| 3 5 CYCLIC NUCLEOTIDE PHOSPHODIESTERASE ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| ACCGAGC,MIR-423 |
TFmiRNA_Targets.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| ACETYLCHOLINE BINDING |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| ACGCACA,MIR-210 |
TFmiRNA_Targets.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| ACTIN FILAMENT BASED MOVEMENT |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| ADP signalling through P2Y purinoceptor 1 |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
12.0 |
12.0 |
8.74 |
| AGCGCAG,MIR-191 |
TFmiRNA_Targets.gmt.txt |
-1.7976931348623157E308 |
0.0 |
7.0 |
7.0 |
5.1 |
| AKT-mediated inactivation of FOXO1A |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| ALDO KETO REDUCTASE ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| AMINE BIOSYNTHETIC PROCESS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
9.0 |
9.0 |
6.56 |
| AMINO ACID DERIVATIVE BIOSYNTHETIC PROCESS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| ANION CATION SYMPORTER ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| ANION CHANNEL ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| ANION TRANSPORT |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
7.0 |
7.0 |
5.1 |
| ANTIOXIDANT ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
8.0 |
8.0 |
5.83 |
| APICAL PLASMA MEMBRANE |
GO_-_Cellular_Component.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| ARYLSULFATASE ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| ATPASE ACTIVITY COUPLED TO TRANSMEMBRANE MOVEMENT OF IONS |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
15.0 |
15.0 |
10.93 |
| ATPASE ACTIVITY COUPLED TO TRANSMEMBRANE MOVEMENT OF IONS PHOSPHORYLATIVE MECHANISM |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
11.0 |
11.0 |
8.01 |
| Acetylcholine Binding And Downstream Events |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Activation of G protein gated Potassium channels |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
7.0 |
7.0 |
5.1 |
| Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| Activation of NOXA and translocation to mitochondria |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| Activation of Nicotinic Acetylcholine Receptors |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Activation of PKB |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Activation of PUMA and translocation to mitochondria |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| Activation of RAS in B Cells |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| Activation of caspases through apoptosome-mediated cleavage |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| Adherens junctions interactions |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Apoptotic factor-mediated response |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| Assembly of the ORC complex at the origin of replication |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| Axonal growth inhibition (RHOA activation) |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| BIOCARTA AMI PATHWAY |
Pathways_-_KEGGBioCarta.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| BIOCARTA CELL2CELL PATHWAY |
Pathways_-_KEGGBioCarta.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| BIOCARTA FEEDER PATHWAY |
Pathways_-_KEGGBioCarta.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| BIOCARTA FIBRINOLYSIS PATHWAY |
Pathways_-_KEGGBioCarta.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| BIOCARTA IL10 PATHWAY |
Pathways_-_KEGGBioCarta.gmt.txt |
-1.7976931348623157E308 |
0.0 |
8.0 |
8.0 |
5.83 |
| BIOCARTA IL22BP PATHWAY |
Pathways_-_KEGGBioCarta.gmt.txt |
-1.7976931348623157E308 |
0.0 |
9.0 |
9.0 |
6.56 |
| BIOCARTA INTRINSIC PATHWAY |
Pathways_-_KEGGBioCarta.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| BIOCARTA PLATELETAPP PATHWAY |
Pathways_-_KEGGBioCarta.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| BIOCARTA PTC1 PATHWAY |
Pathways_-_KEGGBioCarta.gmt.txt |
-1.7976931348623157E308 |
0.0 |
9.0 |
9.0 |
6.56 |
| BIOCARTA SARS PATHWAY |
Pathways_-_KEGGBioCarta.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| BIOPOLYMER BIOSYNTHETIC PROCESS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| BRUSH BORDER |
GO_-_Cellular_Component.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Beta oxidation of butanoyl-CoA to acetyl-CoA |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Bicarbonate transporters |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| Bile acid and bile salt metabolism |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| Binding of RNA by Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| CAGCTG V$AP4 Q5 |
TFmiRNA_Targets.gmt.txt |
-4.0 |
0.01121 |
491.0 |
392.0 |
357.73 |
| CALCIUM ION TRANSMEMBRANE TRANSPORTER ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
7.0 |
7.0 |
5.1 |
| CARBONATE DEHYDRATASE ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| CATION TRANSPORTING ATPASE ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
9.0 |
9.0 |
6.56 |
| CELLULAR POLYSACCHARIDE METABOLIC PROCESS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| CELLULAR PROTEIN COMPLEX DISASSEMBLY |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
11.0 |
11.0 |
8.01 |
| CGCTGCT,MIR-503 |
TFmiRNA_Targets.gmt.txt |
-1.7976931348623157E308 |
0.0 |
9.0 |
9.0 |
6.56 |
| CHLORIDE CHANNEL ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| COFACTOR TRANSPORT |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| COFACTOR TRANSPORTER ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| CONTRACTILE FIBER PART |
GO_-_Cellular_Component.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| CREB phosphorylation through the activation of Adenylate Cyclase |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| CYCLIC NUCLEOTIDE METABOLIC PROCESS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| CYCLIC NUCLEOTIDE PHOSPHODIESTERASE ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| CYTOSOL |
GO_-_Cellular_Component.gmt.txt |
-3.5 |
0.01245 |
123.0 |
105.0 |
89.61 |
| Carnitine synthesis |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Cleavage of the damaged purine |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Coenzyme A biosynthesis |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| Cyclin B2 mediated events |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| Cytochrome c-mediated apoptotic response |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| Cytosolic sulfonation of small molecules |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| DEAMINASE ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| DNA strand elongation |
Pathways_-_Reactome.gmt.txt |
-2.8 |
0.01939 |
28.0 |
26.0 |
20.4 |
| DRUG BINDING |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
10.0 |
10.0 |
7.29 |
| Degradation of cysteine and homocysteine |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| Depurination |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Disinhibition of SNARE formation |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Dissolution of Fibrin Clot |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Downregulation of ERBB4 signaling |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| Downregulation of ERRB2:ERBB3 signaling |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
8.0 |
8.0 |
5.83 |
| E2F-enabled inhibition of pre-replication complex formation |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
10.0 |
10.0 |
7.29 |
| EXTERNAL SIDE OF PLASMA MEMBRANE |
GO_-_Cellular_Component.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| EXTRACELLULAR STRUCTURE ORGANIZATION AND BIOGENESIS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
7.0 |
7.0 |
5.1 |
| Eicosanoid ligand-binding receptors |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| Endosomal/Vacuolar pathway |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| Extension of Telomeres |
Pathways_-_Reactome.gmt.txt |
-2.6 |
0.03244 |
26.0 |
24.0 |
18.94 |
| FATTY ACID BETA OXIDATION |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
11.0 |
11.0 |
8.01 |
| FEMALE GAMETE GENERATION |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| Formation of annular gap junctions |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
7.0 |
7.0 |
5.1 |
| Formyl peptide receptors bind formyl peptides and many other ligands |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| G beta:gamma signalling through PI3Kgamma |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
14.0 |
14.0 |
10.2 |
| G beta:gamma signalling through PLC beta |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
10.0 |
10.0 |
7.29 |
| G protein gated Potassium channels |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
7.0 |
7.0 |
5.1 |
| G-protein beta:gamma signalling |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
16.0 |
16.0 |
11.66 |
| GCANCTGNY V$MYOD Q6 |
TFmiRNA_Targets.gmt.txt |
-5.2 |
9.1E-4 |
299.0 |
249.0 |
217.84 |
| GGGAGGRR V$MAZ Q6 |
TFmiRNA_Targets.gmt.txt |
-4.1 |
0.00965 |
850.0 |
665.0 |
619.29 |
| GGGCGGR V$SP1 Q6 |
TFmiRNA_Targets.gmt.txt |
-4.0 |
0.01121 |
1371.0 |
1055.0 |
998.88 |
| GLUCAN METABOLIC PROCESS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| GLYCOLIPID METABOLIC PROCESS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
7.0 |
7.0 |
5.1 |
| GLYCOSPHINGOLIPID METABOLIC PROCESS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| GTCGATC,MIR-369-5P |
TFmiRNA_Targets.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| Gap junction degradation |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
7.0 |
7.0 |
5.1 |
| Gap junction trafficking |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
9.0 |
9.0 |
6.56 |
| Gap junction trafficking and regulation |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
9.0 |
9.0 |
6.56 |
| Gap-filling DNA repair synthesis and ligation in GG-NER |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
15.0 |
15.0 |
10.93 |
| Gap-filling DNA repair synthesis and ligation in TC-NER |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
15.0 |
15.0 |
10.93 |
| Global Genomic NER (GG-NER) |
Pathways_-_Reactome.gmt.txt |
-2.9 |
0.01526 |
29.0 |
27.0 |
21.13 |
| Glycogen synthesis |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| HDL-mediated lipid transport |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| HISTONE DEACETYLASE BINDING |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
8.0 |
8.0 |
5.83 |
| HIV 2-LTR circle formation |
HIV_Collection.gmt.txt |
-1.7976931348623157E308 |
0.0 |
7.0 |
7.0 |
5.1 |
| HIV Autointegration results in viral DNA circles |
HIV_Collection.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| HIV Integration of viral DNA into host genomic DNA |
HIV_Collection.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| HIV Nef Mediated CD4 Down-regulation |
HIV_Collection.gmt.txt |
-1.7976931348623157E308 |
0.0 |
8.0 |
8.0 |
5.83 |
| HIV Nef Mediated CD8 Down-regulation |
HIV_Collection.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| HIV Nef mediated downregulation of MHC class I complex cell surface expression |
HIV_Collection.gmt.txt |
-1.7976931348623157E308 |
0.0 |
8.0 |
8.0 |
5.83 |
| HIV Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters |
HIV_Collection.gmt.txt |
-1.7976931348623157E308 |
0.0 |
17.0 |
17.0 |
12.39 |
| HIV A0EXJ4 VPU |
HIV_Collection.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| HIV P88795 POL |
HIV_Collection.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| HIV Q9PY17 |
HIV_Collection.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| HYDROLASE ACTIVITY ACTING ON CARBON NITROGEN NOT PEPTIDEBONDSIN CYCLIC AMIDINES |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| Highly calcium permeable nicotinic acetylcholine receptors |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Highly calcium permeable postsynaptic nicotinic acetylcholine receptors |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Host Interactions with Influenza Factors |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| Hypusine synthesis from eIF5A-lysine |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| INORGANIC ANION TRANSMEMBRANE TRANSPORTER ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| INSOLUBLE FRACTION |
GO_-_Cellular_Component.gmt.txt |
-1.7976931348623157E308 |
0.0 |
7.0 |
7.0 |
5.1 |
| INSULIN LIKE GROWTH FACTOR RECEPTOR BINDING |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| INTERLEUKIN 1 SECRETION |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| INTERLEUKIN BINDING |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| INTERLEUKIN RECEPTOR ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| INWARD RECTIFIER POTASSIUM CHANNEL ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
7.0 |
7.0 |
5.1 |
| Inwardly rectifying K+ channels |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
8.0 |
8.0 |
5.83 |
| Ion channel transport |
Pathways_-_Reactome.gmt.txt |
-2.6 |
0.02841 |
19.0 |
18.0 |
13.84 |
| Ion transport by P-type ATPases |
Pathways_-_Reactome.gmt.txt |
-2.5 |
0.03803 |
18.0 |
17.0 |
13.11 |
| KEGG DNA REPLICATION |
Pathways_-_KEGGBioCarta.gmt.txt |
-3.3 |
0.01989 |
32.0 |
30.0 |
23.31 |
| KEGG HEDGEHOG SIGNALING PATHWAY |
Pathways_-_KEGGBioCarta.gmt.txt |
-1.7976931348623157E308 |
0.0 |
21.0 |
21.0 |
15.3 |
| KEGG NUCLEOTIDE EXCISION REPAIR |
Pathways_-_KEGGBioCarta.gmt.txt |
-3.1 |
0.03214 |
37.0 |
34.0 |
26.96 |
| KEGG PANTOTHENATE AND COA BIOSYNTHESIS |
Pathways_-_KEGGBioCarta.gmt.txt |
-1.7976931348623157E308 |
0.0 |
9.0 |
9.0 |
6.56 |
| KEGG PRIMARY BILE ACID BIOSYNTHESIS |
Pathways_-_KEGGBioCarta.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| LEARNING AND OR MEMORY |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| LEUKOCYTE CHEMOTAXIS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Lipoprotein metabolism |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| MACROMOLECULAR COMPLEX DISASSEMBLY |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
12.0 |
12.0 |
8.74 |
| MAINTENANCE OF CELLULAR LOCALIZATION |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
8.0 |
8.0 |
5.83 |
| MAINTENANCE OF CELLULAR PROTEIN LOCALIZATION |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
8.0 |
8.0 |
5.83 |
| MONOCARBOXYLIC ACID TRANSMEMBRANE TRANSPORTER ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| MONOCARBOXYLIC ACID TRANSPORT |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| MORPHOGENESIS OF AN EPITHELIUM |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| MYOFIBRIL |
GO_-_Cellular_Component.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| Metabolism of folate and pterines |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
7.0 |
7.0 |
5.1 |
| Metabolism of vitamins and cofactors |
Pathways_-_Reactome.gmt.txt |
-2.8 |
0.0182 |
35.0 |
32.0 |
25.5 |
| Metabolism of water-soluble vitamins and cofactors |
Pathways_-_Reactome.gmt.txt |
-2.8 |
0.0182 |
35.0 |
32.0 |
25.5 |
| Mitochondrial ABC transporters |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Mitochondrial Protein Import |
Pathways_-_Reactome.gmt.txt |
-2.7 |
0.02284 |
46.0 |
41.0 |
33.51 |
| NEGATIVE REGULATION OF ANGIOGENESIS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| NEGATIVE REGULATION OF IMMUNE SYSTEM PROCESS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| NEGATIVE REGULATION OF INTRACELLULAR TRANSPORT |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| NEGATIVE REGULATION OF PHOSPHATE METABOLIC PROCESS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| NEGATIVE REGULATION OF PHOSPHORYLATION |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| NEUROTRANSMITTER BINDING |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| NEUROTRANSMITTER RECEPTOR ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| NS1 Mediated Effects on Host Pathways |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Nonhomologous End-joining (NHEJ) |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| Nucleotide-like (purinergic) receptors |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| OXIDOREDUCTASE ACTIVITY ACTING ON PEROXIDE AS ACCEPTOR |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| PEPTIDE METABOLIC PROCESS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| PEPTIDE RECEPTOR ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| PHAGOCYTOSIS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| PHOSPHATE TRANSMEMBRANE TRANSPORTER ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| PHOSPHOLIPASE C ACTIVATION |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| PHOSPHOLIPASE C ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| PLASMA MEMBRANE |
GO_-_Cellular_Component.gmt.txt |
-3.0 |
0.03493 |
426.0 |
337.0 |
310.37 |
| POSITIVE REGULATION OF CYTOKINE BIOSYNTHETIC PROCESS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| POSITIVE REGULATION OF PEPTIDYL TYROSINE PHOSPHORYLATION |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| POSITIVE REGULATION OF PROTEIN SECRETION |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| POSITIVE REGULATION OF SECRETION |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| PP2A-mediated dephosphorylation of key metabolic factors |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| PROTEIN AMINO ACID ADP RIBOSYLATION |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
7.0 |
7.0 |
5.1 |
| PROTEIN COMPLEX DISASSEMBLY |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
11.0 |
11.0 |
8.01 |
| PROTEIN SERINE THREONINE PHOSPHATASE COMPLEX |
GO_-_Cellular_Component.gmt.txt |
-1.7976931348623157E308 |
0.0 |
9.0 |
9.0 |
6.56 |
| Post-transcriptional Silencing By Small RNAs |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| Postsynaptic nicotinic acetylcholine receptors |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Pre-NOTCH Expression and Processing |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
24.0 |
24.0 |
17.49 |
| Pre-NOTCH Processing in Golgi |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
14.0 |
14.0 |
10.2 |
| Pre-NOTCH Processing in the Endoplasmic Reticulum |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| Pre-NOTCH Transcription and Translation |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
11.0 |
11.0 |
8.01 |
| Pregnenolone biosynthesis |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Presynaptic function of Kainate receptors |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
10.0 |
10.0 |
7.29 |
| Presynaptic nicotinic acetylcholine receptors |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Processing of DNA ends prior to end rejoining |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| Prostanoid metabolism |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Purine catabolism |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| REGULATION OF ENDOTHELIAL CELL PROLIFERATION |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| REGULATION OF JAK STAT CASCADE |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| REGULATION OF NEUROGENESIS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| REGULATION OF PEPTIDYL TYROSINE PHOSPHORYLATION |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| REGULATION OF SYNAPSE STRUCTURE AND ACTIVITY |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| REGULATION OF TYROSINE PHOSPHORYLATION OF STAT PROTEIN |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| RHO GTPASE ACTIVATOR ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
8.0 |
8.0 |
5.83 |
| RYTTCCTG V$ETS2 B |
TFmiRNA_Targets.gmt.txt |
-4.7 |
0.00278 |
424.0 |
344.0 |
308.92 |
| Reactions specific to the complex N-glycan synthesis pathway |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Recognition and association of DNA glycosylase with site containing an affected purine |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Recruitment of NuMA to mitotic centrosomes |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
9.0 |
9.0 |
6.56 |
| Reduction of cytosolic Ca++ levels |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| Regulation of Insulin Secretion by Acetylcholine |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
7.0 |
7.0 |
5.1 |
| Regulation of Insulin Secretion by Fatty Acids Bound to GPR40 (FFAR1) |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| Regulation of Insulin Secretion by Free Fatty Acids |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| Repair synthesis for gap-filling by DNA polymerase in TC-NER |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
14.0 |
14.0 |
10.2 |
| Repair synthesis of patch ~27-30 bases long by DNA polymerase |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
14.0 |
14.0 |
10.2 |
| Retrograde neurotrophin signalling |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
10.0 |
10.0 |
7.29 |
| SARCOMERE |
GO_-_Cellular_Component.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| SA G1 AND S PHASES |
Pathways_-_KEGGBioCarta.gmt.txt |
-1.7976931348623157E308 |
0.0 |
12.0 |
12.0 |
8.74 |
| SERINE TYPE ENDOPEPTIDASE INHIBITOR ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| SMAC binds to IAPs |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| SMAC-mediated apoptotic response |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| SMAC-mediated dissociation of IAP:caspase complexes |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| SODIUM CHANNEL ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| SPHINGOLIPID BIOSYNTHETIC PROCESS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| STEROID DEHYDROGENASE ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| STEROID DEHYDROGENASE ACTIVITY ACTING ON THE CH OH GROUP OF DONORSNAD OR NADP AS ACCEPTOR |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| ST IL 13 PATHWAY |
Pathways_-_KEGGBioCarta.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| ST INTERLEUKIN 13 PATHWAY |
Pathways_-_KEGGBioCarta.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| ST STAT3 PATHWAY |
Pathways_-_KEGGBioCarta.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| SULFURIC ESTER HYDROLASE ACTIVITY |
GO_-_Molecular_Function.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| SYNAPSE ORGANIZATION AND BIOGENESIS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| SYNAPTOGENESIS |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| Serine biosynthesis |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Signal Transduction |
Pathways_-_Reactome.gmt.txt |
-2.7 |
0.02528 |
549.0 |
428.0 |
399.99 |
| Signaling by NOTCH |
Pathways_-_Reactome.gmt.txt |
-2.6 |
0.03147 |
76.0 |
65.0 |
55.37 |
| Sulfide oxidation to sulfate |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| Synthesis of DNA |
Pathways_-_Reactome.gmt.txt |
-2.4 |
0.0426 |
84.0 |
71.0 |
61.2 |
| Synthesis of bile acids and bile salts |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| Synthesis of dolichyl-phosphate mannose |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| TCCGTCC,MIR-184 |
TFmiRNA_Targets.gmt.txt |
-1.7976931348623157E308 |
0.0 |
8.0 |
8.0 |
5.83 |
| TGGAAA V$NFAT Q4 01 |
TFmiRNA_Targets.gmt.txt |
-3.5 |
0.02607 |
667.0 |
523.0 |
485.96 |
| TRAIL signaling |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| TYROSINE PHOSPHORYLATION OF STAT PROTEIN |
GO_-_Biological_Process.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| Telomere Extension By Telomerase |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| The NLRP3 inflammasome |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| Trafficking of GluR2-containing AMPA receptors |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
9.0 |
9.0 |
6.56 |
| Transmembrane transport of small molecules |
Pathways_-_Reactome.gmt.txt |
-2.8 |
0.01939 |
182.0 |
149.0 |
132.6 |
| Unwinding of DNA |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
9.0 |
9.0 |
6.56 |
| V$ETS Q4 |
TFmiRNA_Targets.gmt.txt |
-3.8 |
0.01364 |
117.0 |
101.0 |
85.24 |
| V$EVI1 06 |
TFmiRNA_Targets.gmt.txt |
-1.7976931348623157E308 |
0.0 |
11.0 |
11.0 |
8.01 |
| V$HOXA3 01 |
TFmiRNA_Targets.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |
| V$LBP1 Q6 |
TFmiRNA_Targets.gmt.txt |
-3.9 |
0.01343 |
69.0 |
62.0 |
50.27 |
| V$STAT3 01 |
TFmiRNA_Targets.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| V$STAT6 01 |
TFmiRNA_Targets.gmt.txt |
-3.4 |
0.03598 |
96.0 |
83.0 |
69.94 |
| Viral dsRNA:TLR3:TRIF Complex Activates TBK1/IKK epsilon |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
5.0 |
5.0 |
3.64 |
| Vitamin B5 (pantothenate) metabolism |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
9.0 |
9.0 |
6.56 |
| Zinc influx into cells by the SLC39 gene family |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
7.0 |
7.0 |
5.1 |
| chr16p |
Chromosomal_Bands.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| chr16p13 |
Chromosomal_Bands.gmt.txt |
-5.1 |
4.4E-4 |
115.0 |
102.0 |
83.79 |
| chr16q11 |
Chromosomal_Bands.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| chr17p13 |
Chromosomal_Bands.gmt.txt |
-3.9 |
0.00521 |
92.0 |
81.0 |
67.03 |
| chr19p13 |
Chromosomal_Bands.gmt.txt |
-6.2 |
4.0E-5 |
222.0 |
191.0 |
161.74 |
| chr19q12 |
Chromosomal_Bands.gmt.txt |
-1.7976931348623157E308 |
0.0 |
7.0 |
7.0 |
5.1 |
| chr4q13 |
Chromosomal_Bands.gmt.txt |
-1.7976931348623157E308 |
0.0 |
9.0 |
9.0 |
6.56 |
| chr4q34 |
Chromosomal_Bands.gmt.txt |
-1.7976931348623157E308 |
0.0 |
7.0 |
7.0 |
5.1 |
| chr6p21 |
Chromosomal_Bands.gmt.txt |
-3.1 |
0.02948 |
160.0 |
133.0 |
116.57 |
| chr6q13 |
Chromosomal_Bands.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| chr7p |
Chromosomal_Bands.gmt.txt |
-1.7976931348623157E308 |
0.0 |
3.0 |
3.0 |
2.19 |
| chrxq12 |
Chromosomal_Bands.gmt.txt |
-1.7976931348623157E308 |
0.0 |
6.0 |
6.0 |
4.37 |
| p38MAPK events |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
8.0 |
8.0 |
5.83 |
| p75NTR regulates axonogenesis |
Pathways_-_Reactome.gmt.txt |
-1.7976931348623157E308 |
0.0 |
4.0 |
4.0 |
2.91 |