
|
-0.004050
|
1.31e-02
|
9.59e-01
|
STRIATED MUSCLE CONTRACTION
|
26
|
1.97e-01
|
3.61e-01
|
0.19500
|
-1.86e-01
|
-0.058000
|
1.00e-01
|
6.09e-01
|
TNFR1 INDUCED NFKAPPAB SIGNALING PATHWAY
|
29
|
3.39e-01
|
5.11e-01
|
0.19500
|
1.16e-01
|
0.157000
|
2.79e-01
|
1.44e-01
|
APC C MEDIATED DEGRADATION OF CELL CYCLE PROTEINS
|
81
|
3.09e-03
|
1.85e-02
|
0.19500
|
1.90e-01
|
0.042000
|
3.11e-03
|
5.13e-01
|
CILIUM ASSEMBLY
|
192
|
4.75e-05
|
8.22e-04
|
0.19500
|
1.79e-01
|
0.076100
|
1.92e-05
|
6.95e-02
|
REGULATION OF BACH1 ACTIVITY
|
11
|
6.79e-01
|
7.88e-01
|
0.19500
|
1.26e-01
|
0.148000
|
4.69e-01
|
3.95e-01
|
SIGNAL REGULATORY PROTEIN FAMILY INTERACTIONS
|
11
|
3.72e-01
|
5.36e-01
|
0.19400
|
1.30e-02
|
0.194000
|
9.41e-01
|
2.66e-01
|
STABILIZATION OF P53
|
54
|
3.94e-03
|
2.18e-02
|
0.19400
|
1.94e-01
|
-0.006590
|
1.36e-02
|
9.33e-01
|
TRANSPORT OF BILE SALTS AND ORGANIC ACIDS METAL IONS AND AMINE COMPOUNDS
|
67
|
7.60e-02
|
1.89e-01
|
0.19400
|
1.60e-01
|
0.109000
|
2.33e-02
|
1.22e-01
|
EUKARYOTIC TRANSLATION INITIATION
|
114
|
6.31e-04
|
6.14e-03
|
0.19400
|
-5.17e-02
|
-0.187000
|
3.40e-01
|
5.79e-04
|
ASSEMBLY OF COLLAGEN FIBRILS AND OTHER MULTIMERIC STRUCTURES
|
52
|
1.30e-01
|
2.73e-01
|
0.19400
|
-1.06e-01
|
-0.162000
|
1.86e-01
|
4.33e-02
|
METHYLATION
|
11
|
4.49e-01
|
6.14e-01
|
0.19300
|
1.90e-01
|
0.038200
|
2.76e-01
|
8.26e-01
|
ACTIVATION OF ANTERIOR HOX GENES IN HINDBRAIN DEVELOPMENT DURING EARLY EMBRYOGENESIS
|
68
|
1.01e-01
|
2.28e-01
|
0.19300
|
-1.35e-01
|
-0.138000
|
5.38e-02
|
4.95e-02
|
ACTIVATION OF THE PRE REPLICATIVE COMPLEX
|
30
|
3.03e-01
|
4.75e-01
|
0.19300
|
1.02e-01
|
0.163000
|
3.31e-01
|
1.22e-01
|
INTERFERON SIGNALING
|
161
|
3.33e-09
|
2.45e-07
|
0.19200
|
-1.88e-01
|
0.040300
|
3.89e-05
|
3.78e-01
|
EFFECTS OF PIP2 HYDROLYSIS
|
27
|
3.23e-02
|
1.04e-01
|
0.19200
|
-4.90e-02
|
0.186000
|
6.60e-01
|
9.46e-02
|
MITOCHONDRIAL FATTY ACID BETA OXIDATION
|
34
|
1.59e-01
|
3.10e-01
|
0.19100
|
1.79e-01
|
0.067900
|
7.10e-02
|
4.93e-01
|
SIGNALING BY FLT3 FUSION PROTEINS
|
19
|
4.58e-01
|
6.20e-01
|
0.19100
|
-1.65e-01
|
-0.096800
|
2.13e-01
|
4.65e-01
|
SENSORY PERCEPTION
|
158
|
2.87e-03
|
1.77e-02
|
0.19100
|
-1.08e-01
|
-0.158000
|
1.91e-02
|
6.31e-04
|
RHOBTB GTPASE CYCLE
|
35
|
3.09e-01
|
4.81e-01
|
0.19000
|
1.24e-01
|
0.145000
|
2.04e-01
|
1.39e-01
|
ANCHORING FIBRIL FORMATION
|
14
|
5.54e-01
|
7.02e-01
|
0.19000
|
-1.66e-01
|
-0.091500
|
2.81e-01
|
5.53e-01
|
INHIBITION OF THE PROTEOLYTIC ACTIVITY OF APC C REQUIRED FOR THE ONSET OF ANAPHASE BY MITOTIC SPINDLE CHECKPOINT COMPONENTS
|
19
|
4.89e-01
|
6.49e-01
|
0.18900
|
1.58e-01
|
0.104000
|
2.32e-01
|
4.34e-01
|
RNA POLYMERASE I PROMOTER ESCAPE
|
50
|
1.13e-01
|
2.48e-01
|
0.18900
|
-8.73e-02
|
-0.168000
|
2.85e-01
|
3.98e-02
|
HEME SIGNALING
|
46
|
1.81e-02
|
6.65e-02
|
0.18900
|
-1.89e-01
|
-0.009410
|
2.65e-02
|
9.12e-01
|
SIGNALING BY GPCR
|
483
|
1.81e-07
|
7.89e-06
|
0.18900
|
1.25e-01
|
0.142000
|
2.72e-06
|
9.39e-08
|
RHO GTPASES ACTIVATE KTN1
|
11
|
5.23e-01
|
6.77e-01
|
0.18900
|
5.61e-02
|
0.181000
|
7.47e-01
|
3.00e-01
|
TOLL LIKE RECEPTOR 9 TLR9 CASCADE
|
91
|
3.44e-03
|
1.99e-02
|
0.18900
|
4.94e-02
|
0.183000
|
4.16e-01
|
2.62e-03
|
SIGNALING BY FGFR4
|
34
|
2.47e-01
|
4.19e-01
|
0.18900
|
1.65e-01
|
0.092900
|
9.67e-02
|
3.49e-01
|
TERMINATION OF TRANSLESION DNA SYNTHESIS
|
32
|
2.48e-01
|
4.19e-01
|
0.18900
|
-1.68e-01
|
-0.086600
|
1.00e-01
|
3.97e-01
|
PHASE I FUNCTIONALIZATION OF COMPOUNDS
|
59
|
1.50e-01
|
2.99e-01
|
0.18800
|
1.32e-01
|
0.135000
|
8.06e-02
|
7.35e-02
|
NF KB IS ACTIVATED AND SIGNALS SURVIVAL
|
12
|
4.97e-01
|
6.56e-01
|
0.18800
|
-5.59e-02
|
-0.180000
|
7.37e-01
|
2.81e-01
|
PYRIMIDINE SALVAGE
|
10
|
7.18e-01
|
8.13e-01
|
0.18800
|
1.21e-01
|
0.144000
|
5.09e-01
|
4.29e-01
|
CRMPS IN SEMA3A SIGNALING
|
16
|
3.97e-01
|
5.62e-01
|
0.18800
|
-1.79e-01
|
-0.056300
|
2.15e-01
|
6.97e-01
|
SUMOYLATION OF UBIQUITINYLATION PROTEINS
|
37
|
1.20e-02
|
4.90e-02
|
0.18800
|
-4.50e-02
|
0.182000
|
6.36e-01
|
5.52e-02
|
CYCLIN D ASSOCIATED EVENTS IN G1
|
45
|
2.14e-01
|
3.77e-01
|
0.18700
|
1.11e-01
|
0.150000
|
1.96e-01
|
8.09e-02
|
PHASE II CONJUGATION OF COMPOUNDS
|
64
|
1.30e-01
|
2.73e-01
|
0.18700
|
1.38e-01
|
0.126000
|
5.63e-02
|
8.10e-02
|
NOREPINEPHRINE NEUROTRANSMITTER RELEASE CYCLE
|
17
|
5.59e-01
|
7.04e-01
|
0.18700
|
1.50e-01
|
0.111000
|
2.84e-01
|
4.28e-01
|
BIOLOGICAL OXIDATIONS
|
126
|
1.91e-02
|
6.89e-02
|
0.18600
|
1.35e-01
|
0.129000
|
9.01e-03
|
1.26e-02
|
CIRCADIAN CLOCK
|
68
|
7.77e-04
|
7.11e-03
|
0.18600
|
-2.42e-02
|
0.185000
|
7.30e-01
|
8.48e-03
|
FREE FATTY ACIDS REGULATE INSULIN SECRETION
|
10
|
5.57e-01
|
7.04e-01
|
0.18600
|
5.20e-02
|
0.178000
|
7.76e-01
|
3.29e-01
|
SCF SKP2 MEDIATED DEGRADATION OF P27 P21
|
59
|
2.92e-03
|
1.77e-02
|
0.18600
|
1.85e-01
|
-0.014600
|
1.39e-02
|
8.46e-01
|
RAC1 GTPASE CYCLE
|
177
|
4.44e-07
|
1.63e-05
|
0.18600
|
1.03e-02
|
0.185000
|
8.14e-01
|
2.13e-05
|
BASIGIN INTERACTIONS
|
22
|
2.61e-01
|
4.33e-01
|
0.18500
|
4.56e-02
|
0.179000
|
7.11e-01
|
1.46e-01
|
NEGATIVE REGULATION OF FGFR1 SIGNALING
|
27
|
4.34e-01
|
5.97e-01
|
0.18400
|
1.26e-01
|
0.134000
|
2.56e-01
|
2.27e-01
|
TRAF6 MEDIATED IRF7 ACTIVATION
|
15
|
1.17e-01
|
2.55e-01
|
0.18400
|
-1.50e-01
|
0.107000
|
3.14e-01
|
4.75e-01
|
REGULATION OF RUNX3 EXPRESSION AND ACTIVITY
|
53
|
5.76e-03
|
2.83e-02
|
0.18400
|
1.83e-01
|
-0.014800
|
2.09e-02
|
8.52e-01
|
METABOLISM OF VITAMINS AND COFACTORS
|
151
|
9.38e-03
|
4.07e-02
|
0.18400
|
1.20e-01
|
0.139000
|
1.08e-02
|
3.28e-03
|
APC C CDH1 MEDIATED DEGRADATION OF CDC20 AND OTHER APC C CDH1 TARGETED PROTEINS IN LATE MITOSIS EARLY G1
|
70
|
4.64e-03
|
2.44e-02
|
0.18300
|
1.82e-01
|
0.017000
|
8.32e-03
|
8.06e-01
|
PEXOPHAGY
|
11
|
7.16e-01
|
8.12e-01
|
0.18300
|
1.26e-01
|
0.133000
|
4.71e-01
|
4.46e-01
|
ROLE OF SECOND MESSENGERS IN NETRIN 1 SIGNALING
|
10
|
3.38e-01
|
5.10e-01
|
0.18300
|
-3.54e-02
|
0.179000
|
8.46e-01
|
3.26e-01
|
EGR2 AND SOX10 MEDIATED INITIATION OF SCHWANN CELL MYELINATION
|
27
|
4.16e-01
|
5.80e-01
|
0.18300
|
1.10e-01
|
0.146000
|
3.24e-01
|
1.89e-01
|
SYNTHESIS OF IP2 IP AND INS IN THE CYTOSOL
|
13
|
2.34e-01
|
4.04e-01
|
0.18200
|
-4.16e-02
|
0.177000
|
7.95e-01
|
2.68e-01
|
ESTROGEN DEPENDENT GENE EXPRESSION
|
107
|
4.04e-02
|
1.22e-01
|
0.18200
|
-1.27e-01
|
-0.131000
|
2.38e-02
|
1.92e-02
|
G ALPHA 12 13 SIGNALLING EVENTS
|
75
|
5.61e-03
|
2.79e-02
|
0.18200
|
2.80e-02
|
0.180000
|
6.75e-01
|
7.06e-03
|
TRAFFICKING OF GLUR2 CONTAINING AMPA RECEPTORS
|
17
|
5.91e-01
|
7.26e-01
|
0.18200
|
1.39e-01
|
0.117000
|
3.20e-01
|
4.03e-01
|
REGULATION OF TP53 ACTIVITY THROUGH ACETYLATION
|
30
|
1.36e-01
|
2.82e-01
|
0.18200
|
3.23e-02
|
0.179000
|
7.60e-01
|
8.97e-02
|
TRANSPORT OF SMALL MOLECULES
|
582
|
1.10e-08
|
6.79e-07
|
0.18100
|
1.07e-01
|
0.147000
|
1.08e-05
|
1.72e-09
|
RHO GTPASE CYCLE
|
422
|
1.06e-11
|
1.78e-09
|
0.18100
|
4.06e-02
|
0.177000
|
1.54e-01
|
5.27e-10
|
ASSEMBLY OF THE HIV VIRION
|
16
|
3.70e-01
|
5.36e-01
|
0.18100
|
1.77e-01
|
0.038700
|
2.21e-01
|
7.88e-01
|
DNA STRAND ELONGATION
|
32
|
1.28e-01
|
2.72e-01
|
0.18100
|
3.49e-02
|
0.178000
|
7.33e-01
|
8.23e-02
|
COLLAGEN DEGRADATION
|
52
|
7.00e-02
|
1.76e-01
|
0.18000
|
-5.73e-02
|
-0.171000
|
4.75e-01
|
3.33e-02
|
GROWTH HORMONE RECEPTOR SIGNALING
|
20
|
4.97e-01
|
6.56e-01
|
0.18000
|
1.53e-01
|
0.095400
|
2.37e-01
|
4.60e-01
|
INNATE IMMUNE SYSTEM
|
779
|
2.16e-10
|
2.54e-08
|
0.18000
|
1.35e-01
|
0.119000
|
1.65e-10
|
1.94e-08
|
SIGNALING BY PDGFRA TRANSMEMBRANE JUXTAMEMBRANE AND KINASE DOMAIN MUTANTS
|
12
|
7.05e-01
|
8.06e-01
|
0.17900
|
1.28e-01
|
0.125000
|
4.43e-01
|
4.52e-01
|
FRS MEDIATED FGFR3 SIGNALING
|
15
|
5.56e-01
|
7.02e-01
|
0.17900
|
1.59e-01
|
0.081800
|
2.86e-01
|
5.83e-01
|
CELL CELL COMMUNICATION
|
106
|
4.92e-03
|
2.53e-02
|
0.17900
|
5.73e-02
|
0.169000
|
3.08e-01
|
2.59e-03
|
L1CAM INTERACTIONS
|
108
|
2.99e-02
|
9.73e-02
|
0.17900
|
1.47e-01
|
0.101000
|
8.13e-03
|
6.93e-02
|
INFLUENZA INFECTION
|
145
|
1.47e-02
|
5.70e-02
|
0.17800
|
-1.17e-01
|
-0.134000
|
1.48e-02
|
5.32e-03
|
ADRENALINE NORADRENALINE INHIBITS INSULIN SECRETION
|
27
|
2.62e-01
|
4.33e-01
|
0.17800
|
1.69e-01
|
0.057600
|
1.30e-01
|
6.05e-01
|
GLUTATHIONE CONJUGATION
|
30
|
4.07e-01
|
5.71e-01
|
0.17800
|
1.39e-01
|
0.111000
|
1.89e-01
|
2.91e-01
|
PCP CE PATHWAY
|
89
|
6.59e-03
|
3.12e-02
|
0.17800
|
1.72e-01
|
0.044000
|
4.98e-03
|
4.73e-01
|
CLASS A 1 RHODOPSIN LIKE RECEPTORS
|
185
|
3.65e-04
|
4.09e-03
|
0.17700
|
1.63e-01
|
0.070200
|
1.34e-04
|
1.00e-01
|
SIGNALING BY MODERATE KINASE ACTIVITY BRAF MUTANTS
|
41
|
2.71e-01
|
4.44e-01
|
0.17700
|
1.01e-01
|
0.146000
|
2.62e-01
|
1.06e-01
|
GLYCOLYSIS
|
67
|
1.51e-01
|
3.00e-01
|
0.17700
|
1.23e-01
|
0.126000
|
8.12e-02
|
7.36e-02
|
SARS COV INFECTIONS
|
140
|
1.67e-02
|
6.23e-02
|
0.17600
|
1.37e-01
|
0.110000
|
5.02e-03
|
2.42e-02
|
SIGNALING BY FGFR2 IN DISEASE
|
37
|
3.34e-01
|
5.06e-01
|
0.17600
|
-1.09e-01
|
-0.139000
|
2.53e-01
|
1.45e-01
|
PI 3K CASCADE FGFR1
|
16
|
2.08e-01
|
3.70e-01
|
0.17600
|
-1.74e-01
|
0.029500
|
2.29e-01
|
8.38e-01
|
AUF1 HNRNP D0 BINDS AND DESTABILIZES MRNA
|
53
|
3.95e-03
|
2.18e-02
|
0.17600
|
1.71e-01
|
-0.041200
|
3.13e-02
|
6.04e-01
|
SIGNALING BY MET
|
74
|
1.27e-02
|
5.10e-02
|
0.17600
|
3.64e-02
|
0.172000
|
5.89e-01
|
1.06e-02
|
SIGNALING BY THE B CELL RECEPTOR BCR
|
103
|
2.16e-02
|
7.56e-02
|
0.17600
|
1.56e-01
|
0.081100
|
6.34e-03
|
1.55e-01
|
S PHASE
|
154
|
1.40e-02
|
5.53e-02
|
0.17500
|
1.27e-01
|
0.121000
|
6.65e-03
|
9.56e-03
|
HIV INFECTION
|
221
|
2.30e-03
|
1.51e-02
|
0.17500
|
1.28e-01
|
0.119000
|
1.06e-03
|
2.36e-03
|
ABORTIVE ELONGATION OF HIV 1 TRANSCRIPT IN THE ABSENCE OF TAT
|
23
|
2.00e-01
|
3.62e-01
|
0.17500
|
-1.60e-02
|
-0.174000
|
8.94e-01
|
1.49e-01
|
SUMOYLATION OF RNA BINDING PROTEINS
|
45
|
2.32e-02
|
8.05e-02
|
0.17400
|
-7.54e-03
|
0.174000
|
9.30e-01
|
4.32e-02
|
SELENOAMINO ACID METABOLISM
|
108
|
8.95e-03
|
3.91e-02
|
0.17400
|
-6.41e-02
|
-0.162000
|
2.50e-01
|
3.62e-03
|
ADP SIGNALLING THROUGH P2Y PURINOCEPTOR 1
|
24
|
2.92e-01
|
4.65e-01
|
0.17400
|
1.67e-01
|
0.048200
|
1.57e-01
|
6.83e-01
|
FGFR1 LIGAND BINDING AND ACTIVATION
|
10
|
7.31e-01
|
8.23e-01
|
0.17400
|
-1.45e-01
|
-0.096400
|
4.29e-01
|
5.98e-01
|
SIGNALING BY RHO GTPASES MIRO GTPASES AND RHOBTB3
|
628
|
2.05e-11
|
3.02e-09
|
0.17400
|
7.06e-02
|
0.159000
|
2.61e-03
|
1.31e-11
|
DNA REPLICATION PRE INITIATION
|
80
|
5.11e-02
|
1.41e-01
|
0.17400
|
1.55e-01
|
0.078300
|
1.66e-02
|
2.26e-01
|
RNA POLYMERASE III TRANSCRIPTION INITIATION FROM TYPE 3 PROMOTER
|
28
|
2.63e-01
|
4.34e-01
|
0.17300
|
-5.48e-02
|
-0.165000
|
6.16e-01
|
1.32e-01
|
TRANSCRIPTIONAL REGULATION OF GRANULOPOIESIS
|
47
|
4.90e-02
|
1.37e-01
|
0.17300
|
-2.41e-02
|
-0.172000
|
7.75e-01
|
4.17e-02
|
SIGNALING BY NOTCH1 HD DOMAIN MUTANTS IN CANCER
|
15
|
6.52e-01
|
7.69e-01
|
0.17300
|
1.36e-01
|
0.108000
|
3.63e-01
|
4.70e-01
|
TRANSLESION SYNTHESIS BY Y FAMILY DNA POLYMERASES BYPASSES LESIONS ON DNA TEMPLATE
|
39
|
2.25e-01
|
3.91e-01
|
0.17300
|
-1.56e-01
|
-0.074900
|
9.20e-02
|
4.18e-01
|
G1 S DNA DAMAGE CHECKPOINTS
|
65
|
1.96e-03
|
1.37e-02
|
0.17300
|
1.70e-01
|
-0.031600
|
1.78e-02
|
6.60e-01
|
RNA POLYMERASE II TRANSCRIPTION TERMINATION
|
65
|
1.38e-02
|
5.49e-02
|
0.17200
|
-1.93e-02
|
-0.171000
|
7.88e-01
|
1.71e-02
|
ADAPTIVE IMMUNE SYSTEM
|
608
|
9.46e-08
|
4.64e-06
|
0.17200
|
1.31e-01
|
0.112000
|
3.83e-08
|
2.79e-06
|
METABOLISM OF NITRIC OXIDE NOS3 ACTIVATION AND REGULATION
|
15
|
4.70e-01
|
6.30e-01
|
0.17100
|
1.65e-01
|
0.046500
|
2.69e-01
|
7.55e-01
|
COMMON PATHWAY OF FIBRIN CLOT FORMATION
|
11
|
6.09e-01
|
7.40e-01
|
0.17100
|
1.61e-01
|
0.056700
|
3.55e-01
|
7.45e-01
|
TP53 REGULATES TRANSCRIPTION OF CELL CYCLE GENES
|
45
|
2.21e-01
|
3.87e-01
|
0.17000
|
1.49e-01
|
0.082700
|
8.47e-02
|
3.37e-01
|
TIE2 SIGNALING
|
17
|
6.39e-01
|
7.58e-01
|
0.17000
|
1.25e-01
|
0.116000
|
3.73e-01
|
4.10e-01
|
ONCOGENIC MAPK SIGNALING
|
77
|
9.92e-02
|
2.25e-01
|
0.17000
|
9.38e-02
|
0.142000
|
1.55e-01
|
3.16e-02
|
DOWNREGULATION OF SMAD2 3 SMAD4 TRANSCRIPTIONAL ACTIVITY
|
23
|
1.67e-01
|
3.19e-01
|
0.17000
|
-1.70e-01
|
0.004690
|
1.59e-01
|
9.69e-01
|
GENE AND PROTEIN EXPRESSION BY JAK STAT SIGNALING AFTER INTERLEUKIN 12 STIMULATION
|
31
|
4.63e-02
|
1.33e-01
|
0.17000
|
1.64e-01
|
-0.043000
|
1.13e-01
|
6.78e-01
|
EPIGENETIC REGULATION OF GENE EXPRESSION
|
106
|
5.02e-02
|
1.39e-01
|
0.17000
|
-1.37e-01
|
-0.100000
|
1.50e-02
|
7.46e-02
|
CYTOSOLIC IRON SULFUR CLUSTER ASSEMBLY
|
13
|
7.05e-01
|
8.06e-01
|
0.16900
|
-1.31e-01
|
-0.108000
|
4.15e-01
|
5.02e-01
|
FGFR1 MUTANT RECEPTOR ACTIVATION
|
26
|
1.71e-01
|
3.23e-01
|
0.16900
|
1.15e-02
|
0.169000
|
9.19e-01
|
1.36e-01
|
REGULATION OF FZD BY UBIQUITINATION
|
19
|
6.10e-01
|
7.40e-01
|
0.16900
|
1.23e-01
|
0.116000
|
3.55e-01
|
3.80e-01
|
RUNX1 INTERACTS WITH CO FACTORS WHOSE PRECISE EFFECT ON RUNX1 TARGETS IS NOT KNOWN
|
37
|
3.43e-01
|
5.12e-01
|
0.16900
|
-9.58e-02
|
-0.139000
|
3.13e-01
|
1.44e-01
|
LYSOSPHINGOLIPID AND LPA RECEPTORS
|
13
|
2.09e-01
|
3.70e-01
|
0.16900
|
1.34e-01
|
-0.102000
|
4.01e-01
|
5.25e-01
|
DEATH RECEPTOR SIGNALLING
|
132
|
2.91e-03
|
1.77e-02
|
0.16900
|
5.44e-02
|
0.160000
|
2.81e-01
|
1.57e-03
|
MITOCHONDRIAL TRANSLATION
|
93
|
7.33e-05
|
1.14e-03
|
0.16800
|
5.32e-02
|
-0.160000
|
3.76e-01
|
7.76e-03
|
TRANSCRIPTIONAL REGULATION BY MECP2
|
59
|
2.50e-02
|
8.49e-02
|
0.16800
|
-1.67e-01
|
-0.019300
|
2.66e-02
|
7.98e-01
|
HEMOSTASIS
|
478
|
5.22e-06
|
1.43e-04
|
0.16800
|
1.09e-01
|
0.128000
|
4.72e-05
|
1.88e-06
|
AQUAPORIN MEDIATED TRANSPORT
|
41
|
2.59e-01
|
4.32e-01
|
0.16800
|
1.47e-01
|
0.080600
|
1.03e-01
|
3.72e-01
|
COLLAGEN BIOSYNTHESIS AND MODIFYING ENZYMES
|
63
|
6.25e-02
|
1.61e-01
|
0.16700
|
-5.32e-02
|
-0.158000
|
4.65e-01
|
2.97e-02
|
SYNAPTIC ADHESION LIKE MOLECULES
|
21
|
4.73e-01
|
6.32e-01
|
0.16700
|
1.50e-01
|
0.071900
|
2.33e-01
|
5.68e-01
|
LONG TERM POTENTIATION
|
23
|
4.07e-01
|
5.71e-01
|
0.16700
|
6.34e-02
|
0.154000
|
5.99e-01
|
2.01e-01
|
PI 3K CASCADE FGFR3
|
13
|
2.53e-01
|
4.27e-01
|
0.16600
|
-6.38e-02
|
0.154000
|
6.90e-01
|
3.37e-01
|
MYOGENESIS
|
25
|
6.35e-02
|
1.64e-01
|
0.16600
|
-7.57e-02
|
0.148000
|
5.12e-01
|
2.00e-01
|
IRF3 MEDIATED INDUCTION OF TYPE I IFN
|
11
|
3.40e-01
|
5.12e-01
|
0.16600
|
4.82e-02
|
-0.159000
|
7.82e-01
|
3.61e-01
|
TRANSLESION SYNTHESIS BY POLK
|
17
|
6.50e-01
|
7.68e-01
|
0.16600
|
-1.24e-01
|
-0.110000
|
3.76e-01
|
4.32e-01
|
SIGNALING BY BRAF AND RAF FUSIONS
|
60
|
1.74e-01
|
3.27e-01
|
0.16600
|
8.94e-02
|
0.140000
|
2.31e-01
|
6.14e-02
|
NUCLEAR SIGNALING BY ERBB4
|
31
|
4.53e-01
|
6.20e-01
|
0.16600
|
1.27e-01
|
0.107000
|
2.23e-01
|
3.04e-01
|
TRANSCRIPTIONAL REGULATION BY RUNX1
|
182
|
2.37e-03
|
1.53e-02
|
0.16600
|
-7.57e-02
|
-0.147000
|
7.85e-02
|
6.23e-04
|
INTERLEUKIN 12 FAMILY SIGNALING
|
43
|
7.93e-02
|
1.93e-01
|
0.16500
|
1.64e-01
|
0.022100
|
6.29e-02
|
8.02e-01
|
REGULATION OF EXPRESSION OF SLITS AND ROBOS
|
162
|
2.49e-05
|
4.80e-04
|
0.16500
|
-9.50e-03
|
-0.165000
|
8.35e-01
|
2.90e-04
|
CONSTITUTIVE SIGNALING BY OVEREXPRESSED ERBB2
|
11
|
2.76e-01
|
4.50e-01
|
0.16500
|
1.18e-01
|
-0.115000
|
4.99e-01
|
5.07e-01
|
INTERLEUKIN 12 SIGNALING
|
37
|
1.12e-01
|
2.46e-01
|
0.16400
|
1.63e-01
|
0.020200
|
8.59e-02
|
8.31e-01
|
DISEASES OF GLYCOSYLATION
|
123
|
2.97e-02
|
9.68e-02
|
0.16400
|
1.39e-01
|
0.088100
|
8.01e-03
|
9.16e-02
|
DEGRADATION OF BETA CATENIN BY THE DESTRUCTION COMPLEX
|
82
|
1.62e-02
|
6.07e-02
|
0.16400
|
1.60e-01
|
0.036200
|
1.23e-02
|
5.71e-01
|
TOLL LIKE RECEPTOR CASCADES
|
138
|
1.48e-02
|
5.70e-02
|
0.16400
|
8.08e-02
|
0.142000
|
1.01e-01
|
3.91e-03
|
RHO GTPASE EFFECTORS
|
251
|
2.46e-03
|
1.56e-02
|
0.16300
|
1.20e-01
|
0.110000
|
1.07e-03
|
2.67e-03
|
CONVERSION FROM APC C CDC20 TO APC C CDH1 IN LATE ANAPHASE
|
19
|
5.59e-01
|
7.04e-01
|
0.16300
|
1.42e-01
|
0.079700
|
2.84e-01
|
5.47e-01
|
CLASS C 3 METABOTROPIC GLUTAMATE PHEROMONE RECEPTORS
|
11
|
7.54e-01
|
8.38e-01
|
0.16300
|
9.84e-02
|
0.130000
|
5.72e-01
|
4.57e-01
|
DEFECTIVE EXT2 CAUSES EXOSTOSES 2
|
14
|
5.16e-01
|
6.72e-01
|
0.16300
|
1.58e-01
|
0.040400
|
3.08e-01
|
7.93e-01
|
TRNA MODIFICATION IN THE NUCLEUS AND CYTOSOL
|
43
|
3.46e-01
|
5.15e-01
|
0.16200
|
-1.03e-01
|
-0.125000
|
2.41e-01
|
1.55e-01
|
TCR SIGNALING
|
101
|
1.49e-02
|
5.74e-02
|
0.16200
|
1.54e-01
|
0.050800
|
7.60e-03
|
3.78e-01
|
C TYPE LECTIN RECEPTORS CLRS
|
112
|
1.38e-02
|
5.49e-02
|
0.16200
|
1.51e-01
|
0.058000
|
5.78e-03
|
2.89e-01
|
P75 NTR RECEPTOR MEDIATED SIGNALLING
|
93
|
5.08e-03
|
2.59e-02
|
0.16200
|
2.04e-02
|
0.160000
|
7.35e-01
|
7.53e-03
|
ORC1 REMOVAL FROM CHROMATIN
|
67
|
2.38e-02
|
8.18e-02
|
0.16200
|
1.60e-01
|
0.022100
|
2.36e-02
|
7.55e-01
|
MITOCHONDRIAL PROTEIN IMPORT
|
63
|
3.73e-02
|
1.15e-01
|
0.16100
|
1.59e-01
|
0.028800
|
2.93e-02
|
6.93e-01
|
ZINC INFLUX INTO CELLS BY THE SLC39 GENE FAMILY
|
10
|
5.01e-01
|
6.58e-01
|
0.16100
|
1.61e-01
|
-0.002690
|
3.78e-01
|
9.88e-01
|
SIGNALING BY FLT3 ITD AND TKD MUTANTS
|
16
|
6.27e-01
|
7.52e-01
|
0.16000
|
-1.39e-01
|
-0.080200
|
3.36e-01
|
5.78e-01
|
MITOTIC PROMETAPHASE
|
177
|
7.80e-03
|
3.51e-02
|
0.16000
|
8.48e-02
|
0.136000
|
5.18e-02
|
1.85e-03
|
ENOS ACTIVATION
|
11
|
5.77e-01
|
7.20e-01
|
0.16000
|
1.57e-01
|
0.031200
|
3.68e-01
|
8.58e-01
|
SWITCHING OF ORIGINS TO A POST REPLICATIVE STATE
|
86
|
1.31e-02
|
5.28e-02
|
0.16000
|
1.57e-01
|
0.029700
|
1.20e-02
|
6.34e-01
|
CDC42 GTPASE CYCLE
|
153
|
8.88e-06
|
2.13e-04
|
0.15900
|
-2.02e-02
|
0.158000
|
6.66e-01
|
7.77e-04
|
MET PROMOTES CELL MOTILITY
|
39
|
2.85e-02
|
9.40e-02
|
0.15900
|
-5.01e-02
|
0.151000
|
5.88e-01
|
1.04e-01
|
ANTIVIRAL MECHANISM BY IFN STIMULATED GENES
|
73
|
2.36e-03
|
1.53e-02
|
0.15900
|
-3.34e-02
|
0.155000
|
6.21e-01
|
2.21e-02
|
INTERLEUKIN 2 FAMILY SIGNALING
|
32
|
3.57e-02
|
1.12e-01
|
0.15900
|
-8.56e-02
|
0.133000
|
4.02e-01
|
1.92e-01
|
INTERLEUKIN 6 FAMILY SIGNALING
|
20
|
5.83e-01
|
7.21e-01
|
0.15800
|
8.39e-02
|
0.134000
|
5.16e-01
|
2.99e-01
|
ACTIVATION OF GENE EXPRESSION BY SREBF SREBP
|
43
|
3.40e-01
|
5.12e-01
|
0.15800
|
9.03e-02
|
0.129000
|
3.06e-01
|
1.43e-01
|
ANTIGEN PROCESSING UBIQUITINATION PROTEASOME DEGRADATION
|
286
|
1.61e-03
|
1.23e-02
|
0.15700
|
1.18e-01
|
0.104000
|
5.90e-04
|
2.52e-03
|
SIGNALING BY PTK6
|
50
|
3.21e-01
|
4.93e-01
|
0.15700
|
1.04e-01
|
0.118000
|
2.02e-01
|
1.50e-01
|
REGULATION OF INNATE IMMUNE RESPONSES TO CYTOSOLIC DNA
|
13
|
2.86e-01
|
4.59e-01
|
0.15700
|
1.42e-01
|
-0.066300
|
3.74e-01
|
6.79e-01
|
DEGRADATION OF AXIN
|
53
|
6.73e-02
|
1.70e-01
|
0.15700
|
1.55e-01
|
0.024800
|
5.12e-02
|
7.55e-01
|
NICOTINAMIDE SALVAGING
|
14
|
2.35e-01
|
4.05e-01
|
0.15700
|
-9.04e-02
|
0.128000
|
5.58e-01
|
4.07e-01
|
DISEASES OF METABOLISM
|
197
|
1.22e-02
|
4.97e-02
|
0.15600
|
1.19e-01
|
0.101000
|
4.16e-03
|
1.42e-02
|
INTERLEUKIN 1 SIGNALING
|
96
|
7.85e-02
|
1.92e-01
|
0.15600
|
1.33e-01
|
0.081200
|
2.43e-02
|
1.69e-01
|
PHASE 2 PLATEAU PHASE
|
10
|
6.10e-01
|
7.40e-01
|
0.15600
|
-1.54e-01
|
-0.026700
|
4.01e-01
|
8.84e-01
|
CELL CELL JUNCTION ORGANIZATION
|
48
|
3.24e-01
|
4.97e-01
|
0.15500
|
9.28e-02
|
0.124000
|
2.66e-01
|
1.37e-01
|
DEGRADATION OF DVL
|
55
|
1.97e-02
|
7.01e-02
|
0.15500
|
1.54e-01
|
-0.017100
|
4.81e-02
|
8.27e-01
|
REGULATION OF IFNA SIGNALING
|
12
|
2.93e-01
|
4.65e-01
|
0.15500
|
-1.21e-01
|
0.096600
|
4.67e-01
|
5.63e-01
|
SIGNALING BY KIT IN DISEASE
|
20
|
3.84e-01
|
5.45e-01
|
0.15500
|
2.83e-02
|
0.152000
|
8.27e-01
|
2.38e-01
|
APOPTOTIC CLEAVAGE OF CELLULAR PROTEINS
|
34
|
4.69e-01
|
6.30e-01
|
0.15500
|
1.18e-01
|
0.100000
|
2.34e-01
|
3.12e-01
|
RNA POLYMERASE III TRANSCRIPTION
|
41
|
2.77e-01
|
4.50e-01
|
0.15500
|
-6.50e-02
|
-0.140000
|
4.72e-01
|
1.20e-01
|
INITIAL TRIGGERING OF COMPLEMENT
|
12
|
7.68e-01
|
8.46e-01
|
0.15500
|
1.03e-01
|
0.116000
|
5.38e-01
|
4.88e-01
|
SUMOYLATION OF DNA DAMAGE RESPONSE AND REPAIR PROTEINS
|
73
|
6.72e-04
|
6.43e-03
|
0.15400
|
-8.92e-02
|
0.126000
|
1.88e-01
|
6.27e-02
|
M PHASE
|
343
|
6.24e-04
|
6.12e-03
|
0.15400
|
1.16e-01
|
0.102000
|
2.30e-04
|
1.24e-03
|
ALPHA PROTEIN KINASE 1 SIGNALING PATHWAY
|
11
|
7.69e-01
|
8.46e-01
|
0.15300
|
8.75e-02
|
0.126000
|
6.16e-01
|
4.69e-01
|
TP53 REGULATES TRANSCRIPTION OF GENES INVOLVED IN G1 CELL CYCLE ARREST
|
13
|
7.06e-01
|
8.06e-01
|
0.15300
|
-7.65e-02
|
-0.133000
|
6.33e-01
|
4.06e-01
|
CLEC7A DECTIN 1 SIGNALING
|
94
|
2.15e-02
|
7.56e-02
|
0.15300
|
1.48e-01
|
0.040200
|
1.32e-02
|
5.00e-01
|
POLYMERASE SWITCHING ON THE C STRAND OF THE TELOMERE
|
25
|
5.75e-01
|
7.18e-01
|
0.15300
|
9.67e-02
|
0.119000
|
4.03e-01
|
3.04e-01
|
NEGATIVE EPIGENETIC REGULATION OF RRNA EXPRESSION
|
68
|
2.02e-01
|
3.63e-01
|
0.15300
|
-8.81e-02
|
-0.125000
|
2.09e-01
|
7.41e-02
|
REGULATION OF COMMISSURAL AXON PATHFINDING BY SLIT AND ROBO
|
10
|
7.25e-01
|
8.19e-01
|
0.15300
|
6.06e-02
|
0.141000
|
7.40e-01
|
4.41e-01
|
THE NLRP3 INFLAMMASOME
|
15
|
3.47e-01
|
5.15e-01
|
0.15300
|
-1.52e-01
|
0.018800
|
3.09e-01
|
9.00e-01
|
RRNA PROCESSING
|
194
|
1.73e-03
|
1.26e-02
|
0.15300
|
-5.76e-02
|
-0.141000
|
1.67e-01
|
6.87e-04
|
INTRINSIC PATHWAY FOR APOPTOSIS
|
52
|
1.63e-01
|
3.15e-01
|
0.15300
|
1.43e-01
|
0.053100
|
7.41e-02
|
5.08e-01
|
ECM PROTEOGLYCANS
|
68
|
2.33e-01
|
4.03e-01
|
0.15300
|
-1.00e-01
|
-0.115000
|
1.52e-01
|
1.01e-01
|
POST TRANSLATIONAL MODIFICATION SYNTHESIS OF GPI ANCHORED PROTEINS
|
62
|
2.41e-01
|
4.11e-01
|
0.15200
|
1.23e-01
|
0.089600
|
9.31e-02
|
2.23e-01
|
NOTCH3 ACTIVATION AND TRANSMISSION OF SIGNAL TO THE NUCLEUS
|
26
|
5.69e-01
|
7.13e-01
|
0.15200
|
9.80e-02
|
0.117000
|
3.87e-01
|
3.03e-01
|
RHO GTPASES ACTIVATE PKNS
|
50
|
3.86e-02
|
1.18e-01
|
0.15200
|
1.00e-02
|
-0.151000
|
9.02e-01
|
6.39e-02
|
EPH EPHRIN MEDIATED REPULSION OF CELLS
|
51
|
3.43e-01
|
5.13e-01
|
0.15200
|
1.03e-01
|
0.111000
|
2.02e-01
|
1.69e-01
|
MET ACTIVATES PTK2 SIGNALING
|
29
|
1.22e-01
|
2.62e-01
|
0.15200
|
-1.50e-01
|
0.025000
|
1.63e-01
|
8.16e-01
|
NUCLEAR RECEPTOR TRANSCRIPTION PATHWAY
|
44
|
3.20e-01
|
4.92e-01
|
0.15200
|
7.65e-02
|
0.131000
|
3.80e-01
|
1.33e-01
|
PURINE CATABOLISM
|
16
|
6.12e-01
|
7.41e-01
|
0.15100
|
1.38e-01
|
0.061900
|
3.38e-01
|
6.68e-01
|
DNA REPLICATION
|
122
|
3.68e-02
|
1.14e-01
|
0.15100
|
1.33e-01
|
0.071800
|
1.10e-02
|
1.71e-01
|
INTERLEUKIN RECEPTOR SHC SIGNALING
|
20
|
3.16e-01
|
4.87e-01
|
0.15100
|
3.70e-03
|
0.151000
|
9.77e-01
|
2.42e-01
|
CELL DEATH SIGNALLING VIA NRAGE NRIF AND NADE
|
72
|
7.48e-03
|
3.43e-02
|
0.15100
|
-1.73e-02
|
0.150000
|
7.99e-01
|
2.79e-02
|
TRANSCRIPTIONAL REGULATION BY E2F6
|
34
|
4.56e-01
|
6.20e-01
|
0.15100
|
8.53e-02
|
0.124000
|
3.90e-01
|
2.10e-01
|
REPRODUCTION
|
80
|
1.72e-01
|
3.26e-01
|
0.15000
|
-9.05e-02
|
-0.120000
|
1.62e-01
|
6.31e-02
|
INTERLEUKIN 15 SIGNALING
|
12
|
5.79e-01
|
7.21e-01
|
0.15000
|
-1.48e-01
|
-0.026800
|
3.75e-01
|
8.72e-01
|
G BETA GAMMA SIGNALLING THROUGH PI3KGAMMA
|
24
|
1.57e-01
|
3.07e-01
|
0.15000
|
1.45e-01
|
-0.037700
|
2.19e-01
|
7.49e-01
|
IL 6 TYPE CYTOKINE RECEPTOR LIGAND INTERACTIONS
|
14
|
7.07e-01
|
8.06e-01
|
0.15000
|
7.69e-02
|
0.128000
|
6.18e-01
|
4.06e-01
|
ADHERENS JUNCTIONS INTERACTIONS
|
30
|
5.01e-01
|
6.58e-01
|
0.14900
|
8.30e-02
|
0.124000
|
4.32e-01
|
2.40e-01
|
METABOLISM OF AMINO ACIDS AND DERIVATIVES
|
314
|
7.71e-05
|
1.16e-03
|
0.14800
|
1.37e-01
|
0.057000
|
3.22e-05
|
8.29e-02
|
FRS MEDIATED FGFR4 SIGNALING
|
15
|
3.17e-01
|
4.88e-01
|
0.14800
|
1.42e-01
|
-0.040900
|
3.41e-01
|
7.84e-01
|
CELL JUNCTION ORGANIZATION
|
73
|
1.25e-01
|
2.67e-01
|
0.14700
|
6.16e-02
|
0.134000
|
3.63e-01
|
4.79e-02
|
ERYTHROPOIETIN ACTIVATES PHOSPHOINOSITIDE 3 KINASE PI3K
|
11
|
3.62e-01
|
5.28e-01
|
0.14700
|
-9.36e-02
|
0.113000
|
5.91e-01
|
5.15e-01
|
CELLULAR RESPONSE TO HYPOXIA
|
72
|
1.58e-02
|
5.93e-02
|
0.14700
|
1.46e-01
|
-0.003770
|
3.17e-02
|
9.56e-01
|
CELL CYCLE MITOTIC
|
478
|
1.10e-04
|
1.57e-03
|
0.14600
|
1.08e-01
|
0.098700
|
5.42e-05
|
2.26e-04
|
FORMATION OF SENESCENCE ASSOCIATED HETEROCHROMATIN FOCI SAHF
|
13
|
3.67e-01
|
5.33e-01
|
0.14600
|
-1.39e-01
|
0.045900
|
3.87e-01
|
7.75e-01
|
SUMOYLATION OF INTRACELLULAR RECEPTORS
|
27
|
4.60e-01
|
6.20e-01
|
0.14600
|
1.33e-01
|
0.058300
|
2.30e-01
|
6.00e-01
|
RRNA PROCESSING IN THE MITOCHONDRION
|
10
|
8.05e-01
|
8.72e-01
|
0.14600
|
8.22e-02
|
0.120000
|
6.53e-01
|
5.11e-01
|
LAGGING STRAND SYNTHESIS
|
20
|
2.56e-01
|
4.29e-01
|
0.14500
|
-2.69e-02
|
0.143000
|
8.35e-01
|
2.68e-01
|
SIGNALING BY ACTIVIN
|
11
|
6.80e-01
|
7.88e-01
|
0.14500
|
4.22e-02
|
0.139000
|
8.09e-01
|
4.25e-01
|
TRAFFICKING AND PROCESSING OF ENDOSOMAL TLR
|
11
|
7.55e-01
|
8.39e-01
|
0.14500
|
1.29e-01
|
0.067300
|
4.60e-01
|
6.99e-01
|
ACTIVATED NOTCH1 TRANSMITS SIGNAL TO THE NUCLEUS
|
32
|
5.23e-01
|
6.77e-01
|
0.14500
|
1.15e-01
|
0.087300
|
2.59e-01
|
3.93e-01
|
CLASS I MHC MEDIATED ANTIGEN PROCESSING PRESENTATION
|
346
|
1.60e-03
|
1.23e-02
|
0.14400
|
1.04e-01
|
0.100000
|
8.80e-04
|
1.42e-03
|
SIGNALING BY ERBB4
|
57
|
2.67e-01
|
4.39e-01
|
0.14400
|
1.24e-01
|
0.073600
|
1.05e-01
|
3.37e-01
|
ASSEMBLY OF THE PRE REPLICATIVE COMPLEX
|
64
|
7.95e-02
|
1.93e-01
|
0.14400
|
1.41e-01
|
0.030300
|
5.12e-02
|
6.75e-01
|
PHASE 0 RAPID DEPOLARISATION
|
28
|
5.90e-01
|
7.25e-01
|
0.14400
|
-1.00e-01
|
-0.104000
|
3.59e-01
|
3.42e-01
|
FORMATION OF INCISION COMPLEX IN GG NER
|
43
|
3.61e-01
|
5.28e-01
|
0.14400
|
1.25e-01
|
0.071400
|
1.56e-01
|
4.18e-01
|
INWARDLY RECTIFYING K CHANNELS
|
32
|
5.38e-01
|
6.90e-01
|
0.14400
|
1.11e-01
|
0.091400
|
2.78e-01
|
3.71e-01
|
SEMA4D INDUCED CELL MIGRATION AND GROWTH CONE COLLAPSE
|
20
|
6.75e-01
|
7.86e-01
|
0.14300
|
-1.13e-01
|
-0.088800
|
3.83e-01
|
4.92e-01
|
ACETYLCHOLINE REGULATES INSULIN SECRETION
|
10
|
5.30e-01
|
6.83e-01
|
0.14300
|
-2.06e-02
|
0.142000
|
9.10e-01
|
4.38e-01
|
BASE EXCISION REPAIR
|
60
|
1.90e-01
|
3.53e-01
|
0.14300
|
-5.76e-02
|
-0.131000
|
4.41e-01
|
7.93e-02
|
NICOTINATE METABOLISM
|
23
|
4.70e-01
|
6.30e-01
|
0.14300
|
4.44e-02
|
0.136000
|
7.12e-01
|
2.59e-01
|
SNRNP ASSEMBLY
|
51
|
1.03e-01
|
2.31e-01
|
0.14300
|
1.81e-02
|
0.142000
|
8.23e-01
|
7.96e-02
|
INTRACELLULAR SIGNALING BY SECOND MESSENGERS
|
284
|
4.44e-03
|
2.36e-02
|
0.14300
|
8.96e-02
|
0.111000
|
9.50e-03
|
1.25e-03
|
RAS PROCESSING
|
24
|
4.87e-01
|
6.47e-01
|
0.14300
|
1.33e-01
|
0.051500
|
2.58e-01
|
6.63e-01
|
ZINC TRANSPORTERS
|
16
|
5.90e-01
|
7.25e-01
|
0.14300
|
1.36e-01
|
0.043800
|
3.46e-01
|
7.62e-01
|
SIGNALING BY RECEPTOR TYROSINE KINASES
|
462
|
1.23e-04
|
1.69e-03
|
0.14300
|
8.46e-02
|
0.115000
|
1.87e-03
|
2.49e-05
|
DNA DAMAGE RECOGNITION IN GG NER
|
38
|
4.45e-01
|
6.09e-01
|
0.14300
|
1.19e-01
|
0.077900
|
2.03e-01
|
4.06e-01
|
SIGNALING BY EGFR IN CANCER
|
22
|
2.60e-01
|
4.33e-01
|
0.14200
|
1.74e-02
|
-0.141000
|
8.88e-01
|
2.51e-01
|
ATF4 ACTIVATES GENES IN RESPONSE TO ENDOPLASMIC RETICULUM STRESS
|
23
|
6.16e-01
|
7.42e-01
|
0.14200
|
-7.85e-02
|
-0.119000
|
5.15e-01
|
3.25e-01
|
PEPTIDE LIGAND BINDING RECEPTORS
|
110
|
5.45e-03
|
2.73e-02
|
0.14200
|
1.42e-01
|
0.010000
|
1.04e-02
|
8.56e-01
|
INTERLEUKIN 20 FAMILY SIGNALING
|
14
|
3.74e-01
|
5.39e-01
|
0.14200
|
-1.37e-01
|
0.038300
|
3.76e-01
|
8.04e-01
|
DECTIN 1 MEDIATED NONCANONICAL NF KB SIGNALING
|
59
|
5.09e-02
|
1.41e-01
|
0.14200
|
1.42e-01
|
0.003620
|
5.99e-02
|
9.62e-01
|
NOD1 2 SIGNALING PATHWAY
|
35
|
2.14e-01
|
3.78e-01
|
0.14100
|
1.68e-02
|
0.140000
|
8.64e-01
|
1.51e-01
|
PI3K EVENTS IN ERBB2 SIGNALING
|
15
|
3.14e-01
|
4.84e-01
|
0.14100
|
-1.28e-01
|
0.059000
|
3.91e-01
|
6.92e-01
|
DEPOSITION OF NEW CENPA CONTAINING NUCLEOSOMES AT THE CENTROMERE
|
40
|
3.01e-01
|
4.74e-01
|
0.14100
|
-4.79e-02
|
-0.132000
|
6.00e-01
|
1.48e-01
|
NEGATIVE REGULATORS OF DDX58 IFIH1 SIGNALING
|
33
|
3.31e-01
|
5.03e-01
|
0.14000
|
3.89e-02
|
0.135000
|
6.99e-01
|
1.80e-01
|
ADORA2B MEDIATED ANTI INFLAMMATORY CYTOKINES PRODUCTION
|
94
|
6.17e-02
|
1.60e-01
|
0.14000
|
1.32e-01
|
0.047600
|
2.75e-02
|
4.26e-01
|
CHAPERONE MEDIATED AUTOPHAGY
|
20
|
3.51e-01
|
5.18e-01
|
0.14000
|
1.40e-01
|
-0.002840
|
2.79e-01
|
9.82e-01
|
POLO LIKE KINASE MEDIATED EVENTS
|
14
|
4.68e-01
|
6.30e-01
|
0.14000
|
1.40e-01
|
-0.006720
|
3.65e-01
|
9.65e-01
|
CELLULAR RESPONSE TO STARVATION
|
146
|
3.62e-03
|
2.07e-02
|
0.14000
|
-2.58e-02
|
-0.137000
|
5.91e-01
|
4.24e-03
|
TOLL LIKE RECEPTOR TLR1 TLR2 CASCADE
|
94
|
7.73e-02
|
1.91e-01
|
0.14000
|
5.33e-02
|
0.129000
|
3.72e-01
|
3.09e-02
|
FOXO MEDIATED TRANSCRIPTION OF OXIDATIVE STRESS METABOLIC AND NEURONAL GENES
|
24
|
5.81e-01
|
7.21e-01
|
0.13900
|
-1.22e-01
|
-0.067500
|
3.01e-01
|
5.67e-01
|
PLASMA LIPOPROTEIN REMODELING
|
14
|
4.92e-01
|
6.52e-01
|
0.13900
|
-9.00e-05
|
0.139000
|
1.00e+00
|
3.67e-01
|
SIGNALING BY FGFR1 IN DISEASE
|
33
|
2.78e-01
|
4.50e-01
|
0.13900
|
2.42e-02
|
0.136000
|
8.10e-01
|
1.75e-01
|
NF KB ACTIVATION THROUGH FADD RIP 1 PATHWAY MEDIATED BY CASPASE 8 AND 10
|
11
|
6.01e-01
|
7.34e-01
|
0.13900
|
-1.38e-01
|
-0.007900
|
4.27e-01
|
9.64e-01
|
O LINKED GLYCOSYLATION
|
85
|
1.89e-01
|
3.51e-01
|
0.13900
|
7.80e-02
|
0.115000
|
2.14e-01
|
6.81e-02
|
TICAM1 RIP1 MEDIATED IKK COMPLEX RECRUITMENT
|
18
|
6.34e-01
|
7.56e-01
|
0.13900
|
1.26e-01
|
0.057700
|
3.55e-01
|
6.72e-01
|
OTHER SEMAPHORIN INTERACTIONS
|
19
|
5.76e-01
|
7.18e-01
|
0.13800
|
-1.30e-01
|
-0.047100
|
3.26e-01
|
7.22e-01
|
SHC1 EVENTS IN ERBB4 SIGNALING
|
13
|
6.40e-01
|
7.59e-01
|
0.13700
|
1.33e-01
|
0.032600
|
4.05e-01
|
8.39e-01
|
MICRORNA MIRNA BIOGENESIS
|
24
|
6.14e-01
|
7.41e-01
|
0.13700
|
-7.20e-02
|
-0.116000
|
5.41e-01
|
3.23e-01
|
IONOTROPIC ACTIVITY OF KAINATE RECEPTORS
|
10
|
7.07e-01
|
8.06e-01
|
0.13700
|
1.33e-01
|
0.031300
|
4.66e-01
|
8.64e-01
|
SHC MEDIATED CASCADE FGFR3
|
13
|
4.57e-01
|
6.20e-01
|
0.13700
|
1.35e-01
|
-0.025000
|
4.01e-01
|
8.76e-01
|
HOMOLOGY DIRECTED REPAIR
|
111
|
4.42e-02
|
1.29e-01
|
0.13700
|
-1.28e-01
|
-0.046900
|
1.95e-02
|
3.93e-01
|
INTERLEUKIN 1 FAMILY SIGNALING
|
123
|
1.07e-01
|
2.38e-01
|
0.13700
|
1.10e-01
|
0.081700
|
3.58e-02
|
1.18e-01
|
PROTEIN PROTEIN INTERACTIONS AT SYNAPSES
|
85
|
1.46e-01
|
2.95e-01
|
0.13700
|
6.29e-02
|
0.121000
|
3.16e-01
|
5.33e-02
|
GLUCAGON TYPE LIGAND RECEPTORS
|
26
|
1.84e-01
|
3.44e-01
|
0.13600
|
3.79e-02
|
-0.131000
|
7.38e-01
|
2.48e-01
|
RHOH GTPASE CYCLE
|
37
|
5.35e-01
|
6.88e-01
|
0.13600
|
1.02e-01
|
0.090000
|
2.85e-01
|
3.44e-01
|
METABOLISM OF FOLATE AND PTERINES
|
15
|
7.38e-01
|
8.28e-01
|
0.13500
|
1.16e-01
|
0.069600
|
4.37e-01
|
6.41e-01
|
MITOTIC PROPHASE
|
97
|
1.99e-01
|
3.62e-01
|
0.13500
|
9.10e-02
|
0.099900
|
1.21e-01
|
8.92e-02
|
PLASMA LIPOPROTEIN ASSEMBLY
|
12
|
7.58e-01
|
8.41e-01
|
0.13500
|
5.90e-02
|
0.121000
|
7.24e-01
|
4.67e-01
|
CROSSLINKING OF COLLAGEN FIBRILS
|
15
|
6.26e-01
|
7.52e-01
|
0.13400
|
-3.58e-02
|
-0.129000
|
8.10e-01
|
3.85e-01
|
NOTCH3 INTRACELLULAR DOMAIN REGULATES TRANSCRIPTION
|
23
|
1.82e-01
|
3.40e-01
|
0.13400
|
-1.13e-01
|
0.071500
|
3.48e-01
|
5.53e-01
|
ION TRANSPORT BY P TYPE ATPASES
|
50
|
9.69e-02
|
2.21e-01
|
0.13300
|
-1.09e-03
|
0.133000
|
9.89e-01
|
1.03e-01
|
CRISTAE FORMATION
|
31
|
1.09e-01
|
2.41e-01
|
0.13300
|
6.37e-02
|
-0.117000
|
5.39e-01
|
2.60e-01
|
DETOXIFICATION OF REACTIVE OXYGEN SPECIES
|
32
|
1.61e-01
|
3.12e-01
|
0.13300
|
2.49e-02
|
-0.131000
|
8.08e-01
|
2.01e-01
|
ASYMMETRIC LOCALIZATION OF PCP PROTEINS
|
62
|
9.11e-02
|
2.13e-01
|
0.13200
|
1.32e-01
|
0.015600
|
7.34e-02
|
8.31e-01
|
INTERLEUKIN 4 AND INTERLEUKIN 13 SIGNALING
|
77
|
2.93e-01
|
4.65e-01
|
0.13200
|
8.95e-02
|
0.097600
|
1.75e-01
|
1.39e-01
|
RUNX3 REGULATES NOTCH SIGNALING
|
13
|
3.80e-01
|
5.43e-01
|
0.13200
|
-1.03e-01
|
0.083100
|
5.22e-01
|
6.04e-01
|
PROCESSING OF CAPPED INTRONLESS PRE MRNA
|
28
|
3.84e-01
|
5.45e-01
|
0.13200
|
-2.51e-02
|
-0.129000
|
8.18e-01
|
2.36e-01
|
G PROTEIN ACTIVATION
|
23
|
1.81e-01
|
3.39e-01
|
0.13200
|
8.61e-02
|
-0.099700
|
4.75e-01
|
4.08e-01
|
HCMV INFECTION
|
106
|
1.82e-01
|
3.40e-01
|
0.13100
|
8.37e-02
|
0.101000
|
1.37e-01
|
7.20e-02
|
RECEPTOR TYPE TYROSINE PROTEIN PHOSPHATASES
|
20
|
5.29e-01
|
6.82e-01
|
0.13100
|
2.98e-02
|
0.128000
|
8.17e-01
|
3.23e-01
|
RNA POLYMERASE III TRANSCRIPTION INITIATION FROM TYPE 1 PROMOTER
|
28
|
3.48e-01
|
5.15e-01
|
0.13100
|
-1.59e-02
|
-0.130000
|
8.85e-01
|
2.34e-01
|
PI3K AKT SIGNALING IN CANCER
|
91
|
1.08e-01
|
2.40e-01
|
0.13100
|
4.88e-02
|
0.121000
|
4.22e-01
|
4.53e-02
|
ACTIVATION OF KAINATE RECEPTORS UPON GLUTAMATE BINDING
|
29
|
4.11e-01
|
5.73e-01
|
0.13100
|
1.27e-01
|
0.032100
|
2.38e-01
|
7.65e-01
|
PROGRAMMED CELL DEATH
|
186
|
6.81e-03
|
3.17e-02
|
0.13100
|
1.24e-01
|
0.041400
|
3.58e-03
|
3.31e-01
|
IKK COMPLEX RECRUITMENT MEDIATED BY RIP1
|
21
|
6.29e-01
|
7.52e-01
|
0.13100
|
1.18e-01
|
0.055900
|
3.49e-01
|
6.57e-01
|
NEGATIVE REGULATION OF FGFR2 SIGNALING
|
28
|
6.50e-01
|
7.68e-01
|
0.13000
|
9.15e-02
|
0.092800
|
4.02e-01
|
3.95e-01
|
NOTCH2 ACTIVATION AND TRANSMISSION OF SIGNAL TO THE NUCLEUS
|
23
|
5.85e-01
|
7.22e-01
|
0.13000
|
1.20e-01
|
0.051300
|
3.20e-01
|
6.70e-01
|
REGULATION OF GENE EXPRESSION IN BETA CELLS
|
12
|
4.34e-01
|
5.97e-01
|
0.13000
|
6.99e-02
|
-0.109000
|
6.75e-01
|
5.13e-01
|
GENE SILENCING BY RNA
|
85
|
2.03e-01
|
3.64e-01
|
0.12900
|
-1.12e-01
|
-0.065100
|
7.51e-02
|
3.00e-01
|
DAP12 INTERACTIONS
|
30
|
3.46e-01
|
5.15e-01
|
0.12900
|
-1.28e-01
|
-0.018700
|
2.26e-01
|
8.59e-01
|
NR1H2 AND NR1H3 MEDIATED SIGNALING
|
38
|
2.62e-01
|
4.33e-01
|
0.12900
|
-1.28e-01
|
-0.018800
|
1.73e-01
|
8.41e-01
|
RNA POLYMERASE I TRANSCRIPTION
|
70
|
2.82e-01
|
4.56e-01
|
0.12900
|
-6.76e-02
|
-0.110000
|
3.28e-01
|
1.12e-01
|
EPHA MEDIATED GROWTH CONE COLLAPSE
|
29
|
5.95e-01
|
7.28e-01
|
0.12900
|
-1.09e-01
|
-0.068000
|
3.08e-01
|
5.26e-01
|
VIRAL MESSENGER RNA SYNTHESIS
|
42
|
5.19e-02
|
1.43e-01
|
0.12800
|
-9.88e-02
|
0.082100
|
2.68e-01
|
3.57e-01
|
CONSTITUTIVE SIGNALING BY LIGAND RESPONSIVE EGFR CANCER VARIANTS
|
19
|
5.01e-01
|
6.58e-01
|
0.12800
|
-1.51e-02
|
-0.127000
|
9.09e-01
|
3.36e-01
|
NUCLEAR EVENTS KINASE AND TRANSCRIPTION FACTOR ACTIVATION
|
58
|
4.00e-01
|
5.64e-01
|
0.12800
|
7.86e-02
|
0.101000
|
3.00e-01
|
1.82e-01
|
MITOCHONDRIAL CALCIUM ION TRANSPORT
|
23
|
6.30e-01
|
7.52e-01
|
0.12800
|
1.14e-01
|
0.058800
|
3.44e-01
|
6.25e-01
|
TRAF6 MEDIATED INDUCTION OF TAK1 COMPLEX WITHIN TLR4 COMPLEX
|
15
|
4.72e-01
|
6.32e-01
|
0.12800
|
-1.67e-02
|
0.127000
|
9.11e-01
|
3.94e-01
|
SIGNALING BY INSULIN RECEPTOR
|
65
|
3.81e-01
|
5.43e-01
|
0.12800
|
9.14e-02
|
0.089800
|
2.03e-01
|
2.11e-01
|
RHO GTPASES ACTIVATE CIT
|
18
|
7.44e-01
|
8.33e-01
|
0.12800
|
-7.35e-02
|
-0.105000
|
5.89e-01
|
4.42e-01
|
INTERLEUKIN 3 INTERLEUKIN 5 AND GM CSF SIGNALING
|
41
|
2.74e-01
|
4.49e-01
|
0.12800
|
2.58e-02
|
0.125000
|
7.75e-01
|
1.66e-01
|
SODIUM CALCIUM EXCHANGERS
|
10
|
5.22e-01
|
6.76e-01
|
0.12800
|
-5.86e-02
|
0.113000
|
7.48e-01
|
5.35e-01
|
SYNTHESIS OF LEUKOTRIENES LT AND EOXINS EX
|
12
|
8.01e-01
|
8.69e-01
|
0.12800
|
-1.10e-01
|
-0.063800
|
5.08e-01
|
7.02e-01
|
GAP FILLING DNA REPAIR SYNTHESIS AND LIGATION IN GG NER
|
25
|
6.92e-01
|
7.98e-01
|
0.12700
|
-8.74e-02
|
-0.092500
|
4.49e-01
|
4.24e-01
|
DISEASES OF SIGNAL TRANSDUCTION BY GROWTH FACTOR RECEPTORS AND SECOND MESSENGERS
|
369
|
3.67e-03
|
2.09e-02
|
0.12700
|
7.67e-02
|
0.101000
|
1.16e-02
|
9.19e-04
|
CHROMATIN MODIFYING ENZYMES
|
222
|
2.91e-03
|
1.77e-02
|
0.12600
|
-1.21e-01
|
-0.035900
|
1.96e-03
|
3.58e-01
|
SIGNALING BY CYTOSOLIC FGFR1 FUSION MUTANTS
|
18
|
3.52e-01
|
5.19e-01
|
0.12500
|
-4.28e-02
|
0.118000
|
7.54e-01
|
3.87e-01
|
APOPTOSIS
|
164
|
1.16e-02
|
4.80e-02
|
0.12500
|
1.21e-01
|
0.032900
|
7.59e-03
|
4.67e-01
|
DISEASES OF IMMUNE SYSTEM
|
25
|
4.44e-01
|
6.09e-01
|
0.12500
|
-1.24e-01
|
-0.020000
|
2.85e-01
|
8.63e-01
|
JOSEPHIN DOMAIN DUBS
|
11
|
6.76e-01
|
7.86e-01
|
0.12500
|
1.24e-01
|
0.012300
|
4.75e-01
|
9.44e-01
|
SUMOYLATION OF IMMUNE RESPONSE PROTEINS
|
11
|
5.36e-01
|
6.88e-01
|
0.12400
|
1.18e-01
|
-0.040900
|
5.00e-01
|
8.14e-01
|
ORGANELLE BIOGENESIS AND MAINTENANCE
|
284
|
4.08e-03
|
2.23e-02
|
0.12400
|
1.12e-01
|
0.054000
|
1.21e-03
|
1.18e-01
|
RNA POLYMERASE I TRANSCRIPTION TERMINATION
|
31
|
6.10e-01
|
7.40e-01
|
0.12400
|
-1.03e-01
|
-0.068300
|
3.20e-01
|
5.11e-01
|
UB SPECIFIC PROCESSING PROTEASES
|
167
|
9.42e-02
|
2.19e-01
|
0.12400
|
9.49e-02
|
0.079000
|
3.45e-02
|
7.83e-02
|
P38MAPK EVENTS
|
13
|
8.24e-01
|
8.83e-01
|
0.12300
|
7.31e-02
|
0.099100
|
6.48e-01
|
5.36e-01
|
COLLAGEN FORMATION
|
79
|
2.23e-01
|
3.89e-01
|
0.12300
|
-5.43e-02
|
-0.110000
|
4.04e-01
|
9.01e-02
|
HS GAG DEGRADATION
|
20
|
4.60e-01
|
6.20e-01
|
0.12300
|
1.23e-01
|
0.000556
|
3.43e-01
|
9.97e-01
|
SUMOYLATION OF TRANSCRIPTION FACTORS
|
18
|
4.07e-01
|
5.71e-01
|
0.12200
|
2.68e-02
|
-0.120000
|
8.44e-01
|
3.80e-01
|
TNFR2 NON CANONICAL NF KB PATHWAY
|
79
|
1.66e-01
|
3.19e-01
|
0.12200
|
1.15e-01
|
0.040700
|
7.75e-02
|
5.31e-01
|
REGULATION OF RUNX2 EXPRESSION AND ACTIVITY
|
68
|
4.68e-02
|
1.34e-01
|
0.12200
|
1.21e-01
|
-0.016100
|
8.57e-02
|
8.18e-01
|
UNBLOCKING OF NMDA RECEPTORS GLUTAMATE BINDING AND ACTIVATION
|
21
|
4.56e-01
|
6.20e-01
|
0.12100
|
2.46e-03
|
0.121000
|
9.84e-01
|
3.35e-01
|
SHC1 EVENTS IN ERBB2 SIGNALING
|
21
|
7.53e-01
|
8.38e-01
|
0.12100
|
9.17e-02
|
0.078300
|
4.67e-01
|
5.34e-01
|
DEREGULATED CDK5 TRIGGERS MULTIPLE NEURODEGENERATIVE PATHWAYS IN ALZHEIMER S DISEASE MODELS
|
19
|
3.06e-01
|
4.77e-01
|
0.12100
|
8.07e-02
|
-0.089500
|
5.42e-01
|
4.99e-01
|
SIGNALING BY FGFR1
|
44
|
5.60e-01
|
7.04e-01
|
0.12000
|
8.86e-02
|
0.081100
|
3.09e-01
|
3.52e-01
|
TGF BETA RECEPTOR SIGNALING IN EMT EPITHELIAL TO MESENCHYMAL TRANSITION
|
16
|
3.76e-01
|
5.40e-01
|
0.12000
|
9.59e-02
|
-0.072300
|
5.07e-01
|
6.16e-01
|
TRANSLATION OF SARS COV 1 STRUCTURAL PROTEINS
|
28
|
6.09e-01
|
7.40e-01
|
0.12000
|
5.48e-02
|
0.107000
|
6.16e-01
|
3.27e-01
|
NEGATIVE REGULATION OF FLT3
|
14
|
4.20e-01
|
5.83e-01
|
0.12000
|
-8.84e-02
|
0.081200
|
5.67e-01
|
5.99e-01
|
PREGNENOLONE BIOSYNTHESIS
|
12
|
7.28e-01
|
8.20e-01
|
0.12000
|
-2.73e-02
|
-0.116000
|
8.70e-01
|
4.85e-01
|
PLATELET AGGREGATION PLUG FORMATION
|
32
|
6.13e-01
|
7.41e-01
|
0.12000
|
6.38e-02
|
0.101000
|
5.32e-01
|
3.23e-01
|
OTHER INTERLEUKIN SIGNALING
|
20
|
4.92e-01
|
6.52e-01
|
0.12000
|
1.19e-01
|
0.004260
|
3.55e-01
|
9.74e-01
|
ANTI INFLAMMATORY RESPONSE FAVOURING LEISHMANIA PARASITE INFECTION
|
118
|
2.03e-01
|
3.64e-01
|
0.11900
|
9.37e-02
|
0.073900
|
7.88e-02
|
1.66e-01
|
EARLY PHASE OF HIV LIFE CYCLE
|
13
|
5.07e-01
|
6.64e-01
|
0.11800
|
4.16e-02
|
-0.111000
|
7.95e-01
|
4.89e-01
|
INTERLEUKIN 7 SIGNALING
|
19
|
7.52e-01
|
8.37e-01
|
0.11800
|
-1.00e-01
|
-0.063100
|
4.50e-01
|
6.34e-01
|
TRP CHANNELS
|
20
|
3.06e-01
|
4.77e-01
|
0.11800
|
-7.20e-02
|
0.093700
|
5.77e-01
|
4.68e-01
|
MITOTIC G2 G2 M PHASES
|
184
|
1.19e-02
|
4.88e-02
|
0.11800
|
1.14e-01
|
0.031200
|
7.74e-03
|
4.66e-01
|
REGULATION OF PTEN GENE TRANSCRIPTION
|
58
|
4.31e-01
|
5.96e-01
|
0.11800
|
9.85e-02
|
0.065100
|
1.95e-01
|
3.92e-01
|
REGULATED PROTEOLYSIS OF P75NTR
|
12
|
8.53e-01
|
9.04e-01
|
0.11700
|
9.27e-02
|
0.072100
|
5.78e-01
|
6.65e-01
|
TFAP2 AP 2 FAMILY REGULATES TRANSCRIPTION OF GROWTH FACTORS AND THEIR RECEPTORS
|
11
|
5.50e-01
|
7.02e-01
|
0.11700
|
5.11e-02
|
-0.106000
|
7.69e-01
|
5.44e-01
|
GRB2 SOS PROVIDES LINKAGE TO MAPK SIGNALING FOR INTEGRINS
|
12
|
4.98e-01
|
6.57e-01
|
0.11700
|
-6.90e-02
|
0.094800
|
6.79e-01
|
5.70e-01
|
TRANSLATION
|
286
|
8.21e-08
|
4.54e-06
|
0.11700
|
9.25e-02
|
-0.071200
|
7.19e-03
|
3.86e-02
|
SHC MEDIATED CASCADE FGFR1
|
16
|
6.14e-01
|
7.41e-01
|
0.11600
|
-1.24e-02
|
-0.116000
|
9.31e-01
|
4.23e-01
|
TELOMERE EXTENSION BY TELOMERASE
|
22
|
4.36e-01
|
5.99e-01
|
0.11600
|
1.16e-01
|
-0.006200
|
3.45e-01
|
9.60e-01
|
SIGNALING BY INTERLEUKINS
|
349
|
1.50e-02
|
5.76e-02
|
0.11600
|
8.22e-02
|
0.082200
|
8.43e-03
|
8.48e-03
|
RIP MEDIATED NFKB ACTIVATION VIA ZBP1
|
15
|
5.82e-01
|
7.21e-01
|
0.11600
|
-2.27e-03
|
0.116000
|
9.88e-01
|
4.36e-01
|
SIGNALING BY ERBB2 ECD MUTANTS
|
16
|
7.01e-01
|
8.04e-01
|
0.11600
|
-3.45e-02
|
-0.111000
|
8.11e-01
|
4.42e-01
|
DNA DOUBLE STRAND BREAK REPAIR
|
140
|
2.49e-02
|
8.49e-02
|
0.11600
|
-1.14e-01
|
-0.022100
|
2.00e-02
|
6.51e-01
|
FGFRL1 MODULATION OF FGFR1 SIGNALING
|
10
|
8.63e-01
|
9.12e-01
|
0.11600
|
-5.99e-02
|
-0.098800
|
7.43e-01
|
5.88e-01
|
ION HOMEOSTASIS
|
50
|
1.43e-01
|
2.91e-01
|
0.11500
|
-1.11e-02
|
0.115000
|
8.92e-01
|
1.60e-01
|
ERBB2 REGULATES CELL MOTILITY
|
14
|
7.74e-01
|
8.51e-01
|
0.11500
|
4.48e-02
|
0.106000
|
7.71e-01
|
4.93e-01
|
FORMATION OF TC NER PRE INCISION COMPLEX
|
53
|
5.25e-01
|
6.78e-01
|
0.11500
|
8.70e-02
|
0.074900
|
2.74e-01
|
3.46e-01
|
CELL CYCLE CHECKPOINTS
|
245
|
4.97e-02
|
1.38e-01
|
0.11500
|
8.92e-02
|
0.072100
|
1.64e-02
|
5.24e-02
|
STING MEDIATED INDUCTION OF HOST IMMUNE RESPONSES
|
14
|
5.03e-01
|
6.60e-01
|
0.11400
|
4.27e-02
|
-0.105000
|
7.82e-01
|
4.95e-01
|
MAPK6 MAPK4 SIGNALING
|
83
|
4.50e-02
|
1.31e-01
|
0.11300
|
1.12e-01
|
-0.011100
|
7.68e-02
|
8.61e-01
|
TICAM1 TRAF6 DEPENDENT INDUCTION OF TAK1 COMPLEX
|
11
|
7.99e-01
|
8.68e-01
|
0.11300
|
3.48e-02
|
0.107000
|
8.41e-01
|
5.38e-01
|
LEISHMANIA INFECTION
|
198
|
8.25e-02
|
1.99e-01
|
0.11200
|
6.44e-02
|
0.092000
|
1.19e-01
|
2.58e-02
|
PTEN REGULATION
|
133
|
6.69e-02
|
1.70e-01
|
0.11200
|
1.07e-01
|
0.033900
|
3.34e-02
|
5.00e-01
|
RUNX1 REGULATES TRANSCRIPTION OF GENES INVOLVED IN DIFFERENTIATION OF HSCS
|
86
|
1.93e-02
|
6.92e-02
|
0.11200
|
3.74e-02
|
-0.105000
|
5.49e-01
|
9.10e-02
|
CELL SURFACE INTERACTIONS AT THE VASCULAR WALL
|
92
|
2.54e-01
|
4.27e-01
|
0.11100
|
5.11e-02
|
0.098400
|
3.98e-01
|
1.03e-01
|
ONCOGENE INDUCED SENESCENCE
|
32
|
6.93e-01
|
7.98e-01
|
0.11100
|
7.09e-02
|
0.085100
|
4.88e-01
|
4.05e-01
|
TRAFFICKING OF AMPA RECEPTORS
|
31
|
6.96e-01
|
8.00e-01
|
0.11100
|
8.72e-02
|
0.067900
|
4.01e-01
|
5.13e-01
|
TRAF6 MEDIATED NF KB ACTIVATION
|
22
|
5.54e-01
|
7.02e-01
|
0.11000
|
-1.10e-01
|
-0.013300
|
3.73e-01
|
9.14e-01
|
DISEASES OF PROGRAMMED CELL DEATH
|
57
|
1.59e-01
|
3.10e-01
|
0.11000
|
1.51e-03
|
-0.110000
|
9.84e-01
|
1.50e-01
|
NOTCH4 INTRACELLULAR DOMAIN REGULATES TRANSCRIPTION
|
20
|
4.34e-01
|
5.97e-01
|
0.11000
|
-1.07e-01
|
0.027900
|
4.09e-01
|
8.29e-01
|
RAF INDEPENDENT MAPK1 3 ACTIVATION
|
21
|
7.75e-01
|
8.51e-01
|
0.11000
|
8.96e-02
|
0.063800
|
4.77e-01
|
6.13e-01
|
CELL CYCLE
|
596
|
1.69e-03
|
1.26e-02
|
0.11000
|
8.22e-02
|
0.072600
|
6.31e-04
|
2.53e-03
|
NOTCH4 ACTIVATION AND TRANSMISSION OF SIGNAL TO THE NUCLEUS
|
12
|
5.43e-01
|
6.94e-01
|
0.11000
|
6.58e-02
|
-0.087700
|
6.93e-01
|
5.99e-01
|
SIGNALING BY WNT
|
272
|
4.36e-03
|
2.33e-02
|
0.11000
|
1.05e-01
|
0.030900
|
2.87e-03
|
3.81e-01
|
SIGNALING BY TGFB FAMILY MEMBERS
|
96
|
2.74e-01
|
4.48e-01
|
0.10900
|
5.39e-02
|
0.094500
|
3.62e-01
|
1.10e-01
|
HIV TRANSCRIPTION ELONGATION
|
42
|
3.47e-01
|
5.15e-01
|
0.10800
|
-1.48e-02
|
-0.107000
|
8.68e-01
|
2.28e-01
|
MAPK FAMILY SIGNALING CASCADES
|
290
|
4.10e-02
|
1.24e-01
|
0.10800
|
6.63e-02
|
0.085200
|
5.24e-02
|
1.27e-02
|
CONSTITUTIVE SIGNALING BY ABERRANT PI3K IN CANCER
|
64
|
1.43e-01
|
2.92e-01
|
0.10800
|
-2.62e-04
|
0.108000
|
9.97e-01
|
1.36e-01
|
HIV LIFE CYCLE
|
142
|
1.91e-01
|
3.54e-01
|
0.10800
|
6.16e-02
|
0.088300
|
2.06e-01
|
6.94e-02
|
POLYMERASE SWITCHING
|
14
|
5.51e-01
|
7.02e-01
|
0.10800
|
-3.60e-02
|
0.101000
|
8.15e-01
|
5.12e-01
|
SMOOTH MUSCLE CONTRACTION
|
33
|
5.68e-01
|
7.12e-01
|
0.10700
|
-3.75e-02
|
-0.100000
|
7.09e-01
|
3.18e-01
|
NCAM SIGNALING FOR NEURITE OUT GROWTH
|
62
|
4.17e-01
|
5.80e-01
|
0.10700
|
-4.84e-02
|
-0.095500
|
5.10e-01
|
1.94e-01
|
ACTIVATION OF MATRIX METALLOPROTEINASES
|
15
|
7.46e-01
|
8.33e-01
|
0.10700
|
1.03e-01
|
0.029200
|
4.91e-01
|
8.45e-01
|
FLT3 SIGNALING IN DISEASE
|
28
|
3.64e-01
|
5.31e-01
|
0.10700
|
-1.05e-01
|
0.017900
|
3.35e-01
|
8.70e-01
|
TRANSCRIPTIONAL REGULATION BY THE AP 2 TFAP2 FAMILY OF TRANSCRIPTION FACTORS
|
33
|
2.00e-01
|
3.62e-01
|
0.10700
|
7.01e-02
|
-0.080400
|
4.86e-01
|
4.24e-01
|
APC CDC20 MEDIATED DEGRADATION OF NEK2A
|
24
|
6.97e-01
|
8.00e-01
|
0.10700
|
9.70e-02
|
0.044100
|
4.11e-01
|
7.08e-01
|
BETA CATENIN INDEPENDENT WNT SIGNALING
|
140
|
1.81e-02
|
6.65e-02
|
0.10600
|
1.06e-01
|
0.001080
|
3.06e-02
|
9.82e-01
|
DEACTIVATION OF THE BETA CATENIN TRANSACTIVATING COMPLEX
|
41
|
3.47e-01
|
5.15e-01
|
0.10500
|
1.05e-01
|
0.008630
|
2.45e-01
|
9.24e-01
|
SIGNALING BY LEPTIN
|
10
|
6.65e-01
|
7.79e-01
|
0.10500
|
-3.56e-02
|
0.099000
|
8.46e-01
|
5.88e-01
|
SIGNALING BY NTRK3 TRKC
|
17
|
6.97e-01
|
8.00e-01
|
0.10500
|
-2.14e-02
|
-0.103000
|
8.78e-01
|
4.63e-01
|
RHO GTPASES ACTIVATE ROCKS
|
19
|
7.68e-01
|
8.46e-01
|
0.10400
|
-4.50e-02
|
-0.093900
|
7.34e-01
|
4.79e-01
|
PHASE 4 RESTING MEMBRANE POTENTIAL
|
14
|
7.75e-01
|
8.51e-01
|
0.10300
|
-9.92e-02
|
-0.028100
|
5.21e-01
|
8.56e-01
|
ACTIVATED TAK1 MEDIATES P38 MAPK ACTIVATION
|
23
|
7.95e-01
|
8.66e-01
|
0.10300
|
7.98e-02
|
0.065000
|
5.08e-01
|
5.89e-01
|
RESOLUTION OF ABASIC SITES AP SITES
|
38
|
6.58e-01
|
7.74e-01
|
0.10300
|
-8.58e-02
|
-0.056300
|
3.60e-01
|
5.48e-01
|
CYTOCHROME P450 ARRANGED BY SUBSTRATE TYPE
|
31
|
2.61e-01
|
4.33e-01
|
0.10300
|
-8.70e-02
|
0.054200
|
4.02e-01
|
6.02e-01
|
REGULATION OF TP53 ACTIVITY
|
152
|
1.36e-01
|
2.82e-01
|
0.10200
|
4.50e-02
|
0.091800
|
3.39e-01
|
5.10e-02
|
SIGNALING BY NOTCH4
|
83
|
1.44e-01
|
2.92e-01
|
0.10200
|
1.01e-01
|
0.010700
|
1.10e-01
|
8.67e-01
|
INFLAMMASOMES
|
19
|
4.93e-01
|
6.52e-01
|
0.10200
|
-9.72e-02
|
0.030800
|
4.63e-01
|
8.16e-01
|
DEUBIQUITINATION
|
241
|
1.07e-01
|
2.37e-01
|
0.10200
|
7.09e-02
|
0.073100
|
5.85e-02
|
5.09e-02
|
SIGNALING BY TYPE 1 INSULIN LIKE GROWTH FACTOR 1 RECEPTOR IGF1R
|
46
|
3.64e-01
|
5.31e-01
|
0.10100
|
-1.00e-01
|
-0.013800
|
2.40e-01
|
8.72e-01
|
REGULATION OF MRNA STABILITY BY PROTEINS THAT BIND AU RICH ELEMENTS
|
83
|
3.38e-02
|
1.08e-01
|
0.10100
|
4.89e-02
|
-0.087900
|
4.42e-01
|
1.66e-01
|
NUCLEOTIDE BINDING DOMAIN LEUCINE RICH REPEAT CONTAINING RECEPTOR NLR SIGNALING PATHWAYS
|
53
|
1.92e-01
|
3.54e-01
|
0.10000
|
-1.51e-02
|
0.099000
|
8.49e-01
|
2.13e-01
|
SIGNALING BY ROBO RECEPTORS
|
207
|
2.48e-03
|
1.57e-02
|
0.10000
|
9.63e-03
|
-0.099500
|
8.12e-01
|
1.37e-02
|
PROCESSIVE SYNTHESIS ON THE C STRAND OF THE TELOMERE
|
19
|
5.39e-01
|
6.90e-01
|
0.09990
|
-1.96e-02
|
0.098000
|
8.82e-01
|
4.60e-01
|
PCNA DEPENDENT LONG PATCH BASE EXCISION REPAIR
|
21
|
7.98e-01
|
8.68e-01
|
0.09960
|
-5.26e-02
|
-0.084600
|
6.76e-01
|
5.02e-01
|
SIGNALING BY CSF3 G CSF
|
29
|
5.64e-01
|
7.07e-01
|
0.09960
|
9.79e-02
|
0.018200
|
3.62e-01
|
8.65e-01
|
NON INTEGRIN MEMBRANE ECM INTERACTIONS
|
57
|
4.55e-01
|
6.20e-01
|
0.09900
|
-9.16e-02
|
-0.037500
|
2.32e-01
|
6.24e-01
|
NEUREXINS AND NEUROLIGINS
|
54
|
3.98e-01
|
5.62e-01
|
0.09890
|
2.59e-02
|
0.095400
|
7.42e-01
|
2.25e-01
|
FANCONI ANEMIA PATHWAY
|
36
|
3.60e-01
|
5.28e-01
|
0.09890
|
-9.85e-02
|
0.008750
|
3.07e-01
|
9.28e-01
|
CONSTITUTIVE SIGNALING BY EGFRVIII
|
15
|
7.19e-01
|
8.13e-01
|
0.09850
|
-9.97e-03
|
-0.098000
|
9.47e-01
|
5.11e-01
|
TRANSCRIPTIONAL REGULATION BY SMALL RNAS
|
64
|
4.59e-01
|
6.20e-01
|
0.09820
|
-8.82e-02
|
-0.043200
|
2.22e-01
|
5.50e-01
|
G PROTEIN BETA GAMMA SIGNALLING
|
31
|
5.95e-01
|
7.28e-01
|
0.09770
|
9.44e-02
|
0.025200
|
3.63e-01
|
8.08e-01
|
NGF STIMULATED TRANSCRIPTION
|
36
|
5.53e-01
|
7.02e-01
|
0.09750
|
9.40e-02
|
0.026000
|
3.29e-01
|
7.87e-01
|
REPRESSION OF WNT TARGET GENES
|
14
|
7.11e-01
|
8.10e-01
|
0.09730
|
-9.41e-04
|
-0.097300
|
9.95e-01
|
5.28e-01
|
GLOBAL GENOME NUCLEOTIDE EXCISION REPAIR GG NER
|
84
|
4.27e-01
|
5.91e-01
|
0.09610
|
8.22e-02
|
0.049800
|
1.93e-01
|
4.30e-01
|
PROCESSING OF DNA DOUBLE STRAND BREAK ENDS
|
74
|
5.02e-01
|
6.59e-01
|
0.09600
|
-7.88e-02
|
-0.054900
|
2.41e-01
|
4.14e-01
|
TELOMERE C STRAND LAGGING STRAND SYNTHESIS
|
33
|
5.73e-01
|
7.16e-01
|
0.09580
|
2.21e-02
|
0.093200
|
8.26e-01
|
3.54e-01
|
SIGNALLING TO RAS
|
19
|
6.57e-01
|
7.74e-01
|
0.09480
|
4.10e-03
|
0.094700
|
9.75e-01
|
4.75e-01
|
MEIOSIS
|
67
|
5.80e-01
|
7.21e-01
|
0.09480
|
-6.79e-02
|
-0.066200
|
3.37e-01
|
3.49e-01
|
DOWNSTREAM SIGNALING OF ACTIVATED FGFR3
|
20
|
8.43e-01
|
9.00e-01
|
0.09470
|
5.88e-02
|
0.074200
|
6.49e-01
|
5.66e-01
|
FLT3 SIGNALING
|
36
|
2.98e-01
|
4.71e-01
|
0.09460
|
-3.45e-02
|
0.088100
|
7.21e-01
|
3.60e-01
|
TNFS BIND THEIR PHYSIOLOGICAL RECEPTORS
|
12
|
8.77e-01
|
9.18e-01
|
0.09450
|
4.32e-02
|
0.084100
|
7.95e-01
|
6.14e-01
|
DNA DAMAGE BYPASS
|
47
|
3.71e-01
|
5.36e-01
|
0.09450
|
-9.43e-02
|
-0.006670
|
2.64e-01
|
9.37e-01
|
ORGANIC CATION ANION ZWITTERION TRANSPORT
|
11
|
8.20e-01
|
8.82e-01
|
0.09440
|
-9.29e-02
|
-0.016400
|
5.94e-01
|
9.25e-01
|
TRANSCRIPTIONAL ACTIVATION OF MITOCHONDRIAL BIOGENESIS
|
54
|
1.29e-01
|
2.73e-01
|
0.09400
|
-6.92e-02
|
0.063700
|
3.79e-01
|
4.19e-01
|
INFECTIOUS DISEASE
|
736
|
2.40e-03
|
1.54e-02
|
0.09230
|
7.53e-02
|
0.053400
|
5.34e-04
|
1.40e-02
|
ION CHANNEL TRANSPORT
|
143
|
1.20e-01
|
2.59e-01
|
0.09230
|
2.40e-02
|
0.089100
|
6.21e-01
|
6.61e-02
|
PRESYNAPTIC FUNCTION OF KAINATE RECEPTORS
|
20
|
7.27e-01
|
8.20e-01
|
0.09220
|
8.99e-02
|
0.020400
|
4.86e-01
|
8.74e-01
|
SUMOYLATION OF CHROMATIN ORGANIZATION PROTEINS
|
60
|
1.15e-01
|
2.50e-01
|
0.09190
|
-6.96e-02
|
0.060000
|
3.51e-01
|
4.22e-01
|
TELOMERE MAINTENANCE
|
81
|
3.41e-01
|
5.12e-01
|
0.09180
|
-2.92e-02
|
-0.087000
|
6.50e-01
|
1.76e-01
|
NOTCH HLH TRANSCRIPTION PATHWAY
|
28
|
5.60e-01
|
7.04e-01
|
0.09160
|
-9.15e-02
|
-0.003660
|
4.02e-01
|
9.73e-01
|
SIGNALING BY ERBB2
|
48
|
6.12e-01
|
7.41e-01
|
0.09130
|
4.16e-02
|
0.081300
|
6.18e-01
|
3.30e-01
|
SIGNALING BY FGFR4 IN DISEASE
|
11
|
7.30e-01
|
8.22e-01
|
0.09110
|
2.33e-02
|
-0.088100
|
8.93e-01
|
6.13e-01
|
PLATELET HOMEOSTASIS
|
78
|
3.02e-01
|
4.74e-01
|
0.09100
|
2.04e-02
|
0.088700
|
7.56e-01
|
1.76e-01
|
IRAK4 DEFICIENCY TLR2 4
|
14
|
8.91e-01
|
9.30e-01
|
0.09030
|
-7.42e-02
|
-0.051400
|
6.31e-01
|
7.39e-01
|
METABOLISM OF STEROID HORMONES
|
21
|
7.99e-01
|
8.68e-01
|
0.08990
|
8.17e-02
|
0.037300
|
5.17e-01
|
7.67e-01
|
MAP2K AND MAPK ACTIVATION
|
36
|
7.18e-01
|
8.13e-01
|
0.08960
|
7.79e-02
|
0.044300
|
4.18e-01
|
6.46e-01
|
TRAF6 MEDIATED IRF7 ACTIVATION IN TLR7 8 OR 9 SIGNALING
|
13
|
6.92e-01
|
7.98e-01
|
0.08880
|
-8.46e-02
|
0.027100
|
5.97e-01
|
8.66e-01
|
HCMV LATE EVENTS
|
68
|
1.44e-01
|
2.92e-01
|
0.08880
|
-2.79e-02
|
0.084300
|
6.91e-01
|
2.29e-01
|
VISUAL PHOTOTRANSDUCTION
|
61
|
1.48e-01
|
2.98e-01
|
0.08830
|
4.18e-02
|
-0.077800
|
5.73e-01
|
2.94e-01
|
FORMATION OF FIBRIN CLOT CLOTTING CASCADE
|
23
|
7.60e-01
|
8.42e-01
|
0.08790
|
-2.92e-02
|
-0.082900
|
8.09e-01
|
4.91e-01
|
NOTCH2 INTRACELLULAR DOMAIN REGULATES TRANSCRIPTION
|
11
|
7.59e-01
|
8.41e-01
|
0.08790
|
-8.62e-02
|
0.017000
|
6.21e-01
|
9.22e-01
|
RUNX2 REGULATES BONE DEVELOPMENT
|
29
|
5.53e-01
|
7.02e-01
|
0.08760
|
-1.48e-03
|
0.087600
|
9.89e-01
|
4.15e-01
|
TRANSLESION SYNTHESIS BY POLH
|
19
|
7.88e-01
|
8.60e-01
|
0.08760
|
-2.61e-02
|
-0.083600
|
8.44e-01
|
5.28e-01
|
ACYL CHAIN REMODELLING OF PS
|
14
|
8.29e-01
|
8.87e-01
|
0.08750
|
2.27e-02
|
0.084500
|
8.83e-01
|
5.84e-01
|
ACTIVATION OF THE MRNA UPON BINDING OF THE CAP BINDING COMPLEX AND EIFS AND SUBSEQUENT BINDING TO 43S
|
59
|
1.47e-01
|
2.95e-01
|
0.08730
|
6.65e-02
|
-0.056600
|
3.77e-01
|
4.52e-01
|
IRS MEDIATED SIGNALLING
|
41
|
2.90e-01
|
4.63e-01
|
0.08670
|
-7.62e-02
|
0.041300
|
3.99e-01
|
6.47e-01
|
SIGNALING BY NOTCH3
|
48
|
3.91e-01
|
5.54e-01
|
0.08660
|
-5.26e-05
|
0.086600
|
9.99e-01
|
2.99e-01
|
TCF DEPENDENT SIGNALING IN RESPONSE TO WNT
|
179
|
4.71e-02
|
1.34e-01
|
0.08660
|
8.62e-02
|
0.007910
|
4.68e-02
|
8.55e-01
|
MUSCLE CONTRACTION
|
160
|
4.51e-02
|
1.31e-01
|
0.08620
|
-8.62e-02
|
0.000526
|
6.00e-02
|
9.91e-01
|
OXIDATIVE STRESS INDUCED SENESCENCE
|
81
|
3.71e-01
|
5.36e-01
|
0.08620
|
-2.53e-02
|
-0.082400
|
6.94e-01
|
2.00e-01
|
AMYLOID FIBER FORMATION
|
61
|
5.18e-01
|
6.73e-01
|
0.08620
|
-3.13e-02
|
-0.080300
|
6.73e-01
|
2.78e-01
|
SIGNALING BY NOTCH2
|
33
|
7.96e-01
|
8.66e-01
|
0.08590
|
6.63e-02
|
0.054600
|
5.10e-01
|
5.88e-01
|
G ALPHA S SIGNALLING EVENTS
|
107
|
4.84e-01
|
6.44e-01
|
0.08550
|
6.56e-02
|
0.054800
|
2.41e-01
|
3.28e-01
|
PRE NOTCH EXPRESSION AND PROCESSING
|
67
|
6.03e-01
|
7.36e-01
|
0.08520
|
-7.11e-02
|
-0.046900
|
3.14e-01
|
5.07e-01
|
CYTOSOLIC SENSORS OF PATHOGEN ASSOCIATED DNA
|
59
|
5.35e-01
|
6.88e-01
|
0.08510
|
-3.05e-02
|
-0.079400
|
6.85e-01
|
2.92e-01
|
REGULATION OF TLR BY ENDOGENOUS LIGAND
|
13
|
6.93e-01
|
7.98e-01
|
0.08490
|
3.59e-02
|
-0.076900
|
8.23e-01
|
6.31e-01
|
PI 3K CASCADE FGFR4
|
13
|
7.51e-01
|
8.37e-01
|
0.08450
|
-8.36e-02
|
0.012200
|
6.02e-01
|
9.39e-01
|
NRIF SIGNALS CELL DEATH FROM THE NUCLEUS
|
16
|
6.23e-01
|
7.49e-01
|
0.08380
|
6.82e-02
|
-0.048700
|
6.37e-01
|
7.36e-01
|
PYROPTOSIS
|
21
|
6.10e-01
|
7.40e-01
|
0.08360
|
1.92e-02
|
-0.081400
|
8.79e-01
|
5.19e-01
|
INTERCONVERSION OF NUCLEOTIDE DI AND TRIPHOSPHATES
|
29
|
5.55e-01
|
7.02e-01
|
0.08320
|
8.28e-02
|
-0.008010
|
4.40e-01
|
9.40e-01
|
SIGNALING BY NOTCH1
|
75
|
5.49e-01
|
7.01e-01
|
0.08310
|
4.03e-02
|
0.072600
|
5.46e-01
|
2.77e-01
|
MEIOTIC SYNAPSIS
|
43
|
7.65e-01
|
8.44e-01
|
0.08300
|
-5.84e-02
|
-0.059000
|
5.08e-01
|
5.03e-01
|
G2 M DNA DAMAGE CHECKPOINT
|
69
|
6.38e-01
|
7.58e-01
|
0.08290
|
-5.17e-02
|
-0.064800
|
4.58e-01
|
3.52e-01
|
AKT PHOSPHORYLATES TARGETS IN THE CYTOSOL
|
14
|
7.92e-01
|
8.64e-01
|
0.08290
|
8.27e-02
|
0.004530
|
5.92e-01
|
9.77e-01
|
RA BIOSYNTHESIS PATHWAY
|
13
|
8.40e-01
|
8.97e-01
|
0.08260
|
-8.11e-02
|
-0.015800
|
6.13e-01
|
9.21e-01
|
RET SIGNALING
|
38
|
7.87e-01
|
8.60e-01
|
0.08240
|
5.36e-02
|
0.062600
|
5.68e-01
|
5.04e-01
|
GAB1 SIGNALOSOME
|
14
|
6.72e-01
|
7.84e-01
|
0.08220
|
-6.75e-02
|
0.047000
|
6.62e-01
|
7.61e-01
|
TRANSCRIPTIONAL ACTIVITY OF SMAD2 SMAD3 SMAD4 HETEROTRIMER
|
43
|
2.89e-01
|
4.63e-01
|
0.08200
|
-6.10e-02
|
0.054900
|
4.89e-01
|
5.34e-01
|
ERBB2 ACTIVATES PTK6 SIGNALING
|
11
|
7.47e-01
|
8.33e-01
|
0.08190
|
-3.64e-02
|
0.073400
|
8.34e-01
|
6.73e-01
|
TP53 REGULATES TRANSCRIPTION OF DNA REPAIR GENES
|
61
|
6.87e-01
|
7.94e-01
|
0.08170
|
-6.15e-02
|
-0.053900
|
4.06e-01
|
4.67e-01
|
INACTIVATION OF CSF3 G CSF SIGNALING
|
24
|
5.09e-01
|
6.65e-01
|
0.08120
|
5.12e-02
|
-0.063100
|
6.64e-01
|
5.93e-01
|
DOWNSTREAM SIGNALING OF ACTIVATED FGFR2
|
24
|
8.49e-01
|
9.01e-01
|
0.08100
|
-6.75e-02
|
-0.044800
|
5.67e-01
|
7.04e-01
|
ENDOGENOUS STEROLS
|
20
|
6.65e-01
|
7.79e-01
|
0.08050
|
-7.95e-02
|
0.012900
|
5.38e-01
|
9.20e-01
|
CARDIAC CONDUCTION
|
107
|
5.32e-02
|
1.46e-01
|
0.08030
|
-6.14e-02
|
0.051700
|
2.73e-01
|
3.56e-01
|
REGULATION OF TP53 ACTIVITY THROUGH METHYLATION
|
18
|
8.97e-01
|
9.36e-01
|
0.08020
|
-5.07e-02
|
-0.062200
|
7.10e-01
|
6.48e-01
|
DISEASES OF MITOTIC CELL CYCLE
|
37
|
8.07e-01
|
8.72e-01
|
0.07990
|
5.80e-02
|
0.055000
|
5.42e-01
|
5.63e-01
|
SIGNALING BY FGFR3 FUSIONS IN CANCER
|
10
|
9.03e-01
|
9.37e-01
|
0.07920
|
2.42e-02
|
0.075400
|
8.95e-01
|
6.80e-01
|
SIGNALING BY FGFR2 IIIA TM
|
19
|
8.61e-01
|
9.11e-01
|
0.07860
|
-3.41e-02
|
-0.070800
|
7.97e-01
|
5.93e-01
|
RECRUITMENT OF NUMA TO MITOTIC CENTROSOMES
|
85
|
5.10e-01
|
6.67e-01
|
0.07840
|
7.09e-02
|
0.033500
|
2.59e-01
|
5.93e-01
|
TRANSCRIPTIONAL REGULATION BY RUNX3
|
94
|
2.75e-01
|
4.49e-01
|
0.07840
|
7.79e-02
|
0.008370
|
1.92e-01
|
8.89e-01
|
POTASSIUM CHANNELS
|
90
|
5.55e-01
|
7.02e-01
|
0.07810
|
6.62e-02
|
0.041500
|
2.78e-01
|
4.96e-01
|
MRNA DECAY BY 3 TO 5 EXORIBONUCLEASE
|
15
|
9.11e-01
|
9.43e-01
|
0.07760
|
-6.44e-02
|
-0.043200
|
6.66e-01
|
7.72e-01
|
OVARIAN TUMOR DOMAIN PROTEASES
|
36
|
8.21e-01
|
8.82e-01
|
0.07750
|
5.69e-02
|
0.052700
|
5.55e-01
|
5.85e-01
|
DOWNREGULATION OF ERBB2 ERBB3 SIGNALING
|
13
|
7.32e-01
|
8.23e-01
|
0.07740
|
-3.63e-02
|
0.068300
|
8.21e-01
|
6.70e-01
|
P75NTR RECRUITS SIGNALLING COMPLEXES
|
12
|
7.76e-01
|
8.51e-01
|
0.07710
|
2.27e-02
|
-0.073700
|
8.92e-01
|
6.59e-01
|
DEGRADATION OF THE EXTRACELLULAR MATRIX
|
110
|
4.22e-01
|
5.85e-01
|
0.07690
|
-3.17e-02
|
-0.070100
|
5.66e-01
|
2.04e-01
|
REGULATED NECROSIS
|
46
|
3.58e-01
|
5.26e-01
|
0.07680
|
2.90e-02
|
-0.071200
|
7.34e-01
|
4.04e-01
|
ZBP1 DAI MEDIATED INDUCTION OF TYPE I IFNS
|
18
|
8.07e-01
|
8.72e-01
|
0.07680
|
1.36e-02
|
0.075600
|
9.20e-01
|
5.79e-01
|
ANTIGEN ACTIVATES B CELL RECEPTOR BCR LEADING TO GENERATION OF SECOND MESSENGERS
|
26
|
6.70e-01
|
7.84e-01
|
0.07680
|
-1.54e-04
|
0.076800
|
9.99e-01
|
4.98e-01
|
APC C CDC20 MEDIATED DEGRADATION OF CYCLIN B
|
21
|
7.65e-01
|
8.44e-01
|
0.07650
|
7.59e-02
|
0.009580
|
5.47e-01
|
9.39e-01
|
MRNA SPLICING
|
188
|
9.71e-03
|
4.20e-02
|
0.07630
|
4.90e-02
|
-0.058500
|
2.47e-01
|
1.67e-01
|
CELLULAR RESPONSE TO CHEMICAL STRESS
|
150
|
2.72e-02
|
9.07e-02
|
0.07620
|
4.20e-02
|
-0.063600
|
3.75e-01
|
1.79e-01
|
SUMOYLATION OF DNA METHYLATION PROTEINS
|
16
|
8.72e-01
|
9.15e-01
|
0.07510
|
-7.05e-02
|
-0.025700
|
6.25e-01
|
8.59e-01
|
FGFR2 ALTERNATIVE SPLICING
|
25
|
6.37e-01
|
7.58e-01
|
0.07480
|
1.38e-02
|
-0.073500
|
9.05e-01
|
5.25e-01
|
FOXO MEDIATED TRANSCRIPTION
|
57
|
4.73e-01
|
6.32e-01
|
0.07400
|
-7.39e-02
|
-0.004450
|
3.35e-01
|
9.54e-01
|
INSULIN RECEPTOR SIGNALLING CASCADE
|
46
|
3.85e-01
|
5.47e-01
|
0.07340
|
-2.95e-02
|
0.067200
|
7.29e-01
|
4.31e-01
|
FRS MEDIATED FGFR2 SIGNALING
|
19
|
8.45e-01
|
9.00e-01
|
0.07320
|
-2.15e-02
|
-0.070000
|
8.71e-01
|
5.97e-01
|
RIPK1 MEDIATED REGULATED NECROSIS
|
25
|
5.83e-01
|
7.21e-01
|
0.07260
|
3.71e-02
|
-0.062400
|
7.48e-01
|
5.89e-01
|
ACETYLCHOLINE NEUROTRANSMITTER RELEASE CYCLE
|
17
|
8.06e-01
|
8.72e-01
|
0.07200
|
3.48e-03
|
0.071900
|
9.80e-01
|
6.08e-01
|
AKT PHOSPHORYLATES TARGETS IN THE NUCLEUS
|
10
|
8.99e-01
|
9.37e-01
|
0.07200
|
1.20e-02
|
0.071000
|
9.47e-01
|
6.98e-01
|
APOPTOTIC EXECUTION PHASE
|
45
|
8.11e-01
|
8.74e-01
|
0.07130
|
5.33e-02
|
0.047400
|
5.37e-01
|
5.82e-01
|
YAP1 AND WWTR1 TAZ STIMULATED GENE EXPRESSION
|
12
|
8.28e-01
|
8.87e-01
|
0.07130
|
-1.05e-02
|
0.070500
|
9.50e-01
|
6.72e-01
|
THE CANONICAL RETINOID CYCLE IN RODS TWILIGHT VISION
|
14
|
9.37e-01
|
9.62e-01
|
0.07120
|
5.15e-02
|
0.049200
|
7.39e-01
|
7.50e-01
|
PURINERGIC SIGNALING IN LEISHMANIASIS INFECTION
|
23
|
6.29e-01
|
7.52e-01
|
0.07110
|
-6.31e-02
|
0.032700
|
6.00e-01
|
7.86e-01
|
UCH PROTEINASES
|
89
|
1.54e-01
|
3.04e-01
|
0.07060
|
5.65e-02
|
-0.042300
|
3.57e-01
|
4.90e-01
|
POTENTIAL THERAPEUTICS FOR SARS
|
77
|
6.10e-01
|
7.40e-01
|
0.07060
|
6.38e-02
|
0.030300
|
3.33e-01
|
6.46e-01
|
CHROMOSOME MAINTENANCE
|
104
|
5.22e-01
|
6.76e-01
|
0.07040
|
-3.09e-02
|
-0.063300
|
5.86e-01
|
2.65e-01
|
SUMOYLATION OF TRANSCRIPTION COFACTORS
|
42
|
6.77e-01
|
7.86e-01
|
0.07010
|
-6.85e-02
|
-0.015000
|
4.42e-01
|
8.66e-01
|
DUAL INCISION IN TC NER
|
65
|
6.61e-01
|
7.76e-01
|
0.06970
|
-6.33e-02
|
-0.029100
|
3.77e-01
|
6.85e-01
|
VOLTAGE GATED POTASSIUM CHANNELS
|
38
|
8.24e-01
|
8.83e-01
|
0.06950
|
3.78e-02
|
0.058300
|
6.87e-01
|
5.34e-01
|
CYTOPROTECTION BY HMOX1
|
119
|
8.79e-02
|
2.07e-01
|
0.06910
|
4.75e-02
|
-0.050200
|
3.71e-01
|
3.45e-01
|
DNA DAMAGE TELOMERE STRESS INDUCED SENESCENCE
|
46
|
6.72e-01
|
7.84e-01
|
0.06890
|
-1.64e-02
|
-0.067000
|
8.48e-01
|
4.32e-01
|
SUMOYLATION
|
168
|
3.63e-02
|
1.13e-01
|
0.06870
|
-5.55e-02
|
0.040500
|
2.15e-01
|
3.66e-01
|
SENESCENCE ASSOCIATED SECRETORY PHENOTYPE SASP
|
66
|
5.28e-01
|
6.82e-01
|
0.06830
|
-1.07e-02
|
-0.067400
|
8.81e-01
|
3.44e-01
|
HCMV EARLY EVENTS
|
83
|
6.71e-01
|
7.84e-01
|
0.06760
|
3.68e-02
|
0.056700
|
5.62e-01
|
3.72e-01
|
HATS ACETYLATE HISTONES
|
96
|
3.09e-01
|
4.81e-01
|
0.06740
|
-6.74e-02
|
0.001970
|
2.54e-01
|
9.73e-01
|
SEROTONIN NEUROTRANSMITTER RELEASE CYCLE
|
18
|
7.62e-01
|
8.43e-01
|
0.06690
|
6.51e-02
|
-0.015600
|
6.33e-01
|
9.09e-01
|
BIOSYNTHESIS OF SPECIALIZED PRORESOLVING MEDIATORS SPMS
|
11
|
9.55e-01
|
9.72e-01
|
0.06590
|
-4.06e-02
|
-0.051900
|
8.15e-01
|
7.66e-01
|
COMPLEMENT CASCADE
|
26
|
9.02e-01
|
9.37e-01
|
0.06570
|
4.96e-02
|
0.043000
|
6.61e-01
|
7.04e-01
|
FCERI MEDIATED CA 2 MOBILIZATION
|
26
|
8.73e-01
|
9.15e-01
|
0.06540
|
3.01e-02
|
0.058100
|
7.90e-01
|
6.08e-01
|
PHOSPHORYLATION OF THE APC C
|
17
|
9.14e-01
|
9.45e-01
|
0.06540
|
5.82e-02
|
0.029700
|
6.78e-01
|
8.32e-01
|
MOLECULES ASSOCIATED WITH ELASTIC FIBRES
|
33
|
5.52e-01
|
7.02e-01
|
0.06520
|
-3.97e-02
|
0.051700
|
6.93e-01
|
6.07e-01
|
CASPASE MEDIATED CLEAVAGE OF CYTOSKELETAL PROTEINS
|
12
|
9.09e-01
|
9.41e-01
|
0.06450
|
6.31e-02
|
0.013300
|
7.05e-01
|
9.36e-01
|
SIGNALING BY NOTCH1 PEST DOMAIN MUTANTS IN CANCER
|
59
|
7.82e-01
|
8.56e-01
|
0.06440
|
3.68e-02
|
0.052800
|
6.25e-01
|
4.83e-01
|
STIMULI SENSING CHANNELS
|
76
|
2.64e-01
|
4.35e-01
|
0.06400
|
-4.35e-02
|
0.046800
|
5.12e-01
|
4.80e-01
|
CELLULAR RESPONSES TO EXTERNAL STIMULI
|
604
|
8.27e-04
|
7.43e-03
|
0.06370
|
6.33e-02
|
-0.007360
|
8.13e-03
|
7.58e-01
|
P75NTR SIGNALS VIA NF KB
|
15
|
8.68e-01
|
9.13e-01
|
0.06360
|
-5.04e-03
|
-0.063400
|
9.73e-01
|
6.71e-01
|
CYTOKINE SIGNALING IN IMMUNE SYSTEM
|
541
|
1.61e-03
|
1.23e-02
|
0.06350
|
-8.09e-03
|
0.063000
|
7.48e-01
|
1.25e-02
|
G2 M CHECKPOINTS
|
136
|
1.69e-01
|
3.21e-01
|
0.06300
|
6.15e-02
|
-0.013500
|
2.16e-01
|
7.86e-01
|
TRNA PROCESSING
|
105
|
4.19e-01
|
5.82e-01
|
0.06260
|
8.93e-03
|
0.062000
|
8.74e-01
|
2.73e-01
|
TRANSCRIPTIONAL REGULATION BY RUNX2
|
108
|
2.31e-01
|
4.01e-01
|
0.06250
|
6.02e-02
|
-0.016800
|
2.80e-01
|
7.63e-01
|
SEMAPHORIN INTERACTIONS
|
64
|
6.29e-01
|
7.52e-01
|
0.06240
|
-6.08e-02
|
-0.014000
|
4.00e-01
|
8.46e-01
|
RESOLUTION OF AP SITES VIA THE MULTIPLE NUCLEOTIDE PATCH REPLACEMENT PATHWAY
|
25
|
9.14e-01
|
9.45e-01
|
0.06240
|
-4.05e-02
|
-0.047500
|
7.26e-01
|
6.81e-01
|
PYRIMIDINE CATABOLISM
|
10
|
9.02e-01
|
9.37e-01
|
0.06210
|
1.43e-03
|
-0.062100
|
9.94e-01
|
7.34e-01
|
REGULATION OF TP53 ACTIVITY THROUGH PHOSPHORYLATION
|
88
|
7.14e-01
|
8.12e-01
|
0.06150
|
-5.05e-02
|
-0.035100
|
4.13e-01
|
5.69e-01
|
SIGNALING BY FGFR
|
74
|
5.82e-01
|
7.21e-01
|
0.06110
|
5.99e-02
|
0.011700
|
3.73e-01
|
8.62e-01
|
REGULATION OF LIPID METABOLISM BY PPARALPHA
|
108
|
1.87e-01
|
3.48e-01
|
0.06040
|
-4.57e-02
|
0.039400
|
4.12e-01
|
4.79e-01
|
FORMATION OF THE EARLY ELONGATION COMPLEX
|
33
|
6.49e-01
|
7.67e-01
|
0.05940
|
2.08e-02
|
-0.055700
|
8.36e-01
|
5.80e-01
|
DNA REPAIR
|
295
|
1.27e-01
|
2.71e-01
|
0.05890
|
-5.81e-02
|
-0.009870
|
8.65e-02
|
7.71e-01
|
IRAK2 MEDIATED ACTIVATION OF TAK1 COMPLEX
|
10
|
8.91e-01
|
9.30e-01
|
0.05860
|
-1.36e-02
|
0.057000
|
9.41e-01
|
7.55e-01
|
ANTIGEN PROCESSING CROSS PRESENTATION
|
96
|
3.62e-01
|
5.28e-01
|
0.05850
|
5.78e-02
|
-0.008810
|
3.28e-01
|
8.81e-01
|
DDX58 IFIH1 MEDIATED INDUCTION OF INTERFERON ALPHA BETA
|
63
|
4.59e-01
|
6.20e-01
|
0.05700
|
-2.20e-02
|
0.052600
|
7.63e-01
|
4.71e-01
|
EXTENSION OF TELOMERES
|
49
|
8.47e-01
|
9.00e-01
|
0.05600
|
2.95e-02
|
0.047600
|
7.21e-01
|
5.64e-01
|
TRANSCRIPTIONAL REGULATION BY VENTX
|
35
|
8.66e-01
|
9.13e-01
|
0.05500
|
-2.19e-02
|
-0.050400
|
8.22e-01
|
6.06e-01
|
DUAL INCISION IN GG NER
|
41
|
7.46e-01
|
8.33e-01
|
0.05490
|
-5.48e-02
|
-0.003790
|
5.44e-01
|
9.67e-01
|
THE CITRIC ACID TCA CYCLE AND RESPIRATORY ELECTRON TRANSPORT
|
172
|
1.49e-01
|
2.99e-01
|
0.05450
|
1.99e-02
|
-0.050800
|
6.54e-01
|
2.51e-01
|
INCRETIN SYNTHESIS SECRETION AND INACTIVATION
|
14
|
8.48e-01
|
9.01e-01
|
0.05430
|
4.81e-02
|
-0.025100
|
7.55e-01
|
8.71e-01
|
ELASTIC FIBRE FORMATION
|
38
|
6.32e-01
|
7.53e-01
|
0.05310
|
-3.94e-02
|
0.035600
|
6.74e-01
|
7.05e-01
|
TP53 REGULATES METABOLIC GENES
|
85
|
6.36e-01
|
7.57e-01
|
0.05310
|
-1.13e-02
|
-0.051900
|
8.57e-01
|
4.09e-01
|
SIGNALING BY FGFR2
|
63
|
6.73e-01
|
7.85e-01
|
0.05270
|
5.25e-02
|
0.005340
|
4.72e-01
|
9.42e-01
|
ANTIMICROBIAL PEPTIDES
|
15
|
9.49e-01
|
9.68e-01
|
0.05230
|
2.25e-02
|
0.047200
|
8.80e-01
|
7.52e-01
|
RUNX2 REGULATES OSTEOBLAST DIFFERENTIATION
|
23
|
9.29e-01
|
9.57e-01
|
0.05170
|
2.42e-02
|
0.045700
|
8.40e-01
|
7.05e-01
|
ACTIVATION OF ATR IN RESPONSE TO REPLICATION STRESS
|
33
|
7.14e-01
|
8.11e-01
|
0.05130
|
-2.15e-02
|
0.046500
|
8.31e-01
|
6.44e-01
|
DOWNSTREAM SIGNALING OF ACTIVATED FGFR4
|
20
|
8.33e-01
|
8.91e-01
|
0.04930
|
4.60e-02
|
-0.017900
|
7.22e-01
|
8.90e-01
|
ANCHORING OF THE BASAL BODY TO THE PLASMA MEMBRANE
|
96
|
4.21e-01
|
5.83e-01
|
0.04900
|
4.55e-02
|
-0.018200
|
4.41e-01
|
7.58e-01
|
RHO GTPASES ACTIVATE PAKS
|
21
|
8.18e-01
|
8.81e-01
|
0.04880
|
4.31e-02
|
-0.023000
|
7.33e-01
|
8.55e-01
|
FORMATION OF RNA POL II ELONGATION COMPLEX
|
57
|
7.35e-01
|
8.25e-01
|
0.04870
|
-4.58e-03
|
-0.048400
|
9.52e-01
|
5.27e-01
|
GRB2 EVENTS IN ERBB2 SIGNALING
|
15
|
8.64e-01
|
9.12e-01
|
0.04840
|
2.62e-02
|
-0.040700
|
8.61e-01
|
7.85e-01
|
SURFACTANT METABOLISM
|
16
|
9.26e-01
|
9.55e-01
|
0.04810
|
4.75e-02
|
0.007420
|
7.42e-01
|
9.59e-01
|
RRNA MODIFICATION IN THE NUCLEUS AND CYTOSOL
|
59
|
7.16e-01
|
8.12e-01
|
0.04550
|
1.85e-03
|
-0.045500
|
9.80e-01
|
5.46e-01
|
NOTCH1 INTRACELLULAR DOMAIN REGULATES TRANSCRIPTION
|
48
|
6.88e-01
|
7.94e-01
|
0.04530
|
-1.74e-02
|
0.041800
|
8.34e-01
|
6.17e-01
|
MRNA CAPPING
|
29
|
9.41e-01
|
9.64e-01
|
0.04480
|
3.75e-02
|
0.024400
|
7.26e-01
|
8.20e-01
|
SMAD2 SMAD3 SMAD4 HETEROTRIMER REGULATES TRANSCRIPTION
|
31
|
8.20e-01
|
8.82e-01
|
0.04440
|
-8.59e-03
|
0.043500
|
9.34e-01
|
6.75e-01
|
TRANSPORT OF MATURE TRANSCRIPT TO CYTOPLASM
|
79
|
8.06e-01
|
8.72e-01
|
0.04430
|
1.70e-02
|
0.040800
|
7.93e-01
|
5.31e-01
|
SYNTHESIS SECRETION AND INACTIVATION OF GLUCAGON LIKE PEPTIDE 1 GLP 1
|
13
|
9.25e-01
|
9.55e-01
|
0.04410
|
6.18e-03
|
-0.043700
|
9.69e-01
|
7.85e-01
|
EXTRACELLULAR MATRIX ORGANIZATION
|
250
|
4.82e-01
|
6.43e-01
|
0.04360
|
-4.12e-02
|
-0.014200
|
2.63e-01
|
6.99e-01
|
SIGNALING BY NUCLEAR RECEPTORS
|
228
|
6.84e-01
|
7.92e-01
|
0.04310
|
3.09e-02
|
0.030100
|
4.22e-01
|
4.35e-01
|
METABOLISM OF RNA
|
644
|
8.33e-03
|
3.72e-02
|
0.04300
|
2.36e-02
|
-0.036000
|
3.09e-01
|
1.21e-01
|
TRANSCRIPTIONAL REGULATION OF WHITE ADIPOCYTE DIFFERENTIATION
|
74
|
5.85e-01
|
7.22e-01
|
0.04290
|
-3.85e-02
|
0.018900
|
5.67e-01
|
7.79e-01
|
SEMA4D IN SEMAPHORIN SIGNALING
|
24
|
8.53e-01
|
9.04e-01
|
0.04280
|
-1.34e-02
|
0.040600
|
9.09e-01
|
7.31e-01
|
DEADENYLATION DEPENDENT MRNA DECAY
|
55
|
6.62e-01
|
7.77e-01
|
0.04270
|
-3.63e-02
|
0.022500
|
6.42e-01
|
7.73e-01
|
REGULATION OF BETA CELL DEVELOPMENT
|
30
|
9.32e-01
|
9.59e-01
|
0.04270
|
-3.85e-02
|
-0.018400
|
7.15e-01
|
8.62e-01
|
CASPASE ACTIVATION VIA EXTRINSIC APOPTOTIC SIGNALLING PATHWAY
|
23
|
8.65e-01
|
9.12e-01
|
0.04240
|
-4.07e-02
|
0.011700
|
7.35e-01
|
9.22e-01
|
MRNA SPLICING MINOR PATHWAY
|
52
|
6.78e-01
|
7.87e-01
|
0.04200
|
3.34e-02
|
-0.025500
|
6.77e-01
|
7.50e-01
|
SIGNALING BY PDGFR IN DISEASE
|
20
|
9.01e-01
|
9.37e-01
|
0.04180
|
-4.62e-03
|
0.041500
|
9.71e-01
|
7.48e-01
|
DISEASES ASSOCIATED WITH O GLYCOSYLATION OF PROTEINS
|
50
|
8.90e-01
|
9.30e-01
|
0.04150
|
-3.80e-02
|
-0.016700
|
6.42e-01
|
8.38e-01
|
TAK1 ACTIVATES NFKB BY PHOSPHORYLATION AND ACTIVATION OF IKKS COMPLEX
|
30
|
9.03e-01
|
9.37e-01
|
0.04150
|
4.08e-02
|
0.007750
|
6.99e-01
|
9.41e-01
|
SIGNALING BY TGF BETA RECEPTOR COMPLEX
|
72
|
7.82e-01
|
8.56e-01
|
0.04130
|
7.38e-03
|
0.040700
|
9.14e-01
|
5.51e-01
|
DNA DOUBLE STRAND BREAK RESPONSE
|
55
|
8.46e-01
|
9.00e-01
|
0.04120
|
1.02e-02
|
0.040000
|
8.96e-01
|
6.08e-01
|
DOWNREGULATION OF TGF BETA RECEPTOR SIGNALING
|
26
|
9.33e-01
|
9.59e-01
|
0.04110
|
3.90e-02
|
0.013100
|
7.31e-01
|
9.08e-01
|
PROCESSING OF CAPPED INTRON CONTAINING PRE MRNA
|
237
|
1.98e-01
|
3.61e-01
|
0.04090
|
3.45e-02
|
-0.021900
|
3.61e-01
|
5.62e-01
|
SIGNALING BY ERYTHROPOIETIN
|
24
|
8.56e-01
|
9.06e-01
|
0.04080
|
-3.69e-02
|
0.017200
|
7.54e-01
|
8.84e-01
|
CA2 PATHWAY
|
59
|
6.59e-01
|
7.75e-01
|
0.04060
|
2.99e-02
|
-0.027500
|
6.92e-01
|
7.15e-01
|
RNA POLYMERASE II TRANSCRIBES SNRNA GENES
|
74
|
7.12e-01
|
8.11e-01
|
0.03940
|
3.92e-02
|
-0.004100
|
5.60e-01
|
9.51e-01
|
GENERATION OF SECOND MESSENGER MOLECULES
|
19
|
9.65e-01
|
9.79e-01
|
0.03930
|
-3.50e-02
|
-0.018000
|
7.92e-01
|
8.92e-01
|
RNA POLYMERASE I TRANSCRIPTION INITIATION
|
47
|
7.43e-01
|
8.33e-01
|
0.03920
|
-3.35e-02
|
0.020400
|
6.92e-01
|
8.09e-01
|
NEGATIVE REGULATION OF TCF DEPENDENT SIGNALING BY WNT LIGAND ANTAGONISTS
|
11
|
9.48e-01
|
9.68e-01
|
0.03710
|
3.55e-02
|
-0.010600
|
8.38e-01
|
9.51e-01
|
NONHOMOLOGOUS END JOINING NHEJ
|
46
|
9.42e-01
|
9.64e-01
|
0.03690
|
-2.89e-02
|
-0.022900
|
7.34e-01
|
7.88e-01
|
DOWNSTREAM SIGNALING OF ACTIVATED FGFR1
|
26
|
9.33e-01
|
9.59e-01
|
0.03570
|
-3.53e-02
|
-0.005610
|
7.56e-01
|
9.61e-01
|
SIGNALING BY NOTCH
|
192
|
6.42e-01
|
7.61e-01
|
0.03490
|
3.41e-02
|
0.007300
|
4.15e-01
|
8.62e-01
|
TGF BETA RECEPTOR SIGNALING ACTIVATES SMADS
|
32
|
8.72e-01
|
9.15e-01
|
0.03460
|
1.02e-02
|
-0.033100
|
9.21e-01
|
7.46e-01
|
SIGNALING BY PDGF
|
56
|
8.44e-01
|
9.00e-01
|
0.03460
|
-3.46e-02
|
-0.000609
|
6.55e-01
|
9.94e-01
|
HIV TRANSCRIPTION INITIATION
|
45
|
8.11e-01
|
8.74e-01
|
0.03410
|
-3.01e-02
|
0.015900
|
7.27e-01
|
8.53e-01
|
NUCLEOTIDE EXCISION REPAIR
|
110
|
7.84e-01
|
8.58e-01
|
0.03240
|
3.20e-02
|
0.004690
|
5.62e-01
|
9.32e-01
|
TP53 REGULATES TRANSCRIPTION OF CELL DEATH GENES
|
37
|
9.42e-01
|
9.64e-01
|
0.03210
|
-3.04e-02
|
-0.010500
|
7.49e-01
|
9.12e-01
|
IRAK1 RECRUITS IKK COMPLEX
|
14
|
9.86e-01
|
9.93e-01
|
0.03210
|
2.01e-02
|
0.025100
|
8.96e-01
|
8.71e-01
|
MITOCHONDRIAL BIOGENESIS
|
92
|
7.45e-01
|
8.33e-01
|
0.03100
|
-3.02e-02
|
0.006940
|
6.17e-01
|
9.08e-01
|
SIGNALING BY ERBB2 IN CANCER
|
25
|
9.75e-01
|
9.88e-01
|
0.03080
|
1.65e-02
|
0.026000
|
8.87e-01
|
8.22e-01
|
METABOLIC DISORDERS OF BIOLOGICAL OXIDATION ENZYMES
|
20
|
9.84e-01
|
9.92e-01
|
0.02980
|
2.21e-02
|
0.020100
|
8.64e-01
|
8.76e-01
|
FRS MEDIATED FGFR1 SIGNALING
|
18
|
9.36e-01
|
9.62e-01
|
0.02950
|
2.44e-02
|
-0.016700
|
8.58e-01
|
9.02e-01
|
APOPTOTIC FACTOR MEDIATED RESPONSE
|
18
|
9.55e-01
|
9.72e-01
|
0.02950
|
2.94e-02
|
-0.003090
|
8.29e-01
|
9.82e-01
|
TP53 REGULATES TRANSCRIPTION OF GENES INVOLVED IN CYTOCHROME C RELEASE
|
19
|
9.79e-01
|
9.90e-01
|
0.02760
|
2.58e-02
|
0.009670
|
8.45e-01
|
9.42e-01
|
RECRUITMENT OF MITOTIC CENTROSOME PROTEINS AND COMPLEXES
|
78
|
9.52e-01
|
9.71e-01
|
0.02610
|
2.00e-02
|
0.016800
|
7.60e-01
|
7.98e-01
|
TRANSCRIPTION COUPLED NUCLEOTIDE EXCISION REPAIR TC NER
|
78
|
9.45e-01
|
9.67e-01
|
0.02580
|
1.36e-02
|
0.022000
|
8.35e-01
|
7.38e-01
|
SENSORY PROCESSING OF SOUND BY OUTER HAIR CELLS OF THE COCHLEA
|
41
|
8.98e-01
|
9.37e-01
|
0.02500
|
-1.43e-02
|
0.020500
|
8.74e-01
|
8.21e-01
|
NERVOUS SYSTEM DEVELOPMENT
|
553
|
3.42e-01
|
5.12e-01
|
0.02310
|
2.15e-02
|
-0.008400
|
3.89e-01
|
7.36e-01
|
METALLOPROTEASE DUBS
|
26
|
9.55e-01
|
9.72e-01
|
0.02230
|
2.13e-02
|
-0.006740
|
8.51e-01
|
9.53e-01
|
SENSORY PROCESSING OF SOUND
|
62
|
9.59e-01
|
9.74e-01
|
0.02220
|
-8.75e-03
|
-0.020400
|
9.05e-01
|
7.81e-01
|
DEVELOPMENTAL BIOLOGY
|
830
|
2.94e-01
|
4.67e-01
|
0.02150
|
4.73e-03
|
-0.021000
|
8.18e-01
|
3.06e-01
|
DAP12 SIGNALING
|
24
|
9.90e-01
|
9.94e-01
|
0.02130
|
-1.62e-02
|
-0.013800
|
8.91e-01
|
9.07e-01
|
RNA POLYMERASE II TRANSCRIPTION
|
1097
|
2.96e-01
|
4.68e-01
|
0.02020
|
-2.01e-02
|
0.001810
|
2.65e-01
|
9.20e-01
|
ABERRANT REGULATION OF MITOTIC G1 S TRANSITION IN CANCER DUE TO RB1 DEFECTS
|
17
|
9.86e-01
|
9.93e-01
|
0.01930
|
1.92e-02
|
0.002290
|
8.91e-01
|
9.87e-01
|
DOWNREGULATION OF ERBB2 SIGNALING
|
28
|
9.56e-01
|
9.72e-01
|
0.01930
|
-1.24e-02
|
0.014800
|
9.09e-01
|
8.92e-01
|
ARACHIDONIC ACID METABOLISM
|
38
|
9.83e-01
|
9.92e-01
|
0.01930
|
8.79e-03
|
0.017200
|
9.25e-01
|
8.55e-01
|
TRANSCRIPTIONAL REGULATION BY TP53
|
343
|
8.69e-01
|
9.13e-01
|
0.01610
|
5.01e-03
|
0.015300
|
8.74e-01
|
6.26e-01
|
SYNDECAN INTERACTIONS
|
27
|
9.92e-01
|
9.96e-01
|
0.01430
|
1.32e-02
|
0.005430
|
9.05e-01
|
9.61e-01
|
ESR MEDIATED SIGNALING
|
171
|
8.67e-01
|
9.13e-01
|
0.01400
|
1.05e-02
|
-0.009290
|
8.13e-01
|
8.34e-01
|
PERK REGULATES GENE EXPRESSION
|
28
|
9.79e-01
|
9.90e-01
|
0.01360
|
1.11e-02
|
-0.007850
|
9.19e-01
|
9.43e-01
|
SIGNALING BY FGFR IN DISEASE
|
57
|
9.80e-01
|
9.90e-01
|
0.01270
|
-1.26e-02
|
-0.001370
|
8.69e-01
|
9.86e-01
|
DOPAMINE NEUROTRANSMITTER RELEASE CYCLE
|
23
|
9.97e-01
|
9.97e-01
|
0.01130
|
5.77e-03
|
0.009660
|
9.62e-01
|
9.36e-01
|
TRANSCRIPTION OF THE HIV GENOME
|
67
|
9.89e-01
|
9.94e-01
|
0.01070
|
9.91e-03
|
0.004010
|
8.89e-01
|
9.55e-01
|
PROCESSING OF INTRONLESS PRE MRNAS
|
19
|
9.93e-01
|
9.96e-01
|
0.00989
|
-3.20e-03
|
0.009360
|
9.81e-01
|
9.44e-01
|
RECOGNITION OF DNA DAMAGE BY PCNA CONTAINING REPLICATION COMPLEX
|
29
|
9.97e-01
|
9.97e-01
|
0.00972
|
-5.63e-03
|
-0.007930
|
9.58e-01
|
9.41e-01
|
CELLULAR SENESCENCE
|
144
|
9.76e-01
|
9.89e-01
|
0.00875
|
1.02e-03
|
0.008690
|
9.83e-01
|
8.57e-01
|
REGULATION OF PLK1 ACTIVITY AT G2 M TRANSITION
|
85
|
9.88e-01
|
9.94e-01
|
0.00590
|
5.12e-03
|
-0.002930
|
9.35e-01
|
9.63e-01
|
AURKA ACTIVATION BY TPX2
|
71
|
9.97e-01
|
9.97e-01
|
0.00315
|
-2.93e-03
|
0.001160
|
9.66e-01
|
9.86e-01
|