date generated: 2020-07-13
Mitch performs unidimensional and multidimensional gene set enrichment analysis. The concept behind this dates to work by Cox and Mann (https://doi.org/10.1186/1471-2105-13-S16-S12). This implementation is suited to R based workflows of multi-omics datasets. This software was developed by Antony Kaspi and Mark Ziemann. Learn more about Mitch at the website: https://github.com/markziemann/Mitch
Here is the first few lines of the input profile.
## x
## A2M 0.4967182
## A4GALT 1.1055218
## AAAS 2.1498692
## AACS -0.8274404
## AADAT 2.7771694
## AAED1 1.1657765
Here are some metrics about the input data profile:
| Profile metrics | |
|---|---|
| num_genesets | 2400 |
| num_genes_in_profile | 13161 |
| duplicated_genes_present | 0 |
| num_profile_genes_in_sets | 7488 |
| num_profile_genes_not_in_sets | 5673 |
Here is a plot of the input profiles. Note the dynamic ranges.
Here is the contour plot of the profile including all detected genes.
Here are some metrics about the gene sets used: GMT file of genesets: ReactomePathways.gmt
| Gene sets metrics | |
|---|---|
| num_genesets | 2400 |
| num_genesets_excluded | 1061 |
| num_genesets_included | 1339 |
Significance is calculated by -log10(p-value). All points shown are FDR<0.05.
Top N= 50 gene sets
| set | setSize | pANOVA | s.dist | p.adjustANOVA |
|---|---|---|---|---|
| Establishment of Sister Chromatid Cohesion | 10 | 8.94e-05 | 0.715 | 1.48e-03 |
| Unwinding of DNA | 12 | 2.56e-05 | 0.702 | 5.12e-04 |
| Mitotic Telophase/Cytokinesis | 12 | 5.57e-05 | 0.672 | 1.04e-03 |
| Viral mRNA Translation | 55 | 4.87e-15 | 0.610 | 2.17e-12 |
| Peptide chain elongation | 55 | 1.22e-14 | 0.601 | 2.72e-12 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | 65 | 2.69e-16 | 0.587 | 1.80e-13 |
| Activation of the pre-replicative complex | 31 | 1.94e-08 | 0.583 | 8.67e-07 |
| Selenocysteine synthesis | 58 | 6.68e-14 | 0.569 | 1.12e-11 |
| Eukaryotic Translation Termination | 58 | 1.86e-13 | 0.559 | 2.76e-11 |
| Glucuronidation | 11 | 1.35e-03 | 0.558 | 1.49e-02 |
| Eukaryotic Translation Elongation | 59 | 6.46e-13 | 0.541 | 7.21e-11 |
| DNA strand elongation | 32 | 1.24e-07 | 0.540 | 4.48e-06 |
| Condensation of Prophase Chromosomes | 13 | 8.83e-04 | 0.533 | 1.01e-02 |
| Condensation of Prometaphase Chromosomes | 11 | 2.38e-03 | 0.529 | 2.34e-02 |
| Dissolution of Fibrin Clot | 10 | 4.58e-03 | 0.518 | 3.90e-02 |
| Polo-like kinase mediated events | 15 | 5.45e-04 | 0.516 | 6.82e-03 |
| Cyclin A/B1/B2 associated events during G2/M transition | 22 | 3.20e-05 | 0.512 | 6.21e-04 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 60 | 9.09e-12 | 0.509 | 5.53e-10 |
| HSF1-dependent transactivation | 32 | 6.86e-07 | -0.507 | 2.14e-05 |
| Formation of a pool of free 40S subunits | 65 | 2.80e-12 | 0.501 | 2.34e-10 |
| Negative regulation of TCF-dependent signaling by WNT ligand antagonists | 11 | 4.71e-03 | -0.492 | 3.99e-02 |
| Processive synthesis on the lagging strand | 15 | 9.79e-04 | 0.492 | 1.10e-02 |
| Activation of ATR in response to replication stress | 35 | 6.51e-07 | 0.486 | 2.08e-05 |
| SRP-dependent cotranslational protein targeting to membrane | 76 | 5.63e-13 | 0.478 | 7.21e-11 |
| L13a-mediated translational silencing of Ceruloplasmin expression | 73 | 1.65e-12 | 0.478 | 1.55e-10 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | 15 | 1.38e-03 | 0.477 | 1.51e-02 |
| Selenoamino acid metabolism | 72 | 3.56e-12 | 0.474 | 2.81e-10 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | 75 | 1.74e-12 | 0.471 | 1.55e-10 |
| Removal of the Flap Intermediate | 14 | 2.31e-03 | 0.470 | 2.29e-02 |
| LGI-ADAM interactions | 11 | 7.18e-03 | -0.468 | 5.29e-02 |
| G0 and Early G1 | 25 | 6.17e-05 | 0.463 | 1.09e-03 |
| Recognition of DNA damage by PCNA-containing replication complex | 28 | 2.89e-05 | 0.457 | 5.70e-04 |
| G1/S-Specific Transcription | 26 | 6.73e-05 | 0.452 | 1.17e-03 |
| Constitutive Signaling by NOTCH1 HD Domain Mutants | 12 | 6.92e-03 | -0.450 | 5.15e-02 |
| Signaling by NOTCH1 HD Domain Mutants in Cancer | 12 | 6.92e-03 | -0.450 | 5.15e-02 |
| Attenuation phase | 22 | 2.67e-04 | -0.449 | 3.73e-03 |
| CDC6 association with the ORC:origin complex | 10 | 1.43e-02 | 0.448 | 8.76e-02 |
| Lagging Strand Synthesis | 20 | 6.21e-04 | 0.442 | 7.63e-03 |
| Cap-dependent Translation Initiation | 81 | 6.39e-12 | 0.442 | 4.50e-10 |
| Eukaryotic Translation Initiation | 81 | 6.39e-12 | 0.442 | 4.50e-10 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 80 | 8.68e-12 | 0.442 | 5.53e-10 |
| Nonsense-Mediated Decay (NMD) | 80 | 8.68e-12 | 0.442 | 5.53e-10 |
| Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | 14 | 4.25e-03 | 0.441 | 3.70e-02 |
| PCNA-Dependent Long Patch Base Excision Repair | 21 | 4.76e-04 | 0.441 | 6.13e-03 |
| Formation of the ternary complex, and subsequently, the 43S complex | 39 | 2.34e-06 | 0.437 | 5.69e-05 |
| Synthesis of PE | 11 | 1.31e-02 | -0.432 | 8.34e-02 |
| Glycogen storage diseases | 11 | 1.36e-02 | -0.430 | 8.54e-02 |
| Interleukin-12 signaling | 35 | 1.31e-05 | 0.426 | 2.79e-04 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | 30 | 6.11e-05 | 0.423 | 1.09e-03 |
| NCAM1 interactions | 29 | 9.65e-05 | -0.418 | 1.54e-03 |
| set | setSize | pANOVA | s.dist | p.adjustANOVA |
|---|---|---|---|---|
| Establishment of Sister Chromatid Cohesion | 10 | 8.94e-05 | 7.15e-01 | 1.48e-03 |
| Unwinding of DNA | 12 | 2.56e-05 | 7.02e-01 | 5.12e-04 |
| Mitotic Telophase/Cytokinesis | 12 | 5.57e-05 | 6.72e-01 | 1.04e-03 |
| Viral mRNA Translation | 55 | 4.87e-15 | 6.10e-01 | 2.17e-12 |
| Peptide chain elongation | 55 | 1.22e-14 | 6.01e-01 | 2.72e-12 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | 65 | 2.69e-16 | 5.87e-01 | 1.80e-13 |
| Activation of the pre-replicative complex | 31 | 1.94e-08 | 5.83e-01 | 8.67e-07 |
| Selenocysteine synthesis | 58 | 6.68e-14 | 5.69e-01 | 1.12e-11 |
| Eukaryotic Translation Termination | 58 | 1.86e-13 | 5.59e-01 | 2.76e-11 |
| Glucuronidation | 11 | 1.35e-03 | 5.58e-01 | 1.49e-02 |
| Eukaryotic Translation Elongation | 59 | 6.46e-13 | 5.41e-01 | 7.21e-11 |
| DNA strand elongation | 32 | 1.24e-07 | 5.40e-01 | 4.48e-06 |
| Condensation of Prophase Chromosomes | 13 | 8.83e-04 | 5.33e-01 | 1.01e-02 |
| Condensation of Prometaphase Chromosomes | 11 | 2.38e-03 | 5.29e-01 | 2.34e-02 |
| Dissolution of Fibrin Clot | 10 | 4.58e-03 | 5.18e-01 | 3.90e-02 |
| Polo-like kinase mediated events | 15 | 5.45e-04 | 5.16e-01 | 6.82e-03 |
| Cyclin A/B1/B2 associated events during G2/M transition | 22 | 3.20e-05 | 5.12e-01 | 6.21e-04 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 60 | 9.09e-12 | 5.09e-01 | 5.53e-10 |
| HSF1-dependent transactivation | 32 | 6.86e-07 | -5.07e-01 | 2.14e-05 |
| Formation of a pool of free 40S subunits | 65 | 2.80e-12 | 5.01e-01 | 2.34e-10 |
| Negative regulation of TCF-dependent signaling by WNT ligand antagonists | 11 | 4.71e-03 | -4.92e-01 | 3.99e-02 |
| Processive synthesis on the lagging strand | 15 | 9.79e-04 | 4.92e-01 | 1.10e-02 |
| Activation of ATR in response to replication stress | 35 | 6.51e-07 | 4.86e-01 | 2.08e-05 |
| SRP-dependent cotranslational protein targeting to membrane | 76 | 5.63e-13 | 4.78e-01 | 7.21e-11 |
| L13a-mediated translational silencing of Ceruloplasmin expression | 73 | 1.65e-12 | 4.78e-01 | 1.55e-10 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | 15 | 1.38e-03 | 4.77e-01 | 1.51e-02 |
| Selenoamino acid metabolism | 72 | 3.56e-12 | 4.74e-01 | 2.81e-10 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | 75 | 1.74e-12 | 4.71e-01 | 1.55e-10 |
| Removal of the Flap Intermediate | 14 | 2.31e-03 | 4.70e-01 | 2.29e-02 |
| LGI-ADAM interactions | 11 | 7.18e-03 | -4.68e-01 | 5.29e-02 |
| G0 and Early G1 | 25 | 6.17e-05 | 4.63e-01 | 1.09e-03 |
| Recognition of DNA damage by PCNA-containing replication complex | 28 | 2.89e-05 | 4.57e-01 | 5.70e-04 |
| G1/S-Specific Transcription | 26 | 6.73e-05 | 4.52e-01 | 1.17e-03 |
| Constitutive Signaling by NOTCH1 HD Domain Mutants | 12 | 6.92e-03 | -4.50e-01 | 5.15e-02 |
| Signaling by NOTCH1 HD Domain Mutants in Cancer | 12 | 6.92e-03 | -4.50e-01 | 5.15e-02 |
| Attenuation phase | 22 | 2.67e-04 | -4.49e-01 | 3.73e-03 |
| CDC6 association with the ORC:origin complex | 10 | 1.43e-02 | 4.48e-01 | 8.76e-02 |
| Lagging Strand Synthesis | 20 | 6.21e-04 | 4.42e-01 | 7.63e-03 |
| Cap-dependent Translation Initiation | 81 | 6.39e-12 | 4.42e-01 | 4.50e-10 |
| Eukaryotic Translation Initiation | 81 | 6.39e-12 | 4.42e-01 | 4.50e-10 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 80 | 8.68e-12 | 4.42e-01 | 5.53e-10 |
| Nonsense-Mediated Decay (NMD) | 80 | 8.68e-12 | 4.42e-01 | 5.53e-10 |
| Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | 14 | 4.25e-03 | 4.41e-01 | 3.70e-02 |
| PCNA-Dependent Long Patch Base Excision Repair | 21 | 4.76e-04 | 4.41e-01 | 6.13e-03 |
| Formation of the ternary complex, and subsequently, the 43S complex | 39 | 2.34e-06 | 4.37e-01 | 5.69e-05 |
| Synthesis of PE | 11 | 1.31e-02 | -4.32e-01 | 8.34e-02 |
| Glycogen storage diseases | 11 | 1.36e-02 | -4.30e-01 | 8.54e-02 |
| Interleukin-12 signaling | 35 | 1.31e-05 | 4.26e-01 | 2.79e-04 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | 30 | 6.11e-05 | 4.23e-01 | 1.09e-03 |
| NCAM1 interactions | 29 | 9.65e-05 | -4.18e-01 | 1.54e-03 |
| Interferon alpha/beta signaling | 45 | 1.53e-06 | 4.14e-01 | 4.01e-05 |
| Collagen chain trimerization | 33 | 3.91e-05 | -4.14e-01 | 7.37e-04 |
| P2Y receptors | 10 | 2.35e-02 | 4.14e-01 | 1.27e-01 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | 46 | 1.32e-06 | 4.12e-01 | 3.67e-05 |
| Ribosomal scanning and start codon recognition | 46 | 1.40e-06 | 4.11e-01 | 3.84e-05 |
| Transcription of E2F targets under negative control by DREAM complex | 18 | 2.74e-03 | 4.08e-01 | 2.60e-02 |
| Termination of translesion DNA synthesis | 29 | 1.44e-04 | 4.08e-01 | 2.16e-03 |
| E2F mediated regulation of DNA replication | 20 | 1.67e-03 | 4.06e-01 | 1.78e-02 |
| Leading Strand Synthesis | 14 | 8.55e-03 | 4.06e-01 | 6.12e-02 |
| Polymerase switching | 14 | 8.55e-03 | 4.06e-01 | 6.12e-02 |
| Translation initiation complex formation | 45 | 3.30e-06 | 4.01e-01 | 7.88e-05 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | 12 | 1.66e-02 | 3.99e-01 | 9.87e-02 |
| Interleukin-12 family signaling | 41 | 1.10e-05 | 3.97e-01 | 2.37e-04 |
| Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | 14 | 1.13e-02 | 3.91e-01 | 7.58e-02 |
| Acetylcholine regulates insulin secretion | 10 | 3.45e-02 | -3.86e-01 | 1.61e-01 |
| Elevation of cytosolic Ca2+ levels | 12 | 2.10e-02 | -3.85e-01 | 1.17e-01 |
| Termination of O-glycan biosynthesis | 10 | 3.56e-02 | -3.84e-01 | 1.64e-01 |
| Mitotic G1 phase and G1/S transition | 135 | 3.17e-14 | 3.79e-01 | 6.06e-12 |
| Activation of AMPK downstream of NMDARs | 10 | 3.85e-02 | -3.78e-01 | 1.72e-01 |
| Gap-filling DNA repair synthesis and ligation in GG-NER | 23 | 1.71e-03 | 3.78e-01 | 1.80e-02 |
| Resolution of AP sites via the multiple-nucleotide patch replacement pathway | 24 | 1.38e-03 | 3.77e-01 | 1.51e-02 |
| Glycogen synthesis | 12 | 2.37e-02 | -3.77e-01 | 1.28e-01 |
| G1/S Transition | 119 | 1.39e-12 | 3.76e-01 | 1.44e-10 |
| Assembly of collagen fibrils and other multimeric structures | 46 | 1.03e-05 | -3.76e-01 | 2.27e-04 |
| DNA Damage Bypass | 44 | 1.77e-05 | 3.74e-01 | 3.65e-04 |
| Phosphorylation of CD3 and TCR zeta chains | 11 | 3.25e-02 | 3.72e-01 | 1.56e-01 |
| MASTL Facilitates Mitotic Progression | 10 | 4.47e-02 | 3.67e-01 | 1.91e-01 |
| Lysine catabolism | 10 | 4.50e-02 | 3.66e-01 | 1.91e-01 |
| S Phase | 152 | 9.15e-15 | 3.65e-01 | 2.45e-12 |
| DNA Replication Pre-Initiation | 77 | 3.22e-08 | 3.65e-01 | 1.39e-06 |
| ATF6 (ATF6-alpha) activates chaperone genes | 10 | 4.67e-02 | 3.63e-01 | 1.97e-01 |
| CD28 dependent Vav1 pathway | 12 | 3.02e-02 | 3.61e-01 | 1.49e-01 |
| Mismatch Repair | 15 | 1.69e-02 | 3.56e-01 | 9.89e-02 |
| Orc1 removal from chromatin | 63 | 1.03e-06 | 3.56e-01 | 3.00e-05 |
| Regulation of expression of SLITs and ROBOs | 121 | 1.92e-11 | 3.54e-01 | 1.11e-09 |
| DNA Replication | 119 | 3.91e-11 | 3.51e-01 | 2.18e-09 |
| Synthesis of DNA | 112 | 1.57e-10 | 3.50e-01 | 8.41e-09 |
| Effects of PIP2 hydrolysis | 22 | 5.03e-03 | -3.46e-01 | 4.24e-02 |
| mitochondrial fatty acid beta-oxidation of saturated fatty acids | 10 | 6.12e-02 | 3.42e-01 | 2.36e-01 |
| Activation of Matrix Metalloproteinases | 17 | 1.47e-02 | -3.42e-01 | 8.98e-02 |
| Synthesis of PC | 24 | 3.84e-03 | -3.41e-01 | 3.43e-02 |
| Metal ion SLC transporters | 21 | 7.66e-03 | 3.36e-01 | 5.60e-02 |
| Deposition of new CENPA-containing nucleosomes at the centromere | 22 | 6.49e-03 | 3.35e-01 | 4.94e-02 |
| Nucleosome assembly | 22 | 6.49e-03 | 3.35e-01 | 4.94e-02 |
| Signaling by Activin | 11 | 5.49e-02 | -3.34e-01 | 2.19e-01 |
| Signaling by FGFR3 fusions in cancer | 10 | 6.77e-02 | 3.34e-01 | 2.50e-01 |
| Early Phase of HIV Life Cycle | 13 | 3.77e-02 | 3.33e-01 | 1.70e-01 |
| ATF6 (ATF6-alpha) activates chaperones | 12 | 4.62e-02 | 3.32e-01 | 1.95e-01 |
| Translesion synthesis by POLK | 15 | 2.58e-02 | 3.32e-01 | 1.35e-01 |
| Pre-NOTCH Processing in Golgi | 16 | 2.18e-02 | -3.31e-01 | 1.20e-01 |
| Cholesterol biosynthesis | 23 | 6.01e-03 | -3.31e-01 | 4.76e-02 |
| Synthesis of IP3 and IP4 in the cytosol | 21 | 9.03e-03 | -3.29e-01 | 6.40e-02 |
| Translesion synthesis by REV1 | 14 | 3.34e-02 | 3.28e-01 | 1.59e-01 |
| ERBB2 Activates PTK6 Signaling | 10 | 7.22e-02 | -3.28e-01 | 2.62e-01 |
| Transcriptional Regulation by E2F6 | 33 | 1.17e-03 | 3.27e-01 | 1.30e-02 |
| Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | 35 | 8.51e-04 | 3.26e-01 | 9.82e-03 |
| Purine salvage | 12 | 5.19e-02 | 3.24e-01 | 2.11e-01 |
| Collagen biosynthesis and modifying enzymes | 52 | 5.90e-05 | -3.22e-01 | 1.08e-03 |
| Translesion synthesis by POLI | 15 | 3.17e-02 | 3.20e-01 | 1.54e-01 |
| ATF4 activates genes in response to endoplasmic reticulum stress | 24 | 6.60e-03 | 3.20e-01 | 4.99e-02 |
| Influenza Viral RNA Transcription and Replication | 96 | 7.97e-08 | 3.17e-01 | 2.97e-06 |
| Assembly of the pre-replicative complex | 61 | 1.91e-05 | 3.17e-01 | 3.87e-04 |
| IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation | 13 | 4.87e-02 | -3.16e-01 | 2.02e-01 |
| TRAF6-mediated induction of TAK1 complex within TLR4 complex | 13 | 4.87e-02 | -3.16e-01 | 2.02e-01 |
| Interleukin-35 Signalling | 10 | 8.53e-02 | 3.14e-01 | 2.91e-01 |
| G2/M Checkpoints | 124 | 1.84e-09 | 3.13e-01 | 9.48e-08 |
| Transport of bile salts and organic acids, metal ions and amine compounds | 51 | 1.13e-04 | 3.13e-01 | 1.75e-03 |
| Formation of Fibrin Clot (Clotting Cascade) | 17 | 2.63e-02 | 3.11e-01 | 1.37e-01 |
| EGR2 and SOX10-mediated initiation of Schwann cell myelination | 21 | 1.36e-02 | -3.11e-01 | 8.54e-02 |
| Influenza Infection | 112 | 1.73e-08 | 3.09e-01 | 8.00e-07 |
| Phase II - Conjugation of compounds | 72 | 6.80e-06 | 3.07e-01 | 1.54e-04 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 89 | 6.21e-07 | 3.06e-01 | 2.03e-05 |
| Resolution of Sister Chromatid Cohesion | 95 | 2.63e-07 | 3.06e-01 | 9.27e-06 |
| Metabolism of Angiotensinogen to Angiotensins | 12 | 6.68e-02 | -3.06e-01 | 2.50e-01 |
| Regulation of FZD by ubiquitination | 13 | 5.76e-02 | -3.04e-01 | 2.25e-01 |
| Common Pathway of Fibrin Clot Formation | 10 | 9.61e-02 | 3.04e-01 | 3.15e-01 |
| Cyclin D associated events in G1 | 41 | 7.74e-04 | 3.04e-01 | 9.26e-03 |
| G1 Phase | 41 | 7.74e-04 | 3.04e-01 | 9.26e-03 |
| Zinc transporters | 13 | 5.95e-02 | 3.02e-01 | 2.31e-01 |
| PERK regulates gene expression | 28 | 5.73e-03 | 3.02e-01 | 4.65e-02 |
| Collagen formation | 72 | 1.38e-05 | -2.96e-01 | 2.89e-04 |
| Signaling by Leptin | 10 | 1.06e-01 | -2.96e-01 | 3.39e-01 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | 50 | 3.22e-04 | 2.94e-01 | 4.38e-03 |
| Initial triggering of complement | 19 | 2.68e-02 | 2.94e-01 | 1.38e-01 |
| Switching of origins to a post-replicative state | 83 | 4.12e-06 | 2.93e-01 | 9.67e-05 |
| Telomere C-strand (Lagging Strand) Synthesis | 33 | 3.68e-03 | 2.92e-01 | 3.30e-02 |
| Defective EXT1 causes exostoses 1, TRPS2 and CHDS | 13 | 6.92e-02 | -2.91e-01 | 2.53e-01 |
| Defective EXT2 causes exostoses 2 | 13 | 6.92e-02 | -2.91e-01 | 2.53e-01 |
| NF-kB is activated and signals survival | 11 | 9.52e-02 | -2.91e-01 | 3.12e-01 |
| Polymerase switching on the C-strand of the telomere | 25 | 1.22e-02 | 2.90e-01 | 8.03e-02 |
| Free fatty acids regulate insulin secretion | 10 | 1.15e-01 | -2.88e-01 | 3.61e-01 |
| Glycogen metabolism | 23 | 1.70e-02 | -2.88e-01 | 9.89e-02 |
| HDR through Homologous Recombination (HRR) | 61 | 1.08e-04 | 2.87e-01 | 1.70e-03 |
| Regulation of IFNA signaling | 12 | 8.71e-02 | 2.85e-01 | 2.96e-01 |
| Heme degradation | 10 | 1.19e-01 | 2.85e-01 | 3.65e-01 |
| Inhibition of replication initiation of damaged DNA by RB1/E2F1 | 12 | 8.82e-02 | 2.84e-01 | 2.98e-01 |
| Removal of the Flap Intermediate from the C-strand | 17 | 4.45e-02 | 2.82e-01 | 1.90e-01 |
| Processive synthesis on the C-strand of the telomere | 19 | 3.37e-02 | 2.81e-01 | 1.59e-01 |
| Processing of DNA double-strand break ends | 58 | 2.35e-04 | 2.79e-01 | 3.32e-03 |
| Retrograde neurotrophin signalling | 14 | 7.47e-02 | -2.75e-01 | 2.66e-01 |
| Cell Cycle Checkpoints | 235 | 6.04e-13 | 2.73e-01 | 7.21e-11 |
| Presynaptic phase of homologous DNA pairing and strand exchange | 37 | 4.11e-03 | 2.73e-01 | 3.65e-02 |
| Assembly of active LPL and LIPC lipase complexes | 11 | 1.20e-01 | -2.71e-01 | 3.65e-01 |
| Homology Directed Repair | 95 | 5.86e-06 | 2.69e-01 | 1.35e-04 |
| Glutamate binding, activation of AMPA receptors and synaptic plasticity | 26 | 1.76e-02 | -2.69e-01 | 1.01e-01 |
| Trafficking of AMPA receptors | 26 | 1.76e-02 | -2.69e-01 | 1.01e-01 |
| Cyclin E associated events during G1/S transition | 75 | 5.98e-05 | 2.68e-01 | 1.08e-03 |
| Diseases of carbohydrate metabolism | 27 | 1.60e-02 | -2.68e-01 | 9.63e-02 |
| CDT1 association with the CDC6:ORC:origin complex | 52 | 8.43e-04 | 2.68e-01 | 9.82e-03 |
| Protein methylation | 11 | 1.25e-01 | 2.67e-01 | 3.78e-01 |
| Major pathway of rRNA processing in the nucleolus and cytosol | 141 | 5.45e-08 | 2.66e-01 | 2.15e-06 |
| G2/M DNA damage checkpoint | 58 | 5.03e-04 | 2.64e-01 | 6.41e-03 |
| Platelet calcium homeostasis | 22 | 3.26e-02 | -2.63e-01 | 1.56e-01 |
| Methylation | 11 | 1.31e-01 | 2.63e-01 | 3.89e-01 |
| WNT5A-dependent internalization of FZD4 | 15 | 7.82e-02 | -2.63e-01 | 2.74e-01 |
| Cyclin A:Cdk2-associated events at S phase entry | 77 | 7.00e-05 | 2.62e-01 | 1.19e-03 |
| Extension of Telomeres | 48 | 1.76e-03 | 2.61e-01 | 1.82e-02 |
| Signaling by WNT in cancer | 28 | 1.69e-02 | -2.61e-01 | 9.89e-02 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | 15 | 8.08e-02 | 2.60e-01 | 2.79e-01 |
| rRNA processing in the nucleus and cytosol | 150 | 4.27e-08 | 2.60e-01 | 1.79e-06 |
| RET signaling | 35 | 8.14e-03 | -2.59e-01 | 5.89e-02 |
| EPHB-mediated forward signaling | 32 | 1.14e-02 | 2.58e-01 | 7.65e-02 |
| KSRP (KHSRP) binds and destabilizes mRNA | 16 | 7.44e-02 | 2.58e-01 | 2.66e-01 |
| Disassembly of the destruction complex and recruitment of AXIN to the membrane | 26 | 2.38e-02 | -2.56e-01 | 1.28e-01 |
| Classical antibody-mediated complement activation | 10 | 1.61e-01 | 2.56e-01 | 4.27e-01 |
| Negative regulation of NOTCH4 signaling | 48 | 2.16e-03 | 2.56e-01 | 2.16e-02 |
| SCF(Skp2)-mediated degradation of p27/p21 | 52 | 1.41e-03 | 2.56e-01 | 1.53e-02 |
| Antigen Presentation: Folding, assembly and peptide loading of class I MHC | 17 | 6.77e-02 | 2.56e-01 | 2.50e-01 |
| PRC2 methylates histones and DNA | 14 | 9.77e-02 | 2.56e-01 | 3.18e-01 |
| Cross-presentation of soluble exogenous antigens (endosomes) | 45 | 3.07e-03 | 2.55e-01 | 2.89e-02 |
| Nucleotide-like (purinergic) receptors | 13 | 1.13e-01 | 2.54e-01 | 3.55e-01 |
| WNT5A-dependent internalization of FZD2, FZD5 and ROR2 | 13 | 1.13e-01 | -2.54e-01 | 3.55e-01 |
| FCGR activation | 16 | 8.04e-02 | 2.53e-01 | 2.79e-01 |
| Separation of Sister Chromatids | 154 | 7.50e-08 | 2.52e-01 | 2.87e-06 |
| Chromosome Maintenance | 82 | 8.36e-05 | 2.52e-01 | 1.40e-03 |
| Homologous DNA Pairing and Strand Exchange | 40 | 6.33e-03 | 2.50e-01 | 4.94e-02 |
| Metabolism of polyamines | 53 | 1.80e-03 | 2.48e-01 | 1.84e-02 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 70 | 3.44e-04 | 2.48e-01 | 4.60e-03 |
| RA biosynthesis pathway | 14 | 1.09e-01 | 2.47e-01 | 3.47e-01 |
| NRAGE signals death through JNK | 54 | 1.74e-03 | -2.46e-01 | 1.82e-02 |
| rRNA processing | 167 | 4.72e-08 | 2.45e-01 | 1.91e-06 |
| IL-6-type cytokine receptor ligand interactions | 12 | 1.42e-01 | 2.45e-01 | 4.00e-01 |
| APC/C-mediated degradation of cell cycle proteins | 81 | 1.49e-04 | 2.44e-01 | 2.16e-03 |
| Regulation of mitotic cell cycle | 81 | 1.49e-04 | 2.44e-01 | 2.16e-03 |
| Regulation of APC/C activators between G1/S and early anaphase | 74 | 3.24e-04 | 2.42e-01 | 4.38e-03 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | 69 | 5.32e-04 | 2.41e-01 | 6.72e-03 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | 83 | 1.47e-04 | 2.41e-01 | 2.16e-03 |
| Amplification of signal from the kinetochores | 83 | 1.47e-04 | 2.41e-01 | 2.16e-03 |
| HSF1 activation | 24 | 4.14e-02 | -2.41e-01 | 1.80e-01 |
| Hyaluronan uptake and degradation | 11 | 1.67e-01 | 2.41e-01 | 4.35e-01 |
| Phosphorylation of the APC/C | 20 | 6.33e-02 | 2.40e-01 | 2.41e-01 |
| TAK1 activates NFkB by phosphorylation and activation of IKKs complex | 25 | 3.81e-02 | -2.40e-01 | 1.71e-01 |
| Interferon gamma signaling | 64 | 9.19e-04 | 2.40e-01 | 1.04e-02 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | 32 | 1.96e-02 | 2.39e-01 | 1.12e-01 |
| STING mediated induction of host immune responses | 12 | 1.54e-01 | 2.38e-01 | 4.13e-01 |
| Cytosolic iron-sulfur cluster assembly | 11 | 1.74e-01 | -2.37e-01 | 4.43e-01 |
| Generation of second messenger molecules | 22 | 5.49e-02 | 2.37e-01 | 2.19e-01 |
| NCAM signaling for neurite out-growth | 49 | 4.22e-03 | -2.36e-01 | 3.69e-02 |
| Killing mechanisms | 10 | 1.96e-01 | -2.36e-01 | 4.78e-01 |
| WNT5:FZD7-mediated leishmania damping | 10 | 1.96e-01 | -2.36e-01 | 4.78e-01 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | 67 | 8.44e-04 | 2.36e-01 | 9.82e-03 |
| Biological oxidations | 139 | 1.67e-06 | 2.36e-01 | 4.30e-05 |
| Carnitine metabolism | 12 | 1.58e-01 | -2.36e-01 | 4.19e-01 |
| Signaling by ERBB2 TMD/JMD mutants | 19 | 7.85e-02 | -2.33e-01 | 2.75e-01 |
| Resolution of D-loop Structures through Holliday Junction Intermediates | 29 | 3.02e-02 | 2.33e-01 | 1.49e-01 |
| Competing endogenous RNAs (ceRNAs) regulate PTEN translation | 10 | 2.03e-01 | -2.33e-01 | 4.88e-01 |
| Metabolism of folate and pterines | 15 | 1.19e-01 | -2.32e-01 | 3.65e-01 |
| Sema4D induced cell migration and growth-cone collapse | 20 | 7.29e-02 | -2.32e-01 | 2.63e-01 |
| Activated NOTCH1 Transmits Signal to the Nucleus | 26 | 4.15e-02 | -2.31e-01 | 1.80e-01 |
| ERBB2 Regulates Cell Motility | 13 | 1.50e-01 | -2.30e-01 | 4.10e-01 |
| Mucopolysaccharidoses | 11 | 1.87e-01 | -2.30e-01 | 4.64e-01 |
| PD-1 signaling | 10 | 2.08e-01 | 2.30e-01 | 4.98e-01 |
| CD28 co-stimulation | 32 | 2.48e-02 | 2.29e-01 | 1.31e-01 |
| Formation of the beta-catenin:TCF transactivating complex | 30 | 2.98e-02 | -2.29e-01 | 1.48e-01 |
| Nicotinamide salvaging | 14 | 1.38e-01 | 2.29e-01 | 3.99e-01 |
| p75NTR signals via NF-kB | 14 | 1.40e-01 | -2.28e-01 | 3.99e-01 |
| Collagen degradation | 25 | 4.92e-02 | -2.27e-01 | 2.03e-01 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | 66 | 1.46e-03 | 2.27e-01 | 1.56e-02 |
| Diseases associated with N-glycosylation of proteins | 16 | 1.17e-01 | -2.26e-01 | 3.62e-01 |
| RIP-mediated NFkB activation via ZBP1 | 17 | 1.07e-01 | -2.26e-01 | 3.41e-01 |
| Activation of RAC1 | 12 | 1.77e-01 | 2.25e-01 | 4.48e-01 |
| Signaling by ROBO receptors | 163 | 7.95e-07 | 2.25e-01 | 2.42e-05 |
| Resolution of D-Loop Structures | 30 | 3.37e-02 | 2.24e-01 | 1.59e-01 |
| Trafficking of GluR2-containing AMPA receptors | 15 | 1.33e-01 | -2.24e-01 | 3.92e-01 |
| Mitotic Spindle Checkpoint | 100 | 1.13e-04 | 2.24e-01 | 1.75e-03 |
| Voltage gated Potassium channels | 26 | 4.85e-02 | -2.24e-01 | 2.02e-01 |
| Antigen processing-Cross presentation | 83 | 4.57e-04 | 2.23e-01 | 5.95e-03 |
| Activation of BAD and translocation to mitochondria | 14 | 1.50e-01 | 2.22e-01 | 4.10e-01 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | 14 | 1.50e-01 | -2.22e-01 | 4.10e-01 |
| Presynaptic depolarization and calcium channel opening | 11 | 2.02e-01 | -2.22e-01 | 4.87e-01 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | 44 | 1.09e-02 | 2.22e-01 | 7.41e-02 |
| Telomere Maintenance | 62 | 2.55e-03 | 2.22e-01 | 2.47e-02 |
| EML4 and NUDC in mitotic spindle formation | 87 | 3.60e-04 | 2.22e-01 | 4.77e-03 |
| Regulation of ornithine decarboxylase (ODC) | 46 | 9.43e-03 | 2.21e-01 | 6.61e-02 |
| Vif-mediated degradation of APOBEC3G | 45 | 1.05e-02 | 2.21e-01 | 7.22e-02 |
| RHO GTPases activate IQGAPs | 10 | 2.28e-01 | 2.20e-01 | 5.16e-01 |
| Laminin interactions | 22 | 7.36e-02 | -2.20e-01 | 2.64e-01 |
| DAP12 signaling | 25 | 5.74e-02 | 2.20e-01 | 2.25e-01 |
| Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol | 14 | 1.55e-01 | 2.19e-01 | 4.16e-01 |
| BBSome-mediated cargo-targeting to cilium | 20 | 9.26e-02 | 2.17e-01 | 3.10e-01 |
| Transferrin endocytosis and recycling | 24 | 6.57e-02 | -2.17e-01 | 2.48e-01 |
| Uptake and actions of bacterial toxins | 24 | 6.63e-02 | -2.17e-01 | 2.49e-01 |
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | 11 | 2.14e-01 | 2.16e-01 | 5.03e-01 |
| Ion homeostasis | 42 | 1.53e-02 | -2.16e-01 | 9.31e-02 |
| Vpu mediated degradation of CD4 | 46 | 1.15e-02 | 2.16e-01 | 7.66e-02 |
| Trafficking and processing of endosomal TLR | 11 | 2.17e-01 | 2.15e-01 | 5.05e-01 |
| Nitric oxide stimulates guanylate cyclase | 19 | 1.06e-01 | -2.14e-01 | 3.39e-01 |
| Ub-specific processing proteases | 165 | 2.21e-06 | 2.14e-01 | 5.47e-05 |
| HDR through Single Strand Annealing (SSA) | 36 | 2.63e-02 | 2.14e-01 | 1.37e-01 |
| Cell Cycle, Mitotic | 458 | 6.70e-15 | 2.14e-01 | 2.24e-12 |
| Costimulation by the CD28 family | 55 | 6.17e-03 | 2.14e-01 | 4.86e-02 |
| Interferon Signaling | 146 | 9.07e-06 | 2.13e-01 | 2.02e-04 |
| Non-integrin membrane-ECM interactions | 40 | 1.99e-02 | -2.13e-01 | 1.13e-01 |
| Diseases associated with glycosylation precursor biosynthesis | 18 | 1.19e-01 | -2.13e-01 | 3.64e-01 |
| PKA activation in glucagon signalling | 16 | 1.41e-01 | -2.12e-01 | 4.00e-01 |
| Nonhomologous End-Joining (NHEJ) | 33 | 3.51e-02 | 2.12e-01 | 1.63e-01 |
| Ubiquitin-dependent degradation of Cyclin D | 46 | 1.32e-02 | 2.11e-01 | 8.35e-02 |
| SCF-beta-TrCP mediated degradation of Emi1 | 49 | 1.06e-02 | 2.11e-01 | 7.29e-02 |
| Organic cation/anion/zwitterion transport | 10 | 2.49e-01 | 2.10e-01 | 5.43e-01 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | 49 | 1.11e-02 | 2.10e-01 | 7.53e-02 |
| Mitochondrial iron-sulfur cluster biogenesis | 12 | 2.10e-01 | -2.09e-01 | 5.01e-01 |
| Selective autophagy | 53 | 8.82e-03 | -2.08e-01 | 6.29e-02 |
| MECP2 regulates neuronal receptors and channels | 12 | 2.12e-01 | 2.08e-01 | 5.03e-01 |
| DNA Double-Strand Break Repair | 123 | 6.98e-05 | 2.08e-01 | 1.19e-03 |
| Heme biosynthesis | 13 | 1.95e-01 | -2.08e-01 | 4.77e-01 |
| Metabolism of amino acids and derivatives | 260 | 9.17e-09 | 2.08e-01 | 4.55e-07 |
| CDK-mediated phosphorylation and removal of Cdc6 | 66 | 3.60e-03 | 2.07e-01 | 3.25e-02 |
| RHO GTPases Activate WASPs and WAVEs | 35 | 3.40e-02 | 2.07e-01 | 1.60e-01 |
| Cellular hexose transport | 12 | 2.14e-01 | -2.07e-01 | 5.03e-01 |
| GAB1 signalosome | 14 | 1.80e-01 | -2.07e-01 | 4.53e-01 |
| Stimuli-sensing channels | 58 | 6.70e-03 | -2.06e-01 | 5.04e-02 |
| MicroRNA (miRNA) biogenesis | 23 | 8.75e-02 | -2.06e-01 | 2.97e-01 |
| Glucagon-type ligand receptors | 17 | 1.42e-01 | -2.06e-01 | 4.00e-01 |
| TP53 Regulates Transcription of Death Receptors and Ligands | 11 | 2.38e-01 | -2.06e-01 | 5.31e-01 |
| Citric acid cycle (TCA cycle) | 22 | 9.51e-02 | 2.06e-01 | 3.12e-01 |
| Degradation of AXIN | 49 | 1.30e-02 | 2.05e-01 | 8.32e-02 |
| MET activates PTK2 signaling | 17 | 1.43e-01 | -2.05e-01 | 4.02e-01 |
| Negative regulation of NMDA receptor-mediated neuronal transmission | 16 | 1.57e-01 | -2.04e-01 | 4.18e-01 |
| Stabilization of p53 | 50 | 1.28e-02 | 2.04e-01 | 8.25e-02 |
| Synthesis of PA | 25 | 7.93e-02 | -2.03e-01 | 2.76e-01 |
| DARPP-32 events | 22 | 9.99e-02 | 2.03e-01 | 3.24e-01 |
| NOTCH2 Activation and Transmission of Signal to the Nucleus | 18 | 1.38e-01 | -2.02e-01 | 3.99e-01 |
| Cell Cycle | 571 | 2.60e-16 | 2.02e-01 | 1.80e-13 |
| Signaling by PDGFRA extracellular domain mutants | 12 | 2.26e-01 | 2.02e-01 | 5.15e-01 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | 12 | 2.26e-01 | 2.02e-01 | 5.15e-01 |
| Regulation of Complement cascade | 33 | 4.57e-02 | 2.01e-01 | 1.94e-01 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | 68 | 4.39e-03 | 2.00e-01 | 3.77e-02 |
| GRB2 events in EGFR signaling | 10 | 2.74e-01 | -2.00e-01 | 5.63e-01 |
| Formation of Senescence-Associated Heterochromatin Foci (SAHF) | 10 | 2.74e-01 | -2.00e-01 | 5.63e-01 |
| EGFR downregulation | 26 | 7.82e-02 | -2.00e-01 | 2.74e-01 |
| ER-Phagosome pathway | 69 | 4.29e-03 | 1.99e-01 | 3.70e-02 |
| HS-GAG degradation | 19 | 1.34e-01 | -1.99e-01 | 3.93e-01 |
| Gastrin-CREB signalling pathway via PKC and MAPK | 16 | 1.69e-01 | -1.99e-01 | 4.38e-01 |
| ZBP1(DAI) mediated induction of type I IFNs | 20 | 1.25e-01 | -1.98e-01 | 3.78e-01 |
| Nucleotide salvage | 21 | 1.16e-01 | 1.98e-01 | 3.61e-01 |
| Ubiquitin Mediated Degradation of Phosphorylated Cdc25A | 46 | 2.02e-02 | 1.98e-01 | 1.13e-01 |
| p53-Independent DNA Damage Response | 46 | 2.02e-02 | 1.98e-01 | 1.13e-01 |
| p53-Independent G1/S DNA damage checkpoint | 46 | 2.02e-02 | 1.98e-01 | 1.13e-01 |
| Mitotic Metaphase and Anaphase | 207 | 1.01e-06 | 1.98e-01 | 3.00e-05 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | 57 | 1.01e-02 | 1.97e-01 | 7.02e-02 |
| IRF3-mediated induction of type I IFN | 10 | 2.81e-01 | 1.97e-01 | 5.70e-01 |
| Defective CFTR causes cystic fibrosis | 52 | 1.41e-02 | 1.97e-01 | 8.73e-02 |
| Extracellular matrix organization | 223 | 4.98e-07 | -1.96e-01 | 1.67e-05 |
| CS/DS degradation | 11 | 2.62e-01 | -1.95e-01 | 5.56e-01 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | 54 | 1.32e-02 | 1.95e-01 | 8.35e-02 |
| Energy dependent regulation of mTOR by LKB1-AMPK | 29 | 6.91e-02 | -1.95e-01 | 2.53e-01 |
| APC/C:Cdc20 mediated degradation of Securin | 62 | 7.99e-03 | 1.95e-01 | 5.82e-02 |
| Mitotic Anaphase | 206 | 1.52e-06 | 1.95e-01 | 4.01e-05 |
| TCR signaling | 99 | 8.42e-04 | 1.94e-01 | 9.82e-03 |
| Defective B4GALT7 causes EDS, progeroid type | 17 | 1.65e-01 | -1.94e-01 | 4.33e-01 |
| Glutathione conjugation | 30 | 6.73e-02 | 1.93e-01 | 2.50e-01 |
| YAP1- and WWTR1 (TAZ)-stimulated gene expression | 15 | 1.96e-01 | -1.93e-01 | 4.78e-01 |
| Meiotic synapsis | 27 | 8.48e-02 | 1.92e-01 | 2.91e-01 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | 17 | 1.72e-01 | 1.91e-01 | 4.42e-01 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | 17 | 1.72e-01 | 1.91e-01 | 4.42e-01 |
| Peroxisomal lipid metabolism | 26 | 9.26e-02 | 1.91e-01 | 3.10e-01 |
| Signaling by PDGF | 47 | 2.42e-02 | -1.90e-01 | 1.28e-01 |
| p53-Dependent G1 DNA Damage Response | 58 | 1.24e-02 | 1.90e-01 | 8.04e-02 |
| p53-Dependent G1/S DNA damage checkpoint | 58 | 1.24e-02 | 1.90e-01 | 8.04e-02 |
| G alpha (12/13) signalling events | 71 | 5.94e-03 | -1.89e-01 | 4.73e-02 |
| Regulation of IFNG signaling | 13 | 2.38e-01 | 1.89e-01 | 5.32e-01 |
| Ion channel transport | 110 | 6.56e-04 | -1.88e-01 | 7.98e-03 |
| G1/S DNA Damage Checkpoints | 60 | 1.17e-02 | 1.88e-01 | 7.77e-02 |
| TRAF6 mediated IRF7 activation | 15 | 2.09e-01 | 1.87e-01 | 5.00e-01 |
| Binding and Uptake of Ligands by Scavenger Receptors | 31 | 7.15e-02 | -1.87e-01 | 2.60e-01 |
| Regulation of RAS by GAPs | 60 | 1.24e-02 | 1.87e-01 | 8.04e-02 |
| Membrane binding and targetting of GAG proteins | 11 | 2.84e-01 | -1.87e-01 | 5.72e-01 |
| Synthesis And Processing Of GAG, GAGPOL Polyproteins | 11 | 2.84e-01 | -1.87e-01 | 5.72e-01 |
| Inactivation of APC/C via direct inhibition of the APC/C complex | 21 | 1.39e-01 | 1.87e-01 | 3.99e-01 |
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | 21 | 1.39e-01 | 1.87e-01 | 3.99e-01 |
| APC/C:Cdc20 mediated degradation of Cyclin B | 22 | 1.30e-01 | 1.86e-01 | 3.87e-01 |
| Cristae formation | 11 | 2.85e-01 | 1.86e-01 | 5.72e-01 |
| Biosynthesis of specialized proresolving mediators (SPMs) | 14 | 2.28e-01 | 1.86e-01 | 5.16e-01 |
| Aquaporin-mediated transport | 37 | 5.04e-02 | -1.86e-01 | 2.06e-01 |
| Autodegradation of the E3 ubiquitin ligase COP1 | 46 | 2.99e-02 | 1.85e-01 | 1.48e-01 |
| RHO GTPases Activate NADPH Oxidases | 19 | 1.63e-01 | 1.85e-01 | 4.29e-01 |
| O-glycosylation of TSR domain-containing proteins | 32 | 7.05e-02 | -1.85e-01 | 2.57e-01 |
| SUMOylation of DNA replication proteins | 40 | 4.33e-02 | 1.85e-01 | 1.86e-01 |
| Creation of C4 and C2 activators | 12 | 2.68e-01 | 1.85e-01 | 5.58e-01 |
| Initiation of Nuclear Envelope (NE) Reformation | 19 | 1.63e-01 | 1.85e-01 | 4.30e-01 |
| Deadenylation of mRNA | 24 | 1.18e-01 | 1.85e-01 | 3.62e-01 |
| A tetrasaccharide linker sequence is required for GAG synthesis | 21 | 1.43e-01 | -1.85e-01 | 4.02e-01 |
| Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) | 24 | 1.18e-01 | 1.85e-01 | 3.62e-01 |
| DAP12 interactions | 28 | 9.29e-02 | 1.84e-01 | 3.10e-01 |
| Arachidonic acid metabolism | 38 | 5.04e-02 | 1.83e-01 | 2.06e-01 |
| Deubiquitination | 238 | 1.21e-06 | 1.83e-01 | 3.44e-05 |
| Regulation of Apoptosis | 47 | 2.99e-02 | 1.83e-01 | 1.48e-01 |
| Downstream TCR signaling | 78 | 5.26e-03 | 1.83e-01 | 4.40e-02 |
| Resolution of Abasic Sites (AP sites) | 37 | 5.46e-02 | 1.83e-01 | 2.19e-01 |
| Mitotic Prometaphase | 175 | 3.55e-05 | 1.82e-01 | 6.79e-04 |
| Interleukin-6 family signaling | 18 | 1.82e-01 | 1.82e-01 | 4.57e-01 |
| Ca2+ pathway | 54 | 2.15e-02 | -1.81e-01 | 1.19e-01 |
| SHC-mediated cascade:FGFR1 | 12 | 2.80e-01 | 1.80e-01 | 5.68e-01 |
| Scavenging by Class A Receptors | 14 | 2.46e-01 | -1.79e-01 | 5.42e-01 |
| Inactivation, recovery and regulation of the phototransduction cascade | 19 | 1.77e-01 | -1.79e-01 | 4.48e-01 |
| The phototransduction cascade | 19 | 1.77e-01 | -1.79e-01 | 4.48e-01 |
| HS-GAG biosynthesis | 23 | 1.38e-01 | -1.79e-01 | 3.99e-01 |
| Class B/2 (Secretin family receptors) | 45 | 3.83e-02 | -1.79e-01 | 1.72e-01 |
| Dual Incision in GG-NER | 39 | 5.39e-02 | 1.79e-01 | 2.17e-01 |
| Post-chaperonin tubulin folding pathway | 17 | 2.03e-01 | -1.78e-01 | 4.88e-01 |
| Defective B3GALTL causes Peters-plus syndrome (PpS) | 31 | 8.61e-02 | -1.78e-01 | 2.93e-01 |
| Signaling by the B Cell Receptor (BCR) | 104 | 1.77e-03 | 1.78e-01 | 1.82e-02 |
| TRAF6 mediated NF-kB activation | 22 | 1.52e-01 | -1.77e-01 | 4.12e-01 |
| Diseases associated with the TLR signaling cascade | 22 | 1.52e-01 | -1.76e-01 | 4.12e-01 |
| Diseases of Immune System | 22 | 1.52e-01 | -1.76e-01 | 4.12e-01 |
| Golgi Cisternae Pericentriolar Stack Reorganization | 14 | 2.54e-01 | 1.76e-01 | 5.50e-01 |
| Signaling by EGFR in Cancer | 20 | 1.73e-01 | -1.76e-01 | 4.43e-01 |
| Antimicrobial peptides | 14 | 2.56e-01 | 1.76e-01 | 5.50e-01 |
| Defects in vitamin and cofactor metabolism | 19 | 1.86e-01 | -1.75e-01 | 4.64e-01 |
| Peptide hormone metabolism | 54 | 2.67e-02 | -1.74e-01 | 1.38e-01 |
| Glucagon-like Peptide-1 (GLP1) regulates insulin secretion | 34 | 7.91e-02 | -1.74e-01 | 2.76e-01 |
| Degradation of GLI1 by the proteasome | 53 | 2.86e-02 | 1.74e-01 | 1.45e-01 |
| Integration of energy metabolism | 91 | 4.18e-03 | -1.74e-01 | 3.68e-02 |
| Activation of gene expression by SREBF (SREBP) | 41 | 5.43e-02 | -1.74e-01 | 2.18e-01 |
| HDMs demethylate histones | 21 | 1.70e-01 | -1.73e-01 | 4.39e-01 |
| NOTCH3 Activation and Transmission of Signal to the Nucleus | 22 | 1.61e-01 | -1.73e-01 | 4.27e-01 |
| Heparan sulfate/heparin (HS-GAG) metabolism | 41 | 5.60e-02 | -1.73e-01 | 2.22e-01 |
| Cellular response to heat stress | 87 | 5.58e-03 | -1.72e-01 | 4.59e-02 |
| DAG and IP3 signaling | 39 | 6.31e-02 | -1.72e-01 | 2.41e-01 |
| Glutathione synthesis and recycling | 11 | 3.26e-01 | 1.71e-01 | 6.26e-01 |
| Base Excision Repair | 45 | 4.71e-02 | 1.71e-01 | 1.98e-01 |
| Translation of structural proteins | 26 | 1.32e-01 | -1.71e-01 | 3.91e-01 |
| Cytochrome c-mediated apoptotic response | 10 | 3.50e-01 | -1.71e-01 | 6.56e-01 |
| Caspase activation via extrinsic apoptotic signalling pathway | 24 | 1.50e-01 | -1.70e-01 | 4.10e-01 |
| Cell-extracellular matrix interactions | 16 | 2.40e-01 | -1.70e-01 | 5.34e-01 |
| Complement cascade | 37 | 7.45e-02 | 1.70e-01 | 2.66e-01 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | 13 | 2.90e-01 | 1.69e-01 | 5.79e-01 |
| Degradation of DVL | 50 | 3.87e-02 | 1.69e-01 | 1.72e-01 |
| APC-Cdc20 mediated degradation of Nek2A | 24 | 1.53e-01 | 1.69e-01 | 4.13e-01 |
| Interleukin-10 signaling | 26 | 1.40e-01 | 1.67e-01 | 3.99e-01 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | 33 | 9.65e-02 | -1.67e-01 | 3.15e-01 |
| GLI3 is processed to GLI3R by the proteasome | 52 | 3.73e-02 | 1.67e-01 | 1.69e-01 |
| Uptake and function of anthrax toxins | 11 | 3.40e-01 | -1.66e-01 | 6.43e-01 |
| Regulation of RUNX2 expression and activity | 64 | 2.16e-02 | 1.66e-01 | 1.19e-01 |
| Pre-NOTCH Expression and Processing | 47 | 4.93e-02 | -1.66e-01 | 2.03e-01 |
| Regulation of TP53 Activity through Methylation | 14 | 2.83e-01 | -1.66e-01 | 5.72e-01 |
| Defective B3GAT3 causes JDSSDHD | 17 | 2.41e-01 | -1.64e-01 | 5.35e-01 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | 62 | 2.56e-02 | 1.64e-01 | 1.35e-01 |
| NIK-->noncanonical NF-kB signaling | 52 | 4.11e-02 | 1.64e-01 | 1.79e-01 |
| The NLRP3 inflammasome | 14 | 2.89e-01 | -1.64e-01 | 5.79e-01 |
| Hh mutants that don't undergo autocatalytic processing are degraded by ERAD | 48 | 5.03e-02 | 1.63e-01 | 2.06e-01 |
| Autodegradation of Cdh1 by Cdh1:APC/C | 58 | 3.18e-02 | 1.63e-01 | 1.54e-01 |
| Regulation of RUNX3 expression and activity | 48 | 5.11e-02 | 1.63e-01 | 2.08e-01 |
| PI3K events in ERBB2 signaling | 14 | 2.94e-01 | -1.62e-01 | 5.84e-01 |
| Degradation of the extracellular matrix | 73 | 1.69e-02 | -1.62e-01 | 9.89e-02 |
| GRB2 events in ERBB2 signaling | 14 | 2.96e-01 | -1.61e-01 | 5.86e-01 |
| Visual phototransduction | 54 | 4.05e-02 | -1.61e-01 | 1.77e-01 |
| p38MAPK events | 12 | 3.34e-01 | 1.61e-01 | 6.35e-01 |
| Glycerophospholipid biosynthesis | 96 | 6.42e-03 | -1.61e-01 | 4.94e-02 |
| Role of LAT2/NTAL/LAB on calcium mobilization | 14 | 2.98e-01 | 1.61e-01 | 5.90e-01 |
| Abortive elongation of HIV-1 transcript in the absence of Tat | 22 | 1.97e-01 | -1.59e-01 | 4.78e-01 |
| NGF-stimulated transcription | 34 | 1.09e-01 | -1.59e-01 | 3.46e-01 |
| Global Genome Nucleotide Excision Repair (GG-NER) | 80 | 1.41e-02 | 1.59e-01 | 8.73e-02 |
| Phase I - Functionalization of compounds | 63 | 2.93e-02 | 1.59e-01 | 1.48e-01 |
| Thromboxane signalling through TP receptor | 20 | 2.19e-01 | -1.59e-01 | 5.08e-01 |
| FCGR3A-mediated phagocytosis | 61 | 3.28e-02 | 1.58e-01 | 1.56e-01 |
| Leishmania phagocytosis | 61 | 3.28e-02 | 1.58e-01 | 1.56e-01 |
| Parasite infection | 61 | 3.28e-02 | 1.58e-01 | 1.56e-01 |
| Miscellaneous transport and binding events | 19 | 2.33e-01 | -1.58e-01 | 5.24e-01 |
| Antiviral mechanism by IFN-stimulated genes | 70 | 2.27e-02 | 1.58e-01 | 1.23e-01 |
| Activation of SMO | 14 | 3.07e-01 | -1.58e-01 | 6.05e-01 |
| p75NTR recruits signalling complexes | 11 | 3.66e-01 | -1.57e-01 | 6.78e-01 |
| Processing of Intronless Pre-mRNAs | 17 | 2.62e-01 | 1.57e-01 | 5.56e-01 |
| Interleukin-6 signaling | 10 | 3.89e-01 | 1.57e-01 | 6.98e-01 |
| Assembly Of The HIV Virion | 13 | 3.28e-01 | -1.57e-01 | 6.27e-01 |
| Acyl chain remodelling of PE | 16 | 2.79e-01 | 1.56e-01 | 5.68e-01 |
| Gap-filling DNA repair synthesis and ligation in TC-NER | 61 | 3.51e-02 | 1.56e-01 | 1.63e-01 |
| Olfactory Signaling Pathway | 14 | 3.12e-01 | -1.56e-01 | 6.08e-01 |
| Regulation of insulin secretion | 64 | 3.09e-02 | -1.56e-01 | 1.51e-01 |
| Signaling by ERBB2 ECD mutants | 15 | 2.95e-01 | -1.56e-01 | 5.86e-01 |
| Regulation of TLR by endogenous ligand | 10 | 3.94e-01 | -1.56e-01 | 6.98e-01 |
| Hh mutants abrogate ligand secretion | 50 | 5.69e-02 | 1.56e-01 | 2.23e-01 |
| Chemokine receptors bind chemokines | 30 | 1.40e-01 | 1.56e-01 | 3.99e-01 |
| RAB geranylgeranylation | 49 | 5.98e-02 | 1.56e-01 | 2.31e-01 |
| Downregulation of ERBB2 signaling | 24 | 1.87e-01 | -1.55e-01 | 4.64e-01 |
| COPII-mediated vesicle transport | 59 | 3.92e-02 | -1.55e-01 | 1.74e-01 |
| Cell death signalling via NRAGE, NRIF and NADE | 68 | 2.70e-02 | -1.55e-01 | 1.38e-01 |
| M Phase | 323 | 1.84e-06 | 1.55e-01 | 4.64e-05 |
| RHO GTPases Activate Formins | 109 | 5.35e-03 | 1.55e-01 | 4.45e-02 |
| Adherens junctions interactions | 14 | 3.19e-01 | -1.54e-01 | 6.18e-01 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 17 | 2.73e-01 | -1.53e-01 | 5.63e-01 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | 17 | 2.73e-01 | -1.53e-01 | 5.63e-01 |
| FGFR2 mutant receptor activation | 23 | 2.03e-01 | -1.53e-01 | 4.88e-01 |
| Degradation of GLI2 by the proteasome | 52 | 5.66e-02 | 1.53e-01 | 2.23e-01 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | 48 | 6.70e-02 | 1.53e-01 | 2.50e-01 |
| Downstream signaling events of B Cell Receptor (BCR) | 73 | 2.40e-02 | 1.53e-01 | 1.28e-01 |
| Diseases of metabolism | 181 | 4.02e-04 | -1.53e-01 | 5.28e-03 |
| SUMOylation of intracellular receptors | 26 | 1.78e-01 | 1.53e-01 | 4.50e-01 |
| Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon | 14 | 3.23e-01 | -1.53e-01 | 6.23e-01 |
| Adenylate cyclase activating pathway | 10 | 4.04e-01 | -1.52e-01 | 7.07e-01 |
| Ion transport by P-type ATPases | 36 | 1.16e-01 | -1.52e-01 | 3.61e-01 |
| Meiosis | 47 | 7.29e-02 | 1.51e-01 | 2.63e-01 |
| Telomere C-strand synthesis initiation | 12 | 3.66e-01 | 1.51e-01 | 6.78e-01 |
| Signaling by EGFR | 45 | 8.12e-02 | -1.50e-01 | 2.80e-01 |
| ABC transporter disorders | 63 | 3.94e-02 | 1.50e-01 | 1.74e-01 |
| Signaling by ERBB2 KD Mutants | 22 | 2.24e-01 | -1.50e-01 | 5.12e-01 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | 23 | 2.14e-01 | -1.50e-01 | 5.03e-01 |
| mRNA 3'-end processing | 52 | 6.26e-02 | 1.49e-01 | 2.40e-01 |
| Diseases of glycosylation | 112 | 6.44e-03 | -1.49e-01 | 4.94e-02 |
| SHC1 events in ERBB2 signaling | 20 | 2.49e-01 | -1.49e-01 | 5.43e-01 |
| Meiotic recombination | 22 | 2.27e-01 | 1.49e-01 | 5.16e-01 |
| Post-translational protein phosphorylation | 72 | 2.95e-02 | -1.49e-01 | 1.48e-01 |
| Metabolism of nitric oxide: NOS3 activation and regulation | 15 | 3.20e-01 | 1.48e-01 | 6.19e-01 |
| Inflammasomes | 19 | 2.64e-01 | -1.48e-01 | 5.58e-01 |
| Cobalamin (Cbl, vitamin B12) transport and metabolism | 12 | 3.75e-01 | -1.48e-01 | 6.86e-01 |
| Defects in cobalamin (B12) metabolism | 11 | 3.96e-01 | -1.48e-01 | 6.98e-01 |
| Dectin-1 mediated noncanonical NF-kB signaling | 53 | 6.36e-02 | 1.47e-01 | 2.41e-01 |
| Sema4D in semaphorin signaling | 24 | 2.12e-01 | -1.47e-01 | 5.03e-01 |
| tRNA Aminoacylation | 24 | 2.13e-01 | -1.47e-01 | 5.03e-01 |
| Signaling by FGFR4 in disease | 10 | 4.22e-01 | 1.47e-01 | 7.21e-01 |
| CD28 dependent PI3K/Akt signaling | 21 | 2.46e-01 | 1.46e-01 | 5.42e-01 |
| SUMOylation | 150 | 2.04e-03 | 1.46e-01 | 2.06e-02 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) | 34 | 1.40e-01 | -1.46e-01 | 3.99e-01 |
| CaM pathway | 33 | 1.46e-01 | -1.46e-01 | 4.07e-01 |
| Calmodulin induced events | 33 | 1.46e-01 | -1.46e-01 | 4.07e-01 |
| SUMO E3 ligases SUMOylate target proteins | 144 | 2.56e-03 | 1.46e-01 | 2.47e-02 |
| Caspase-mediated cleavage of cytoskeletal proteins | 12 | 3.82e-01 | -1.46e-01 | 6.94e-01 |
| Phase 2 - plateau phase | 19 | 2.73e-01 | -1.45e-01 | 5.63e-01 |
| Formation of the Early Elongation Complex | 32 | 1.56e-01 | -1.45e-01 | 4.16e-01 |
| Formation of the HIV-1 Early Elongation Complex | 32 | 1.56e-01 | -1.45e-01 | 4.16e-01 |
| ER to Golgi Anterograde Transport | 121 | 5.94e-03 | -1.45e-01 | 4.73e-02 |
| UCH proteinases | 78 | 2.71e-02 | 1.45e-01 | 1.38e-01 |
| PI-3K cascade:FGFR1 | 12 | 3.85e-01 | 1.45e-01 | 6.95e-01 |
| Regulation of PTEN mRNA translation | 11 | 4.06e-01 | -1.45e-01 | 7.07e-01 |
| Post NMDA receptor activation events | 55 | 6.38e-02 | -1.45e-01 | 2.41e-01 |
| Intra-Golgi traffic | 40 | 1.16e-01 | -1.44e-01 | 3.61e-01 |
| Glycosphingolipid metabolism | 34 | 1.47e-01 | -1.44e-01 | 4.09e-01 |
| Translesion Synthesis by POLH | 16 | 3.20e-01 | 1.44e-01 | 6.19e-01 |
| Activated NTRK2 signals through FRS2 and FRS3 | 10 | 4.33e-01 | -1.43e-01 | 7.27e-01 |
| FCERI mediated NF-kB activation | 72 | 3.60e-02 | 1.43e-01 | 1.66e-01 |
| Listeria monocytogenes entry into host cells | 17 | 3.08e-01 | -1.43e-01 | 6.06e-01 |
| Plasma lipoprotein remodeling | 15 | 3.40e-01 | -1.42e-01 | 6.43e-01 |
| SHC1 events in EGFR signaling | 11 | 4.14e-01 | -1.42e-01 | 7.17e-01 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | 36 | 1.40e-01 | 1.42e-01 | 3.99e-01 |
| Diseases of mitotic cell cycle | 36 | 1.40e-01 | 1.42e-01 | 3.99e-01 |
| Regulation of TP53 Degradation | 32 | 1.65e-01 | 1.42e-01 | 4.32e-01 |
| Platelet homeostasis | 71 | 3.93e-02 | -1.42e-01 | 1.74e-01 |
| RNA Polymerase II Transcription Termination | 61 | 5.65e-02 | 1.41e-01 | 2.23e-01 |
| Metalloprotease DUBs | 18 | 3.00e-01 | 1.41e-01 | 5.92e-01 |
| Transcription-Coupled Nucleotide Excision Repair (TC-NER) | 75 | 3.65e-02 | 1.40e-01 | 1.67e-01 |
| Mitochondrial tRNA aminoacylation | 18 | 3.05e-01 | -1.40e-01 | 6.01e-01 |
| Unblocking of NMDA receptors, glutamate binding and activation | 15 | 3.49e-01 | -1.40e-01 | 6.55e-01 |
| Deadenylation-dependent mRNA decay | 54 | 7.62e-02 | 1.40e-01 | 2.68e-01 |
| Telomere Extension By Telomerase | 21 | 2.68e-01 | 1.40e-01 | 5.58e-01 |
| Dual incision in TC-NER | 62 | 5.78e-02 | 1.39e-01 | 2.25e-01 |
| DNA Repair | 267 | 9.38e-05 | 1.39e-01 | 1.53e-03 |
| Biosynthesis of DHA-derived SPMs | 12 | 4.03e-01 | 1.39e-01 | 7.07e-01 |
| Keratan sulfate/keratin metabolism | 26 | 2.22e-01 | -1.39e-01 | 5.12e-01 |
| Insulin processing | 21 | 2.72e-01 | -1.38e-01 | 5.63e-01 |
| Translation | 230 | 3.17e-04 | 1.38e-01 | 4.38e-03 |
| Cytosolic sulfonation of small molecules | 15 | 3.54e-01 | 1.38e-01 | 6.62e-01 |
| Cell junction organization | 51 | 8.83e-02 | -1.38e-01 | 2.98e-01 |
| FCERI mediated Ca+2 mobilization | 27 | 2.15e-01 | 1.38e-01 | 5.03e-01 |
| Thrombin signalling through proteinase activated receptors (PARs) | 26 | 2.24e-01 | -1.38e-01 | 5.12e-01 |
| Ras activation upon Ca2+ influx through NMDA receptor | 15 | 3.56e-01 | -1.38e-01 | 6.65e-01 |
| Regulation of actin dynamics for phagocytic cup formation | 63 | 5.99e-02 | 1.37e-01 | 2.31e-01 |
| Metabolism of RNA | 601 | 1.43e-08 | 1.37e-01 | 6.86e-07 |
| Signaling by NOTCH4 | 74 | 4.30e-02 | 1.36e-01 | 1.86e-01 |
| Peroxisomal protein import | 55 | 8.12e-02 | 1.36e-01 | 2.80e-01 |
| IRE1alpha activates chaperones | 49 | 9.97e-02 | -1.36e-01 | 3.24e-01 |
| DCC mediated attractive signaling | 13 | 3.97e-01 | 1.36e-01 | 6.98e-01 |
| Activation of PPARGC1A (PGC-1alpha) by phosphorylation | 10 | 4.57e-01 | -1.36e-01 | 7.47e-01 |
| Processing of Capped Intronless Pre-mRNA | 26 | 2.32e-01 | 1.35e-01 | 5.24e-01 |
| Incretin synthesis, secretion, and inactivation | 12 | 4.18e-01 | -1.35e-01 | 7.19e-01 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | 78 | 3.96e-02 | -1.35e-01 | 1.74e-01 |
| Regulation of PTEN stability and activity | 62 | 6.71e-02 | 1.35e-01 | 2.50e-01 |
| Amino acid transport across the plasma membrane | 23 | 2.66e-01 | 1.34e-01 | 5.58e-01 |
| Elastic fibre formation | 38 | 1.53e-01 | -1.34e-01 | 4.13e-01 |
| Diseases associated with O-glycosylation of proteins | 44 | 1.25e-01 | -1.34e-01 | 3.78e-01 |
| Interleukin-2 family signaling | 34 | 1.80e-01 | 1.33e-01 | 4.53e-01 |
| Glycogen breakdown (glycogenolysis) | 14 | 3.90e-01 | -1.33e-01 | 6.98e-01 |
| PKA activation | 17 | 3.45e-01 | -1.32e-01 | 6.49e-01 |
| Host Interactions of HIV factors | 112 | 1.68e-02 | 1.31e-01 | 9.89e-02 |
| Rho GTPase cycle | 129 | 1.04e-02 | -1.31e-01 | 7.22e-02 |
| Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. | 103 | 2.20e-02 | 1.31e-01 | 1.20e-01 |
| Regulated proteolysis of p75NTR | 11 | 4.53e-01 | -1.31e-01 | 7.44e-01 |
| G2/M Transition | 173 | 3.13e-03 | 1.31e-01 | 2.93e-02 |
| BMAL1:CLOCK,NPAS2 activates circadian gene expression | 24 | 2.70e-01 | 1.30e-01 | 5.59e-01 |
| Physiological factors | 11 | 4.55e-01 | -1.30e-01 | 7.45e-01 |
| PLC beta mediated events | 49 | 1.15e-01 | -1.30e-01 | 3.61e-01 |
| CLEC7A (Dectin-1) induces NFAT activation | 10 | 4.77e-01 | 1.30e-01 | 7.56e-01 |
| Infection with Mycobacterium tuberculosis | 23 | 2.82e-01 | 1.30e-01 | 5.70e-01 |
| activated TAK1 mediates p38 MAPK activation | 18 | 3.42e-01 | -1.29e-01 | 6.45e-01 |
| Activation of NF-kappaB in B cells | 61 | 8.15e-02 | 1.29e-01 | 2.80e-01 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | 13 | 4.21e-01 | -1.29e-01 | 7.21e-01 |
| G beta:gamma signalling through PLC beta | 16 | 3.73e-01 | -1.29e-01 | 6.85e-01 |
| Mitotic G2-G2/M phases | 175 | 3.43e-03 | 1.29e-01 | 3.13e-02 |
| XBP1(S) activates chaperone genes | 47 | 1.28e-01 | -1.28e-01 | 3.82e-01 |
| Sema3A PAK dependent Axon repulsion | 16 | 3.74e-01 | -1.28e-01 | 6.85e-01 |
| PECAM1 interactions | 11 | 4.61e-01 | 1.28e-01 | 7.48e-01 |
| Disorders of developmental biology | 11 | 4.62e-01 | 1.28e-01 | 7.48e-01 |
| Loss of function of MECP2 in Rett syndrome | 11 | 4.62e-01 | 1.28e-01 | 7.48e-01 |
| Pervasive developmental disorders | 11 | 4.62e-01 | 1.28e-01 | 7.48e-01 |
| Smooth Muscle Contraction | 36 | 1.86e-01 | -1.27e-01 | 4.64e-01 |
| Respiratory electron transport | 97 | 3.04e-02 | 1.27e-01 | 1.49e-01 |
| mRNA decay by 3' to 5' exoribonuclease | 15 | 3.94e-01 | 1.27e-01 | 6.98e-01 |
| The canonical retinoid cycle in rods (twilight vision) | 10 | 4.87e-01 | -1.27e-01 | 7.65e-01 |
| Gluconeogenesis | 27 | 2.54e-01 | -1.27e-01 | 5.50e-01 |
| InlB-mediated entry of Listeria monocytogenes into host cell | 13 | 4.29e-01 | -1.27e-01 | 7.23e-01 |
| Constitutive Signaling by EGFRvIII | 15 | 3.97e-01 | -1.26e-01 | 6.98e-01 |
| Signaling by EGFRvIII in Cancer | 15 | 3.97e-01 | -1.26e-01 | 6.98e-01 |
| Prolactin receptor signaling | 11 | 4.68e-01 | -1.26e-01 | 7.53e-01 |
| Negative regulators of DDX58/IFIH1 signaling | 30 | 2.33e-01 | 1.26e-01 | 5.24e-01 |
| Deactivation of the beta-catenin transactivating complex | 35 | 1.98e-01 | -1.26e-01 | 4.80e-01 |
| Adaptive Immune System | 585 | 2.82e-07 | 1.25e-01 | 9.68e-06 |
| RHO GTPases activate KTN1 | 10 | 4.93e-01 | -1.25e-01 | 7.67e-01 |
| Nucleotide Excision Repair | 105 | 2.71e-02 | 1.25e-01 | 1.38e-01 |
| TP53 Regulates Transcription of Cell Cycle Genes | 46 | 1.43e-01 | 1.25e-01 | 4.02e-01 |
| NR1H2 and NR1H3-mediated signaling | 37 | 1.89e-01 | -1.25e-01 | 4.66e-01 |
| Ephrin signaling | 19 | 3.47e-01 | -1.25e-01 | 6.52e-01 |
| Pentose phosphate pathway | 13 | 4.37e-01 | 1.24e-01 | 7.29e-01 |
| mRNA Splicing - Major Pathway | 168 | 5.65e-03 | 1.24e-01 | 4.61e-02 |
| Kinesins | 38 | 1.86e-01 | 1.24e-01 | 4.64e-01 |
| Apoptotic factor-mediated response | 13 | 4.40e-01 | -1.24e-01 | 7.32e-01 |
| Signaling by FGFR2 IIIa TM | 18 | 3.64e-01 | -1.24e-01 | 6.77e-01 |
| mRNA Capping | 28 | 2.61e-01 | -1.23e-01 | 5.56e-01 |
| Cellular response to hypoxia | 64 | 9.08e-02 | 1.22e-01 | 3.06e-01 |
| Syndecan interactions | 20 | 3.44e-01 | -1.22e-01 | 6.48e-01 |
| Defective B3GALT6 causes EDSP2 and SEMDJL1 | 17 | 3.83e-01 | -1.22e-01 | 6.94e-01 |
| G-protein mediated events | 50 | 1.36e-01 | -1.22e-01 | 3.97e-01 |
| Neurexins and neuroligins | 38 | 1.94e-01 | -1.22e-01 | 4.77e-01 |
| Chondroitin sulfate/dermatan sulfate metabolism | 42 | 1.73e-01 | -1.22e-01 | 4.43e-01 |
| Vasopressin regulates renal water homeostasis via Aquaporins | 34 | 2.24e-01 | -1.21e-01 | 5.12e-01 |
| SHC-mediated cascade:FGFR3 | 12 | 4.69e-01 | 1.21e-01 | 7.54e-01 |
| Chondroitin sulfate biosynthesis | 16 | 4.04e-01 | -1.21e-01 | 7.07e-01 |
| RHO GTPase Effectors | 220 | 2.13e-03 | 1.21e-01 | 2.14e-02 |
| Reproduction | 57 | 1.17e-01 | 1.20e-01 | 3.62e-01 |
| Macroautophagy | 104 | 3.48e-02 | -1.20e-01 | 1.63e-01 |
| Regulation of KIT signaling | 16 | 4.06e-01 | 1.20e-01 | 7.07e-01 |
| NOTCH4 Intracellular Domain Regulates Transcription | 18 | 3.79e-01 | -1.20e-01 | 6.92e-01 |
| mRNA Splicing | 176 | 6.37e-03 | 1.20e-01 | 4.94e-02 |
| SUMOylation of DNA damage response and repair proteins | 66 | 9.44e-02 | 1.19e-01 | 3.11e-01 |
| Synaptic adhesion-like molecules | 17 | 3.96e-01 | -1.19e-01 | 6.98e-01 |
| Mitochondrial Fatty Acid Beta-Oxidation | 32 | 2.47e-01 | 1.18e-01 | 5.42e-01 |
| Signaling by ERBB2 in Cancer | 23 | 3.26e-01 | -1.18e-01 | 6.27e-01 |
| Glucose metabolism | 77 | 7.33e-02 | -1.18e-01 | 2.64e-01 |
| Pre-NOTCH Transcription and Translation | 32 | 2.48e-01 | -1.18e-01 | 5.42e-01 |
| Degradation of beta-catenin by the destruction complex | 76 | 7.58e-02 | 1.18e-01 | 2.68e-01 |
| CRMPs in Sema3A signaling | 15 | 4.30e-01 | -1.18e-01 | 7.23e-01 |
| Signaling by Retinoic Acid | 33 | 2.44e-01 | 1.17e-01 | 5.40e-01 |
| PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases | 13 | 4.64e-01 | 1.17e-01 | 7.51e-01 |
| Reduction of cytosolic Ca++ levels | 10 | 5.21e-01 | -1.17e-01 | 7.82e-01 |
| FOXO-mediated transcription of cell cycle genes | 16 | 4.18e-01 | -1.17e-01 | 7.19e-01 |
| COPI-mediated anterograde transport | 77 | 7.61e-02 | -1.17e-01 | 2.68e-01 |
| TRAF3-dependent IRF activation pathway | 13 | 4.66e-01 | 1.17e-01 | 7.52e-01 |
| G alpha (z) signalling events | 39 | 2.07e-01 | -1.17e-01 | 4.96e-01 |
| Signaling by NOTCH1 | 66 | 1.02e-01 | -1.17e-01 | 3.30e-01 |
| Transport to the Golgi and subsequent modification | 146 | 1.54e-02 | -1.16e-01 | 9.35e-02 |
| Sialic acid metabolism | 25 | 3.15e-01 | -1.16e-01 | 6.14e-01 |
| Synthesis, secretion, and deacylation of Ghrelin | 11 | 5.05e-01 | 1.16e-01 | 7.75e-01 |
| rRNA processing in the mitochondrion | 17 | 4.09e-01 | 1.16e-01 | 7.10e-01 |
| MET activates RAP1 and RAC1 | 11 | 5.07e-01 | 1.15e-01 | 7.75e-01 |
| Signaling by NOTCH3 | 44 | 1.87e-01 | -1.15e-01 | 4.64e-01 |
| Regulation of TP53 Expression and Degradation | 33 | 2.53e-01 | 1.15e-01 | 5.49e-01 |
| Signaling by FGFR3 in disease | 16 | 4.28e-01 | 1.14e-01 | 7.23e-01 |
| Signaling by FGFR3 point mutants in cancer | 16 | 4.28e-01 | 1.14e-01 | 7.23e-01 |
| Pyruvate metabolism and Citric Acid (TCA) cycle | 50 | 1.62e-01 | 1.14e-01 | 4.28e-01 |
| The citric acid (TCA) cycle and respiratory electron transport | 149 | 1.62e-02 | 1.14e-01 | 9.70e-02 |
| Hedgehog ligand biogenesis | 53 | 1.50e-01 | 1.14e-01 | 4.10e-01 |
| eNOS activation | 11 | 5.15e-01 | 1.13e-01 | 7.80e-01 |
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes | 25 | 3.27e-01 | 1.13e-01 | 6.27e-01 |
| Spry regulation of FGF signaling | 14 | 4.63e-01 | -1.13e-01 | 7.50e-01 |
| Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | 10 | 5.36e-01 | 1.13e-01 | 7.96e-01 |
| Regulation of signaling by CBL | 18 | 4.07e-01 | 1.13e-01 | 7.07e-01 |
| Regulation of innate immune responses to cytosolic DNA | 11 | 5.18e-01 | 1.13e-01 | 7.81e-01 |
| Metabolism of carbohydrates | 234 | 3.17e-03 | -1.12e-01 | 2.94e-02 |
| Cargo trafficking to the periciliary membrane | 45 | 1.93e-01 | 1.12e-01 | 4.75e-01 |
| Regulation of beta-cell development | 22 | 3.63e-01 | -1.12e-01 | 6.75e-01 |
| Pyrimidine salvage | 10 | 5.40e-01 | 1.12e-01 | 8.00e-01 |
| Regulation of TP53 Activity through Association with Co-factors | 12 | 5.02e-01 | -1.12e-01 | 7.74e-01 |
| ISG15 antiviral mechanism | 62 | 1.30e-01 | 1.11e-01 | 3.85e-01 |
| CTLA4 inhibitory signaling | 21 | 3.77e-01 | 1.11e-01 | 6.89e-01 |
| Ca-dependent events | 35 | 2.55e-01 | -1.11e-01 | 5.50e-01 |
| Biotin transport and metabolism | 11 | 5.23e-01 | -1.11e-01 | 7.84e-01 |
| Class I MHC mediated antigen processing & presentation | 324 | 6.21e-04 | 1.11e-01 | 7.63e-03 |
| Insulin receptor recycling | 19 | 4.02e-01 | -1.11e-01 | 7.06e-01 |
| Regulation of HSF1-mediated heat shock response | 70 | 1.12e-01 | -1.10e-01 | 3.55e-01 |
| Fc epsilon receptor (FCERI) signaling | 121 | 3.73e-02 | 1.10e-01 | 1.69e-01 |
| Signaling by KIT in disease | 20 | 3.96e-01 | 1.10e-01 | 6.98e-01 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | 20 | 3.96e-01 | 1.10e-01 | 6.98e-01 |
| Lewis blood group biosynthesis | 11 | 5.29e-01 | 1.10e-01 | 7.89e-01 |
| Signaling by BRAF and RAF fusions | 56 | 1.57e-01 | -1.09e-01 | 4.18e-01 |
| Signaling by NTRKs | 123 | 3.67e-02 | -1.09e-01 | 1.68e-01 |
| Formation of Incision Complex in GG-NER | 40 | 2.32e-01 | 1.09e-01 | 5.24e-01 |
| Retinoid metabolism and transport | 27 | 3.28e-01 | -1.09e-01 | 6.27e-01 |
| Processing of Capped Intron-Containing Pre-mRNA | 221 | 5.56e-03 | 1.09e-01 | 4.59e-02 |
| RIPK1-mediated regulated necrosis | 14 | 4.84e-01 | 1.08e-01 | 7.61e-01 |
| Regulated Necrosis | 14 | 4.84e-01 | 1.08e-01 | 7.61e-01 |
| Asparagine N-linked glycosylation | 249 | 3.41e-03 | -1.08e-01 | 3.13e-02 |
| Regulation of cholesterol biosynthesis by SREBP (SREBF) | 54 | 1.70e-01 | -1.08e-01 | 4.39e-01 |
| Transcriptional regulation by RUNX2 | 108 | 5.31e-02 | 1.08e-01 | 2.15e-01 |
| Prefoldin mediated transfer of substrate to CCT/TriC | 24 | 3.61e-01 | 1.08e-01 | 6.72e-01 |
| Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein | 68 | 1.26e-01 | -1.07e-01 | 3.79e-01 |
| Oncogenic MAPK signaling | 72 | 1.16e-01 | -1.07e-01 | 3.61e-01 |
| DNA Double Strand Break Response | 39 | 2.47e-01 | 1.07e-01 | 5.42e-01 |
| Transcriptional Regulation by VENTX | 36 | 2.67e-01 | -1.07e-01 | 5.58e-01 |
| Keratan sulfate biosynthesis | 21 | 3.99e-01 | -1.06e-01 | 7.01e-01 |
| Response of EIF2AK1 (HRI) to heme deficiency | 14 | 4.91e-01 | 1.06e-01 | 7.67e-01 |
| Autophagy | 116 | 4.87e-02 | -1.06e-01 | 2.02e-01 |
| Potential therapeutics for SARS | 35 | 2.79e-01 | 1.06e-01 | 5.68e-01 |
| Acyl chain remodelling of PG | 11 | 5.44e-01 | -1.06e-01 | 8.04e-01 |
| Gamma carboxylation, hypusine formation and arylsulfatase activation | 31 | 3.09e-01 | -1.06e-01 | 6.06e-01 |
| p75 NTR receptor-mediated signalling | 85 | 9.35e-02 | -1.05e-01 | 3.10e-01 |
| FGFR2 alternative splicing | 24 | 3.72e-01 | -1.05e-01 | 6.85e-01 |
| Negative regulation of MET activity | 19 | 4.27e-01 | -1.05e-01 | 7.23e-01 |
| Muscle contraction | 159 | 2.24e-02 | -1.05e-01 | 1.22e-01 |
| HDACs deacetylate histones | 30 | 3.19e-01 | 1.05e-01 | 6.18e-01 |
| Glycosaminoglycan metabolism | 96 | 7.54e-02 | -1.05e-01 | 2.68e-01 |
| Acyl chain remodelling of PC | 18 | 4.40e-01 | 1.05e-01 | 7.32e-01 |
| tRNA processing in the mitochondrion | 16 | 4.67e-01 | 1.05e-01 | 7.53e-01 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | 80 | 1.05e-01 | 1.05e-01 | 3.38e-01 |
| Inositol phosphate metabolism | 43 | 2.34e-01 | -1.05e-01 | 5.25e-01 |
| Neddylation | 210 | 9.14e-03 | 1.05e-01 | 6.44e-02 |
| Diseases of DNA repair | 10 | 5.68e-01 | -1.04e-01 | 8.21e-01 |
| cGMP effects | 13 | 5.15e-01 | -1.04e-01 | 7.80e-01 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | 36 | 2.79e-01 | -1.04e-01 | 5.68e-01 |
| Receptor Mediated Mitophagy | 11 | 5.49e-01 | -1.04e-01 | 8.08e-01 |
| RAS processing | 20 | 4.21e-01 | 1.04e-01 | 7.21e-01 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat | 38 | 2.68e-01 | -1.04e-01 | 5.58e-01 |
| HIV Transcription Elongation | 38 | 2.68e-01 | -1.04e-01 | 5.58e-01 |
| Tat-mediated elongation of the HIV-1 transcript | 38 | 2.68e-01 | -1.04e-01 | 5.58e-01 |
| ECM proteoglycans | 42 | 2.44e-01 | -1.04e-01 | 5.41e-01 |
| Interleukin-7 signaling | 20 | 4.22e-01 | -1.04e-01 | 7.21e-01 |
| Processing of SMDT1 | 15 | 4.89e-01 | 1.03e-01 | 7.65e-01 |
| Interleukin-15 signaling | 14 | 5.07e-01 | 1.02e-01 | 7.75e-01 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | 47 | 2.25e-01 | -1.02e-01 | 5.14e-01 |
| Sphingolipid metabolism | 67 | 1.48e-01 | -1.02e-01 | 4.09e-01 |
| Protein-protein interactions at synapses | 62 | 1.69e-01 | -1.01e-01 | 4.37e-01 |
| Glycolysis | 59 | 1.80e-01 | -1.01e-01 | 4.53e-01 |
| Aggrephagy | 17 | 4.72e-01 | -1.01e-01 | 7.54e-01 |
| Interleukin-37 signaling | 18 | 4.61e-01 | -1.00e-01 | 7.48e-01 |
| MyD88 cascade initiated on plasma membrane | 78 | 1.28e-01 | -9.98e-02 | 3.82e-01 |
| Toll Like Receptor 10 (TLR10) Cascade | 78 | 1.28e-01 | -9.98e-02 | 3.82e-01 |
| Toll Like Receptor 5 (TLR5) Cascade | 78 | 1.28e-01 | -9.98e-02 | 3.82e-01 |
| B-WICH complex positively regulates rRNA expression | 32 | 3.32e-01 | 9.92e-02 | 6.32e-01 |
| Glucagon signaling in metabolic regulation | 27 | 3.74e-01 | -9.89e-02 | 6.85e-01 |
| O-linked glycosylation | 70 | 1.54e-01 | -9.87e-02 | 4.13e-01 |
| NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 11 | 5.71e-01 | 9.87e-02 | 8.25e-01 |
| Negative regulation of FGFR2 signaling | 23 | 4.15e-01 | -9.82e-02 | 7.18e-01 |
| ER Quality Control Compartment (ERQC) | 18 | 4.71e-01 | -9.81e-02 | 7.54e-01 |
| Diseases associated with glycosaminoglycan metabolism | 35 | 3.16e-01 | -9.80e-02 | 6.14e-01 |
| Potassium Channels | 64 | 1.77e-01 | -9.76e-02 | 4.49e-01 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 26 | 3.90e-01 | 9.75e-02 | 6.98e-01 |
| Rap1 signalling | 15 | 5.14e-01 | -9.74e-02 | 7.80e-01 |
| RNA Pol II CTD phosphorylation and interaction with CE | 26 | 3.91e-01 | -9.72e-02 | 6.98e-01 |
| RNA Pol II CTD phosphorylation and interaction with CE during HIV infection | 26 | 3.91e-01 | -9.72e-02 | 6.98e-01 |
| Vitamin B5 (pantothenate) metabolism | 15 | 5.15e-01 | 9.72e-02 | 7.80e-01 |
| TNFR2 non-canonical NF-kB pathway | 75 | 1.46e-01 | 9.71e-02 | 4.07e-01 |
| Neuronal System | 262 | 7.18e-03 | -9.68e-02 | 5.29e-02 |
| ABC-family proteins mediated transport | 86 | 1.23e-01 | 9.64e-02 | 3.74e-01 |
| Infectious disease | 574 | 9.46e-05 | 9.62e-02 | 1.53e-03 |
| FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | 22 | 4.35e-01 | -9.61e-02 | 7.27e-01 |
| Cytochrome P450 - arranged by substrate type | 33 | 3.41e-01 | 9.58e-02 | 6.45e-01 |
| Maturation of nucleoprotein | 10 | 6.01e-01 | 9.55e-02 | 8.43e-01 |
| Regulation of TP53 Activity through Phosphorylation | 87 | 1.25e-01 | 9.52e-02 | 3.78e-01 |
| Synthesis of bile acids and bile salts | 24 | 4.24e-01 | 9.42e-02 | 7.23e-01 |
| Nucleobase catabolism | 31 | 3.66e-01 | 9.40e-02 | 6.78e-01 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | 18 | 4.92e-01 | 9.36e-02 | 7.67e-01 |
| Negative epigenetic regulation of rRNA expression | 48 | 2.64e-01 | 9.32e-02 | 5.58e-01 |
| TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 85 | 1.39e-01 | -9.30e-02 | 3.99e-01 |
| Amine ligand-binding receptors | 13 | 5.62e-01 | 9.30e-02 | 8.16e-01 |
| FRS-mediated FGFR2 signaling | 16 | 5.20e-01 | -9.29e-02 | 7.82e-01 |
| GPVI-mediated activation cascade | 30 | 3.80e-01 | 9.26e-02 | 6.93e-01 |
| Hedgehog 'on' state | 75 | 1.67e-01 | 9.24e-02 | 4.35e-01 |
| NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux | 30 | 3.83e-01 | -9.20e-02 | 6.94e-01 |
| SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 27 | 4.09e-01 | 9.18e-02 | 7.10e-01 |
| Fcgamma receptor (FCGR) dependent phagocytosis | 86 | 1.42e-01 | 9.17e-02 | 4.00e-01 |
| Integrin cell surface interactions | 52 | 2.58e-01 | -9.07e-02 | 5.54e-01 |
| TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway | 12 | 5.87e-01 | -9.07e-02 | 8.36e-01 |
| Activation of G protein gated Potassium channels | 21 | 4.75e-01 | 9.01e-02 | 7.55e-01 |
| G protein gated Potassium channels | 21 | 4.75e-01 | 9.01e-02 | 7.55e-01 |
| Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits | 21 | 4.75e-01 | 9.01e-02 | 7.55e-01 |
| Circadian Clock | 63 | 2.17e-01 | 9.01e-02 | 5.05e-01 |
| Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 39 | 3.31e-01 | 9.01e-02 | 6.31e-01 |
| Interaction between L1 and Ankyrins | 23 | 4.55e-01 | -9.00e-02 | 7.45e-01 |
| Activation of NMDA receptors and postsynaptic events | 64 | 2.14e-01 | -9.00e-02 | 5.03e-01 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 52 | 2.62e-01 | -8.99e-02 | 5.56e-01 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | 52 | 2.62e-01 | -8.99e-02 | 5.56e-01 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 52 | 2.62e-01 | -8.99e-02 | 5.56e-01 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | 52 | 2.62e-01 | -8.99e-02 | 5.56e-01 |
| Signaling by NOTCH1 in Cancer | 52 | 2.62e-01 | -8.99e-02 | 5.56e-01 |
| Nuclear Events (kinase and transcription factor activation) | 56 | 2.45e-01 | -8.99e-02 | 5.41e-01 |
| Metabolism of nucleotides | 87 | 1.48e-01 | 8.99e-02 | 4.09e-01 |
| RUNX3 regulates NOTCH signaling | 14 | 5.63e-01 | -8.94e-02 | 8.16e-01 |
| Antigen processing: Ubiquitination & Proteasome degradation | 274 | 1.13e-02 | 8.93e-02 | 7.58e-02 |
| Downstream signaling of activated FGFR1 | 22 | 4.70e-01 | 8.90e-02 | 7.54e-01 |
| MTOR signalling | 40 | 3.31e-01 | -8.89e-02 | 6.31e-01 |
| Sulfur amino acid metabolism | 22 | 4.71e-01 | 8.87e-02 | 7.54e-01 |
| Signaling by TGF-beta Receptor Complex | 67 | 2.10e-01 | 8.87e-02 | 5.00e-01 |
| rRNA modification in the nucleus and cytosol | 53 | 2.65e-01 | 8.85e-02 | 5.58e-01 |
| Synthesis of PIPs at the late endosome membrane | 11 | 6.12e-01 | 8.84e-02 | 8.48e-01 |
| Regulation of necroptotic cell death | 12 | 5.97e-01 | 8.81e-02 | 8.40e-01 |
| Bile acid and bile salt metabolism | 27 | 4.30e-01 | 8.78e-02 | 7.23e-01 |
| Nicotinate metabolism | 25 | 4.49e-01 | 8.75e-02 | 7.40e-01 |
| Long-term potentiation | 18 | 5.22e-01 | -8.73e-02 | 7.82e-01 |
| Notch-HLH transcription pathway | 25 | 4.51e-01 | -8.71e-02 | 7.41e-01 |
| alpha-linolenic (omega3) and linoleic (omega6) acid metabolism | 10 | 6.33e-01 | -8.71e-02 | 8.65e-01 |
| alpha-linolenic acid (ALA) metabolism | 10 | 6.33e-01 | -8.71e-02 | 8.65e-01 |
| Cardiac conduction | 100 | 1.33e-01 | -8.71e-02 | 3.92e-01 |
| Synthesis of Prostaglandins (PG) and Thromboxanes (TX) | 11 | 6.18e-01 | -8.68e-02 | 8.51e-01 |
| Transport of Mature Transcript to Cytoplasm | 74 | 2.00e-01 | 8.63e-02 | 4.83e-01 |
| Downregulation of TGF-beta receptor signaling | 24 | 4.68e-01 | 8.56e-02 | 7.53e-01 |
| Caspase activation via Death Receptors in the presence of ligand | 15 | 5.66e-01 | -8.56e-02 | 8.21e-01 |
| Transcriptional regulation of pluripotent stem cells | 16 | 5.54e-01 | 8.55e-02 | 8.11e-01 |
| Carboxyterminal post-translational modifications of tubulin | 26 | 4.51e-01 | -8.54e-02 | 7.41e-01 |
| Branched-chain amino acid catabolism | 21 | 4.98e-01 | 8.54e-02 | 7.72e-01 |
| Synthesis of substrates in N-glycan biosythesis | 54 | 2.78e-01 | -8.54e-02 | 5.68e-01 |
| PI-3K cascade:FGFR3 | 12 | 6.09e-01 | 8.52e-02 | 8.48e-01 |
| Late endosomal microautophagy | 26 | 4.57e-01 | -8.43e-02 | 7.47e-01 |
| Signaling by GPCR | 437 | 2.69e-03 | -8.43e-02 | 2.58e-02 |
| Disorders of transmembrane transporters | 133 | 9.44e-02 | 8.42e-02 | 3.11e-01 |
| Response of Mtb to phagocytosis | 20 | 5.16e-01 | 8.40e-02 | 7.80e-01 |
| Synthesis of IP2, IP, and Ins in the cytosol | 14 | 5.87e-01 | -8.38e-02 | 8.36e-01 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | 38 | 3.72e-01 | 8.38e-02 | 6.85e-01 |
| Dopamine Neurotransmitter Release Cycle | 16 | 5.62e-01 | 8.37e-02 | 8.16e-01 |
| Transcriptional regulation of granulopoiesis | 28 | 4.45e-01 | 8.35e-02 | 7.36e-01 |
| Semaphorin interactions | 63 | 2.55e-01 | -8.30e-02 | 5.50e-01 |
| p130Cas linkage to MAPK signaling for integrins | 12 | 6.19e-01 | 8.28e-02 | 8.51e-01 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | 65 | 2.49e-01 | 8.28e-02 | 5.43e-01 |
| Positive epigenetic regulation of rRNA expression | 45 | 3.38e-01 | 8.26e-02 | 6.42e-01 |
| MyD88 dependent cascade initiated on endosome | 86 | 1.88e-01 | -8.23e-02 | 4.64e-01 |
| Toll Like Receptor 7/8 (TLR7/8) Cascade | 86 | 1.88e-01 | -8.23e-02 | 4.64e-01 |
| Fatty acyl-CoA biosynthesis | 24 | 4.88e-01 | -8.19e-02 | 7.65e-01 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 17 | 5.60e-01 | 8.17e-02 | 8.15e-01 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | 20 | 5.28e-01 | 8.16e-02 | 7.88e-01 |
| Protein ubiquitination | 56 | 2.92e-01 | 8.15e-02 | 5.82e-01 |
| Signaling by ERBB2 | 43 | 3.56e-01 | -8.15e-02 | 6.64e-01 |
| TP53 Regulates Metabolic Genes | 83 | 2.01e-01 | -8.13e-02 | 4.86e-01 |
| Metabolism of steroid hormones | 18 | 5.52e-01 | 8.11e-02 | 8.10e-01 |
| Formation of RNA Pol II elongation complex | 53 | 3.10e-01 | -8.06e-02 | 6.06e-01 |
| RNA Polymerase II Transcription Elongation | 53 | 3.10e-01 | -8.06e-02 | 6.06e-01 |
| Signaling by NOTCH2 | 27 | 4.69e-01 | -8.06e-02 | 7.53e-01 |
| C-type lectin receptors (CLRs) | 110 | 1.45e-01 | 8.05e-02 | 4.07e-01 |
| E3 ubiquitin ligases ubiquitinate target proteins | 39 | 3.85e-01 | 8.04e-02 | 6.95e-01 |
| Presynaptic function of Kainate receptors | 17 | 5.71e-01 | -7.94e-02 | 8.25e-01 |
| The role of Nef in HIV-1 replication and disease pathogenesis | 25 | 4.92e-01 | 7.94e-02 | 7.67e-01 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | 20 | 5.39e-01 | 7.93e-02 | 8.00e-01 |
| Beta-catenin phosphorylation cascade | 16 | 5.83e-01 | -7.93e-02 | 8.35e-01 |
| Signaling by Receptor Tyrosine Kinases | 420 | 5.80e-03 | -7.90e-02 | 4.68e-02 |
| SUMOylation of transcription factors | 15 | 5.96e-01 | 7.90e-02 | 8.40e-01 |
| mRNA decay by 5' to 3' exoribonuclease | 15 | 5.97e-01 | 7.88e-02 | 8.40e-01 |
| Gene Silencing by RNA | 61 | 2.89e-01 | -7.85e-02 | 5.79e-01 |
| EPH-ephrin mediated repulsion of cells | 44 | 3.70e-01 | -7.82e-02 | 6.83e-01 |
| Protein localization | 145 | 1.05e-01 | 7.82e-02 | 3.38e-01 |
| Signaling by NTRK1 (TRKA) | 107 | 1.64e-01 | -7.80e-02 | 4.30e-01 |
| Receptor-type tyrosine-protein phosphatases | 14 | 6.14e-01 | -7.79e-02 | 8.48e-01 |
| Mitotic Prophase | 77 | 2.39e-01 | 7.77e-02 | 5.32e-01 |
| Suppression of phagosomal maturation | 11 | 6.57e-01 | -7.73e-02 | 8.84e-01 |
| Negative regulation of FGFR4 signaling | 20 | 5.50e-01 | -7.73e-02 | 8.08e-01 |
| Chaperone Mediated Autophagy | 15 | 6.08e-01 | -7.64e-02 | 8.48e-01 |
| G alpha (s) signalling events | 86 | 2.22e-01 | -7.63e-02 | 5.12e-01 |
| Formation of HIV elongation complex in the absence of HIV Tat | 40 | 4.05e-01 | -7.61e-02 | 7.07e-01 |
| Oxidative Stress Induced Senescence | 60 | 3.09e-01 | -7.61e-02 | 6.06e-01 |
| Toll Like Receptor 9 (TLR9) Cascade | 89 | 2.16e-01 | -7.60e-02 | 5.05e-01 |
| Regulation of TNFR1 signaling | 27 | 4.95e-01 | 7.58e-02 | 7.68e-01 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 89 | 2.18e-01 | -7.57e-02 | 5.05e-01 |
| Toll Like Receptor 2 (TLR2) Cascade | 89 | 2.18e-01 | -7.57e-02 | 5.05e-01 |
| Toll Like Receptor TLR1:TLR2 Cascade | 89 | 2.18e-01 | -7.57e-02 | 5.05e-01 |
| Toll Like Receptor TLR6:TLR2 Cascade | 89 | 2.18e-01 | -7.57e-02 | 5.05e-01 |
| Pyrimidine catabolism | 10 | 6.80e-01 | 7.55e-02 | 8.88e-01 |
| NOTCH1 Intracellular Domain Regulates Transcription | 43 | 3.93e-01 | -7.53e-02 | 6.98e-01 |
| Beta-oxidation of very long chain fatty acids | 10 | 6.82e-01 | -7.49e-02 | 8.88e-01 |
| CLEC7A (Dectin-1) signaling | 89 | 2.23e-01 | 7.48e-02 | 5.12e-01 |
| Neutrophil degranulation | 360 | 1.60e-02 | 7.43e-02 | 9.63e-02 |
| FOXO-mediated transcription of cell death genes | 14 | 6.31e-01 | 7.42e-02 | 8.63e-01 |
| Transmission across Chemical Synapses | 173 | 9.33e-02 | -7.42e-02 | 3.10e-01 |
| Phospholipid metabolism | 174 | 9.35e-02 | -7.39e-02 | 3.10e-01 |
| Plasma lipoprotein assembly, remodeling, and clearance | 47 | 3.82e-01 | -7.38e-02 | 6.94e-01 |
| Activation of BH3-only proteins | 27 | 5.08e-01 | 7.37e-02 | 7.75e-01 |
| Interconversion of nucleotide di- and triphosphates | 24 | 5.33e-01 | 7.35e-02 | 7.94e-01 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | 39 | 4.30e-01 | -7.31e-02 | 7.23e-01 |
| Signaling by RAS mutants | 39 | 4.30e-01 | -7.31e-02 | 7.23e-01 |
| Signaling by moderate kinase activity BRAF mutants | 39 | 4.30e-01 | -7.31e-02 | 7.23e-01 |
| Signaling downstream of RAS mutants | 39 | 4.30e-01 | -7.31e-02 | 7.23e-01 |
| G-protein activation | 19 | 5.82e-01 | -7.29e-02 | 8.35e-01 |
| Pausing and recovery of Tat-mediated HIV elongation | 26 | 5.20e-01 | -7.29e-02 | 7.82e-01 |
| Tat-mediated HIV elongation arrest and recovery | 26 | 5.20e-01 | -7.29e-02 | 7.82e-01 |
| Association of TriC/CCT with target proteins during biosynthesis | 36 | 4.50e-01 | 7.28e-02 | 7.41e-01 |
| Constitutive Signaling by AKT1 E17K in Cancer | 26 | 5.25e-01 | -7.20e-02 | 7.86e-01 |
| GPCR downstream signalling | 404 | 1.40e-02 | -7.17e-02 | 8.69e-02 |
| Mitophagy | 25 | 5.36e-01 | -7.15e-02 | 7.96e-01 |
| CREB1 phosphorylation through the activation of Adenylate Cyclase | 11 | 6.81e-01 | -7.15e-02 | 8.88e-01 |
| SARS-CoV-1 Infection | 43 | 4.18e-01 | -7.14e-02 | 7.19e-01 |
| Interactions of Rev with host cellular proteins | 31 | 4.92e-01 | 7.13e-02 | 7.67e-01 |
| Metabolism of non-coding RNA | 48 | 3.94e-01 | 7.12e-02 | 6.98e-01 |
| snRNP Assembly | 48 | 3.94e-01 | 7.12e-02 | 6.98e-01 |
| Nuclear Pore Complex (NPC) Disassembly | 31 | 4.94e-01 | 7.10e-02 | 7.67e-01 |
| Signaling by WNT | 228 | 6.82e-02 | -7.04e-02 | 2.51e-01 |
| Cell-Cell communication | 82 | 2.75e-01 | -6.98e-02 | 5.64e-01 |
| COPI-independent Golgi-to-ER retrograde traffic | 30 | 5.09e-01 | -6.97e-02 | 7.75e-01 |
| Transcriptional Regulation by MECP2 | 46 | 4.17e-01 | -6.92e-02 | 7.19e-01 |
| Fatty acid metabolism | 134 | 1.68e-01 | 6.91e-02 | 4.37e-01 |
| TCF dependent signaling in response to WNT | 147 | 1.49e-01 | -6.91e-02 | 4.10e-01 |
| RUNX2 regulates bone development | 28 | 5.28e-01 | -6.90e-02 | 7.88e-01 |
| SLBP independent Processing of Histone Pre-mRNAs | 10 | 7.06e-01 | -6.88e-02 | 9.04e-01 |
| Metabolism of fat-soluble vitamins | 31 | 5.09e-01 | -6.86e-02 | 7.75e-01 |
| Detoxification of Reactive Oxygen Species | 30 | 5.17e-01 | 6.83e-02 | 7.81e-01 |
| Assembly and cell surface presentation of NMDA receptors | 17 | 6.26e-01 | -6.82e-02 | 8.59e-01 |
| Growth hormone receptor signaling | 19 | 6.07e-01 | -6.82e-02 | 8.47e-01 |
| Glutamate Neurotransmitter Release Cycle | 17 | 6.28e-01 | -6.80e-02 | 8.60e-01 |
| GRB2:SOS provides linkage to MAPK signaling for Integrins | 12 | 6.84e-01 | 6.78e-02 | 8.88e-01 |
| ADP signalling through P2Y purinoceptor 1 | 21 | 5.91e-01 | -6.77e-02 | 8.39e-01 |
| Signaling by FGFR2 | 58 | 3.74e-01 | -6.76e-02 | 6.85e-01 |
| MyD88-independent TLR4 cascade | 91 | 2.66e-01 | -6.76e-02 | 5.58e-01 |
| TRIF(TICAM1)-mediated TLR4 signaling | 91 | 2.66e-01 | -6.76e-02 | 5.58e-01 |
| Nephrin family interactions | 19 | 6.12e-01 | 6.73e-02 | 8.48e-01 |
| Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | 16 | 6.43e-01 | 6.69e-02 | 8.75e-01 |
| G alpha (q) signalling events | 126 | 1.96e-01 | -6.68e-02 | 4.78e-01 |
| Glutamate and glutamine metabolism | 12 | 6.89e-01 | -6.67e-02 | 8.89e-01 |
| Interleukin receptor SHC signaling | 21 | 5.98e-01 | 6.66e-02 | 8.40e-01 |
| Amino acids regulate mTORC1 | 48 | 4.26e-01 | -6.65e-02 | 7.23e-01 |
| NS1 Mediated Effects on Host Pathways | 33 | 5.12e-01 | 6.60e-02 | 7.79e-01 |
| Erythropoietin activates RAS | 13 | 6.81e-01 | 6.58e-02 | 8.88e-01 |
| Retrograde transport at the Trans-Golgi-Network | 45 | 4.48e-01 | -6.54e-02 | 7.40e-01 |
| HIV Infection | 205 | 1.08e-01 | 6.53e-02 | 3.44e-01 |
| TBC/RABGAPs | 40 | 4.76e-01 | -6.51e-02 | 7.56e-01 |
| NOD1/2 Signaling Pathway | 29 | 5.45e-01 | -6.49e-02 | 8.04e-01 |
| Intraflagellar transport | 36 | 5.02e-01 | 6.47e-02 | 7.74e-01 |
| Purine catabolism | 17 | 6.45e-01 | 6.46e-02 | 8.76e-01 |
| Surfactant metabolism | 14 | 6.77e-01 | -6.43e-02 | 8.88e-01 |
| NOTCH3 Intracellular Domain Regulates Transcription | 23 | 5.94e-01 | -6.42e-02 | 8.40e-01 |
| Cellular responses to external stimuli | 429 | 2.39e-02 | 6.40e-02 | 1.28e-01 |
| RNA Polymerase III Transcription Termination | 23 | 5.96e-01 | 6.40e-02 | 8.40e-01 |
| RHO GTPases Activate ROCKs | 19 | 6.30e-01 | -6.39e-02 | 8.62e-01 |
| ABC transporters in lipid homeostasis | 14 | 6.79e-01 | 6.38e-02 | 8.88e-01 |
| TGF-beta receptor signaling activates SMADs | 29 | 5.53e-01 | 6.37e-02 | 8.11e-01 |
| Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) | 11 | 7.16e-01 | -6.35e-02 | 9.10e-01 |
| CASP8 activity is inhibited | 10 | 7.29e-01 | 6.33e-02 | 9.18e-01 |
| Dimerization of procaspase-8 | 10 | 7.29e-01 | 6.33e-02 | 9.18e-01 |
| Regulation by c-FLIP | 10 | 7.29e-01 | 6.33e-02 | 9.18e-01 |
| Innate Immune System | 759 | 3.39e-03 | 6.33e-02 | 3.13e-02 |
| FCERI mediated MAPK activation | 30 | 5.50e-01 | 6.31e-02 | 8.08e-01 |
| Inhibition of DNA recombination at telomere | 20 | 6.26e-01 | 6.30e-02 | 8.59e-01 |
| FRS-mediated FGFR1 signaling | 14 | 6.84e-01 | 6.29e-02 | 8.88e-01 |
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 23 | 6.03e-01 | -6.27e-02 | 8.44e-01 |
| Signaling by FGFR2 in disease | 33 | 5.35e-01 | -6.25e-02 | 7.96e-01 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 15 | 6.75e-01 | 6.24e-02 | 8.88e-01 |
| SUMOylation of DNA methylation proteins | 16 | 6.66e-01 | -6.24e-02 | 8.88e-01 |
| DNA Damage/Telomere Stress Induced Senescence | 26 | 5.84e-01 | 6.20e-02 | 8.35e-01 |
| Cellular responses to stress | 424 | 2.95e-02 | 6.20e-02 | 1.48e-01 |
| Synthesis of PIPs at the plasma membrane | 51 | 4.44e-01 | 6.20e-02 | 7.36e-01 |
| Regulation of RUNX1 Expression and Activity | 17 | 6.58e-01 | -6.20e-02 | 8.85e-01 |
| Postmitotic nuclear pore complex (NPC) reformation | 25 | 5.92e-01 | 6.19e-02 | 8.39e-01 |
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | 16 | 6.68e-01 | 6.19e-02 | 8.88e-01 |
| Metabolism of water-soluble vitamins and cofactors | 104 | 2.77e-01 | -6.18e-02 | 5.67e-01 |
| Regulation of MECP2 expression and activity | 28 | 5.73e-01 | -6.15e-02 | 8.27e-01 |
| Complex I biogenesis | 54 | 4.35e-01 | 6.15e-02 | 7.27e-01 |
| Hyaluronan metabolism | 14 | 6.91e-01 | 6.14e-02 | 8.89e-01 |
| PINK1-PRKN Mediated Mitophagy | 18 | 6.52e-01 | -6.14e-02 | 8.80e-01 |
| LDL clearance | 15 | 6.84e-01 | -6.08e-02 | 8.88e-01 |
| Other interleukin signaling | 19 | 6.48e-01 | 6.06e-02 | 8.79e-01 |
| Epigenetic regulation of gene expression | 84 | 3.42e-01 | 6.01e-02 | 6.45e-01 |
| N-Glycan antennae elongation | 13 | 7.09e-01 | 5.98e-02 | 9.05e-01 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 27 | 5.91e-01 | -5.97e-02 | 8.39e-01 |
| Downregulation of ERBB2:ERBB3 signaling | 11 | 7.32e-01 | -5.96e-02 | 9.19e-01 |
| FRS-mediated FGFR4 signaling | 13 | 7.10e-01 | -5.96e-02 | 9.05e-01 |
| Toll Like Receptor 4 (TLR4) Cascade | 117 | 2.69e-01 | -5.93e-02 | 5.58e-01 |
| Sphingolipid de novo biosynthesis | 33 | 5.57e-01 | -5.91e-02 | 8.13e-01 |
| Transport of the SLBP independent Mature mRNA | 30 | 5.76e-01 | -5.90e-02 | 8.30e-01 |
| Neurotransmitter receptors and postsynaptic signal transmission | 130 | 2.47e-01 | -5.89e-02 | 5.42e-01 |
| Keratinization | 24 | 6.18e-01 | 5.88e-02 | 8.51e-01 |
| Signaling by Interleukins | 351 | 6.18e-02 | 5.84e-02 | 2.37e-01 |
| Beta-catenin independent WNT signaling | 131 | 2.51e-01 | -5.82e-02 | 5.46e-01 |
| Immune System | 1550 | 1.93e-04 | 5.82e-02 | 2.75e-03 |
| RMTs methylate histone arginines | 29 | 5.89e-01 | -5.80e-02 | 8.38e-01 |
| NoRC negatively regulates rRNA expression | 45 | 5.08e-01 | 5.71e-02 | 7.75e-01 |
| Signalling to RAS | 19 | 6.68e-01 | 5.69e-02 | 8.88e-01 |
| Metabolism of vitamins and cofactors | 153 | 2.31e-01 | -5.62e-02 | 5.23e-01 |
| HCMV Early Events | 53 | 4.81e-01 | 5.60e-02 | 7.60e-01 |
| Signalling to ERKs | 32 | 5.83e-01 | 5.60e-02 | 8.35e-01 |
| Signal Transduction | 1761 | 1.50e-04 | -5.60e-02 | 2.16e-03 |
| RNA Polymerase I Transcription Termination | 30 | 5.97e-01 | -5.58e-02 | 8.40e-01 |
| JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 | 17 | 6.91e-01 | -5.58e-02 | 8.89e-01 |
| Repression of WNT target genes | 12 | 7.39e-01 | -5.55e-02 | 9.23e-01 |
| Crosslinking of collagen fibrils | 10 | 7.62e-01 | -5.53e-02 | 9.23e-01 |
| Cell recruitment (pro-inflammatory response) | 19 | 6.80e-01 | -5.47e-02 | 8.88e-01 |
| Purinergic signaling in leishmaniasis infection | 19 | 6.80e-01 | -5.47e-02 | 8.88e-01 |
| Class A/1 (Rhodopsin-like receptors) | 125 | 2.96e-01 | 5.43e-02 | 5.86e-01 |
| PKA-mediated phosphorylation of CREB | 19 | 6.84e-01 | -5.40e-02 | 8.88e-01 |
| TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain | 11 | 7.57e-01 | -5.38e-02 | 9.23e-01 |
| RUNX2 regulates osteoblast differentiation | 22 | 6.63e-01 | -5.37e-02 | 8.88e-01 |
| SLC-mediated transmembrane transport | 165 | 2.36e-01 | 5.37e-02 | 5.28e-01 |
| Triglyceride metabolism | 23 | 6.56e-01 | -5.36e-02 | 8.84e-01 |
| RNA polymerase II transcribes snRNA genes | 70 | 4.40e-01 | -5.35e-02 | 7.32e-01 |
| Rev-mediated nuclear export of HIV RNA | 30 | 6.13e-01 | 5.34e-02 | 8.48e-01 |
| Mitochondrial translation | 91 | 3.83e-01 | -5.30e-02 | 6.94e-01 |
| Transcriptional regulation by RUNX1 | 155 | 2.56e-01 | 5.29e-02 | 5.51e-01 |
| Tight junction interactions | 11 | 7.62e-01 | 5.28e-02 | 9.23e-01 |
| Apoptotic cleavage of cellular proteins | 33 | 6.00e-01 | -5.28e-02 | 8.42e-01 |
| IKK complex recruitment mediated by RIP1 | 19 | 6.93e-01 | -5.23e-02 | 8.89e-01 |
| IRAK4 deficiency (TLR2/4) | 11 | 7.64e-01 | -5.22e-02 | 9.23e-01 |
| MHC class II antigen presentation | 90 | 3.95e-01 | 5.19e-02 | 6.98e-01 |
| MAPK targets/ Nuclear events mediated by MAP kinases | 31 | 6.18e-01 | 5.18e-02 | 8.51e-01 |
| Inwardly rectifying K+ channels | 26 | 6.50e-01 | 5.15e-02 | 8.80e-01 |
| Ovarian tumor domain proteases | 34 | 6.04e-01 | 5.15e-02 | 8.45e-01 |
| Signal transduction by L1 | 21 | 6.85e-01 | 5.11e-02 | 8.88e-01 |
| Adenylate cyclase inhibitory pathway | 14 | 7.41e-01 | -5.11e-02 | 9.23e-01 |
| Glyoxylate metabolism and glycine degradation | 24 | 6.66e-01 | -5.09e-02 | 8.88e-01 |
| Regulation of TP53 Activity | 148 | 2.90e-01 | 5.05e-02 | 5.79e-01 |
| Cell surface interactions at the vascular wall | 96 | 3.95e-01 | 5.03e-02 | 6.98e-01 |
| Interleukin-20 family signaling | 15 | 7.38e-01 | -4.98e-02 | 9.23e-01 |
| Nuclear signaling by ERBB4 | 27 | 6.55e-01 | -4.97e-02 | 8.84e-01 |
| MET receptor recycling | 10 | 7.88e-01 | -4.92e-02 | 9.35e-01 |
| Signaling by NTRK3 (TRKC) | 17 | 7.26e-01 | -4.91e-02 | 9.18e-01 |
| Interleukin-17 signaling | 63 | 5.03e-01 | -4.88e-02 | 7.74e-01 |
| Calnexin/calreticulin cycle | 23 | 6.87e-01 | -4.86e-02 | 8.88e-01 |
| Generic Transcription Pathway | 868 | 1.72e-02 | 4.83e-02 | 9.99e-02 |
| L1CAM interactions | 88 | 4.35e-01 | -4.82e-02 | 7.27e-01 |
| RNA Polymerase II Transcription | 982 | 1.22e-02 | 4.80e-02 | 8.03e-02 |
| Transcriptional regulation by RUNX3 | 89 | 4.35e-01 | 4.79e-02 | 7.27e-01 |
| Class I peroxisomal membrane protein import | 19 | 7.18e-01 | 4.78e-02 | 9.12e-01 |
| Plasma lipoprotein clearance | 24 | 6.87e-01 | -4.76e-02 | 8.88e-01 |
| Cargo recognition for clathrin-mediated endocytosis | 85 | 4.49e-01 | -4.76e-02 | 7.40e-01 |
| Vesicle-mediated transport | 568 | 5.52e-02 | -4.75e-02 | 2.19e-01 |
| Oncogene Induced Senescence | 29 | 6.59e-01 | -4.73e-02 | 8.85e-01 |
| Negative regulation of MAPK pathway | 40 | 6.05e-01 | -4.73e-02 | 8.45e-01 |
| Diseases of signal transduction by growth factor receptors and second messengers | 336 | 1.39e-01 | -4.72e-02 | 3.99e-01 |
| Metabolism of proteins | 1573 | 2.45e-03 | 4.70e-02 | 2.39e-02 |
| Estrogen-dependent gene expression | 83 | 4.60e-01 | -4.70e-02 | 7.48e-01 |
| VEGFA-VEGFR2 Pathway | 90 | 4.45e-01 | 4.67e-02 | 7.36e-01 |
| Cytokine Signaling in Immune system | 662 | 4.31e-02 | 4.66e-02 | 1.86e-01 |
| Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) | 26 | 6.82e-01 | -4.65e-02 | 8.88e-01 |
| Regulation of Glucokinase by Glucokinase Regulatory Protein | 26 | 6.82e-01 | -4.65e-02 | 8.88e-01 |
| Misspliced GSK3beta mutants stabilize beta-catenin | 14 | 7.64e-01 | -4.65e-02 | 9.23e-01 |
| S33 mutants of beta-catenin aren't phosphorylated | 14 | 7.64e-01 | -4.65e-02 | 9.23e-01 |
| S37 mutants of beta-catenin aren't phosphorylated | 14 | 7.64e-01 | -4.65e-02 | 9.23e-01 |
| S45 mutants of beta-catenin aren't phosphorylated | 14 | 7.64e-01 | -4.65e-02 | 9.23e-01 |
| T41 mutants of beta-catenin aren't phosphorylated | 14 | 7.64e-01 | -4.65e-02 | 9.23e-01 |
| phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex | 14 | 7.64e-01 | -4.65e-02 | 9.23e-01 |
| SHC-mediated cascade:FGFR4 | 11 | 7.91e-01 | 4.62e-02 | 9.35e-01 |
| NRIF signals cell death from the nucleus | 14 | 7.67e-01 | 4.58e-02 | 9.23e-01 |
| MAPK6/MAPK4 signaling | 79 | 4.83e-01 | 4.57e-02 | 7.61e-01 |
| Tie2 Signaling | 16 | 7.53e-01 | 4.55e-02 | 9.23e-01 |
| Post-translational modification: synthesis of GPI-anchored proteins | 60 | 5.45e-01 | -4.53e-02 | 8.04e-01 |
| G beta:gamma signalling through CDC42 | 16 | 7.56e-01 | -4.50e-02 | 9.23e-01 |
| PI-3K cascade:FGFR2 | 14 | 7.71e-01 | -4.50e-02 | 9.24e-01 |
| tRNA processing in the nucleus | 52 | 5.75e-01 | -4.50e-02 | 8.29e-01 |
| NEP/NS2 Interacts with the Cellular Export Machinery | 27 | 6.88e-01 | 4.47e-02 | 8.88e-01 |
| AURKA Activation by TPX2 | 71 | 5.16e-01 | 4.46e-02 | 7.80e-01 |
| Mitochondrial translation initiation | 85 | 4.78e-01 | -4.46e-02 | 7.57e-01 |
| N-glycan trimming in the ER and Calnexin/Calreticulin cycle | 31 | 6.69e-01 | -4.44e-02 | 8.88e-01 |
| COPI-dependent Golgi-to-ER retrograde traffic | 76 | 5.04e-01 | 4.44e-02 | 7.75e-01 |
| Regulation of PTEN gene transcription | 59 | 5.58e-01 | -4.42e-02 | 8.13e-01 |
| DNA Damage Recognition in GG-NER | 35 | 6.52e-01 | 4.41e-02 | 8.80e-01 |
| RNA Polymerase III Transcription Initiation From Type 1 Promoter | 28 | 6.87e-01 | 4.41e-02 | 8.88e-01 |
| Adrenaline,noradrenaline inhibits insulin secretion | 22 | 7.22e-01 | -4.38e-02 | 9.14e-01 |
| Transcriptional Regulation by TP53 | 333 | 1.74e-01 | 4.36e-02 | 4.44e-01 |
| Toll Like Receptor 3 (TLR3) Cascade | 87 | 4.84e-01 | -4.35e-02 | 7.61e-01 |
| Cleavage of the damaged purine | 11 | 8.03e-01 | 4.35e-02 | 9.36e-01 |
| Depurination | 11 | 8.03e-01 | 4.35e-02 | 9.36e-01 |
| Recognition and association of DNA glycosylase with site containing an affected purine | 11 | 8.03e-01 | 4.35e-02 | 9.36e-01 |
| PI Metabolism | 79 | 5.06e-01 | 4.33e-02 | 7.75e-01 |
| Regulation of FOXO transcriptional activity by acetylation | 10 | 8.13e-01 | 4.32e-02 | 9.40e-01 |
| G alpha (i) signalling events | 208 | 2.84e-01 | -4.32e-02 | 5.72e-01 |
| Formation of the cornified envelope | 18 | 7.52e-01 | -4.31e-02 | 9.23e-01 |
| RNA Polymerase I Promoter Escape | 30 | 6.84e-01 | -4.30e-02 | 8.88e-01 |
| Cellular Senescence | 118 | 4.21e-01 | -4.30e-02 | 7.21e-01 |
| PCP/CE pathway | 85 | 4.95e-01 | -4.28e-02 | 7.68e-01 |
| Gene expression (Transcription) | 1100 | 1.94e-02 | 4.25e-02 | 1.11e-01 |
| TNFR1-induced proapoptotic signaling | 13 | 7.91e-01 | -4.25e-02 | 9.35e-01 |
| ERK/MAPK targets | 22 | 7.31e-01 | 4.24e-02 | 9.18e-01 |
| Downstream signaling of activated FGFR3 | 19 | 7.50e-01 | 4.22e-02 | 9.23e-01 |
| Mitochondrial translation elongation | 85 | 5.02e-01 | -4.22e-02 | 7.74e-01 |
| SHC1 events in ERBB4 signaling | 12 | 8.01e-01 | 4.21e-02 | 9.36e-01 |
| Formation of TC-NER Pre-Incision Complex | 50 | 6.08e-01 | 4.20e-02 | 8.47e-01 |
| Regulation of localization of FOXO transcription factors | 12 | 8.04e-01 | 4.14e-02 | 9.36e-01 |
| ADORA2B mediated anti-inflammatory cytokines production | 62 | 5.78e-01 | -4.09e-02 | 8.31e-01 |
| Hedgehog 'off' state | 91 | 5.01e-01 | 4.08e-02 | 7.74e-01 |
| Viral Messenger RNA Synthesis | 38 | 6.64e-01 | -4.07e-02 | 8.88e-01 |
| Signaling by PDGFR in disease | 20 | 7.53e-01 | 4.07e-02 | 9.23e-01 |
| RNA Polymerase II Pre-transcription Events | 75 | 5.44e-01 | -4.06e-02 | 8.04e-01 |
| ADP signalling through P2Y purinoceptor 12 | 18 | 7.66e-01 | 4.06e-02 | 9.23e-01 |
| Downstream signaling of activated FGFR2 | 21 | 7.48e-01 | -4.06e-02 | 9.23e-01 |
| Signaling by NODAL | 13 | 8.05e-01 | -3.96e-02 | 9.36e-01 |
| TNFs bind their physiological receptors | 11 | 8.21e-01 | -3.94e-02 | 9.44e-01 |
| HCMV Infection | 74 | 5.59e-01 | 3.93e-02 | 8.15e-01 |
| TNF signaling | 37 | 6.85e-01 | 3.86e-02 | 8.88e-01 |
| TP53 Regulates Transcription of Cell Death Genes | 36 | 6.90e-01 | 3.84e-02 | 8.89e-01 |
| Estrogen-dependent nuclear events downstream of ESR-membrane signaling | 21 | 7.62e-01 | 3.81e-02 | 9.23e-01 |
| Mitochondrial calcium ion transport | 20 | 7.68e-01 | 3.81e-02 | 9.23e-01 |
| G beta:gamma signalling through BTK | 14 | 8.07e-01 | -3.77e-02 | 9.37e-01 |
| Membrane Trafficking | 538 | 1.39e-01 | -3.76e-02 | 3.99e-01 |
| GABA receptor activation | 40 | 6.81e-01 | 3.76e-02 | 8.88e-01 |
| Post-translational protein modification | 1124 | 3.70e-02 | 3.76e-02 | 1.68e-01 |
| Synthesis of pyrophosphates in the cytosol | 10 | 8.37e-01 | -3.75e-02 | 9.49e-01 |
| Death Receptor Signalling | 123 | 4.74e-01 | -3.75e-02 | 7.55e-01 |
| Golgi Associated Vesicle Biogenesis | 52 | 6.45e-01 | -3.70e-02 | 8.76e-01 |
| Transport of the SLBP Dependant Mature mRNA | 31 | 7.22e-01 | -3.70e-02 | 9.14e-01 |
| RORA activates gene expression | 17 | 7.92e-01 | -3.69e-02 | 9.35e-01 |
| Signaling by FGFR1 in disease | 31 | 7.22e-01 | 3.69e-02 | 9.14e-01 |
| FGFR1 mutant receptor activation | 24 | 7.59e-01 | 3.62e-02 | 9.23e-01 |
| Signaling by NOTCH | 160 | 4.30e-01 | -3.62e-02 | 7.23e-01 |
| Molecules associated with elastic fibres | 28 | 7.41e-01 | -3.61e-02 | 9.23e-01 |
| N-glycan antennae elongation in the medial/trans-Golgi | 20 | 7.81e-01 | 3.58e-02 | 9.33e-01 |
| Metabolism | 1629 | 1.97e-02 | 3.56e-02 | 1.12e-01 |
| RHO GTPases activate CIT | 19 | 7.90e-01 | 3.54e-02 | 9.35e-01 |
| HIV elongation arrest and recovery | 28 | 7.46e-01 | -3.53e-02 | 9.23e-01 |
| Pausing and recovery of HIV elongation | 28 | 7.46e-01 | -3.53e-02 | 9.23e-01 |
| Fanconi Anemia Pathway | 31 | 7.35e-01 | 3.52e-02 | 9.21e-01 |
| Platelet Aggregation (Plug Formation) | 25 | 7.61e-01 | 3.52e-02 | 9.23e-01 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | 56 | 6.52e-01 | -3.49e-02 | 8.80e-01 |
| MAPK family signaling cascades | 272 | 3.24e-01 | -3.49e-02 | 6.24e-01 |
| Toll-like Receptor Cascades | 133 | 4.93e-01 | -3.45e-02 | 7.67e-01 |
| Nuclear Receptor transcription pathway | 44 | 6.93e-01 | 3.44e-02 | 8.89e-01 |
| Activation of the AP-1 family of transcription factors | 10 | 8.51e-01 | 3.44e-02 | 9.56e-01 |
| Recycling pathway of L1 | 27 | 7.58e-01 | -3.43e-02 | 9.23e-01 |
| TRP channels | 12 | 8.37e-01 | 3.42e-02 | 9.49e-01 |
| Signaling by Insulin receptor | 59 | 6.51e-01 | -3.41e-02 | 8.80e-01 |
| MyD88 deficiency (TLR2/4) | 10 | 8.53e-01 | -3.39e-02 | 9.56e-01 |
| ERKs are inactivated | 13 | 8.33e-01 | 3.38e-02 | 9.49e-01 |
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | 13 | 8.33e-01 | -3.38e-02 | 9.49e-01 |
| Activation of GABAB receptors | 35 | 7.30e-01 | 3.37e-02 | 9.18e-01 |
| GABA B receptor activation | 35 | 7.30e-01 | 3.37e-02 | 9.18e-01 |
| Cytosolic sensors of pathogen-associated DNA | 57 | 6.61e-01 | -3.36e-02 | 8.87e-01 |
| Downstream signal transduction | 28 | 7.59e-01 | -3.35e-02 | 9.23e-01 |
| Signaling by cytosolic FGFR1 fusion mutants | 18 | 8.06e-01 | -3.34e-02 | 9.37e-01 |
| CaMK IV-mediated phosphorylation of CREB | 10 | 8.55e-01 | 3.34e-02 | 9.56e-01 |
| VEGFR2 mediated cell proliferation | 19 | 8.02e-01 | -3.32e-02 | 9.36e-01 |
| Regulation of TP53 Activity through Acetylation | 29 | 7.57e-01 | -3.32e-02 | 9.23e-01 |
| CD209 (DC-SIGN) signaling | 19 | 8.03e-01 | -3.30e-02 | 9.36e-01 |
| Metabolism of porphyrins | 22 | 7.90e-01 | -3.28e-02 | 9.35e-01 |
| Metabolism of steroids | 111 | 5.53e-01 | -3.26e-02 | 8.11e-01 |
| Signaling by Rho GTPases | 339 | 3.09e-01 | 3.23e-02 | 6.06e-01 |
| Activation of kainate receptors upon glutamate binding | 24 | 7.86e-01 | -3.21e-02 | 9.35e-01 |
| Platelet sensitization by LDL | 15 | 8.30e-01 | -3.20e-02 | 9.48e-01 |
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | 18 | 8.14e-01 | 3.20e-02 | 9.40e-01 |
| AKT phosphorylates targets in the cytosol | 14 | 8.38e-01 | -3.15e-02 | 9.49e-01 |
| Transport of vitamins, nucleosides, and related molecules | 29 | 7.70e-01 | -3.13e-02 | 9.24e-01 |
| MAP2K and MAPK activation | 34 | 7.55e-01 | -3.10e-02 | 9.23e-01 |
| Purine ribonucleoside monophosphate biosynthesis | 12 | 8.53e-01 | 3.08e-02 | 9.56e-01 |
| PPARA activates gene expression | 110 | 5.78e-01 | 3.08e-02 | 8.31e-01 |
| Blood group systems biosynthesis | 13 | 8.52e-01 | -2.98e-02 | 9.56e-01 |
| Mitochondrial translation termination | 85 | 6.37e-01 | -2.97e-02 | 8.67e-01 |
| Regulation of lipid metabolism by PPARalpha | 112 | 5.93e-01 | 2.93e-02 | 8.39e-01 |
| Base-Excision Repair, AP Site Formation | 18 | 8.31e-01 | -2.90e-02 | 9.48e-01 |
| G beta:gamma signalling through PI3Kgamma | 21 | 8.18e-01 | 2.90e-02 | 9.44e-01 |
| Negative regulation of FGFR3 signaling | 21 | 8.19e-01 | -2.88e-02 | 9.44e-01 |
| Triglyceride catabolism | 15 | 8.48e-01 | 2.87e-02 | 9.55e-01 |
| Nuclear import of Rev protein | 28 | 7.94e-01 | 2.85e-02 | 9.35e-01 |
| Transport of small molecules | 506 | 2.90e-01 | -2.77e-02 | 5.79e-01 |
| Metabolism of cofactors | 19 | 8.35e-01 | 2.77e-02 | 9.49e-01 |
| RHO GTPases activate PAKs | 21 | 8.27e-01 | 2.76e-02 | 9.48e-01 |
| HIV Transcription Initiation | 45 | 7.49e-01 | -2.76e-02 | 9.23e-01 |
| RNA Polymerase II HIV Promoter Escape | 45 | 7.49e-01 | -2.76e-02 | 9.23e-01 |
| RNA Polymerase II Promoter Escape | 45 | 7.49e-01 | -2.76e-02 | 9.23e-01 |
| RNA Polymerase II Transcription Initiation | 45 | 7.49e-01 | -2.76e-02 | 9.23e-01 |
| RNA Polymerase II Transcription Initiation And Promoter Clearance | 45 | 7.49e-01 | -2.76e-02 | 9.23e-01 |
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | 45 | 7.49e-01 | -2.76e-02 | 9.23e-01 |
| Fertilization | 10 | 8.80e-01 | -2.75e-02 | 9.70e-01 |
| Transport of inorganic cations/anions and amino acids/oligopeptides | 75 | 6.83e-01 | -2.73e-02 | 8.88e-01 |
| Signaling by MET | 61 | 7.14e-01 | 2.72e-02 | 9.10e-01 |
| Mitochondrial protein import | 59 | 7.21e-01 | 2.69e-02 | 9.14e-01 |
| Downregulation of SMAD2/3:SMAD4 transcriptional activity | 20 | 8.35e-01 | 2.69e-02 | 9.49e-01 |
| Nuclear Envelope (NE) Reassembly | 65 | 7.10e-01 | 2.67e-02 | 9.05e-01 |
| ESR-mediated signaling | 144 | 5.82e-01 | -2.66e-02 | 8.35e-01 |
| FLT3 Signaling | 246 | 4.75e-01 | -2.65e-02 | 7.55e-01 |
| mTORC1-mediated signalling | 23 | 8.26e-01 | 2.65e-02 | 9.48e-01 |
| trans-Golgi Network Vesicle Budding | 67 | 7.08e-01 | -2.65e-02 | 9.05e-01 |
| Cilium Assembly | 171 | 5.55e-01 | 2.62e-02 | 8.11e-01 |
| Signaling by FGFR in disease | 52 | 7.45e-01 | -2.61e-02 | 9.23e-01 |
| Regulation of PLK1 Activity at G2/M Transition | 84 | 6.80e-01 | 2.61e-02 | 8.88e-01 |
| Synthesis of PIPs at the Golgi membrane | 15 | 8.62e-01 | -2.59e-02 | 9.61e-01 |
| Regulation of glycolysis by fructose 2,6-bisphosphate metabolism | 11 | 8.84e-01 | -2.54e-02 | 9.70e-01 |
| Signaling by Non-Receptor Tyrosine Kinases | 49 | 7.58e-01 | -2.54e-02 | 9.23e-01 |
| Signaling by PTK6 | 49 | 7.58e-01 | -2.54e-02 | 9.23e-01 |
| Budding and maturation of HIV virion | 24 | 8.30e-01 | -2.54e-02 | 9.48e-01 |
| Interleukin-2 signaling | 11 | 8.85e-01 | 2.52e-02 | 9.70e-01 |
| Prostacyclin signalling through prostacyclin receptor | 15 | 8.67e-01 | -2.49e-02 | 9.63e-01 |
| Signaling by FGFR1 | 38 | 7.94e-01 | 2.45e-02 | 9.35e-01 |
| TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 16 | 8.65e-01 | -2.45e-02 | 9.62e-01 |
| Intracellular signaling by second messengers | 276 | 4.87e-01 | -2.44e-02 | 7.65e-01 |
| Formation of tubulin folding intermediates by CCT/TriC | 19 | 8.54e-01 | 2.44e-02 | 9.56e-01 |
| Striated Muscle Contraction | 29 | 8.21e-01 | -2.43e-02 | 9.44e-01 |
| Anti-inflammatory response favouring Leishmania parasite infection | 97 | 6.80e-01 | -2.43e-02 | 8.88e-01 |
| Leishmania parasite growth and survival | 97 | 6.80e-01 | -2.43e-02 | 8.88e-01 |
| Apoptosis | 149 | 6.11e-01 | 2.42e-02 | 8.48e-01 |
| Interleukin-1 signaling | 90 | 6.92e-01 | 2.42e-02 | 8.89e-01 |
| Netrin-1 signaling | 42 | 7.87e-01 | -2.42e-02 | 9.35e-01 |
| TICAM1, RIP1-mediated IKK complex recruitment | 16 | 8.68e-01 | 2.40e-02 | 9.63e-01 |
| SLC transporter disorders | 70 | 7.30e-01 | 2.39e-02 | 9.18e-01 |
| Programmed Cell Death | 152 | 6.12e-01 | 2.39e-02 | 8.48e-01 |
| RNA Polymerase I Transcription Initiation | 45 | 7.84e-01 | -2.36e-02 | 9.35e-01 |
| Transport of Mature mRNA Derived from an Intronless Transcript | 37 | 8.04e-01 | -2.36e-02 | 9.36e-01 |
| IGF1R signaling cascade | 40 | 7.97e-01 | 2.35e-02 | 9.36e-01 |
| Nuclear Envelope Breakdown | 48 | 7.80e-01 | 2.34e-02 | 9.32e-01 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | 38 | 8.04e-01 | -2.33e-02 | 9.36e-01 |
| Metabolic disorders of biological oxidation enzymes | 20 | 8.58e-01 | 2.32e-02 | 9.58e-01 |
| Constitutive Signaling by Overexpressed ERBB2 | 10 | 8.99e-01 | -2.31e-02 | 9.73e-01 |
| RAB GEFs exchange GTP for GDP on RABs | 84 | 7.16e-01 | 2.30e-02 | 9.10e-01 |
| Signaling by NTRK2 (TRKB) | 22 | 8.54e-01 | -2.26e-02 | 9.56e-01 |
| GPCR ligand binding | 173 | 6.12e-01 | -2.24e-02 | 8.48e-01 |
| Cell-cell junction organization | 27 | 8.41e-01 | -2.23e-02 | 9.51e-01 |
| Basigin interactions | 20 | 8.63e-01 | -2.23e-02 | 9.61e-01 |
| Transcriptional regulation by small RNAs | 42 | 8.04e-01 | -2.21e-02 | 9.36e-01 |
| FOXO-mediated transcription | 55 | 7.78e-01 | -2.20e-02 | 9.32e-01 |
| SUMOylation of chromatin organization proteins | 49 | 7.92e-01 | 2.17e-02 | 9.35e-01 |
| Synthesis of PIPs at the early endosome membrane | 16 | 8.81e-01 | 2.16e-02 | 9.70e-01 |
| Platelet activation, signaling and aggregation | 212 | 5.90e-01 | -2.16e-02 | 8.38e-01 |
| RNA Polymerase III Abortive And Retractive Initiation | 41 | 8.13e-01 | 2.14e-02 | 9.40e-01 |
| RNA Polymerase III Transcription | 41 | 8.13e-01 | 2.14e-02 | 9.40e-01 |
| TICAM1-dependent activation of IRF3/IRF7 | 10 | 9.07e-01 | 2.13e-02 | 9.73e-01 |
| PTEN Regulation | 132 | 6.73e-01 | 2.13e-02 | 8.88e-01 |
| RHO GTPases activate PKNs | 32 | 8.35e-01 | -2.12e-02 | 9.49e-01 |
| SUMOylation of transcription cofactors | 39 | 8.19e-01 | 2.12e-02 | 9.44e-01 |
| Transcription of the HIV genome | 64 | 7.70e-01 | -2.11e-02 | 9.24e-01 |
| Signaling by FGFR4 | 30 | 8.41e-01 | -2.11e-02 | 9.51e-01 |
| Opioid Signalling | 78 | 7.48e-01 | -2.11e-02 | 9.23e-01 |
| Regulation of pyruvate dehydrogenase (PDH) complex | 15 | 8.88e-01 | -2.10e-02 | 9.71e-01 |
| Gap junction trafficking | 14 | 8.92e-01 | -2.09e-02 | 9.71e-01 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | 35 | 8.30e-01 | 2.09e-02 | 9.48e-01 |
| Signaling by ERBB4 | 45 | 8.09e-01 | -2.09e-02 | 9.38e-01 |
| MAP kinase activation | 60 | 7.80e-01 | -2.09e-02 | 9.32e-01 |
| Late Phase of HIV Life Cycle | 121 | 6.96e-01 | -2.06e-02 | 8.92e-01 |
| mRNA Splicing - Minor Pathway | 48 | 8.07e-01 | -2.04e-02 | 9.37e-01 |
| Transcriptional regulation of white adipocyte differentiation | 77 | 7.58e-01 | 2.03e-02 | 9.23e-01 |
| SUMOylation of SUMOylation proteins | 29 | 8.51e-01 | 2.02e-02 | 9.56e-01 |
| Signal regulatory protein family interactions | 13 | 9.00e-01 | 2.01e-02 | 9.73e-01 |
| Metabolism of lipids | 578 | 4.17e-01 | -2.00e-02 | 7.19e-01 |
| PI3K Cascade | 32 | 8.47e-01 | -1.98e-02 | 9.55e-01 |
| SUMOylation of immune response proteins | 11 | 9.10e-01 | -1.97e-02 | 9.73e-01 |
| SARS-CoV Infections | 77 | 7.65e-01 | 1.97e-02 | 9.23e-01 |
| Phase 0 - rapid depolarisation | 33 | 8.46e-01 | -1.95e-02 | 9.55e-01 |
| Serotonin Neurotransmitter Release Cycle | 11 | 9.12e-01 | -1.93e-02 | 9.74e-01 |
| Depolymerisation of the Nuclear Lamina | 15 | 8.98e-01 | 1.92e-02 | 9.73e-01 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | 19 | 8.86e-01 | -1.91e-02 | 9.70e-01 |
| Neurodegenerative Diseases | 19 | 8.86e-01 | -1.91e-02 | 9.70e-01 |
| PKMTs methylate histone lysines | 37 | 8.41e-01 | 1.91e-02 | 9.51e-01 |
| Diseases of programmed cell death | 20 | 8.83e-01 | -1.89e-02 | 9.70e-01 |
| Signaling by TGFB family members | 87 | 7.68e-01 | 1.84e-02 | 9.23e-01 |
| Acyl chain remodelling of PS | 14 | 9.06e-01 | 1.82e-02 | 9.73e-01 |
| VxPx cargo-targeting to cilium | 18 | 8.94e-01 | -1.81e-02 | 9.72e-01 |
| Organelle biogenesis and maintenance | 241 | 6.34e-01 | 1.79e-02 | 8.65e-01 |
| O-linked glycosylation of mucins | 33 | 8.62e-01 | -1.75e-02 | 9.61e-01 |
| Chromatin modifying enzymes | 186 | 6.88e-01 | -1.71e-02 | 8.88e-01 |
| Chromatin organization | 186 | 6.88e-01 | -1.71e-02 | 8.88e-01 |
| TP53 Regulates Transcription of DNA Repair Genes | 57 | 8.23e-01 | 1.71e-02 | 9.46e-01 |
| Signaling by SCF-KIT | 42 | 8.50e-01 | 1.69e-02 | 9.56e-01 |
| Cleavage of the damaged pyrimidine | 16 | 9.07e-01 | 1.69e-02 | 9.73e-01 |
| Depyrimidination | 16 | 9.07e-01 | 1.69e-02 | 9.73e-01 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | 16 | 9.07e-01 | 1.69e-02 | 9.73e-01 |
| Chaperonin-mediated protein folding | 81 | 7.96e-01 | 1.66e-02 | 9.36e-01 |
| RAF/MAP kinase cascade | 232 | 6.64e-01 | -1.66e-02 | 8.88e-01 |
| tRNA modification in the nucleus and cytosol | 38 | 8.60e-01 | 1.65e-02 | 9.60e-01 |
| RAF-independent MAPK1/3 activation | 21 | 8.97e-01 | 1.64e-02 | 9.73e-01 |
| Signal amplification | 29 | 8.79e-01 | -1.63e-02 | 9.70e-01 |
| Platelet degranulation | 102 | 7.80e-01 | 1.60e-02 | 9.32e-01 |
| Signaling by RAF1 mutants | 35 | 8.72e-01 | -1.58e-02 | 9.65e-01 |
| Frs2-mediated activation | 12 | 9.25e-01 | -1.56e-02 | 9.80e-01 |
| Cargo concentration in the ER | 23 | 8.98e-01 | -1.55e-02 | 9.73e-01 |
| RNA Polymerase III Transcription Initiation From Type 2 Promoter | 27 | 8.91e-01 | 1.53e-02 | 9.71e-01 |
| Factors involved in megakaryocyte development and platelet production | 104 | 7.89e-01 | 1.52e-02 | 9.35e-01 |
| Hemostasis | 453 | 5.85e-01 | -1.51e-02 | 8.35e-01 |
| TNFR1-induced NFkappaB signaling pathway | 24 | 8.99e-01 | 1.49e-02 | 9.73e-01 |
| Signaling by VEGF | 98 | 8.02e-01 | 1.47e-02 | 9.36e-01 |
| Rab regulation of trafficking | 114 | 7.87e-01 | -1.47e-02 | 9.35e-01 |
| SHC-mediated cascade:FGFR2 | 14 | 9.25e-01 | -1.46e-02 | 9.80e-01 |
| Lysosome Vesicle Biogenesis | 31 | 8.91e-01 | -1.42e-02 | 9.71e-01 |
| Axon guidance | 437 | 6.19e-01 | 1.40e-02 | 8.51e-01 |
| Clathrin-mediated endocytosis | 122 | 7.94e-01 | -1.37e-02 | 9.35e-01 |
| Unfolded Protein Response (UPR) | 84 | 8.29e-01 | 1.37e-02 | 9.48e-01 |
| RNA Polymerase I Transcription | 49 | 8.72e-01 | -1.34e-02 | 9.65e-01 |
| Intrinsic Pathway for Apoptosis | 44 | 8.81e-01 | 1.31e-02 | 9.70e-01 |
| IRS-related events triggered by IGF1R | 39 | 8.89e-01 | 1.29e-02 | 9.71e-01 |
| Signaling by BMP | 21 | 9.18e-01 | -1.29e-02 | 9.78e-01 |
| EPHA-mediated growth cone collapse | 14 | 9.36e-01 | 1.24e-02 | 9.83e-01 |
| PIWI-interacting RNA (piRNA) biogenesis | 18 | 9.28e-01 | 1.24e-02 | 9.80e-01 |
| MAPK1/MAPK3 signaling | 237 | 7.45e-01 | -1.23e-02 | 9.23e-01 |
| Prolonged ERK activation events | 14 | 9.37e-01 | -1.23e-02 | 9.83e-01 |
| Vpr-mediated nuclear import of PICs | 29 | 9.09e-01 | -1.22e-02 | 9.73e-01 |
| AKT phosphorylates targets in the nucleus | 10 | 9.47e-01 | 1.21e-02 | 9.85e-01 |
| Golgi-to-ER retrograde transport | 106 | 8.31e-01 | 1.20e-02 | 9.48e-01 |
| Recruitment of NuMA to mitotic centrosomes | 79 | 8.54e-01 | 1.20e-02 | 9.56e-01 |
| FRS-mediated FGFR3 signaling | 14 | 9.39e-01 | 1.18e-02 | 9.85e-01 |
| Advanced glycosylation endproduct receptor signaling | 10 | 9.49e-01 | 1.16e-02 | 9.85e-01 |
| Translation of Replicase and Assembly of the Replication Transcription Complex | 12 | 9.45e-01 | 1.15e-02 | 9.85e-01 |
| Myogenesis | 23 | 9.26e-01 | -1.12e-02 | 9.80e-01 |
| Loss of Nlp from mitotic centrosomes | 68 | 8.75e-01 | 1.11e-02 | 9.67e-01 |
| Loss of proteins required for interphase microtubule organization from the centrosome | 68 | 8.75e-01 | 1.11e-02 | 9.67e-01 |
| RNA Polymerase III Transcription Initiation | 36 | 9.09e-01 | -1.11e-02 | 9.73e-01 |
| RNA Polymerase III Chain Elongation | 18 | 9.35e-01 | 1.10e-02 | 9.83e-01 |
| FCGR3A-mediated IL10 synthesis | 40 | 9.05e-01 | 1.09e-02 | 9.73e-01 |
| EPH-Ephrin signaling | 84 | 8.68e-01 | -1.05e-02 | 9.63e-01 |
| MET activates RAS signaling | 10 | 9.55e-01 | -1.02e-02 | 9.85e-01 |
| Iron uptake and transport | 48 | 9.04e-01 | 1.00e-02 | 9.73e-01 |
| Export of Viral Ribonucleoproteins from Nucleus | 28 | 9.27e-01 | 1.00e-02 | 9.80e-01 |
| Signaling by FGFR3 | 31 | 9.24e-01 | 9.94e-03 | 9.80e-01 |
| Insulin receptor signalling cascade | 41 | 9.14e-01 | 9.75e-03 | 9.74e-01 |
| Interactions of Vpr with host cellular proteins | 31 | 9.27e-01 | -9.56e-03 | 9.80e-01 |
| Leishmania infection | 171 | 8.30e-01 | 9.54e-03 | 9.48e-01 |
| VLDLR internalisation and degradation | 11 | 9.57e-01 | 9.43e-03 | 9.86e-01 |
| Interleukin-4 and Interleukin-13 signaling | 86 | 8.80e-01 | -9.40e-03 | 9.70e-01 |
| AMER1 mutants destabilize the destruction complex | 13 | 9.53e-01 | 9.37e-03 | 9.85e-01 |
| APC truncation mutants have impaired AXIN binding | 13 | 9.53e-01 | 9.37e-03 | 9.85e-01 |
| AXIN missense mutants destabilize the destruction complex | 13 | 9.53e-01 | 9.37e-03 | 9.85e-01 |
| AXIN mutants destabilize the destruction complex, activating WNT signaling | 13 | 9.53e-01 | 9.37e-03 | 9.85e-01 |
| Truncations of AMER1 destabilize the destruction complex | 13 | 9.53e-01 | 9.37e-03 | 9.85e-01 |
| truncated APC mutants destabilize the destruction complex | 13 | 9.53e-01 | 9.37e-03 | 9.85e-01 |
| Synthesis of glycosylphosphatidylinositol (GPI) | 18 | 9.45e-01 | 9.32e-03 | 9.85e-01 |
| Transcriptional activation of mitochondrial biogenesis | 50 | 9.12e-01 | -9.04e-03 | 9.74e-01 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 84 | 8.89e-01 | -8.83e-03 | 9.71e-01 |
| RNA Polymerase III Transcription Initiation From Type 3 Promoter | 28 | 9.36e-01 | -8.71e-03 | 9.83e-01 |
| Senescence-Associated Secretory Phenotype (SASP) | 44 | 9.21e-01 | -8.67e-03 | 9.79e-01 |
| Apoptotic execution phase | 41 | 9.24e-01 | -8.60e-03 | 9.80e-01 |
| TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain | 19 | 9.49e-01 | 8.47e-03 | 9.85e-01 |
| Role of phospholipids in phagocytosis | 27 | 9.40e-01 | 8.41e-03 | 9.85e-01 |
| PI3K/AKT Signaling in Cancer | 84 | 8.94e-01 | -8.39e-03 | 9.72e-01 |
| SUMOylation of ubiquitinylation proteins | 33 | 9.35e-01 | 8.17e-03 | 9.83e-01 |
| Signaling by FGFR | 67 | 9.08e-01 | -8.15e-03 | 9.73e-01 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | 41 | 9.30e-01 | 7.92e-03 | 9.80e-01 |
| Response to elevated platelet cytosolic Ca2+ | 107 | 8.89e-01 | 7.79e-03 | 9.71e-01 |
| Downstream signaling of activated FGFR4 | 18 | 9.55e-01 | -7.74e-03 | 9.85e-01 |
| Constitutive Signaling by Aberrant PI3K in Cancer | 57 | 9.20e-01 | 7.68e-03 | 9.79e-01 |
| Norepinephrine Neurotransmitter Release Cycle | 11 | 9.65e-01 | 7.54e-03 | 9.87e-01 |
| Signaling by Hedgehog | 120 | 8.87e-01 | -7.51e-03 | 9.71e-01 |
| PI-3K cascade:FGFR4 | 11 | 9.66e-01 | 7.49e-03 | 9.87e-01 |
| Disease | 1139 | 6.79e-01 | 7.41e-03 | 8.88e-01 |
| Transport of Ribonucleoproteins into the Host Nucleus | 27 | 9.47e-01 | 7.37e-03 | 9.85e-01 |
| Neurotransmitter release cycle | 32 | 9.43e-01 | -7.32e-03 | 9.85e-01 |
| HIV Life Cycle | 133 | 8.85e-01 | 7.26e-03 | 9.70e-01 |
| Nucleobase biosynthesis | 15 | 9.62e-01 | 7.12e-03 | 9.87e-01 |
| Negative regulation of the PI3K/AKT network | 91 | 9.07e-01 | 7.08e-03 | 9.73e-01 |
| Synthesis of very long-chain fatty acyl-CoAs | 14 | 9.65e-01 | -6.78e-03 | 9.87e-01 |
| Transport of Mature mRNAs Derived from Intronless Transcripts | 38 | 9.44e-01 | -6.57e-03 | 9.85e-01 |
| Anchoring of the basal body to the plasma membrane | 92 | 9.14e-01 | -6.55e-03 | 9.74e-01 |
| Extra-nuclear estrogen signaling | 65 | 9.30e-01 | 6.33e-03 | 9.80e-01 |
| RAF activation | 34 | 9.52e-01 | -5.99e-03 | 9.85e-01 |
| SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs | 11 | 9.73e-01 | -5.96e-03 | 9.87e-01 |
| RNA Polymerase I Promoter Clearance | 48 | 9.44e-01 | -5.89e-03 | 9.85e-01 |
| HCMV Late Events | 48 | 9.44e-01 | -5.88e-03 | 9.85e-01 |
| Centrosome maturation | 80 | 9.29e-01 | 5.77e-03 | 9.80e-01 |
| Recruitment of mitotic centrosome proteins and complexes | 80 | 9.29e-01 | 5.77e-03 | 9.80e-01 |
| Pyruvate metabolism | 26 | 9.60e-01 | 5.74e-03 | 9.87e-01 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | 169 | 9.01e-01 | -5.56e-03 | 9.73e-01 |
| Amyloid fiber formation | 36 | 9.54e-01 | 5.55e-03 | 9.85e-01 |
| MET promotes cell motility | 28 | 9.60e-01 | -5.49e-03 | 9.87e-01 |
| WNT ligand biogenesis and trafficking | 14 | 9.72e-01 | -5.39e-03 | 9.87e-01 |
| Negative regulation of FGFR1 signaling | 21 | 9.67e-01 | 5.28e-03 | 9.87e-01 |
| G-protein beta:gamma signalling | 28 | 9.62e-01 | 5.25e-03 | 9.87e-01 |
| Plasma lipoprotein assembly | 10 | 9.78e-01 | 5.06e-03 | 9.90e-01 |
| Other semaphorin interactions | 19 | 9.72e-01 | 4.70e-03 | 9.87e-01 |
| Degradation of cysteine and homocysteine | 12 | 9.78e-01 | 4.68e-03 | 9.90e-01 |
| Gap junction trafficking and regulation | 16 | 9.75e-01 | -4.56e-03 | 9.88e-01 |
| Signaling by Erythropoietin | 24 | 9.69e-01 | -4.54e-03 | 9.87e-01 |
| PIP3 activates AKT signaling | 238 | 9.09e-01 | 4.33e-03 | 9.73e-01 |
| Keratan sulfate degradation | 10 | 9.81e-01 | 4.32e-03 | 9.92e-01 |
| Endosomal Sorting Complex Required For Transport (ESCRT) | 27 | 9.72e-01 | -3.94e-03 | 9.87e-01 |
| IRS-mediated signalling | 36 | 9.69e-01 | 3.81e-03 | 9.87e-01 |
| Signaling by high-kinase activity BRAF mutants | 30 | 9.75e-01 | -3.30e-03 | 9.88e-01 |
| SUMOylation of RNA binding proteins | 41 | 9.72e-01 | 3.13e-03 | 9.87e-01 |
| Integrin signaling | 24 | 9.80e-01 | 3.01e-03 | 9.91e-01 |
| Mitochondrial biogenesis | 70 | 9.66e-01 | -2.92e-03 | 9.87e-01 |
| tRNA processing | 107 | 9.63e-01 | 2.61e-03 | 9.87e-01 |
| Peptide ligand-binding receptors | 72 | 9.70e-01 | 2.55e-03 | 9.87e-01 |
| MAP3K8 (TPL2)-dependent MAPK1/3 activation | 14 | 9.87e-01 | -2.48e-03 | 9.95e-01 |
| Nervous system development | 455 | 9.49e-01 | 1.77e-03 | 9.85e-01 |
| VEGFR2 mediated vascular permeability | 27 | 9.89e-01 | -1.57e-03 | 9.96e-01 |
| Signaling by Hippo | 20 | 9.91e-01 | -1.47e-03 | 9.96e-01 |
| Protein folding | 87 | 9.83e-01 | 1.34e-03 | 9.92e-01 |
| Activation of HOX genes during differentiation | 54 | 9.91e-01 | 8.90e-04 | 9.96e-01 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | 54 | 9.91e-01 | 8.90e-04 | 9.96e-01 |
| Developmental Biology | 686 | 9.71e-01 | -8.23e-04 | 9.87e-01 |
| Signaling by Nuclear Receptors | 200 | 9.87e-01 | 6.89e-04 | 9.95e-01 |
| Asymmetric localization of PCP proteins | 58 | 9.93e-01 | -6.88e-04 | 9.96e-01 |
| NOTCH4 Activation and Transmission of Signal to the Nucleus | 11 | 9.97e-01 | 6.01e-04 | 9.99e-01 |
| Interleukin-1 family signaling | 115 | 9.92e-01 | -5.74e-04 | 9.96e-01 |
| Endogenous sterols | 19 | 9.97e-01 | 5.69e-04 | 9.99e-01 |
| HATs acetylate histones | 75 | 9.98e-01 | 1.47e-04 | 1.00e+00 |
| ROS and RNS production in phagocytes | 28 | 9.99e-01 | -1.25e-04 | 1.00e+00 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | 51 | 1.00e+00 | -2.99e-05 | 1.00e+00 |
Establishment of Sister Chromatid Cohesion
| 339 | |
|---|---|
| set | Establishment of Sister Chromatid Cohesion |
| setSize | 10 |
| pANOVA | 8.94e-05 |
| s.dist | 0.715 |
| p.adjustANOVA | 0.00148 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RAD21 | 6600 |
| STAG2 | 6332 |
| PDS5B | 5886 |
| SMC1A | 5757 |
| STAG1 | 5623 |
| CDCA5 | 5608 |
| ESCO2 | 5506 |
| ESCO1 | 5283 |
| SMC3 | 4863 |
| PDS5A | -2866 |
| GeneID | Gene Rank |
|---|---|
| RAD21 | 6600 |
| STAG2 | 6332 |
| PDS5B | 5886 |
| SMC1A | 5757 |
| STAG1 | 5623 |
| CDCA5 | 5608 |
| ESCO2 | 5506 |
| ESCO1 | 5283 |
| SMC3 | 4863 |
| PDS5A | -2866 |
Unwinding of DNA
| 1278 | |
|---|---|
| set | Unwinding of DNA |
| setSize | 12 |
| pANOVA | 2.56e-05 |
| s.dist | 0.702 |
| p.adjustANOVA | 0.000512 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| MCM6 | 6416 |
| GINS4 | 6023 |
| CDC45 | 5799 |
| MCM4 | 5715 |
| MCM5 | 5639 |
| GINS1 | 5456 |
| MCM7 | 5116 |
| MCM2 | 4543 |
| MCM3 | 3995 |
| GINS2 | 3810 |
| MCM8 | 2679 |
| GINS3 | 2030 |
| GeneID | Gene Rank |
|---|---|
| MCM6 | 6416 |
| GINS4 | 6023 |
| CDC45 | 5799 |
| MCM4 | 5715 |
| MCM5 | 5639 |
| GINS1 | 5456 |
| MCM7 | 5116 |
| MCM2 | 4543 |
| MCM3 | 3995 |
| GINS2 | 3810 |
| MCM8 | 2679 |
| GINS3 | 2030 |
Mitotic Telophase/Cytokinesis
| 663 | |
|---|---|
| set | Mitotic Telophase/Cytokinesis |
| setSize | 12 |
| pANOVA | 5.57e-05 |
| s.dist | 0.672 |
| p.adjustANOVA | 0.00104 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RAD21 | 6600 |
| STAG2 | 6332 |
| PDS5B | 5886 |
| KIF23 | 5807 |
| SMC1A | 5757 |
| STAG1 | 5623 |
| SMC3 | 4863 |
| PLK1 | 4607 |
| NIPBL | 4350 |
| KIF20A | 4294 |
| MAU2 | 3612 |
| PDS5A | -2866 |
| GeneID | Gene Rank |
|---|---|
| RAD21 | 6600 |
| STAG2 | 6332 |
| PDS5B | 5886 |
| KIF23 | 5807 |
| SMC1A | 5757 |
| STAG1 | 5623 |
| SMC3 | 4863 |
| PLK1 | 4607 |
| NIPBL | 4350 |
| KIF20A | 4294 |
| MAU2 | 3612 |
| PDS5A | -2866 |
Viral mRNA Translation
| 1289 | |
|---|---|
| set | Viral mRNA Translation |
| setSize | 55 |
| pANOVA | 4.87e-15 |
| s.dist | 0.61 |
| p.adjustANOVA | 2.17e-12 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| DNAJC3 | 5104 |
| RPS18 | 5100 |
| RPS20 | 5062 |
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| DNAJC3 | 5104 |
| RPS18 | 5100 |
| RPS20 | 5062 |
| RPS5 | 4999 |
| RPS8 | 4889 |
| RPL11 | 4820 |
| RPL3L | 4800 |
| RPL8 | 4610 |
| RPS13 | 4582 |
| RPL34 | 4469 |
| RPL37A | 4369 |
| RPL30 | 4353 |
| RPS19 | 4331 |
| RPL19 | 4310 |
| GRSF1 | 4137 |
| RPLP2 | 4122 |
| RPL35A | 4089 |
| RPS6 | 4076 |
| RPL18A | 4046 |
| RPL14 | 3980 |
| RPS9 | 3818 |
| RPL38 | 3732 |
| RPS21 | 3125 |
| RPS11 | 3037 |
| RPS16 | 2931 |
| RPL31 | 2728 |
| RPS15 | 2680 |
| RPS14 | 2662 |
| FAU | 2504 |
| RPL15 | 2190 |
| RPS26 | 2036 |
| RPS27A | 2027 |
| RPL22 | 1849 |
| RPL28 | 1575 |
| RPL18 | 1455 |
| RPL37 | 775 |
| RPL3 | -198 |
| RPS29 | -668 |
Peptide chain elongation
| 790 | |
|---|---|
| set | Peptide chain elongation |
| setSize | 55 |
| pANOVA | 1.22e-14 |
| s.dist | 0.601 |
| p.adjustANOVA | 2.72e-12 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| EEF1A1 | 5200 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| RPS18 | 5100 |
| RPS20 | 5062 |
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| EEF1A1 | 5200 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| RPS18 | 5100 |
| RPS20 | 5062 |
| RPS5 | 4999 |
| RPS8 | 4889 |
| RPL11 | 4820 |
| RPL3L | 4800 |
| RPL8 | 4610 |
| RPS13 | 4582 |
| RPL34 | 4469 |
| RPL37A | 4369 |
| RPL30 | 4353 |
| RPS19 | 4331 |
| RPL19 | 4310 |
| RPLP2 | 4122 |
| RPL35A | 4089 |
| RPS6 | 4076 |
| RPL18A | 4046 |
| RPL14 | 3980 |
| RPS9 | 3818 |
| RPL38 | 3732 |
| RPS21 | 3125 |
| RPS11 | 3037 |
| RPS16 | 2931 |
| RPL31 | 2728 |
| RPS15 | 2680 |
| RPS14 | 2662 |
| FAU | 2504 |
| RPL15 | 2190 |
| RPS26 | 2036 |
| RPS27A | 2027 |
| RPL22 | 1849 |
| RPL28 | 1575 |
| RPL18 | 1455 |
| EEF2 | 786 |
| RPL37 | 775 |
| RPL3 | -198 |
| RPS29 | -668 |
Response of EIF2AK4 (GCN2) to amino acid deficiency
| 986 | |
|---|---|
| set | Response of EIF2AK4 (GCN2) to amino acid deficiency |
| setSize | 65 |
| pANOVA | 2.69e-16 |
| s.dist | 0.587 |
| p.adjustANOVA | 1.8e-13 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| DDIT3 | 6673 |
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| ATF4 | 6272 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| ATF2 | 5661 |
| RPL7 | 5591 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| GeneID | Gene Rank |
|---|---|
| DDIT3 | 6673 |
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| ATF4 | 6272 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| ATF2 | 5661 |
| RPL7 | 5591 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| RPS18 | 5100 |
| RPS20 | 5062 |
| RPS5 | 4999 |
| EIF2S1 | 4996 |
| RPS8 | 4889 |
| RPL11 | 4820 |
| RPL3L | 4800 |
| RPL8 | 4610 |
| RPS13 | 4582 |
| TRIB3 | 4577 |
| RPL34 | 4469 |
| RPL37A | 4369 |
| RPL30 | 4353 |
| RPS19 | 4331 |
| RPL19 | 4310 |
| RPLP2 | 4122 |
| RPL35A | 4089 |
| RPS6 | 4076 |
| RPL18A | 4046 |
| RPL14 | 3980 |
| EIF2S2 | 3887 |
| CEBPB | 3882 |
| RPS9 | 3818 |
| RPL38 | 3732 |
| RPS21 | 3125 |
| RPS11 | 3037 |
| RPS16 | 2931 |
| EIF2AK4 | 2782 |
| RPL31 | 2728 |
| RPS15 | 2680 |
| RPS14 | 2662 |
| FAU | 2504 |
| IMPACT | 2224 |
| RPL15 | 2190 |
| RPS26 | 2036 |
| RPS27A | 2027 |
| CEBPG | 1967 |
| RPL22 | 1849 |
| RPL28 | 1575 |
| RPL18 | 1455 |
| ASNS | 935 |
| RPL37 | 775 |
| RPL3 | -198 |
| RPS29 | -668 |
| ATF3 | -3157 |
Activation of the pre-replicative complex
| 53 | |
|---|---|
| set | Activation of the pre-replicative complex |
| setSize | 31 |
| pANOVA | 1.94e-08 |
| s.dist | 0.583 |
| p.adjustANOVA | 8.67e-07 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| POLA1 | 6512 |
| MCM6 | 6416 |
| RPA2 | 6100 |
| CDC6 | 5816 |
| CDC45 | 5799 |
| MCM4 | 5715 |
| MCM5 | 5639 |
| PRIM1 | 5620 |
| POLE | 5575 |
| POLE3 | 5574 |
| CDK2 | 5572 |
| ORC2 | 5275 |
| CDT1 | 5203 |
| MCM7 | 5116 |
| POLE4 | 4549 |
| MCM2 | 4543 |
| MCM10 | 4343 |
| ORC3 | 4206 |
| MCM3 | 3995 |
| CDC7 | 3718 |
| GeneID | Gene Rank |
|---|---|
| POLA1 | 6512 |
| MCM6 | 6416 |
| RPA2 | 6100 |
| CDC6 | 5816 |
| CDC45 | 5799 |
| MCM4 | 5715 |
| MCM5 | 5639 |
| PRIM1 | 5620 |
| POLE | 5575 |
| POLE3 | 5574 |
| CDK2 | 5572 |
| ORC2 | 5275 |
| CDT1 | 5203 |
| MCM7 | 5116 |
| POLE4 | 4549 |
| MCM2 | 4543 |
| MCM10 | 4343 |
| ORC3 | 4206 |
| MCM3 | 3995 |
| CDC7 | 3718 |
| ORC6 | 3213 |
| ORC5 | 3106 |
| DBF4 | 2779 |
| MCM8 | 2679 |
| RPA1 | 2677 |
| RPA3 | 1952 |
| POLE2 | 1625 |
| ORC4 | 1442 |
| GMNN | 1415 |
| PRIM2 | 285 |
| POLA2 | -3033 |
Selenocysteine synthesis
| 1037 | |
|---|---|
| set | Selenocysteine synthesis |
| setSize | 58 |
| pANOVA | 6.68e-14 |
| s.dist | 0.569 |
| p.adjustANOVA | 1.12e-11 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| PSTK | 5969 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| RPS18 | 5100 |
| RPS20 | 5062 |
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| PSTK | 5969 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| RPS18 | 5100 |
| RPS20 | 5062 |
| RPS5 | 4999 |
| RPS8 | 4889 |
| RPL11 | 4820 |
| RPL3L | 4800 |
| RPL8 | 4610 |
| RPS13 | 4582 |
| RPL34 | 4469 |
| RPL37A | 4369 |
| RPL30 | 4353 |
| RPS19 | 4331 |
| RPL19 | 4310 |
| RPLP2 | 4122 |
| RPL35A | 4089 |
| RPS6 | 4076 |
| RPL18A | 4046 |
| RPL14 | 3980 |
| RPS9 | 3818 |
| RPL38 | 3732 |
| RPS21 | 3125 |
| RPS11 | 3037 |
| RPS16 | 2931 |
| RPL31 | 2728 |
| RPS15 | 2680 |
| RPS14 | 2662 |
| FAU | 2504 |
| RPL15 | 2190 |
| RPS26 | 2036 |
| RPS27A | 2027 |
| EEFSEC | 2014 |
| RPL22 | 1849 |
| RPL28 | 1575 |
| RPL18 | 1455 |
| SECISBP2 | 1247 |
| SEPHS2 | 1245 |
| RPL37 | 775 |
| RPL3 | -198 |
| RPS29 | -668 |
| SEPSECS | -4554 |
Eukaryotic Translation Termination
| 344 | |
|---|---|
| set | Eukaryotic Translation Termination |
| setSize | 58 |
| pANOVA | 1.86e-13 |
| s.dist | 0.559 |
| p.adjustANOVA | 2.76e-11 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| RPS18 | 5100 |
| RPS20 | 5062 |
| RPS5 | 4999 |
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| RPS18 | 5100 |
| RPS20 | 5062 |
| RPS5 | 4999 |
| RPS8 | 4889 |
| RPL11 | 4820 |
| RPL3L | 4800 |
| RPL8 | 4610 |
| RPS13 | 4582 |
| RPL34 | 4469 |
| RPL37A | 4369 |
| RPL30 | 4353 |
| RPS19 | 4331 |
| RPL19 | 4310 |
| RPLP2 | 4122 |
| RPL35A | 4089 |
| RPS6 | 4076 |
| RPL18A | 4046 |
| RPL14 | 3980 |
| N6AMT1 | 3929 |
| RPS9 | 3818 |
| RPL38 | 3732 |
| RPS21 | 3125 |
| RPS11 | 3037 |
| RPS16 | 2931 |
| RPL31 | 2728 |
| RPS15 | 2680 |
| RPS14 | 2662 |
| FAU | 2504 |
| RPL15 | 2190 |
| ETF1 | 2162 |
| RPS26 | 2036 |
| RPS27A | 2027 |
| GSPT1 | 1864 |
| RPL22 | 1849 |
| RPL28 | 1575 |
| RPL18 | 1455 |
| RPL37 | 775 |
| RPL3 | -198 |
| RPS29 | -668 |
| GSPT2 | -1207 |
| APEH | -4725 |
Glucuronidation
| 440 | |
|---|---|
| set | Glucuronidation |
| setSize | 11 |
| pANOVA | 0.00135 |
| s.dist | 0.558 |
| p.adjustANOVA | 0.0149 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| UGT3A1 | 6714.5 |
| UGT3A2 | 6714.5 |
| UGT1A10 | 5030.5 |
| UGT1A7 | 5030.5 |
| UGT1A8 | 5030.5 |
| UGT1A9 | 5030.5 |
| UGT1A6 | 3947.0 |
| SLC35D1 | 3277.0 |
| ABHD10 | 2437.0 |
| UGDH | 2303.0 |
| UGP2 | -3431.0 |
| GeneID | Gene Rank |
|---|---|
| UGT3A1 | 6714.5 |
| UGT3A2 | 6714.5 |
| UGT1A10 | 5030.5 |
| UGT1A7 | 5030.5 |
| UGT1A8 | 5030.5 |
| UGT1A9 | 5030.5 |
| UGT1A6 | 3947.0 |
| SLC35D1 | 3277.0 |
| ABHD10 | 2437.0 |
| UGDH | 2303.0 |
| UGP2 | -3431.0 |
Eukaryotic Translation Elongation
| 342 | |
|---|---|
| set | Eukaryotic Translation Elongation |
| setSize | 59 |
| pANOVA | 6.46e-13 |
| s.dist | 0.541 |
| p.adjustANOVA | 7.21e-11 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| EEF1A1 | 5200 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| RPS18 | 5100 |
| RPS20 | 5062 |
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| EEF1A1 | 5200 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| RPS18 | 5100 |
| RPS20 | 5062 |
| RPS5 | 4999 |
| RPS8 | 4889 |
| RPL11 | 4820 |
| RPL3L | 4800 |
| RPL8 | 4610 |
| RPS13 | 4582 |
| RPL34 | 4469 |
| RPL37A | 4369 |
| RPL30 | 4353 |
| RPS19 | 4331 |
| RPL19 | 4310 |
| EEF1B2 | 4126 |
| RPLP2 | 4122 |
| RPL35A | 4089 |
| RPS6 | 4076 |
| RPL18A | 4046 |
| RPL14 | 3980 |
| RPS9 | 3818 |
| RPL38 | 3732 |
| RPS21 | 3125 |
| RPS11 | 3037 |
| RPS16 | 2931 |
| RPL31 | 2728 |
| RPS15 | 2680 |
| RPS14 | 2662 |
| FAU | 2504 |
| RPL15 | 2190 |
| RPS26 | 2036 |
| RPS27A | 2027 |
| RPL22 | 1849 |
| RPL28 | 1575 |
| RPL18 | 1455 |
| EEF2 | 786 |
| RPL37 | 775 |
| RPL3 | -198 |
| RPS29 | -668 |
| EEF1G | -2431 |
| EEF1D | -2481 |
| EEF1A2 | -6090 |
DNA strand elongation
| 244 | |
|---|---|
| set | DNA strand elongation |
| setSize | 32 |
| pANOVA | 1.24e-07 |
| s.dist | 0.54 |
| p.adjustANOVA | 4.48e-06 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| POLA1 | 6512 |
| MCM6 | 6416 |
| PCNA | 6290 |
| RPA2 | 6100 |
| GINS4 | 6023 |
| CDC45 | 5799 |
| MCM4 | 5715 |
| MCM5 | 5639 |
| PRIM1 | 5620 |
| GINS1 | 5456 |
| RFC2 | 5411 |
| LIG1 | 5337 |
| MCM7 | 5116 |
| POLD3 | 4916 |
| MCM2 | 4543 |
| MCM3 | 3995 |
| GINS2 | 3810 |
| FEN1 | 3622 |
| POLD2 | 3621 |
| RFC5 | 3279 |
| GeneID | Gene Rank |
|---|---|
| POLA1 | 6512 |
| MCM6 | 6416 |
| PCNA | 6290 |
| RPA2 | 6100 |
| GINS4 | 6023 |
| CDC45 | 5799 |
| MCM4 | 5715 |
| MCM5 | 5639 |
| PRIM1 | 5620 |
| GINS1 | 5456 |
| RFC2 | 5411 |
| LIG1 | 5337 |
| MCM7 | 5116 |
| POLD3 | 4916 |
| MCM2 | 4543 |
| MCM3 | 3995 |
| GINS2 | 3810 |
| FEN1 | 3622 |
| POLD2 | 3621 |
| RFC5 | 3279 |
| POLD4 | 2902 |
| MCM8 | 2679 |
| RPA1 | 2677 |
| GINS3 | 2030 |
| POLD1 | 2021 |
| DNA2 | 1978 |
| RPA3 | 1952 |
| RFC4 | 1833 |
| RFC1 | 1775 |
| PRIM2 | 285 |
| RFC3 | -1905 |
| POLA2 | -3033 |
Condensation of Prophase Chromosomes
| 203 | |
|---|---|
| set | Condensation of Prophase Chromosomes |
| setSize | 13 |
| pANOVA | 0.000883 |
| s.dist | 0.533 |
| p.adjustANOVA | 0.0101 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CCNB1 | 6494 |
| SMC2 | 6419 |
| NCAPG2 | 6376 |
| CDK1 | 5752 |
| SET | 5532 |
| SMC4 | 5130 |
| PLK1 | 4607 |
| NCAPH2 | 3678 |
| NCAPD3 | 3291 |
| H2AFX | 3183 |
| PHF8 | 69 |
| RB1 | -1343 |
| MCPH1 | -1647 |
| GeneID | Gene Rank |
|---|---|
| CCNB1 | 6494 |
| SMC2 | 6419 |
| NCAPG2 | 6376 |
| CDK1 | 5752 |
| SET | 5532 |
| SMC4 | 5130 |
| PLK1 | 4607 |
| NCAPH2 | 3678 |
| NCAPD3 | 3291 |
| H2AFX | 3183 |
| PHF8 | 69 |
| RB1 | -1343 |
| MCPH1 | -1647 |
Condensation of Prometaphase Chromosomes
| 202 | |
|---|---|
| set | Condensation of Prometaphase Chromosomes |
| setSize | 11 |
| pANOVA | 0.00238 |
| s.dist | 0.529 |
| p.adjustANOVA | 0.0234 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CCNB1 | 6494.0 |
| SMC2 | 6419.0 |
| NCAPG | 6386.0 |
| NCAPH | 6079.0 |
| CDK1 | 5752.0 |
| SMC4 | 5130.0 |
| CCNB2 | 4898.0 |
| CSNK2A2 | 701.0 |
| NCAPD2 | 584.0 |
| CSNK2B | -339.5 |
| CSNK2A1 | -2137.0 |
| GeneID | Gene Rank |
|---|---|
| CCNB1 | 6494.0 |
| SMC2 | 6419.0 |
| NCAPG | 6386.0 |
| NCAPH | 6079.0 |
| CDK1 | 5752.0 |
| SMC4 | 5130.0 |
| CCNB2 | 4898.0 |
| CSNK2A2 | 701.0 |
| NCAPD2 | 584.0 |
| CSNK2B | -339.5 |
| CSNK2A1 | -2137.0 |
Dissolution of Fibrin Clot
| 294 | |
|---|---|
| set | Dissolution of Fibrin Clot |
| setSize | 10 |
| pANOVA | 0.00458 |
| s.dist | 0.518 |
| p.adjustANOVA | 0.039 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| SERPINF2 | 6608 |
| S100A10 | 6293 |
| SERPINE1 | 5541 |
| ANXA2 | 5133 |
| PLAUR | 5058 |
| SERPINE2 | 4099 |
| SERPINB6 | 3102 |
| SERPINB8 | 2295 |
| PLAU | 1267 |
| PLAT | -3795 |
| GeneID | Gene Rank |
|---|---|
| SERPINF2 | 6608 |
| S100A10 | 6293 |
| SERPINE1 | 5541 |
| ANXA2 | 5133 |
| PLAUR | 5058 |
| SERPINE2 | 4099 |
| SERPINB6 | 3102 |
| SERPINB8 | 2295 |
| PLAU | 1267 |
| PLAT | -3795 |
Polo-like kinase mediated events
| 814 | |
|---|---|
| set | Polo-like kinase mediated events |
| setSize | 15 |
| pANOVA | 0.000545 |
| s.dist | 0.516 |
| p.adjustANOVA | 0.00682 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| WEE1 | 6719 |
| CCNB1 | 6494 |
| LIN52 | 6193 |
| MYBL2 | 5599 |
| CENPF | 5326 |
| RBBP4 | 5147 |
| CCNB2 | 4898 |
| FOXM1 | 4897 |
| PLK1 | 4607 |
| LIN9 | 3491 |
| LIN54 | 2783 |
| PKMYT1 | 1250 |
| CDC25A | -152 |
| EP300 | -262 |
| LIN37 | -3826 |
| GeneID | Gene Rank |
|---|---|
| WEE1 | 6719 |
| CCNB1 | 6494 |
| LIN52 | 6193 |
| MYBL2 | 5599 |
| CENPF | 5326 |
| RBBP4 | 5147 |
| CCNB2 | 4898 |
| FOXM1 | 4897 |
| PLK1 | 4607 |
| LIN9 | 3491 |
| LIN54 | 2783 |
| PKMYT1 | 1250 |
| CDC25A | -152 |
| EP300 | -262 |
| LIN37 | -3826 |
Cyclin A/B1/B2 associated events during G2/M transition
| 220 | |
|---|---|
| set | Cyclin A/B1/B2 associated events during G2/M transition |
| setSize | 22 |
| pANOVA | 3.2e-05 |
| s.dist | 0.512 |
| p.adjustANOVA | 0.000621 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| WEE1 | 6719 |
| CCNB1 | 6494 |
| CCNA2 | 6489 |
| XPO1 | 6429 |
| CDC25B | 6277 |
| CDK1 | 5752 |
| CDK2 | 5572 |
| CCNB2 | 4898 |
| FOXM1 | 4897 |
| PLK1 | 4607 |
| PPP2R1B | 4341 |
| PPP2CA | 4328 |
| CCNH | 3657 |
| PPP2CB | 3439 |
| CDK7 | 2131 |
| PPME1 | 1417 |
| PKMYT1 | 1250 |
| MNAT1 | 1064 |
| PPP2R2A | 872 |
| CDC25A | -152 |
| GeneID | Gene Rank |
|---|---|
| WEE1 | 6719 |
| CCNB1 | 6494 |
| CCNA2 | 6489 |
| XPO1 | 6429 |
| CDC25B | 6277 |
| CDK1 | 5752 |
| CDK2 | 5572 |
| CCNB2 | 4898 |
| FOXM1 | 4897 |
| PLK1 | 4607 |
| PPP2R1B | 4341 |
| PPP2CA | 4328 |
| CCNH | 3657 |
| PPP2CB | 3439 |
| CDK7 | 2131 |
| PPME1 | 1417 |
| PKMYT1 | 1250 |
| MNAT1 | 1064 |
| PPP2R2A | 872 |
| CDC25A | -152 |
| LCMT1 | -233 |
| PPP2R1A | -2809 |
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC)
| 725 | |
|---|---|
| set | Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) |
| setSize | 60 |
| pANOVA | 9.09e-12 |
| s.dist | 0.509 |
| p.adjustANOVA | 5.53e-10 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| RPS18 | 5100 |
| RPS20 | 5062 |
| RPS5 | 4999 |
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| RPS18 | 5100 |
| RPS20 | 5062 |
| RPS5 | 4999 |
| RPS8 | 4889 |
| RPL11 | 4820 |
| RPL3L | 4800 |
| RPL8 | 4610 |
| RPS13 | 4582 |
| RPL34 | 4469 |
| RPL37A | 4369 |
| RPL30 | 4353 |
| RPS19 | 4331 |
| RPL19 | 4310 |
| RPLP2 | 4122 |
| RPL35A | 4089 |
| RPS6 | 4076 |
| RPL18A | 4046 |
| RPL14 | 3980 |
| RPS9 | 3818 |
| RPL38 | 3732 |
| RPS21 | 3125 |
| RPS11 | 3037 |
| RPS16 | 2931 |
| RPL31 | 2728 |
| RPS15 | 2680 |
| RPS14 | 2662 |
| FAU | 2504 |
| RPL15 | 2190 |
| ETF1 | 2162 |
| RPS26 | 2036 |
| RPS27A | 2027 |
| GSPT1 | 1864 |
| RPL22 | 1849 |
| RPL28 | 1575 |
| RPL18 | 1455 |
| RPL37 | 775 |
| RPL3 | -198 |
| RPS29 | -668 |
| NCBP1 | -1003 |
| GSPT2 | -1207 |
| UPF1 | -3282 |
| EIF4G1 | -3686 |
| NCBP2 | -4668 |
HSF1-dependent transactivation
| 476 | |
|---|---|
| set | HSF1-dependent transactivation |
| setSize | 32 |
| pANOVA | 6.86e-07 |
| s.dist | -0.507 |
| p.adjustANOVA | 2.14e-05 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| HSPB8 | -6339.0 |
| CAMK2B | -6330.0 |
| HSPH1 | -6239.0 |
| HSF1 | -6178.0 |
| HSPA1L | -6041.0 |
| HSPA1A | -5937.5 |
| HSPA1B | -5937.5 |
| CRYAB | -5933.0 |
| SERPINH1 | -5894.0 |
| RPTOR | -5776.0 |
| FKBP4 | -5661.0 |
| HSP90AB1 | -5490.0 |
| CAMK2G | -5251.0 |
| CRYBA4 | -5240.0 |
| HSPA2 | -5016.0 |
| MLST8 | -4683.0 |
| DNAJB6 | -4396.0 |
| HSP90AA1 | -3889.0 |
| COL4A6 | -3732.0 |
| MTOR | -3559.0 |
| GeneID | Gene Rank |
|---|---|
| HSPB8 | -6339.0 |
| CAMK2B | -6330.0 |
| HSPH1 | -6239.0 |
| HSF1 | -6178.0 |
| HSPA1L | -6041.0 |
| HSPA1A | -5937.5 |
| HSPA1B | -5937.5 |
| CRYAB | -5933.0 |
| SERPINH1 | -5894.0 |
| RPTOR | -5776.0 |
| FKBP4 | -5661.0 |
| HSP90AB1 | -5490.0 |
| CAMK2G | -5251.0 |
| CRYBA4 | -5240.0 |
| HSPA2 | -5016.0 |
| MLST8 | -4683.0 |
| DNAJB6 | -4396.0 |
| HSP90AA1 | -3889.0 |
| COL4A6 | -3732.0 |
| MTOR | -3559.0 |
| CAMK2D | -2834.0 |
| CREBBP | -2187.0 |
| HSBP1 | -1978.0 |
| HSPA8 | -1092.0 |
| DNAJB1 | -908.0 |
| EP300 | -262.0 |
| AKT1S1 | -258.0 |
| CAMK2A | 862.0 |
| TNFRSF21 | 2049.0 |
| MRPL18 | 2785.0 |
| DEDD2 | 4658.0 |
| PTGES3 | 5102.0 |
Formation of a pool of free 40S subunits
| 382 | |
|---|---|
| set | Formation of a pool of free 40S subunits |
| setSize | 65 |
| pANOVA | 2.8e-12 |
| s.dist | 0.501 |
| p.adjustANOVA | 2.34e-10 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| EIF3E | 5539 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| RPS18 | 5100 |
| RPS20 | 5062 |
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577.0 |
| RPS12 | 6555.0 |
| RPL10 | 6544.0 |
| RPS27L | 6535.0 |
| RPS27 | 6213.0 |
| RPL36A | 6168.0 |
| RPS24 | 6142.0 |
| RPS15A | 6000.0 |
| RPS4X | 5880.0 |
| RPL4 | 5769.0 |
| RPL5 | 5750.0 |
| RPL7 | 5591.0 |
| EIF3E | 5539.0 |
| RPL32 | 5477.0 |
| RPL26 | 5321.0 |
| RPS23 | 5172.0 |
| RPL23 | 5139.0 |
| RPS3 | 5117.0 |
| RPS18 | 5100.0 |
| RPS20 | 5062.0 |
| RPS5 | 4999.0 |
| RPS8 | 4889.0 |
| RPL11 | 4820.0 |
| RPL3L | 4800.0 |
| RPL8 | 4610.0 |
| RPS13 | 4582.0 |
| RPL34 | 4469.0 |
| RPL37A | 4369.0 |
| RPL30 | 4353.0 |
| RPS19 | 4331.0 |
| RPL19 | 4310.0 |
| EIF3M | 4156.0 |
| RPLP2 | 4122.0 |
| RPL35A | 4089.0 |
| RPS6 | 4076.0 |
| RPL18A | 4046.0 |
| RPL14 | 3980.0 |
| RPS9 | 3818.0 |
| RPL38 | 3732.0 |
| EIF3H | 3301.0 |
| RPS21 | 3125.0 |
| RPS11 | 3037.0 |
| RPS16 | 2931.0 |
| RPL31 | 2728.0 |
| RPS15 | 2680.0 |
| RPS14 | 2662.0 |
| EIF3F | 2512.0 |
| FAU | 2504.0 |
| RPL15 | 2190.0 |
| RPS26 | 2036.0 |
| RPS27A | 2027.0 |
| RPL22 | 1849.0 |
| RPL28 | 1575.0 |
| RPL18 | 1455.0 |
| RPL37 | 775.0 |
| EIF3G | 675.0 |
| EIF3I | 488.0 |
| EIF3K | -23.0 |
| RPL3 | -198.0 |
| RPS29 | -668.0 |
| EIF3A | -942.0 |
| EIF3D | -1521.0 |
| EIF3B | -2568.0 |
| EIF3C | -3429.5 |
| EIF3L | -4005.0 |
Negative regulation of TCF-dependent signaling by WNT ligand antagonists
| 706 | |
|---|---|
| set | Negative regulation of TCF-dependent signaling by WNT ligand antagonists |
| setSize | 11 |
| pANOVA | 0.00471 |
| s.dist | -0.492 |
| p.adjustANOVA | 0.0399 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| KREMEN1 | -6335.0 |
| LRP5 | -5909.5 |
| WNT9A | -5315.0 |
| WNT5A | -5200.0 |
| SOST | -4235.0 |
| SFRP2 | -3821.0 |
| LRP6 | -3028.0 |
| KREMEN2 | -2339.0 |
| WIF1 | -1755.0 |
| WNT4 | 1883.0 |
| SFRP1 | 2165.0 |
| GeneID | Gene Rank |
|---|---|
| KREMEN1 | -6335.0 |
| LRP5 | -5909.5 |
| WNT9A | -5315.0 |
| WNT5A | -5200.0 |
| SOST | -4235.0 |
| SFRP2 | -3821.0 |
| LRP6 | -3028.0 |
| KREMEN2 | -2339.0 |
| WIF1 | -1755.0 |
| WNT4 | 1883.0 |
| SFRP1 | 2165.0 |
Processive synthesis on the lagging strand
| 839 | |
|---|---|
| set | Processive synthesis on the lagging strand |
| setSize | 15 |
| pANOVA | 0.000979 |
| s.dist | 0.492 |
| p.adjustANOVA | 0.011 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| POLA1 | 6512 |
| PCNA | 6290 |
| RPA2 | 6100 |
| PRIM1 | 5620 |
| LIG1 | 5337 |
| POLD3 | 4916 |
| FEN1 | 3622 |
| POLD2 | 3621 |
| POLD4 | 2902 |
| RPA1 | 2677 |
| POLD1 | 2021 |
| DNA2 | 1978 |
| RPA3 | 1952 |
| PRIM2 | 285 |
| POLA2 | -3033 |
| GeneID | Gene Rank |
|---|---|
| POLA1 | 6512 |
| PCNA | 6290 |
| RPA2 | 6100 |
| PRIM1 | 5620 |
| LIG1 | 5337 |
| POLD3 | 4916 |
| FEN1 | 3622 |
| POLD2 | 3621 |
| POLD4 | 2902 |
| RPA1 | 2677 |
| POLD1 | 2021 |
| DNA2 | 1978 |
| RPA3 | 1952 |
| PRIM2 | 285 |
| POLA2 | -3033 |
Activation of ATR in response to replication stress
| 35 | |
|---|---|
| set | Activation of ATR in response to replication stress |
| setSize | 35 |
| pANOVA | 6.51e-07 |
| s.dist | 0.486 |
| p.adjustANOVA | 2.08e-05 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| MCM6 | 6416 |
| RPA2 | 6100 |
| CDC6 | 5816 |
| CDC45 | 5799 |
| MCM4 | 5715 |
| MCM5 | 5639 |
| CDK2 | 5572 |
| RFC2 | 5411 |
| ORC2 | 5275 |
| RAD17 | 5255 |
| MCM7 | 5116 |
| CLSPN | 4553 |
| MCM2 | 4543 |
| MCM10 | 4343 |
| ORC3 | 4206 |
| MCM3 | 3995 |
| CDC7 | 3718 |
| RFC5 | 3279 |
| ORC6 | 3213 |
| ORC5 | 3106 |
| GeneID | Gene Rank |
|---|---|
| MCM6 | 6416 |
| RPA2 | 6100 |
| CDC6 | 5816 |
| CDC45 | 5799 |
| MCM4 | 5715 |
| MCM5 | 5639 |
| CDK2 | 5572 |
| RFC2 | 5411 |
| ORC2 | 5275 |
| RAD17 | 5255 |
| MCM7 | 5116 |
| CLSPN | 4553 |
| MCM2 | 4543 |
| MCM10 | 4343 |
| ORC3 | 4206 |
| MCM3 | 3995 |
| CDC7 | 3718 |
| RFC5 | 3279 |
| ORC6 | 3213 |
| ORC5 | 3106 |
| RAD9A | 2924 |
| DBF4 | 2779 |
| MCM8 | 2679 |
| RPA1 | 2677 |
| HUS1 | 2545 |
| ATR | 2460 |
| CHEK1 | 2267 |
| RPA3 | 1952 |
| RFC4 | 1833 |
| ORC4 | 1442 |
| RAD1 | 1208 |
| ATRIP | 548 |
| CDC25A | -152 |
| RFC3 | -1905 |
| RAD9B | -3263 |
SRP-dependent cotranslational protein targeting to membrane
| 1018 | |
|---|---|
| set | SRP-dependent cotranslational protein targeting to membrane |
| setSize | 76 |
| pANOVA | 5.63e-13 |
| s.dist | 0.478 |
| p.adjustANOVA | 7.21e-11 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| TRAM1 | 5865 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| SEC11A | 5559 |
| RPL32 | 5477 |
| SRP54 | 5436 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| TRAM1 | 5865 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| SEC11A | 5559 |
| RPL32 | 5477 |
| SRP54 | 5436 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| RPS18 | 5100 |
| RPS20 | 5062 |
| SRP72 | 5053 |
| RPS5 | 4999 |
| RPS8 | 4889 |
| RPL11 | 4820 |
| RPL3L | 4800 |
| SSR4 | 4753 |
| SSR3 | 4638 |
| RPL8 | 4610 |
| RPS13 | 4582 |
| RPL34 | 4469 |
| RPL37A | 4369 |
| RPL30 | 4353 |
| RPS19 | 4331 |
| RPL19 | 4310 |
| RPLP2 | 4122 |
| RPL35A | 4089 |
| RPS6 | 4076 |
| RPL18A | 4046 |
| RPL14 | 3980 |
| RPS9 | 3818 |
| RPL38 | 3732 |
| SEC61G | 3595 |
| SEC61A2 | 3541 |
| RPS21 | 3125 |
| RPS11 | 3037 |
| SPCS2 | 2945 |
| RPS16 | 2931 |
| RPL31 | 2728 |
| RPS15 | 2680 |
| RPS14 | 2662 |
| FAU | 2504 |
| RPL15 | 2190 |
| SPCS3 | 2118 |
| SRP9 | 2075 |
| RPS26 | 2036 |
| RPS27A | 2027 |
| RPL22 | 1849 |
| SEC11C | 1631 |
| RPL28 | 1575 |
| SRP19 | 1462 |
| RPL18 | 1455 |
| RPL37 | 775 |
| SRP14 | 243 |
| SRP68 | 198 |
| RPL3 | -198 |
| SPCS1 | -416 |
| RPS29 | -668 |
| SSR1 | -1144 |
| SEC61A1 | -1302 |
| RPN2 | -1773 |
| SSR2 | -2413 |
| DDOST | -3106 |
| RPN1 | -3802 |
| SRPRB | -4722 |
L13a-mediated translational silencing of Ceruloplasmin expression
| 571 | |
|---|---|
| set | L13a-mediated translational silencing of Ceruloplasmin expression |
| setSize | 73 |
| pANOVA | 1.65e-12 |
| s.dist | 0.478 |
| p.adjustANOVA | 1.55e-10 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| EIF4A1 | 6352 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| EIF3E | 5539 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| RPS18 | 5100 |
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577.0 |
| RPS12 | 6555.0 |
| RPL10 | 6544.0 |
| RPS27L | 6535.0 |
| EIF4A1 | 6352.0 |
| RPS27 | 6213.0 |
| RPL36A | 6168.0 |
| RPS24 | 6142.0 |
| RPS15A | 6000.0 |
| RPS4X | 5880.0 |
| RPL4 | 5769.0 |
| RPL5 | 5750.0 |
| RPL7 | 5591.0 |
| EIF3E | 5539.0 |
| RPL32 | 5477.0 |
| RPL26 | 5321.0 |
| RPS23 | 5172.0 |
| RPL23 | 5139.0 |
| RPS3 | 5117.0 |
| RPS18 | 5100.0 |
| RPS20 | 5062.0 |
| RPS5 | 4999.0 |
| EIF2S1 | 4996.0 |
| RPS8 | 4889.0 |
| RPL11 | 4820.0 |
| RPL3L | 4800.0 |
| RPL8 | 4610.0 |
| RPS13 | 4582.0 |
| RPL34 | 4469.0 |
| RPL37A | 4369.0 |
| RPL30 | 4353.0 |
| RPS19 | 4331.0 |
| RPL19 | 4310.0 |
| EIF3M | 4156.0 |
| RPLP2 | 4122.0 |
| RPL35A | 4089.0 |
| RPS6 | 4076.0 |
| RPL18A | 4046.0 |
| EIF4B | 3994.0 |
| RPL14 | 3980.0 |
| EIF2S2 | 3887.0 |
| RPS9 | 3818.0 |
| RPL38 | 3732.0 |
| EIF3H | 3301.0 |
| RPS21 | 3125.0 |
| RPS11 | 3037.0 |
| RPS16 | 2931.0 |
| RPL31 | 2728.0 |
| RPS15 | 2680.0 |
| RPS14 | 2662.0 |
| EIF4H | 2589.0 |
| EIF3F | 2512.0 |
| FAU | 2504.0 |
| RPL15 | 2190.0 |
| RPS26 | 2036.0 |
| RPS27A | 2027.0 |
| RPL22 | 1849.0 |
| RPL28 | 1575.0 |
| RPL18 | 1455.0 |
| EIF4A2 | 1422.0 |
| RPL37 | 775.0 |
| EIF3G | 675.0 |
| EIF3I | 488.0 |
| EIF3K | -23.0 |
| RPL3 | -198.0 |
| RPS29 | -668.0 |
| EIF3A | -942.0 |
| EIF3D | -1521.0 |
| EIF3B | -2568.0 |
| EIF4E | -3260.0 |
| EIF3C | -3429.5 |
| EIF4G1 | -3686.0 |
| EIF3L | -4005.0 |
Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1
| 1227 | |
|---|---|
| set | Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 |
| setSize | 15 |
| pANOVA | 0.00138 |
| s.dist | 0.477 |
| p.adjustANOVA | 0.0151 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TFDP2 | 6504.0 |
| CCNA2 | 6489.0 |
| RBL1 | 6216.0 |
| LIN52 | 6193.0 |
| CDK1 | 5752.0 |
| E2F1 | 5631.0 |
| MYBL2 | 5599.0 |
| RBBP4 | 5147.0 |
| RBL2 | 4767.0 |
| LIN9 | 3491.0 |
| LIN54 | 2783.0 |
| E2F5 | 2291.0 |
| E2F4 | -2498.0 |
| LIN37 | -3826.0 |
| TFDP1 | -5186.5 |
| GeneID | Gene Rank |
|---|---|
| TFDP2 | 6504.0 |
| CCNA2 | 6489.0 |
| RBL1 | 6216.0 |
| LIN52 | 6193.0 |
| CDK1 | 5752.0 |
| E2F1 | 5631.0 |
| MYBL2 | 5599.0 |
| RBBP4 | 5147.0 |
| RBL2 | 4767.0 |
| LIN9 | 3491.0 |
| LIN54 | 2783.0 |
| E2F5 | 2291.0 |
| E2F4 | -2498.0 |
| LIN37 | -3826.0 |
| TFDP1 | -5186.5 |
Selenoamino acid metabolism
| 1036 | |
|---|---|
| set | Selenoamino acid metabolism |
| setSize | 72 |
| pANOVA | 3.56e-12 |
| s.dist | 0.474 |
| p.adjustANOVA | 2.81e-10 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| PSTK | 5969 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| RPS18 | 5100 |
| CBS | 5099 |
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577.0 |
| RPS12 | 6555.0 |
| RPL10 | 6544.0 |
| RPS27L | 6535.0 |
| RPS27 | 6213.0 |
| RPL36A | 6168.0 |
| RPS24 | 6142.0 |
| RPS15A | 6000.0 |
| PSTK | 5969.0 |
| RPS4X | 5880.0 |
| RPL4 | 5769.0 |
| RPL5 | 5750.0 |
| RPL7 | 5591.0 |
| RPL32 | 5477.0 |
| RPL26 | 5321.0 |
| RPS23 | 5172.0 |
| RPL23 | 5139.0 |
| RPS3 | 5117.0 |
| RPS18 | 5100.0 |
| CBS | 5099.0 |
| RPS20 | 5062.0 |
| RPS5 | 4999.0 |
| CTH | 4893.0 |
| RPS8 | 4889.0 |
| RPL11 | 4820.0 |
| RPL3L | 4800.0 |
| GNMT | 4656.0 |
| RPL8 | 4610.0 |
| RPS13 | 4582.0 |
| RPL34 | 4469.0 |
| HNMT | 4371.0 |
| RPL37A | 4369.0 |
| RPL30 | 4353.0 |
| RPS19 | 4331.0 |
| RPL19 | 4310.0 |
| RPLP2 | 4122.0 |
| RPL35A | 4089.0 |
| RPS6 | 4076.0 |
| RPL18A | 4046.0 |
| RPL14 | 3980.0 |
| RPS9 | 3818.0 |
| RPL38 | 3732.0 |
| RPS21 | 3125.0 |
| RPS11 | 3037.0 |
| RPS16 | 2931.0 |
| AHCY | 2811.0 |
| RPL31 | 2728.0 |
| RPS15 | 2680.0 |
| RPS14 | 2662.0 |
| FAU | 2504.0 |
| RPL15 | 2190.0 |
| RPS26 | 2036.0 |
| RPS27A | 2027.0 |
| EEFSEC | 2014.0 |
| NNMT | 1942.0 |
| RPL22 | 1849.0 |
| RPL28 | 1575.0 |
| PAPSS2 | 1488.0 |
| RPL18 | 1455.0 |
| SECISBP2 | 1247.0 |
| SEPHS2 | 1245.0 |
| RPL37 | 775.0 |
| AIMP1 | 406.0 |
| EEF1E1 | 218.5 |
| RPL3 | -198.0 |
| RPS29 | -668.0 |
| PAPSS1 | -1112.0 |
| TXNRD1 | -2127.0 |
| AIMP2 | -3345.0 |
| SEPSECS | -4554.0 |
| GSR | -4617.0 |
| SCLY | -5290.0 |
GTP hydrolysis and joining of the 60S ribosomal subunit
| 422 | |
|---|---|
| set | GTP hydrolysis and joining of the 60S ribosomal subunit |
| setSize | 75 |
| pANOVA | 1.74e-12 |
| s.dist | 0.471 |
| p.adjustANOVA | 1.55e-10 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| EIF4A1 | 6352 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| EIF5 | 5902 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| EIF3E | 5539 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577.0 |
| RPS12 | 6555.0 |
| RPL10 | 6544.0 |
| RPS27L | 6535.0 |
| EIF4A1 | 6352.0 |
| RPS27 | 6213.0 |
| RPL36A | 6168.0 |
| RPS24 | 6142.0 |
| RPS15A | 6000.0 |
| EIF5 | 5902.0 |
| RPS4X | 5880.0 |
| RPL4 | 5769.0 |
| RPL5 | 5750.0 |
| RPL7 | 5591.0 |
| EIF3E | 5539.0 |
| RPL32 | 5477.0 |
| RPL26 | 5321.0 |
| RPS23 | 5172.0 |
| RPL23 | 5139.0 |
| RPS3 | 5117.0 |
| RPS18 | 5100.0 |
| RPS20 | 5062.0 |
| RPS5 | 4999.0 |
| EIF2S1 | 4996.0 |
| RPS8 | 4889.0 |
| RPL11 | 4820.0 |
| RPL3L | 4800.0 |
| RPL8 | 4610.0 |
| RPS13 | 4582.0 |
| RPL34 | 4469.0 |
| RPL37A | 4369.0 |
| RPL30 | 4353.0 |
| RPS19 | 4331.0 |
| RPL19 | 4310.0 |
| EIF3M | 4156.0 |
| RPLP2 | 4122.0 |
| RPL35A | 4089.0 |
| RPS6 | 4076.0 |
| RPL18A | 4046.0 |
| EIF4B | 3994.0 |
| RPL14 | 3980.0 |
| EIF2S2 | 3887.0 |
| RPS9 | 3818.0 |
| RPL38 | 3732.0 |
| EIF3H | 3301.0 |
| RPS21 | 3125.0 |
| RPS11 | 3037.0 |
| RPS16 | 2931.0 |
| RPL31 | 2728.0 |
| RPS15 | 2680.0 |
| RPS14 | 2662.0 |
| EIF4H | 2589.0 |
| EIF3F | 2512.0 |
| FAU | 2504.0 |
| RPL15 | 2190.0 |
| RPS26 | 2036.0 |
| RPS27A | 2027.0 |
| RPL22 | 1849.0 |
| RPL28 | 1575.0 |
| RPL18 | 1455.0 |
| EIF4A2 | 1422.0 |
| RPL37 | 775.0 |
| EIF3G | 675.0 |
| EIF3I | 488.0 |
| EIF3K | -23.0 |
| RPL3 | -198.0 |
| RPS29 | -668.0 |
| EIF3A | -942.0 |
| EIF3D | -1521.0 |
| EIF3B | -2568.0 |
| EIF5B | -2738.0 |
| EIF4E | -3260.0 |
| EIF3C | -3429.5 |
| EIF4G1 | -3686.0 |
| EIF3L | -4005.0 |
Removal of the Flap Intermediate
| 973 | |
|---|---|
| set | Removal of the Flap Intermediate |
| setSize | 14 |
| pANOVA | 0.00231 |
| s.dist | 0.47 |
| p.adjustANOVA | 0.0229 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| POLA1 | 6512 |
| PCNA | 6290 |
| RPA2 | 6100 |
| PRIM1 | 5620 |
| POLD3 | 4916 |
| FEN1 | 3622 |
| POLD2 | 3621 |
| POLD4 | 2902 |
| RPA1 | 2677 |
| POLD1 | 2021 |
| DNA2 | 1978 |
| RPA3 | 1952 |
| PRIM2 | 285 |
| POLA2 | -3033 |
| GeneID | Gene Rank |
|---|---|
| POLA1 | 6512 |
| PCNA | 6290 |
| RPA2 | 6100 |
| PRIM1 | 5620 |
| POLD3 | 4916 |
| FEN1 | 3622 |
| POLD2 | 3621 |
| POLD4 | 2902 |
| RPA1 | 2677 |
| POLD1 | 2021 |
| DNA2 | 1978 |
| RPA3 | 1952 |
| PRIM2 | 285 |
| POLA2 | -3033 |
LGI-ADAM interactions
| 574 | |
|---|---|
| set | LGI-ADAM interactions |
| setSize | 11 |
| pANOVA | 0.00718 |
| s.dist | -0.468 |
| p.adjustANOVA | 0.0529 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| LGI1 | -6159 |
| ADAM11 | -6067 |
| STX1B | -5608 |
| LGI4 | -5284 |
| LGI3 | -4643 |
| LGI2 | -4508 |
| STX1A | -2845 |
| ADAM23 | -1841 |
| DLG4 | -1769 |
| CACNG2 | 115 |
| ADAM22 | 6455 |
| GeneID | Gene Rank |
|---|---|
| LGI1 | -6159 |
| ADAM11 | -6067 |
| STX1B | -5608 |
| LGI4 | -5284 |
| LGI3 | -4643 |
| LGI2 | -4508 |
| STX1A | -2845 |
| ADAM23 | -1841 |
| DLG4 | -1769 |
| CACNG2 | 115 |
| ADAM22 | 6455 |
G0 and Early G1
| 404 | |
|---|---|
| set | G0 and Early G1 |
| setSize | 25 |
| pANOVA | 6.17e-05 |
| s.dist | 0.463 |
| p.adjustANOVA | 0.00109 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| MAX | 6562 |
| TFDP2 | 6504 |
| CCNA2 | 6489 |
| PCNA | 6290 |
| RBL1 | 6216 |
| LIN52 | 6193 |
| CDC6 | 5816 |
| CDK1 | 5752 |
| E2F1 | 5631 |
| MYBL2 | 5599 |
| CDK2 | 5572 |
| TOP2A | 5473 |
| RBBP4 | 5147 |
| RBL2 | 4767 |
| CCNE2 | 3602 |
| LIN9 | 3491 |
| LIN54 | 2783 |
| DYRK1A | 2724 |
| E2F5 | 2291 |
| CDC25A | -152 |
| GeneID | Gene Rank |
|---|---|
| MAX | 6562.0 |
| TFDP2 | 6504.0 |
| CCNA2 | 6489.0 |
| PCNA | 6290.0 |
| RBL1 | 6216.0 |
| LIN52 | 6193.0 |
| CDC6 | 5816.0 |
| CDK1 | 5752.0 |
| E2F1 | 5631.0 |
| MYBL2 | 5599.0 |
| CDK2 | 5572.0 |
| TOP2A | 5473.0 |
| RBBP4 | 5147.0 |
| RBL2 | 4767.0 |
| CCNE2 | 3602.0 |
| LIN9 | 3491.0 |
| LIN54 | 2783.0 |
| DYRK1A | 2724.0 |
| E2F5 | 2291.0 |
| CDC25A | -152.0 |
| CCNE1 | -892.0 |
| E2F4 | -2498.0 |
| LIN37 | -3826.0 |
| MYC | -4460.0 |
| TFDP1 | -5186.5 |
Recognition of DNA damage by PCNA-containing replication complex
| 918 | |
|---|---|
| set | Recognition of DNA damage by PCNA-containing replication complex |
| setSize | 28 |
| pANOVA | 2.89e-05 |
| s.dist | 0.457 |
| p.adjustANOVA | 0.00057 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PCNA | 6290 |
| UBE2B | 6136 |
| RPA2 | 6100 |
| CUL4B | 5748 |
| POLE | 5575 |
| POLE3 | 5574 |
| RFC2 | 5411 |
| DTL | 5004 |
| POLD3 | 4916 |
| USP1 | 4805 |
| RAD18 | 4562 |
| POLE4 | 4549 |
| RBX1 | 3837 |
| POLD2 | 3621 |
| RFC5 | 3279 |
| POLD4 | 2902 |
| WDR48 | 2758 |
| RPA1 | 2677 |
| RPS27A | 2027 |
| POLD1 | 2021 |
| GeneID | Gene Rank |
|---|---|
| PCNA | 6290 |
| UBE2B | 6136 |
| RPA2 | 6100 |
| CUL4B | 5748 |
| POLE | 5575 |
| POLE3 | 5574 |
| RFC2 | 5411 |
| DTL | 5004 |
| POLD3 | 4916 |
| USP1 | 4805 |
| RAD18 | 4562 |
| POLE4 | 4549 |
| RBX1 | 3837 |
| POLD2 | 3621 |
| RFC5 | 3279 |
| POLD4 | 2902 |
| WDR48 | 2758 |
| RPA1 | 2677 |
| RPS27A | 2027 |
| POLD1 | 2021 |
| RPA3 | 1952 |
| RFC4 | 1833 |
| RFC1 | 1775 |
| POLE2 | 1625 |
| DDB1 | 1560 |
| CUL4A | 71 |
| RFC3 | -1905 |
| UBC | -6404 |
G1/S-Specific Transcription
| 408 | |
|---|---|
| set | G1/S-Specific Transcription |
| setSize | 26 |
| pANOVA | 6.73e-05 |
| s.dist | 0.452 |
| p.adjustANOVA | 0.00117 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| POLA1 | 6512.0 |
| TFDP2 | 6504.0 |
| PCNA | 6290.0 |
| RBL1 | 6216.0 |
| LIN52 | 6193.0 |
| CDC6 | 5816.0 |
| CDC45 | 5799.0 |
| CDK1 | 5752.0 |
| RRM2 | 5739.0 |
| TK1 | 5665.0 |
| E2F1 | 5631.0 |
| CDT1 | 5203.0 |
| FBXO5 | 5187.0 |
| RBBP4 | 5147.0 |
| RBL2 | 4767.0 |
| DHFR | 3663.5 |
| LIN9 | 3491.0 |
| LIN54 | 2783.0 |
| E2F5 | 2291.0 |
| CDC25A | -152.0 |
| GeneID | Gene Rank |
|---|---|
| POLA1 | 6512.0 |
| TFDP2 | 6504.0 |
| PCNA | 6290.0 |
| RBL1 | 6216.0 |
| LIN52 | 6193.0 |
| CDC6 | 5816.0 |
| CDC45 | 5799.0 |
| CDK1 | 5752.0 |
| RRM2 | 5739.0 |
| TK1 | 5665.0 |
| E2F1 | 5631.0 |
| CDT1 | 5203.0 |
| FBXO5 | 5187.0 |
| RBBP4 | 5147.0 |
| RBL2 | 4767.0 |
| DHFR | 3663.5 |
| LIN9 | 3491.0 |
| LIN54 | 2783.0 |
| E2F5 | 2291.0 |
| CDC25A | -152.0 |
| CCNE1 | -892.0 |
| E2F6 | -2305.0 |
| E2F4 | -2498.0 |
| TYMS | -2640.0 |
| LIN37 | -3826.0 |
| TFDP1 | -5186.5 |
Constitutive Signaling by NOTCH1 HD Domain Mutants
| 208 | |
|---|---|
| set | Constitutive Signaling by NOTCH1 HD Domain Mutants |
| setSize | 12 |
| pANOVA | 0.00692 |
| s.dist | -0.45 |
| p.adjustANOVA | 0.0515 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| UBC | -6404 |
| DLL1 | -6028 |
| ADAM17 | -5641 |
| NOTCH1 | -5482 |
| DLL4 | -5274 |
| JAG2 | -4948 |
| JAG1 | -2597 |
| NEURL1B | -2029 |
| MIB2 | -954 |
| ADAM10 | -825 |
| RPS27A | 2027 |
| MIB1 | 4489 |
| GeneID | Gene Rank |
|---|---|
| UBC | -6404 |
| DLL1 | -6028 |
| ADAM17 | -5641 |
| NOTCH1 | -5482 |
| DLL4 | -5274 |
| JAG2 | -4948 |
| JAG1 | -2597 |
| NEURL1B | -2029 |
| MIB2 | -954 |
| ADAM10 | -825 |
| RPS27A | 2027 |
| MIB1 | 4489 |
Signaling by NOTCH1 HD Domain Mutants in Cancer
| 1088 | |
|---|---|
| set | Signaling by NOTCH1 HD Domain Mutants in Cancer |
| setSize | 12 |
| pANOVA | 0.00692 |
| s.dist | -0.45 |
| p.adjustANOVA | 0.0515 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| UBC | -6404 |
| DLL1 | -6028 |
| ADAM17 | -5641 |
| NOTCH1 | -5482 |
| DLL4 | -5274 |
| JAG2 | -4948 |
| JAG1 | -2597 |
| NEURL1B | -2029 |
| MIB2 | -954 |
| ADAM10 | -825 |
| RPS27A | 2027 |
| MIB1 | 4489 |
| GeneID | Gene Rank |
|---|---|
| UBC | -6404 |
| DLL1 | -6028 |
| ADAM17 | -5641 |
| NOTCH1 | -5482 |
| DLL4 | -5274 |
| JAG2 | -4948 |
| JAG1 | -2597 |
| NEURL1B | -2029 |
| MIB2 | -954 |
| ADAM10 | -825 |
| RPS27A | 2027 |
| MIB1 | 4489 |
Attenuation phase
| 93 | |
|---|---|
| set | Attenuation phase |
| setSize | 22 |
| pANOVA | 0.000267 |
| s.dist | -0.449 |
| p.adjustANOVA | 0.00373 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| HSPH1 | -6239.0 |
| HSF1 | -6178.0 |
| HSPA1L | -6041.0 |
| HSPA1A | -5937.5 |
| HSPA1B | -5937.5 |
| SERPINH1 | -5894.0 |
| FKBP4 | -5661.0 |
| HSP90AB1 | -5490.0 |
| CRYBA4 | -5240.0 |
| HSPA2 | -5016.0 |
| DNAJB6 | -4396.0 |
| HSP90AA1 | -3889.0 |
| COL4A6 | -3732.0 |
| CREBBP | -2187.0 |
| HSBP1 | -1978.0 |
| HSPA8 | -1092.0 |
| DNAJB1 | -908.0 |
| EP300 | -262.0 |
| TNFRSF21 | 2049.0 |
| MRPL18 | 2785.0 |
| GeneID | Gene Rank |
|---|---|
| HSPH1 | -6239.0 |
| HSF1 | -6178.0 |
| HSPA1L | -6041.0 |
| HSPA1A | -5937.5 |
| HSPA1B | -5937.5 |
| SERPINH1 | -5894.0 |
| FKBP4 | -5661.0 |
| HSP90AB1 | -5490.0 |
| CRYBA4 | -5240.0 |
| HSPA2 | -5016.0 |
| DNAJB6 | -4396.0 |
| HSP90AA1 | -3889.0 |
| COL4A6 | -3732.0 |
| CREBBP | -2187.0 |
| HSBP1 | -1978.0 |
| HSPA8 | -1092.0 |
| DNAJB1 | -908.0 |
| EP300 | -262.0 |
| TNFRSF21 | 2049.0 |
| MRPL18 | 2785.0 |
| DEDD2 | 4658.0 |
| PTGES3 | 5102.0 |
CDC6 association with the ORC:origin complex
| 124 | |
|---|---|
| set | CDC6 association with the ORC:origin complex |
| setSize | 10 |
| pANOVA | 0.0143 |
| s.dist | 0.448 |
| p.adjustANOVA | 0.0876 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CDC6 | 5816 |
| E2F1 | 5631 |
| E2F2 | 5537 |
| ORC2 | 5275 |
| ORC3 | 4206 |
| ORC6 | 3213 |
| ORC5 | 3106 |
| MCM8 | 2679 |
| ORC4 | 1442 |
| E2F3 | -5927 |
| GeneID | Gene Rank |
|---|---|
| CDC6 | 5816 |
| E2F1 | 5631 |
| E2F2 | 5537 |
| ORC2 | 5275 |
| ORC3 | 4206 |
| ORC6 | 3213 |
| ORC5 | 3106 |
| MCM8 | 2679 |
| ORC4 | 1442 |
| E2F3 | -5927 |
Lagging Strand Synthesis
| 575 | |
|---|---|
| set | Lagging Strand Synthesis |
| setSize | 20 |
| pANOVA | 0.000621 |
| s.dist | 0.442 |
| p.adjustANOVA | 0.00763 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| POLA1 | 6512 |
| PCNA | 6290 |
| RPA2 | 6100 |
| PRIM1 | 5620 |
| RFC2 | 5411 |
| LIG1 | 5337 |
| POLD3 | 4916 |
| FEN1 | 3622 |
| POLD2 | 3621 |
| RFC5 | 3279 |
| POLD4 | 2902 |
| RPA1 | 2677 |
| POLD1 | 2021 |
| DNA2 | 1978 |
| RPA3 | 1952 |
| RFC4 | 1833 |
| RFC1 | 1775 |
| PRIM2 | 285 |
| RFC3 | -1905 |
| POLA2 | -3033 |
| GeneID | Gene Rank |
|---|---|
| POLA1 | 6512 |
| PCNA | 6290 |
| RPA2 | 6100 |
| PRIM1 | 5620 |
| RFC2 | 5411 |
| LIG1 | 5337 |
| POLD3 | 4916 |
| FEN1 | 3622 |
| POLD2 | 3621 |
| RFC5 | 3279 |
| POLD4 | 2902 |
| RPA1 | 2677 |
| POLD1 | 2021 |
| DNA2 | 1978 |
| RPA3 | 1952 |
| RFC4 | 1833 |
| RFC1 | 1775 |
| PRIM2 | 285 |
| RFC3 | -1905 |
| POLA2 | -3033 |
Cap-dependent Translation Initiation
| 144 | |
|---|---|
| set | Cap-dependent Translation Initiation |
| setSize | 81 |
| pANOVA | 6.39e-12 |
| s.dist | 0.442 |
| p.adjustANOVA | 4.5e-10 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| EIF4A1 | 6352 |
| EIF4EBP1 | 6235 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| EIF5 | 5902 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| EIF3E | 5539 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577.0 |
| RPS12 | 6555.0 |
| RPL10 | 6544.0 |
| RPS27L | 6535.0 |
| EIF4A1 | 6352.0 |
| EIF4EBP1 | 6235.0 |
| RPS27 | 6213.0 |
| RPL36A | 6168.0 |
| RPS24 | 6142.0 |
| RPS15A | 6000.0 |
| EIF5 | 5902.0 |
| RPS4X | 5880.0 |
| RPL4 | 5769.0 |
| RPL5 | 5750.0 |
| RPL7 | 5591.0 |
| EIF3E | 5539.0 |
| RPL32 | 5477.0 |
| RPL26 | 5321.0 |
| RPS23 | 5172.0 |
| RPL23 | 5139.0 |
| RPS3 | 5117.0 |
| RPS18 | 5100.0 |
| RPS20 | 5062.0 |
| RPS5 | 4999.0 |
| EIF2S1 | 4996.0 |
| RPS8 | 4889.0 |
| RPL11 | 4820.0 |
| RPL3L | 4800.0 |
| RPL8 | 4610.0 |
| RPS13 | 4582.0 |
| RPL34 | 4469.0 |
| RPL37A | 4369.0 |
| RPL30 | 4353.0 |
| RPS19 | 4331.0 |
| RPL19 | 4310.0 |
| EIF3M | 4156.0 |
| RPLP2 | 4122.0 |
| RPL35A | 4089.0 |
| RPS6 | 4076.0 |
| RPL18A | 4046.0 |
| EIF4B | 3994.0 |
| RPL14 | 3980.0 |
| EIF2S2 | 3887.0 |
| RPS9 | 3818.0 |
| RPL38 | 3732.0 |
| EIF3H | 3301.0 |
| RPS21 | 3125.0 |
| RPS11 | 3037.0 |
| RPS16 | 2931.0 |
| EIF2B1 | 2752.0 |
| RPL31 | 2728.0 |
| RPS15 | 2680.0 |
| RPS14 | 2662.0 |
| EIF4H | 2589.0 |
| EIF3F | 2512.0 |
| FAU | 2504.0 |
| RPL15 | 2190.0 |
| RPS26 | 2036.0 |
| RPS27A | 2027.0 |
| RPL22 | 1849.0 |
| RPL28 | 1575.0 |
| RPL18 | 1455.0 |
| EIF4A2 | 1422.0 |
| EIF2B5 | 1193.0 |
| RPL37 | 775.0 |
| EIF3G | 675.0 |
| EIF3I | 488.0 |
| EIF3K | -23.0 |
| RPL3 | -198.0 |
| RPS29 | -668.0 |
| EIF3A | -942.0 |
| EIF2B3 | -1274.0 |
| EIF3D | -1521.0 |
| EIF2B2 | -1728.0 |
| EIF3B | -2568.0 |
| EIF5B | -2738.0 |
| EIF4E | -3260.0 |
| EIF3C | -3429.5 |
| EIF2B4 | -3461.0 |
| EIF4G1 | -3686.0 |
| EIF3L | -4005.0 |
Eukaryotic Translation Initiation
| 343 | |
|---|---|
| set | Eukaryotic Translation Initiation |
| setSize | 81 |
| pANOVA | 6.39e-12 |
| s.dist | 0.442 |
| p.adjustANOVA | 4.5e-10 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| EIF4A1 | 6352 |
| EIF4EBP1 | 6235 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| EIF5 | 5902 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RPL7 | 5591 |
| EIF3E | 5539 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RPL23 | 5139 |
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577.0 |
| RPS12 | 6555.0 |
| RPL10 | 6544.0 |
| RPS27L | 6535.0 |
| EIF4A1 | 6352.0 |
| EIF4EBP1 | 6235.0 |
| RPS27 | 6213.0 |
| RPL36A | 6168.0 |
| RPS24 | 6142.0 |
| RPS15A | 6000.0 |
| EIF5 | 5902.0 |
| RPS4X | 5880.0 |
| RPL4 | 5769.0 |
| RPL5 | 5750.0 |
| RPL7 | 5591.0 |
| EIF3E | 5539.0 |
| RPL32 | 5477.0 |
| RPL26 | 5321.0 |
| RPS23 | 5172.0 |
| RPL23 | 5139.0 |
| RPS3 | 5117.0 |
| RPS18 | 5100.0 |
| RPS20 | 5062.0 |
| RPS5 | 4999.0 |
| EIF2S1 | 4996.0 |
| RPS8 | 4889.0 |
| RPL11 | 4820.0 |
| RPL3L | 4800.0 |
| RPL8 | 4610.0 |
| RPS13 | 4582.0 |
| RPL34 | 4469.0 |
| RPL37A | 4369.0 |
| RPL30 | 4353.0 |
| RPS19 | 4331.0 |
| RPL19 | 4310.0 |
| EIF3M | 4156.0 |
| RPLP2 | 4122.0 |
| RPL35A | 4089.0 |
| RPS6 | 4076.0 |
| RPL18A | 4046.0 |
| EIF4B | 3994.0 |
| RPL14 | 3980.0 |
| EIF2S2 | 3887.0 |
| RPS9 | 3818.0 |
| RPL38 | 3732.0 |
| EIF3H | 3301.0 |
| RPS21 | 3125.0 |
| RPS11 | 3037.0 |
| RPS16 | 2931.0 |
| EIF2B1 | 2752.0 |
| RPL31 | 2728.0 |
| RPS15 | 2680.0 |
| RPS14 | 2662.0 |
| EIF4H | 2589.0 |
| EIF3F | 2512.0 |
| FAU | 2504.0 |
| RPL15 | 2190.0 |
| RPS26 | 2036.0 |
| RPS27A | 2027.0 |
| RPL22 | 1849.0 |
| RPL28 | 1575.0 |
| RPL18 | 1455.0 |
| EIF4A2 | 1422.0 |
| EIF2B5 | 1193.0 |
| RPL37 | 775.0 |
| EIF3G | 675.0 |
| EIF3I | 488.0 |
| EIF3K | -23.0 |
| RPL3 | -198.0 |
| RPS29 | -668.0 |
| EIF3A | -942.0 |
| EIF2B3 | -1274.0 |
| EIF3D | -1521.0 |
| EIF2B2 | -1728.0 |
| EIF3B | -2568.0 |
| EIF5B | -2738.0 |
| EIF4E | -3260.0 |
| EIF3C | -3429.5 |
| EIF2B4 | -3461.0 |
| EIF4G1 | -3686.0 |
| EIF3L | -4005.0 |
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC)
| 724 | |
|---|---|
| set | Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) |
| setSize | 80 |
| pANOVA | 8.68e-12 |
| s.dist | 0.442 |
| p.adjustANOVA | 5.53e-10 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| PNRC2 | 6454 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RBM8A | 5635 |
| RPL7 | 5591 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RNPS1 | 5168 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| PNRC2 | 6454 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RBM8A | 5635 |
| RPL7 | 5591 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RNPS1 | 5168 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| RPS18 | 5100 |
| RPS20 | 5062 |
| RPS5 | 4999 |
| RPS8 | 4889 |
| SMG1 | 4874 |
| MAGOHB | 4865 |
| RPL11 | 4820 |
| RPL3L | 4800 |
| RPL8 | 4610 |
| RPS13 | 4582 |
| RPL34 | 4469 |
| RPL37A | 4369 |
| RPL30 | 4353 |
| MAGOH | 4333 |
| RPS19 | 4331 |
| PPP2CA | 4328 |
| RPL19 | 4310 |
| RPLP2 | 4122 |
| RPL35A | 4089 |
| RPS6 | 4076 |
| RPL18A | 4046 |
| RPL14 | 3980 |
| UPF2 | 3963 |
| RPS9 | 3818 |
| RPL38 | 3732 |
| SMG5 | 3334 |
| RPS21 | 3125 |
| RPS11 | 3037 |
| RPS16 | 2931 |
| RPL31 | 2728 |
| RPS15 | 2680 |
| RPS14 | 2662 |
| FAU | 2504 |
| UPF3A | 2471 |
| RPL15 | 2190 |
| ETF1 | 2162 |
| RPS26 | 2036 |
| RPS27A | 2027 |
| SMG8 | 2015 |
| GSPT1 | 1864 |
| RPL22 | 1849 |
| RPL28 | 1575 |
| RPL18 | 1455 |
| CASC3 | 1093 |
| PPP2R2A | 872 |
| RPL37 | 775 |
| SMG6 | 536 |
| RPL3 | -198 |
| RPS29 | -668 |
| NCBP1 | -1003 |
| GSPT2 | -1207 |
| UPF3B | -1360 |
| EIF4A3 | -1480 |
| SMG7 | -2289 |
| PPP2R1A | -2809 |
| SMG9 | -3069 |
| UPF1 | -3282 |
| EIF4G1 | -3686 |
| NCBP2 | -4668 |
| DCP1A | -4832 |
Nonsense-Mediated Decay (NMD)
| 726 | |
|---|---|
| set | Nonsense-Mediated Decay (NMD) |
| setSize | 80 |
| pANOVA | 8.68e-12 |
| s.dist | 0.442 |
| p.adjustANOVA | 5.53e-10 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| PNRC2 | 6454 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RBM8A | 5635 |
| RPL7 | 5591 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RNPS1 | 5168 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| GeneID | Gene Rank |
|---|---|
| RPL22L1 | 6577 |
| RPS12 | 6555 |
| RPL10 | 6544 |
| RPS27L | 6535 |
| PNRC2 | 6454 |
| RPS27 | 6213 |
| RPL36A | 6168 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| RPL4 | 5769 |
| RPL5 | 5750 |
| RBM8A | 5635 |
| RPL7 | 5591 |
| RPL32 | 5477 |
| RPL26 | 5321 |
| RPS23 | 5172 |
| RNPS1 | 5168 |
| RPL23 | 5139 |
| RPS3 | 5117 |
| RPS18 | 5100 |
| RPS20 | 5062 |
| RPS5 | 4999 |
| RPS8 | 4889 |
| SMG1 | 4874 |
| MAGOHB | 4865 |
| RPL11 | 4820 |
| RPL3L | 4800 |
| RPL8 | 4610 |
| RPS13 | 4582 |
| RPL34 | 4469 |
| RPL37A | 4369 |
| RPL30 | 4353 |
| MAGOH | 4333 |
| RPS19 | 4331 |
| PPP2CA | 4328 |
| RPL19 | 4310 |
| RPLP2 | 4122 |
| RPL35A | 4089 |
| RPS6 | 4076 |
| RPL18A | 4046 |
| RPL14 | 3980 |
| UPF2 | 3963 |
| RPS9 | 3818 |
| RPL38 | 3732 |
| SMG5 | 3334 |
| RPS21 | 3125 |
| RPS11 | 3037 |
| RPS16 | 2931 |
| RPL31 | 2728 |
| RPS15 | 2680 |
| RPS14 | 2662 |
| FAU | 2504 |
| UPF3A | 2471 |
| RPL15 | 2190 |
| ETF1 | 2162 |
| RPS26 | 2036 |
| RPS27A | 2027 |
| SMG8 | 2015 |
| GSPT1 | 1864 |
| RPL22 | 1849 |
| RPL28 | 1575 |
| RPL18 | 1455 |
| CASC3 | 1093 |
| PPP2R2A | 872 |
| RPL37 | 775 |
| SMG6 | 536 |
| RPL3 | -198 |
| RPS29 | -668 |
| NCBP1 | -1003 |
| GSPT2 | -1207 |
| UPF3B | -1360 |
| EIF4A3 | -1480 |
| SMG7 | -2289 |
| PPP2R1A | -2809 |
| SMG9 | -3069 |
| UPF1 | -3282 |
| EIF4G1 | -3686 |
| NCBP2 | -4668 |
| DCP1A | -4832 |
Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha)
| 643 | |
|---|---|
| set | Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) |
| setSize | 14 |
| pANOVA | 0.00425 |
| s.dist | 0.441 |
| p.adjustANOVA | 0.037 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PCNA | 6290 |
| RPA2 | 6100 |
| LIG1 | 5337 |
| EXO1 | 5265 |
| POLD3 | 4916 |
| MSH2 | 4185 |
| POLD2 | 3621 |
| POLD4 | 2902 |
| RPA1 | 2677 |
| POLD1 | 2021 |
| RPA3 | 1952 |
| PMS2 | 1644 |
| MSH6 | -734 |
| MLH1 | -3389 |
| GeneID | Gene Rank |
|---|---|
| PCNA | 6290 |
| RPA2 | 6100 |
| LIG1 | 5337 |
| EXO1 | 5265 |
| POLD3 | 4916 |
| MSH2 | 4185 |
| POLD2 | 3621 |
| POLD4 | 2902 |
| RPA1 | 2677 |
| POLD1 | 2021 |
| RPA3 | 1952 |
| PMS2 | 1644 |
| MSH6 | -734 |
| MLH1 | -3389 |
PCNA-Dependent Long Patch Base Excision Repair
| 759 | |
|---|---|
| set | PCNA-Dependent Long Patch Base Excision Repair |
| setSize | 21 |
| pANOVA | 0.000476 |
| s.dist | 0.441 |
| p.adjustANOVA | 0.00613 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PCNA | 6290 |
| RPA2 | 6100 |
| POLE | 5575 |
| POLE3 | 5574 |
| RFC2 | 5411 |
| LIG1 | 5337 |
| POLD3 | 4916 |
| POLE4 | 4549 |
| FEN1 | 3622 |
| POLD2 | 3621 |
| RFC5 | 3279 |
| POLD4 | 2902 |
| RPA1 | 2677 |
| POLD1 | 2021 |
| RPA3 | 1952 |
| RFC4 | 1833 |
| RFC1 | 1775 |
| POLE2 | 1625 |
| POLB | -826 |
| RFC3 | -1905 |
| GeneID | Gene Rank |
|---|---|
| PCNA | 6290 |
| RPA2 | 6100 |
| POLE | 5575 |
| POLE3 | 5574 |
| RFC2 | 5411 |
| LIG1 | 5337 |
| POLD3 | 4916 |
| POLE4 | 4549 |
| FEN1 | 3622 |
| POLD2 | 3621 |
| RFC5 | 3279 |
| POLD4 | 2902 |
| RPA1 | 2677 |
| POLD1 | 2021 |
| RPA3 | 1952 |
| RFC4 | 1833 |
| RFC1 | 1775 |
| POLE2 | 1625 |
| POLB | -826 |
| RFC3 | -1905 |
| APEX1 | -2297 |
Formation of the ternary complex, and subsequently, the 43S complex
| 387 | |
|---|---|
| set | Formation of the ternary complex, and subsequently, the 43S complex |
| setSize | 39 |
| pANOVA | 2.34e-06 |
| s.dist | 0.437 |
| p.adjustANOVA | 5.69e-05 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS12 | 6555 |
| RPS27L | 6535 |
| RPS27 | 6213 |
| RPS24 | 6142 |
| RPS15A | 6000 |
| RPS4X | 5880 |
| EIF3E | 5539 |
| RPS23 | 5172 |
| RPS3 | 5117 |
| RPS18 | 5100 |
| RPS20 | 5062 |
| RPS5 | 4999 |
| EIF2S1 | 4996 |
| RPS8 | 4889 |
| RPS13 | 4582 |
| RPS19 | 4331 |
| EIF3M | 4156 |
| RPS6 | 4076 |
| EIF2S2 | 3887 |
| RPS9 | 3818 |
| GeneID | Gene Rank |
|---|---|
| RPS12 | 6555.0 |
| RPS27L | 6535.0 |
| RPS27 | 6213.0 |
| RPS24 | 6142.0 |
| RPS15A | 6000.0 |
| RPS4X | 5880.0 |
| EIF3E | 5539.0 |
| RPS23 | 5172.0 |
| RPS3 | 5117.0 |
| RPS18 | 5100.0 |
| RPS20 | 5062.0 |
| RPS5 | 4999.0 |
| EIF2S1 | 4996.0 |
| RPS8 | 4889.0 |
| RPS13 | 4582.0 |
| RPS19 | 4331.0 |
| EIF3M | 4156.0 |
| RPS6 | 4076.0 |
| EIF2S2 | 3887.0 |
| RPS9 | 3818.0 |
| EIF3H | 3301.0 |
| RPS21 | 3125.0 |
| RPS11 | 3037.0 |
| RPS16 | 2931.0 |
| RPS15 | 2680.0 |
| RPS14 | 2662.0 |
| EIF3F | 2512.0 |
| FAU | 2504.0 |
| RPS26 | 2036.0 |
| RPS27A | 2027.0 |
| EIF3G | 675.0 |
| EIF3I | 488.0 |
| EIF3K | -23.0 |
| RPS29 | -668.0 |
| EIF3A | -942.0 |
| EIF3D | -1521.0 |
| EIF3B | -2568.0 |
| EIF3C | -3429.5 |
| EIF3L | -4005.0 |
Synthesis of PE
| 1147 | |
|---|---|
| set | Synthesis of PE |
| setSize | 11 |
| pANOVA | 0.0131 |
| s.dist | -0.432 |
| p.adjustANOVA | 0.0834 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| LPIN1 | -6414.0 |
| PCYT2 | -6112.0 |
| PHOSPHO1 | -5980.0 |
| LPIN2 | -4562.0 |
| PISD | -4297.0 |
| LPIN3 | -2291.0 |
| ETNK2 | -2088.0 |
| ETNK1 | -1213.0 |
| CHKB | -1185.5 |
| CHKA | -970.0 |
| CEPT1 | 5562.0 |
| GeneID | Gene Rank |
|---|---|
| LPIN1 | -6414.0 |
| PCYT2 | -6112.0 |
| PHOSPHO1 | -5980.0 |
| LPIN2 | -4562.0 |
| PISD | -4297.0 |
| LPIN3 | -2291.0 |
| ETNK2 | -2088.0 |
| ETNK1 | -1213.0 |
| CHKB | -1185.5 |
| CHKA | -970.0 |
| CEPT1 | 5562.0 |
Glycogen storage diseases
| 449 | |
|---|---|
| set | Glycogen storage diseases |
| setSize | 11 |
| pANOVA | 0.0136 |
| s.dist | -0.43 |
| p.adjustANOVA | 0.0854 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| UBC | -6404 |
| GYS1 | -6290 |
| PPP1R3C | -5637 |
| GAA | -5242 |
| G6PC3 | -4922 |
| NHLRC1 | -3330 |
| GBE1 | -2001 |
| EPM2A | -1087 |
| GYG1 | 637 |
| RPS27A | 2027 |
| SLC37A4 | 2876 |
| GeneID | Gene Rank |
|---|---|
| UBC | -6404 |
| GYS1 | -6290 |
| PPP1R3C | -5637 |
| GAA | -5242 |
| G6PC3 | -4922 |
| NHLRC1 | -3330 |
| GBE1 | -2001 |
| EPM2A | -1087 |
| GYG1 | 637 |
| RPS27A | 2027 |
| SLC37A4 | 2876 |
Interleukin-12 signaling
| 540 | |
|---|---|
| set | Interleukin-12 signaling |
| setSize | 35 |
| pANOVA | 1.31e-05 |
| s.dist | 0.426 |
| p.adjustANOVA | 0.000279 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RAP1B | 6480.0 |
| VAMP7 | 6230.0 |
| PPIA | 6072.0 |
| GSTA2 | 5867.5 |
| PDCD4 | 5835.0 |
| CDC42 | 5339.0 |
| SNRPA1 | 5209.0 |
| ANXA2 | 5133.0 |
| LCP1 | 5065.0 |
| PITPNA | 4954.0 |
| HNRNPF | 4847.0 |
| HSPA9 | 4673.0 |
| STAT4 | 4147.0 |
| PAK2 | 3941.0 |
| TCP1 | 3864.0 |
| HNRNPA2B1 | 3762.0 |
| PSME2 | 3632.0 |
| JAK2 | 3607.0 |
| MSN | 3127.0 |
| LMNB1 | 3110.0 |
| GeneID | Gene Rank |
|---|---|
| RAP1B | 6480.0 |
| VAMP7 | 6230.0 |
| PPIA | 6072.0 |
| GSTA2 | 5867.5 |
| PDCD4 | 5835.0 |
| CDC42 | 5339.0 |
| SNRPA1 | 5209.0 |
| ANXA2 | 5133.0 |
| LCP1 | 5065.0 |
| PITPNA | 4954.0 |
| HNRNPF | 4847.0 |
| HSPA9 | 4673.0 |
| STAT4 | 4147.0 |
| PAK2 | 3941.0 |
| TCP1 | 3864.0 |
| HNRNPA2B1 | 3762.0 |
| PSME2 | 3632.0 |
| JAK2 | 3607.0 |
| MSN | 3127.0 |
| LMNB1 | 3110.0 |
| CFL1 | 2998.0 |
| RALA | 2628.0 |
| TYK2 | 2564.0 |
| SOD1 | 2540.0 |
| MTAP | 2054.5 |
| JAK1 | 1996.0 |
| BOLA2 | 929.5 |
| P4HB | 882.0 |
| ARF1 | 843.0 |
| AIP | 732.0 |
| MIF | 561.0 |
| CNN2 | -799.0 |
| TALDO1 | -1596.0 |
| SOD2 | -2765.0 |
| GSTO1 | -5235.0 |
Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation
| 430 | |
|---|---|
| set | Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation |
| setSize | 30 |
| pANOVA | 6.11e-05 |
| s.dist | 0.423 |
| p.adjustANOVA | 0.00109 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RAP1B | 6480.0 |
| PPIA | 6072.0 |
| GSTA2 | 5867.5 |
| PDCD4 | 5835.0 |
| CDC42 | 5339.0 |
| SNRPA1 | 5209.0 |
| ANXA2 | 5133.0 |
| LCP1 | 5065.0 |
| PITPNA | 4954.0 |
| HNRNPF | 4847.0 |
| HSPA9 | 4673.0 |
| STAT4 | 4147.0 |
| PAK2 | 3941.0 |
| TCP1 | 3864.0 |
| HNRNPA2B1 | 3762.0 |
| PSME2 | 3632.0 |
| MSN | 3127.0 |
| LMNB1 | 3110.0 |
| CFL1 | 2998.0 |
| RALA | 2628.0 |
| GeneID | Gene Rank |
|---|---|
| RAP1B | 6480.0 |
| PPIA | 6072.0 |
| GSTA2 | 5867.5 |
| PDCD4 | 5835.0 |
| CDC42 | 5339.0 |
| SNRPA1 | 5209.0 |
| ANXA2 | 5133.0 |
| LCP1 | 5065.0 |
| PITPNA | 4954.0 |
| HNRNPF | 4847.0 |
| HSPA9 | 4673.0 |
| STAT4 | 4147.0 |
| PAK2 | 3941.0 |
| TCP1 | 3864.0 |
| HNRNPA2B1 | 3762.0 |
| PSME2 | 3632.0 |
| MSN | 3127.0 |
| LMNB1 | 3110.0 |
| CFL1 | 2998.0 |
| RALA | 2628.0 |
| SOD1 | 2540.0 |
| MTAP | 2054.5 |
| BOLA2 | 929.5 |
| ARF1 | 843.0 |
| AIP | 732.0 |
| MIF | 561.0 |
| CNN2 | -799.0 |
| TALDO1 | -1596.0 |
| SOD2 | -2765.0 |
| GSTO1 | -5235.0 |
NCAM1 interactions
| 677 | |
|---|---|
| set | NCAM1 interactions |
| setSize | 29 |
| pANOVA | 9.65e-05 |
| s.dist | -0.418 |
| p.adjustANOVA | 0.00154 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PRNP | -6350 |
| COL4A2 | -6166 |
| COL4A1 | -6153 |
| COL4A3 | -6151 |
| COL4A4 | -5975 |
| CACNB1 | -5659 |
| COL6A3 | -5552 |
| CACNA1H | -5403 |
| CACNA1D | -5368 |
| COL6A6 | -5131 |
| COL6A2 | -4669 |
| CACNA1C | -4631 |
| NRTN | -4489 |
| COL4A5 | -4162 |
| COL6A1 | -3959 |
| CACNA1S | -3639 |
| CNTN2 | -3016 |
| GFRA4 | -1418 |
| CACNB4 | -1238 |
| GFRA1 | -1121 |
| GeneID | Gene Rank |
|---|---|
| PRNP | -6350 |
| COL4A2 | -6166 |
| COL4A1 | -6153 |
| COL4A3 | -6151 |
| COL4A4 | -5975 |
| CACNB1 | -5659 |
| COL6A3 | -5552 |
| CACNA1H | -5403 |
| CACNA1D | -5368 |
| COL6A6 | -5131 |
| COL6A2 | -4669 |
| CACNA1C | -4631 |
| NRTN | -4489 |
| COL4A5 | -4162 |
| COL6A1 | -3959 |
| CACNA1S | -3639 |
| CNTN2 | -3016 |
| GFRA4 | -1418 |
| CACNB4 | -1238 |
| GFRA1 | -1121 |
| AGRN | -1106 |
| CACNB3 | -82 |
| CACNA1G | 316 |
| ST8SIA2 | 1001 |
| NCAM1 | 1697 |
| NCAN | 1786 |
| ST8SIA4 | 2324 |
| GFRA2 | 2522 |
| CACNB2 | 6616 |
Here is the session info with all the versions of packages used.
sessionInfo()
## R version 4.0.2 (2020-06-22)
## Platform: x86_64-pc-linux-gnu (64-bit)
## Running under: Ubuntu 18.04.4 LTS
##
## Matrix products: default
## BLAS: /usr/lib/x86_64-linux-gnu/blas/libblas.so.3.7.1
## LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.7.1
##
## locale:
## [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
## [3] LC_TIME=en_US.UTF-8 LC_COLLATE=en_US.UTF-8
## [5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
## [7] LC_PAPER=en_US.UTF-8 LC_NAME=C
## [9] LC_ADDRESS=C LC_TELEPHONE=C
## [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
##
## attached base packages:
## [1] stats4 parallel stats graphics grDevices utils datasets
## [8] methods base
##
## other attached packages:
## [1] pkgload_1.1.0 GGally_2.0.0
## [3] beeswarm_0.2.3 gtools_3.8.2
## [5] echarts4r_0.3.2 mitch_1.0.6
## [7] fgsea_1.14.0 gplots_3.0.3
## [9] DESeq2_1.28.1 SummarizedExperiment_1.18.1
## [11] DelayedArray_0.14.0 matrixStats_0.56.0
## [13] Biobase_2.48.0 GenomicRanges_1.40.0
## [15] GenomeInfoDb_1.24.2 IRanges_2.22.2
## [17] S4Vectors_0.26.1 BiocGenerics_0.34.0
## [19] reshape2_1.4.4 forcats_0.5.0
## [21] stringr_1.4.0 dplyr_1.0.0
## [23] purrr_0.3.4 readr_1.3.1
## [25] tidyr_1.1.0 tibble_3.0.1
## [27] ggplot2_3.3.2 tidyverse_1.3.0
## [29] locfit_1.5-9.4 statmod_1.4.34
## [31] plyr_1.8.6
##
## loaded via a namespace (and not attached):
## [1] colorspace_1.4-1 ellipsis_0.3.1 rprojroot_1.3-2
## [4] XVector_0.28.0 fs_1.4.2 rstudioapi_0.11
## [7] bit64_0.9-7 AnnotationDbi_1.50.1 fansi_0.4.1
## [10] lubridate_1.7.9 xml2_1.3.2 splines_4.0.2
## [13] geneplotter_1.66.0 knitr_1.29 jsonlite_1.7.0
## [16] broom_0.5.6 annotate_1.66.0 dbplyr_1.4.4
## [19] shiny_1.5.0 compiler_4.0.2 httr_1.4.1
## [22] backports_1.1.8 assertthat_0.2.1 Matrix_1.2-18
## [25] fastmap_1.0.1 cli_2.0.2 later_1.1.0.1
## [28] htmltools_0.5.0 tools_4.0.2 gtable_0.3.0
## [31] glue_1.4.1 GenomeInfoDbData_1.2.3 fastmatch_1.1-0
## [34] Rcpp_1.0.4.6 cellranger_1.1.0 vctrs_0.3.1
## [37] gdata_2.18.0 nlme_3.1-148 xfun_0.15
## [40] testthat_2.3.2 rvest_0.3.5 mime_0.9
## [43] lifecycle_0.2.0 XML_3.99-0.3 zlibbioc_1.34.0
## [46] MASS_7.3-51.6 scales_1.1.1 hms_0.5.3
## [49] promises_1.1.1 RColorBrewer_1.1-2 yaml_2.2.1
## [52] memoise_1.1.0 gridExtra_2.3 reshape_0.8.8
## [55] stringi_1.4.6 RSQLite_2.2.0 highr_0.8
## [58] genefilter_1.70.0 desc_1.2.0 caTools_1.18.0
## [61] BiocParallel_1.22.0 rlang_0.4.6 pkgconfig_2.0.3
## [64] bitops_1.0-6 evaluate_0.14 lattice_0.20-41
## [67] htmlwidgets_1.5.1 bit_1.1-15.2 tidyselect_1.1.0
## [70] magrittr_1.5 R6_2.4.1 generics_0.0.2
## [73] DBI_1.1.0 pillar_1.4.4 haven_2.3.1
## [76] withr_2.2.0 survival_3.2-3 RCurl_1.98-1.2
## [79] modelr_0.1.8 crayon_1.3.4 KernSmooth_2.23-17
## [82] rmarkdown_2.3 grid_4.0.2 readxl_1.3.1
## [85] data.table_1.12.8 blob_1.2.1 reprex_0.3.0
## [88] digest_0.6.25 pbmcapply_1.5.0 xtable_1.8-4
## [91] httpuv_1.5.4 munsell_0.5.0
END of report