date generated: 2022-05-18
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.
## metric
## TSC22D1 -9.436620
## EHMT2 -10.903254
## ZNRD1 -6.147915
## NCRNA00171 -6.147915
## RGL2 -5.215929
## CFLAR -7.577876
Here are some metrics about the input data profile:
| Profile metrics | |
|---|---|
| num_genesets | 2546 |
| num_genes_in_profile | 12012 |
| duplicated_genes_present | 0 |
| num_profile_genes_in_sets | 5835 |
| num_profile_genes_not_in_sets | 6177 |
Here is a plot of the input profiles. Note the dynamic ranges.
Here is the contour plot of the profile including all detected genes.
| Gene sets metrics | |
|---|---|
| num_genesets | 2546 |
| num_genesets_excluded | 1344 |
| num_genesets_included | 1202 |
Significance is calculated by -log10(p-value). All points shown are FDR<0.05.
Significance is calculated by -log10(p-value). Top N sets shown irrespective of FDR.
| set | setSize | pANOVA | s.dist | p.adjustANOVA |
|---|---|---|---|---|
| Condensation of Prometaphase Chromosomes | 10 | 2.89e-03 | -0.544 | 0.02100 |
| HDR through MMEJ (alt-NHEJ) | 11 | 2.04e-03 | -0.537 | 0.01810 |
| NOTCH2 Activation and Transmission of Signal to the Nucleus | 12 | 1.40e-03 | -0.532 | 0.01400 |
| p75NTR signals via NF-kB | 11 | 3.89e-03 | -0.502 | 0.02580 |
| VLDLR internalisation and degradation | 11 | 5.70e-03 | -0.481 | 0.03370 |
| SARS-CoV-2 modulates autophagy | 11 | 6.55e-03 | -0.473 | 0.03630 |
| RHO GTPases Activate ROCKs | 13 | 4.08e-03 | -0.460 | 0.02670 |
| RIPK1-mediated regulated necrosis | 25 | 8.38e-05 | -0.454 | 0.00198 |
| Regulation of necroptotic cell death | 25 | 8.38e-05 | -0.454 | 0.00198 |
| Voltage gated Potassium channels | 13 | 5.90e-03 | 0.441 | 0.03460 |
| Negative regulation of FLT3 | 13 | 6.51e-03 | -0.436 | 0.03630 |
| Signaling by NOTCH2 | 18 | 1.44e-03 | -0.433 | 0.01400 |
| Meiotic recombination | 19 | 1.12e-03 | -0.432 | 0.01210 |
| Caspase activation via Death Receptors in the presence of ligand | 10 | 1.81e-02 | -0.431 | 0.07400 |
| Glyoxylate metabolism and glycine degradation | 19 | 1.39e-03 | -0.423 | 0.01400 |
| NOTCH3 Activation and Transmission of Signal to the Nucleus | 15 | 5.19e-03 | -0.417 | 0.03150 |
| CTNNB1 S33 mutants aren’t phosphorylated | 13 | 1.03e-02 | -0.411 | 0.04930 |
| CTNNB1 S37 mutants aren’t phosphorylated | 13 | 1.03e-02 | -0.411 | 0.04930 |
| CTNNB1 S45 mutants aren’t phosphorylated | 13 | 1.03e-02 | -0.411 | 0.04930 |
| CTNNB1 T41 mutants aren’t phosphorylated | 13 | 1.03e-02 | -0.411 | 0.04930 |
| Signaling by CTNNB1 phospho-site mutants | 13 | 1.03e-02 | -0.411 | 0.04930 |
| Signaling by GSK3beta mutants | 13 | 1.03e-02 | -0.411 | 0.04930 |
| Golgi Cisternae Pericentriolar Stack Reorganization | 14 | 7.95e-03 | -0.410 | 0.04170 |
| Defects in vitamin and cofactor metabolism | 16 | 5.94e-03 | -0.397 | 0.03460 |
| APC truncation mutants have impaired AXIN binding | 12 | 2.09e-02 | -0.385 | 0.08090 |
| AXIN missense mutants destabilize the destruction complex | 12 | 2.09e-02 | -0.385 | 0.08090 |
| Signaling by AMER1 mutants | 12 | 2.09e-02 | -0.385 | 0.08090 |
| Signaling by APC mutants | 12 | 2.09e-02 | -0.385 | 0.08090 |
| Signaling by AXIN mutants | 12 | 2.09e-02 | -0.385 | 0.08090 |
| Truncations of AMER1 destabilize the destruction complex | 12 | 2.09e-02 | -0.385 | 0.08090 |
| NRIF signals cell death from the nucleus | 14 | 1.28e-02 | -0.384 | 0.05800 |
| Glycogen storage diseases | 10 | 3.64e-02 | -0.382 | 0.12400 |
| SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 27 | 6.33e-04 | -0.380 | 0.00746 |
| Gap-filling DNA repair synthesis and ligation in GG-NER | 23 | 1.65e-03 | -0.379 | 0.01540 |
| Translesion synthesis by POLK | 15 | 1.20e-02 | -0.374 | 0.05550 |
| Impaired BRCA2 binding to RAD51 | 32 | 2.65e-04 | -0.372 | 0.00426 |
| HDR through Single Strand Annealing (SSA) | 35 | 2.48e-04 | -0.358 | 0.00420 |
| Beta-catenin phosphorylation cascade | 15 | 1.66e-02 | -0.357 | 0.06940 |
| Cobalamin (Cbl, vitamin B12) transport and metabolism | 11 | 4.13e-02 | -0.355 | 0.13500 |
| mRNA decay by 3’ to 5’ exoribonuclease | 14 | 2.20e-02 | -0.353 | 0.08410 |
| Glycogen synthesis | 11 | 4.25e-02 | -0.353 | 0.13700 |
| APC/C:Cdc20 mediated degradation of Cyclin B | 22 | 4.81e-03 | -0.347 | 0.02990 |
| Chaperone Mediated Autophagy | 12 | 3.83e-02 | -0.345 | 0.12800 |
| Translation of Structural Proteins | 27 | 1.93e-03 | -0.345 | 0.01740 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 14 | 2.57e-02 | -0.344 | 0.09420 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | 14 | 2.57e-02 | -0.344 | 0.09420 |
| Spry regulation of FGF signaling | 15 | 2.17e-02 | -0.342 | 0.08350 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | 18 | 1.24e-02 | -0.340 | 0.05650 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 15 | 2.28e-02 | -0.339 | 0.08690 |
| Defective homologous recombination repair (HRR) due to BRCA2 loss of function | 37 | 3.52e-04 | -0.339 | 0.00492 |
| set | setSize | pANOVA | s.dist | p.adjustANOVA |
|---|---|---|---|---|
| Condensation of Prometaphase Chromosomes | 10 | 2.89e-03 | -5.44e-01 | 2.10e-02 |
| HDR through MMEJ (alt-NHEJ) | 11 | 2.04e-03 | -5.37e-01 | 1.81e-02 |
| NOTCH2 Activation and Transmission of Signal to the Nucleus | 12 | 1.40e-03 | -5.32e-01 | 1.40e-02 |
| p75NTR signals via NF-kB | 11 | 3.89e-03 | -5.02e-01 | 2.58e-02 |
| VLDLR internalisation and degradation | 11 | 5.70e-03 | -4.81e-01 | 3.37e-02 |
| SARS-CoV-2 modulates autophagy | 11 | 6.55e-03 | -4.73e-01 | 3.63e-02 |
| RHO GTPases Activate ROCKs | 13 | 4.08e-03 | -4.60e-01 | 2.67e-02 |
| RIPK1-mediated regulated necrosis | 25 | 8.38e-05 | -4.54e-01 | 1.98e-03 |
| Regulation of necroptotic cell death | 25 | 8.38e-05 | -4.54e-01 | 1.98e-03 |
| Voltage gated Potassium channels | 13 | 5.90e-03 | 4.41e-01 | 3.46e-02 |
| Negative regulation of FLT3 | 13 | 6.51e-03 | -4.36e-01 | 3.63e-02 |
| Signaling by NOTCH2 | 18 | 1.44e-03 | -4.33e-01 | 1.40e-02 |
| Meiotic recombination | 19 | 1.12e-03 | -4.32e-01 | 1.21e-02 |
| Caspase activation via Death Receptors in the presence of ligand | 10 | 1.81e-02 | -4.31e-01 | 7.40e-02 |
| Glyoxylate metabolism and glycine degradation | 19 | 1.39e-03 | -4.23e-01 | 1.40e-02 |
| NOTCH3 Activation and Transmission of Signal to the Nucleus | 15 | 5.19e-03 | -4.17e-01 | 3.15e-02 |
| CTNNB1 S33 mutants aren’t phosphorylated | 13 | 1.03e-02 | -4.11e-01 | 4.93e-02 |
| CTNNB1 S37 mutants aren’t phosphorylated | 13 | 1.03e-02 | -4.11e-01 | 4.93e-02 |
| CTNNB1 S45 mutants aren’t phosphorylated | 13 | 1.03e-02 | -4.11e-01 | 4.93e-02 |
| CTNNB1 T41 mutants aren’t phosphorylated | 13 | 1.03e-02 | -4.11e-01 | 4.93e-02 |
| Signaling by CTNNB1 phospho-site mutants | 13 | 1.03e-02 | -4.11e-01 | 4.93e-02 |
| Signaling by GSK3beta mutants | 13 | 1.03e-02 | -4.11e-01 | 4.93e-02 |
| Golgi Cisternae Pericentriolar Stack Reorganization | 14 | 7.95e-03 | -4.10e-01 | 4.17e-02 |
| Defects in vitamin and cofactor metabolism | 16 | 5.94e-03 | -3.97e-01 | 3.46e-02 |
| APC truncation mutants have impaired AXIN binding | 12 | 2.09e-02 | -3.85e-01 | 8.09e-02 |
| AXIN missense mutants destabilize the destruction complex | 12 | 2.09e-02 | -3.85e-01 | 8.09e-02 |
| Signaling by AMER1 mutants | 12 | 2.09e-02 | -3.85e-01 | 8.09e-02 |
| Signaling by APC mutants | 12 | 2.09e-02 | -3.85e-01 | 8.09e-02 |
| Signaling by AXIN mutants | 12 | 2.09e-02 | -3.85e-01 | 8.09e-02 |
| Truncations of AMER1 destabilize the destruction complex | 12 | 2.09e-02 | -3.85e-01 | 8.09e-02 |
| NRIF signals cell death from the nucleus | 14 | 1.28e-02 | -3.84e-01 | 5.80e-02 |
| Glycogen storage diseases | 10 | 3.64e-02 | -3.82e-01 | 1.24e-01 |
| SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 27 | 6.33e-04 | -3.80e-01 | 7.46e-03 |
| Gap-filling DNA repair synthesis and ligation in GG-NER | 23 | 1.65e-03 | -3.79e-01 | 1.54e-02 |
| Translesion synthesis by POLK | 15 | 1.20e-02 | -3.74e-01 | 5.55e-02 |
| Impaired BRCA2 binding to RAD51 | 32 | 2.65e-04 | -3.72e-01 | 4.26e-03 |
| HDR through Single Strand Annealing (SSA) | 35 | 2.48e-04 | -3.58e-01 | 4.20e-03 |
| Beta-catenin phosphorylation cascade | 15 | 1.66e-02 | -3.57e-01 | 6.94e-02 |
| Cobalamin (Cbl, vitamin B12) transport and metabolism | 11 | 4.13e-02 | -3.55e-01 | 1.35e-01 |
| mRNA decay by 3’ to 5’ exoribonuclease | 14 | 2.20e-02 | -3.53e-01 | 8.41e-02 |
| Glycogen synthesis | 11 | 4.25e-02 | -3.53e-01 | 1.37e-01 |
| APC/C:Cdc20 mediated degradation of Cyclin B | 22 | 4.81e-03 | -3.47e-01 | 2.99e-02 |
| Chaperone Mediated Autophagy | 12 | 3.83e-02 | -3.45e-01 | 1.28e-01 |
| Translation of Structural Proteins | 27 | 1.93e-03 | -3.45e-01 | 1.74e-02 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 14 | 2.57e-02 | -3.44e-01 | 9.42e-02 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | 14 | 2.57e-02 | -3.44e-01 | 9.42e-02 |
| Spry regulation of FGF signaling | 15 | 2.17e-02 | -3.42e-01 | 8.35e-02 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | 18 | 1.24e-02 | -3.40e-01 | 5.65e-02 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 15 | 2.28e-02 | -3.39e-01 | 8.69e-02 |
| Defective homologous recombination repair (HRR) due to BRCA2 loss of function | 37 | 3.52e-04 | -3.39e-01 | 4.92e-03 |
| Diseases of DNA Double-Strand Break Repair | 37 | 3.52e-04 | -3.39e-01 | 4.92e-03 |
| NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 11 | 5.19e-02 | -3.38e-01 | 1.58e-01 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | 64 | 2.87e-06 | -3.38e-01 | 1.64e-04 |
| Amyloid fiber formation | 27 | 2.34e-03 | -3.38e-01 | 2.00e-02 |
| Presynaptic phase of homologous DNA pairing and strand exchange | 36 | 4.82e-04 | -3.36e-01 | 5.97e-03 |
| Sema4D induced cell migration and growth-cone collapse | 12 | 4.39e-02 | -3.36e-01 | 1.39e-01 |
| Resolution of AP sites via the multiple-nucleotide patch replacement pathway | 20 | 9.56e-03 | -3.35e-01 | 4.81e-02 |
| Translesion Synthesis by POLH | 17 | 1.76e-02 | -3.32e-01 | 7.24e-02 |
| Translesion synthesis by REV1 | 14 | 3.18e-02 | -3.31e-01 | 1.11e-01 |
| Homologous DNA Pairing and Strand Exchange | 39 | 3.45e-04 | -3.31e-01 | 4.92e-03 |
| Mucopolysaccharidoses | 10 | 6.98e-02 | 3.31e-01 | 1.92e-01 |
| Meiosis | 42 | 2.34e-04 | -3.28e-01 | 4.01e-03 |
| EGFR downregulation | 20 | 1.18e-02 | -3.25e-01 | 5.51e-02 |
| Class I peroxisomal membrane protein import | 19 | 1.49e-02 | -3.23e-01 | 6.46e-02 |
| Autodegradation of Cdh1 by Cdh1:APC/C | 56 | 3.75e-05 | -3.18e-01 | 1.45e-03 |
| GAB1 signalosome | 10 | 8.11e-02 | 3.18e-01 | 2.12e-01 |
| Ubiquitin Mediated Degradation of Phosphorylated Cdc25A | 44 | 2.70e-04 | -3.17e-01 | 4.26e-03 |
| p53-Independent DNA Damage Response | 44 | 2.70e-04 | -3.17e-01 | 4.26e-03 |
| p53-Independent G1/S DNA damage checkpoint | 44 | 2.70e-04 | -3.17e-01 | 4.26e-03 |
| Erythropoietin activates RAS | 10 | 8.31e-02 | -3.16e-01 | 2.15e-01 |
| Recognition of DNA damage by PCNA-containing replication complex | 26 | 5.32e-03 | -3.16e-01 | 3.21e-02 |
| Diseases of mitotic cell cycle | 34 | 1.48e-03 | -3.15e-01 | 1.42e-02 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | 52 | 8.64e-05 | -3.15e-01 | 2.00e-03 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | 18 | 2.12e-02 | -3.14e-01 | 8.17e-02 |
| Assembly of collagen fibrils and other multimeric structures | 14 | 4.23e-02 | 3.13e-01 | 1.37e-01 |
| Pexophagy | 11 | 7.22e-02 | -3.13e-01 | 1.97e-01 |
| APC-Cdc20 mediated degradation of Nek2A | 24 | 8.17e-03 | -3.12e-01 | 4.22e-02 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | 42 | 4.90e-04 | -3.11e-01 | 6.01e-03 |
| Processing of DNA double-strand break ends | 55 | 6.69e-05 | -3.11e-01 | 1.87e-03 |
| APC/C:Cdc20 mediated degradation of Securin | 58 | 4.68e-05 | -3.09e-01 | 1.52e-03 |
| Ubiquitin-dependent degradation of Cyclin D | 44 | 3.94e-04 | -3.09e-01 | 5.26e-03 |
| PCNA-Dependent Long Patch Base Excision Repair | 18 | 2.36e-02 | -3.08e-01 | 8.89e-02 |
| Striated Muscle Contraction | 10 | 9.24e-02 | -3.07e-01 | 2.34e-01 |
| Apoptotic cleavage of cellular proteins | 25 | 7.84e-03 | -3.07e-01 | 4.15e-02 |
| Autodegradation of the E3 ubiquitin ligase COP1 | 44 | 4.31e-04 | -3.07e-01 | 5.49e-03 |
| G2/M DNA damage checkpoint | 54 | 1.11e-04 | -3.04e-01 | 2.24e-03 |
| Initiation of Nuclear Envelope (NE) Reformation | 17 | 3.02e-02 | -3.04e-01 | 1.07e-01 |
| SCF(Skp2)-mediated degradation of p27/p21 | 52 | 1.66e-04 | -3.02e-01 | 2.98e-03 |
| JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 | 12 | 7.03e-02 | 3.02e-01 | 1.93e-01 |
| SUMOylation of transcription factors | 13 | 6.07e-02 | -3.00e-01 | 1.77e-01 |
| Frs2-mediated activation | 11 | 8.50e-02 | -3.00e-01 | 2.19e-01 |
| Cyclin A/B1/B2 associated events during G2/M transition | 22 | 1.50e-02 | -2.99e-01 | 6.51e-02 |
| Regulation of TP53 Expression and Degradation | 34 | 2.56e-03 | -2.99e-01 | 2.06e-02 |
| Stabilization of p53 | 49 | 2.99e-04 | -2.99e-01 | 4.55e-03 |
| STING mediated induction of host immune responses | 10 | 1.03e-01 | 2.98e-01 | 2.54e-01 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 66 | 3.19e-05 | -2.96e-01 | 1.28e-03 |
| Translesion synthesis by POLI | 15 | 4.73e-02 | -2.96e-01 | 1.47e-01 |
| Regulation of TP53 Activity through Phosphorylation | 79 | 5.61e-06 | -2.96e-01 | 2.70e-04 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | 33 | 3.30e-03 | -2.95e-01 | 2.29e-02 |
| Cyclin D associated events in G1 | 41 | 1.07e-03 | -2.95e-01 | 1.17e-02 |
| G1 Phase | 41 | 1.07e-03 | -2.95e-01 | 1.17e-02 |
| RHO GTPases Activate WASPs and WAVEs | 29 | 6.05e-03 | -2.94e-01 | 3.48e-02 |
| Phosphorylation of the APC/C | 18 | 3.06e-02 | -2.94e-01 | 1.08e-01 |
| TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain | 18 | 3.07e-02 | -2.94e-01 | 1.08e-01 |
| G1/S DNA Damage Checkpoints | 58 | 1.10e-04 | -2.94e-01 | 2.24e-03 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | 35 | 2.65e-03 | -2.93e-01 | 2.06e-02 |
| DNA Double Strand Break Response | 36 | 2.42e-03 | -2.92e-01 | 2.03e-02 |
| CDK-mediated phosphorylation and removal of Cdc6 | 62 | 7.12e-05 | -2.92e-01 | 1.87e-03 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | 65 | 4.83e-05 | -2.92e-01 | 1.53e-03 |
| RUNX3 regulates p14-ARF | 10 | 1.10e-01 | -2.91e-01 | 2.67e-01 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | 63 | 6.40e-05 | -2.91e-01 | 1.87e-03 |
| p53-Dependent G1 DNA Damage Response | 56 | 1.65e-04 | -2.91e-01 | 2.98e-03 |
| p53-Dependent G1/S DNA damage checkpoint | 56 | 1.65e-04 | -2.91e-01 | 2.98e-03 |
| HDR through Homologous Recombination (HRR) | 60 | 9.83e-05 | -2.91e-01 | 2.15e-03 |
| Regulation of TP53 Degradation | 33 | 3.99e-03 | -2.90e-01 | 2.62e-02 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 19 | 3.03e-02 | -2.87e-01 | 1.07e-01 |
| Base Excision Repair | 38 | 2.23e-03 | -2.87e-01 | 1.91e-02 |
| PKA activation | 10 | 1.17e-01 | 2.87e-01 | 2.80e-01 |
| APC/C-mediated degradation of cell cycle proteins | 77 | 1.41e-05 | -2.86e-01 | 6.03e-04 |
| Regulation of mitotic cell cycle | 77 | 1.41e-05 | -2.86e-01 | 6.03e-04 |
| Zinc transporters | 12 | 8.60e-02 | -2.86e-01 | 2.20e-01 |
| RHO GTPases activate PAKs | 13 | 7.45e-02 | -2.86e-01 | 2.00e-01 |
| Resolution of Abasic Sites (AP sites) | 31 | 5.97e-03 | -2.85e-01 | 3.46e-02 |
| Signaling by NOTCH3 | 30 | 7.03e-03 | -2.84e-01 | 3.86e-02 |
| Miscellaneous transport and binding events | 14 | 6.59e-02 | -2.84e-01 | 1.86e-01 |
| SRP-dependent cotranslational protein targeting to membrane | 88 | 4.28e-06 | -2.84e-01 | 2.34e-04 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | 62 | 1.17e-04 | -2.83e-01 | 2.31e-03 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | 15 | 5.95e-02 | -2.81e-01 | 1.75e-01 |
| Signaling by FGFR3 | 26 | 1.37e-02 | -2.79e-01 | 6.12e-02 |
| Homology Directed Repair | 90 | 5.02e-06 | -2.79e-01 | 2.62e-04 |
| Caspase activation via extrinsic apoptotic signalling pathway | 15 | 6.20e-02 | -2.78e-01 | 1.80e-01 |
| Apoptotic factor-mediated response | 16 | 5.44e-02 | -2.78e-01 | 1.63e-01 |
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | 46 | 1.19e-03 | -2.76e-01 | 1.27e-02 |
| HDMs demethylate histones | 15 | 6.65e-02 | -2.74e-01 | 1.87e-01 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | 57 | 3.63e-04 | -2.73e-01 | 5.01e-03 |
| Cyclin A:Cdk2-associated events at S phase entry | 74 | 5.26e-05 | -2.72e-01 | 1.62e-03 |
| Regulation of PTEN stability and activity | 56 | 4.38e-04 | -2.72e-01 | 5.49e-03 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | 16 | 6.08e-02 | -2.71e-01 | 1.77e-01 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | 16 | 6.08e-02 | -2.71e-01 | 1.77e-01 |
| SCF-beta-TrCP mediated degradation of Emi1 | 47 | 1.37e-03 | -2.70e-01 | 1.40e-02 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | 46 | 1.54e-03 | -2.70e-01 | 1.46e-02 |
| Prefoldin mediated transfer of substrate to CCT/TriC | 17 | 5.43e-02 | -2.69e-01 | 1.63e-01 |
| DNA Damage Recognition in GG-NER | 35 | 5.90e-03 | -2.69e-01 | 3.46e-02 |
| Fanconi Anemia Pathway | 31 | 9.90e-03 | -2.68e-01 | 4.92e-02 |
| Degradation of DVL | 48 | 1.36e-03 | -2.67e-01 | 1.40e-02 |
| Apoptotic execution phase | 33 | 8.08e-03 | -2.66e-01 | 4.20e-02 |
| Senescence-Associated Secretory Phenotype (SASP) | 42 | 2.83e-03 | -2.66e-01 | 2.10e-02 |
| Endosomal/Vacuolar pathway | 10 | 1.46e-01 | 2.65e-01 | 3.32e-01 |
| Hh mutants are degraded by ERAD | 47 | 1.65e-03 | -2.65e-01 | 1.54e-02 |
| Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 39 | 4.19e-03 | -2.65e-01 | 2.69e-02 |
| Regulated Necrosis | 43 | 2.66e-03 | -2.65e-01 | 2.06e-02 |
| Regulation of Apoptosis | 45 | 2.15e-03 | -2.64e-01 | 1.87e-02 |
| RNA Polymerase I Transcription Initiation | 40 | 3.87e-03 | -2.64e-01 | 2.58e-02 |
| Cross-presentation of soluble exogenous antigens (endosomes) | 38 | 4.88e-03 | -2.64e-01 | 2.99e-02 |
| Signaling by EGFR in Cancer | 16 | 6.79e-02 | -2.64e-01 | 1.89e-01 |
| Activation of ATR in response to replication stress | 36 | 6.43e-03 | -2.62e-01 | 3.63e-02 |
| Removal of the Flap Intermediate from the C-strand | 15 | 7.92e-02 | -2.62e-01 | 2.09e-01 |
| Gap junction trafficking and regulation | 11 | 1.33e-01 | 2.62e-01 | 3.08e-01 |
| Cyclin E associated events during G1/S transition | 72 | 1.31e-04 | -2.61e-01 | 2.49e-03 |
| SARS-CoV-1 Infection | 46 | 2.23e-03 | -2.61e-01 | 1.91e-02 |
| IKK complex recruitment mediated by RIP1 | 17 | 6.27e-02 | -2.61e-01 | 1.80e-01 |
| Elevation of cytosolic Ca2+ levels | 10 | 1.56e-01 | 2.59e-01 | 3.43e-01 |
| Vpu mediated degradation of CD4 | 44 | 2.94e-03 | -2.59e-01 | 2.10e-02 |
| RNA Polymerase I Promoter Clearance | 44 | 2.94e-03 | -2.59e-01 | 2.10e-02 |
| RNA Polymerase I Transcription | 44 | 2.94e-03 | -2.59e-01 | 2.10e-02 |
| mRNA decay by 5’ to 3’ exoribonuclease | 15 | 8.22e-02 | -2.59e-01 | 2.14e-01 |
| Reproduction | 48 | 1.90e-03 | -2.59e-01 | 1.74e-02 |
| SUMOylation of immune response proteins | 10 | 1.56e-01 | -2.59e-01 | 3.43e-01 |
| Regulation of ornithine decarboxylase (ODC) | 43 | 3.31e-03 | -2.59e-01 | 2.29e-02 |
| Degradation of AXIN | 47 | 2.15e-03 | -2.59e-01 | 1.87e-02 |
| Regulation of RAS by GAPs | 56 | 8.16e-04 | -2.59e-01 | 9.26e-03 |
| FLT3 signaling in disease | 24 | 2.88e-02 | -2.58e-01 | 1.03e-01 |
| BBSome-mediated cargo-targeting to cilium | 19 | 5.17e-02 | -2.58e-01 | 1.58e-01 |
| Transport of vitamins, nucleosides, and related molecules | 21 | 4.09e-02 | 2.58e-01 | 1.34e-01 |
| Response of Mtb to phagocytosis | 20 | 4.60e-02 | -2.58e-01 | 1.44e-01 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | 46 | 2.54e-03 | -2.57e-01 | 2.06e-02 |
| Potassium Channels | 30 | 1.48e-02 | 2.57e-01 | 6.46e-02 |
| Heme biosynthesis | 10 | 1.60e-01 | -2.57e-01 | 3.48e-01 |
| Downregulation of ERBB2:ERBB3 signaling | 10 | 1.60e-01 | -2.57e-01 | 3.48e-01 |
| Methylation | 10 | 1.61e-01 | -2.56e-01 | 3.49e-01 |
| Vif-mediated degradation of APOBEC3G | 43 | 3.78e-03 | -2.55e-01 | 2.56e-02 |
| Removal of the Flap Intermediate | 12 | 1.27e-01 | -2.54e-01 | 2.99e-01 |
| Signaling by FGFR1 | 28 | 2.01e-02 | -2.54e-01 | 7.98e-02 |
| Signaling by FGFR4 | 25 | 2.81e-02 | -2.54e-01 | 1.01e-01 |
| Leading Strand Synthesis | 12 | 1.28e-01 | -2.54e-01 | 3.00e-01 |
| Polymerase switching | 12 | 1.28e-01 | -2.54e-01 | 3.00e-01 |
| Signaling by NOTCH4 | 68 | 3.11e-04 | -2.53e-01 | 4.68e-03 |
| TRAF6 mediated NF-kB activation | 19 | 5.68e-02 | -2.52e-01 | 1.69e-01 |
| G2/M Checkpoints | 119 | 2.23e-06 | -2.51e-01 | 1.34e-04 |
| Asymmetric localization of PCP proteins | 51 | 1.91e-03 | -2.51e-01 | 1.74e-02 |
| PI3K Cascade | 19 | 5.79e-02 | 2.51e-01 | 1.72e-01 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 84 | 6.95e-05 | -2.51e-01 | 1.87e-03 |
| Regulation of APC/C activators between G1/S and early anaphase | 70 | 2.98e-04 | -2.50e-01 | 4.55e-03 |
| Transcription of E2F targets under negative control by DREAM complex | 18 | 6.64e-02 | -2.50e-01 | 1.87e-01 |
| Plasma lipoprotein clearance | 24 | 3.53e-02 | -2.48e-01 | 1.21e-01 |
| Lagging Strand Synthesis | 17 | 7.71e-02 | -2.48e-01 | 2.05e-01 |
| Glycogen metabolism | 17 | 7.74e-02 | -2.47e-01 | 2.05e-01 |
| Degradation of GLI2 by the proteasome | 50 | 2.68e-03 | -2.45e-01 | 2.06e-02 |
| GLI3 is processed to GLI3R by the proteasome | 50 | 2.68e-03 | -2.45e-01 | 2.06e-02 |
| Separation of Sister Chromatids | 147 | 3.34e-07 | -2.44e-01 | 2.86e-05 |
| RMTs methylate histone arginines | 25 | 3.45e-02 | -2.44e-01 | 1.19e-01 |
| Formation of a pool of free 40S subunits | 78 | 1.99e-04 | -2.44e-01 | 3.52e-03 |
| Deadenylation-dependent mRNA decay | 52 | 2.48e-03 | -2.43e-01 | 2.06e-02 |
| Regulation of actin dynamics for phagocytic cup formation | 44 | 5.37e-03 | -2.43e-01 | 3.21e-02 |
| Meiotic synapsis | 25 | 3.59e-02 | -2.42e-01 | 1.22e-01 |
| Degradation of beta-catenin by the destruction complex | 68 | 5.51e-04 | -2.42e-01 | 6.70e-03 |
| DNA Replication Pre-Initiation | 90 | 7.46e-05 | -2.42e-01 | 1.87e-03 |
| Sensory processing of sound by outer hair cells of the cochlea | 18 | 7.57e-02 | 2.42e-01 | 2.02e-01 |
| Diseases associated with N-glycosylation of proteins | 18 | 7.58e-02 | -2.42e-01 | 2.02e-01 |
| Association of TriC/CCT with target proteins during biosynthesis | 29 | 2.48e-02 | -2.41e-01 | 9.13e-02 |
| Infection with Mycobacterium tuberculosis | 22 | 5.08e-02 | -2.40e-01 | 1.56e-01 |
| Polo-like kinase mediated events | 15 | 1.07e-01 | -2.40e-01 | 2.61e-01 |
| Defective CFTR causes cystic fibrosis | 52 | 2.71e-03 | -2.40e-01 | 2.06e-02 |
| Degradation of GLI1 by the proteasome | 51 | 3.09e-03 | -2.40e-01 | 2.20e-02 |
| Caspase-mediated cleavage of cytoskeletal proteins | 10 | 1.90e-01 | -2.39e-01 | 3.84e-01 |
| TICAM1, RIP1-mediated IKK complex recruitment | 17 | 8.76e-02 | -2.39e-01 | 2.23e-01 |
| Purine salvage | 11 | 1.70e-01 | -2.39e-01 | 3.60e-01 |
| Hh mutants abrogate ligand secretion | 49 | 3.83e-03 | -2.39e-01 | 2.57e-02 |
| Signaling by Erythropoietin | 19 | 7.17e-02 | -2.39e-01 | 1.96e-01 |
| SUMOylation of ubiquitinylation proteins | 37 | 1.24e-02 | -2.38e-01 | 5.65e-02 |
| RNA Polymerase I Transcription Termination | 25 | 3.97e-02 | -2.38e-01 | 1.31e-01 |
| Mitochondrial tRNA aminoacylation | 18 | 8.10e-02 | -2.37e-01 | 2.12e-01 |
| Assembly of the pre-replicative complex | 76 | 3.51e-04 | -2.37e-01 | 4.92e-03 |
| Oncogene Induced Senescence | 30 | 2.47e-02 | -2.37e-01 | 9.13e-02 |
| DNA Double-Strand Break Repair | 117 | 1.00e-05 | -2.37e-01 | 4.64e-04 |
| Negative regulation of NOTCH4 signaling | 48 | 4.58e-03 | -2.37e-01 | 2.87e-02 |
| Diseases of DNA repair | 45 | 6.10e-03 | -2.36e-01 | 3.49e-02 |
| FCERI mediated MAPK activation | 23 | 5.01e-02 | -2.36e-01 | 1.54e-01 |
| Major pathway of rRNA processing in the nucleolus and cytosol | 152 | 5.54e-07 | -2.36e-01 | 4.44e-05 |
| DNA strand elongation | 28 | 3.08e-02 | -2.36e-01 | 1.08e-01 |
| Negative regulation of FGFR1 signaling | 18 | 8.35e-02 | -2.36e-01 | 2.15e-01 |
| Negative regulation of FGFR2 signaling | 18 | 8.35e-02 | -2.36e-01 | 2.15e-01 |
| Negative regulation of FGFR3 signaling | 18 | 8.35e-02 | -2.36e-01 | 2.15e-01 |
| Negative regulation of FGFR4 signaling | 18 | 8.35e-02 | -2.36e-01 | 2.15e-01 |
| Degradation of the extracellular matrix | 35 | 1.64e-02 | 2.34e-01 | 6.87e-02 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | 14 | 1.29e-01 | -2.34e-01 | 3.01e-01 |
| Signaling by Leptin | 10 | 2.00e-01 | -2.34e-01 | 3.95e-01 |
| Regulation of TP53 Activity through Methylation | 17 | 9.53e-02 | -2.34e-01 | 2.40e-01 |
| S Phase | 141 | 1.80e-06 | -2.33e-01 | 1.20e-04 |
| Long-term potentiation | 11 | 1.81e-01 | 2.33e-01 | 3.73e-01 |
| Calnexin/calreticulin cycle | 23 | 5.32e-02 | -2.33e-01 | 1.61e-01 |
| Chaperonin-mediated protein folding | 57 | 2.48e-03 | -2.32e-01 | 2.06e-02 |
| Formation of the ternary complex, and subsequently, the 43S complex | 40 | 1.13e-02 | -2.32e-01 | 5.30e-02 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | 13 | 1.49e-01 | -2.31e-01 | 3.37e-01 |
| Ion transport by P-type ATPases | 27 | 3.84e-02 | -2.30e-01 | 1.28e-01 |
| Synthesis of DNA | 106 | 4.36e-05 | -2.30e-01 | 1.52e-03 |
| Ovarian tumor domain proteases | 29 | 3.21e-02 | -2.30e-01 | 1.11e-01 |
| Transcriptional regulation by RUNX3 | 75 | 5.84e-04 | -2.30e-01 | 7.01e-03 |
| ERKs are inactivated | 11 | 1.87e-01 | -2.29e-01 | 3.82e-01 |
| RNA Polymerase I Promoter Escape | 27 | 3.91e-02 | -2.29e-01 | 1.30e-01 |
| Defective HDR through Homologous Recombination (HRR) due to BRCA1 loss-of-function | 22 | 6.26e-02 | -2.29e-01 | 1.80e-01 |
| Defective HDR through Homologous Recombination (HRR) due to PALB2 loss of function | 22 | 6.26e-02 | -2.29e-01 | 1.80e-01 |
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function | 22 | 6.26e-02 | -2.29e-01 | 1.80e-01 |
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function | 22 | 6.26e-02 | -2.29e-01 | 1.80e-01 |
| Impaired BRCA2 binding to PALB2 | 22 | 6.26e-02 | -2.29e-01 | 1.80e-01 |
| DCC mediated attractive signaling | 11 | 1.90e-01 | 2.28e-01 | 3.84e-01 |
| Platelet sensitization by LDL | 13 | 1.54e-01 | -2.28e-01 | 3.42e-01 |
| PKA-mediated phosphorylation of CREB | 11 | 1.91e-01 | 2.28e-01 | 3.84e-01 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | 12 | 1.73e-01 | -2.27e-01 | 3.62e-01 |
| L13a-mediated translational silencing of Ceruloplasmin expression | 87 | 2.57e-04 | -2.27e-01 | 4.26e-03 |
| Regulation of RUNX2 expression and activity | 57 | 3.17e-03 | -2.26e-01 | 2.23e-02 |
| RHOBTB1 GTPase cycle | 18 | 9.72e-02 | -2.26e-01 | 2.44e-01 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 16 | 1.22e-01 | -2.24e-01 | 2.90e-01 |
| rRNA processing in the nucleus and cytosol | 159 | 1.22e-06 | -2.23e-01 | 9.13e-05 |
| DNA Replication | 113 | 4.37e-05 | -2.23e-01 | 1.52e-03 |
| Cell Cycle Checkpoints | 228 | 7.61e-09 | -2.23e-01 | 1.14e-06 |
| TNFs bind their physiological receptors | 10 | 2.23e-01 | 2.23e-01 | 4.23e-01 |
| Peptide chain elongation | 69 | 1.40e-03 | -2.22e-01 | 1.40e-02 |
| Mitotic Anaphase | 195 | 9.14e-08 | -2.22e-01 | 9.53e-06 |
| Constitutive Signaling by EGFRvIII | 10 | 2.23e-01 | -2.22e-01 | 4.23e-01 |
| Signaling by EGFRvIII in Cancer | 10 | 2.23e-01 | -2.22e-01 | 4.23e-01 |
| Deactivation of the beta-catenin transactivating complex | 28 | 4.20e-02 | -2.22e-01 | 1.37e-01 |
| Cytochrome c-mediated apoptotic response | 11 | 2.02e-01 | -2.22e-01 | 3.99e-01 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 41 | 1.40e-02 | -2.22e-01 | 6.12e-02 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | 41 | 1.40e-02 | -2.22e-01 | 6.12e-02 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 41 | 1.40e-02 | -2.22e-01 | 6.12e-02 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | 41 | 1.40e-02 | -2.22e-01 | 6.12e-02 |
| Signaling by NOTCH1 in Cancer | 41 | 1.40e-02 | -2.22e-01 | 6.12e-02 |
| Global Genome Nucleotide Excision Repair (GG-NER) | 76 | 8.41e-04 | -2.22e-01 | 9.45e-03 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | 88 | 3.30e-04 | -2.22e-01 | 4.84e-03 |
| Regulation of RUNX3 expression and activity | 49 | 7.32e-03 | -2.21e-01 | 3.95e-02 |
| Switching of origins to a post-replicative state | 81 | 6.28e-04 | -2.20e-01 | 7.46e-03 |
| Signaling by ERBB2 ECD mutants | 10 | 2.29e-01 | -2.20e-01 | 4.28e-01 |
| Mitotic Metaphase and Anaphase | 196 | 1.24e-07 | -2.20e-01 | 1.15e-05 |
| Cleavage of the damaged pyrimidine | 14 | 1.55e-01 | -2.20e-01 | 3.42e-01 |
| Depyrimidination | 14 | 1.55e-01 | -2.20e-01 | 3.42e-01 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | 14 | 1.55e-01 | -2.20e-01 | 3.42e-01 |
| Smooth Muscle Contraction | 19 | 9.79e-02 | -2.19e-01 | 2.45e-01 |
| Mitochondrial iron-sulfur cluster biogenesis | 12 | 1.90e-01 | -2.18e-01 | 3.84e-01 |
| Positive epigenetic regulation of rRNA expression | 40 | 1.71e-02 | -2.18e-01 | 7.10e-02 |
| Mitotic G1 phase and G1/S transition | 129 | 2.01e-05 | -2.18e-01 | 8.35e-04 |
| G0 and Early G1 | 24 | 6.58e-02 | -2.17e-01 | 1.86e-01 |
| Dectin-1 mediated noncanonical NF-kB signaling | 52 | 6.83e-03 | -2.17e-01 | 3.76e-02 |
| Complex I biogenesis | 43 | 1.39e-02 | -2.17e-01 | 6.12e-02 |
| Unwinding of DNA | 11 | 2.13e-01 | -2.17e-01 | 4.13e-01 |
| Notch-HLH transcription pathway | 21 | 8.57e-02 | -2.17e-01 | 2.20e-01 |
| RIP-mediated NFkB activation via ZBP1 | 14 | 1.62e-01 | -2.16e-01 | 3.51e-01 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | 53 | 6.56e-03 | -2.16e-01 | 3.63e-02 |
| NIK–>noncanonical NF-kB signaling | 51 | 7.71e-03 | -2.16e-01 | 4.10e-02 |
| Metabolism of polyamines | 48 | 9.85e-03 | -2.15e-01 | 4.91e-02 |
| DNA Damage/Telomere Stress Induced Senescence | 24 | 6.80e-02 | -2.15e-01 | 1.89e-01 |
| Translation | 238 | 1.31e-08 | -2.15e-01 | 1.57e-06 |
| Inactivation of APC/C via direct inhibition of the APC/C complex | 19 | 1.05e-01 | -2.15e-01 | 2.58e-01 |
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | 19 | 1.05e-01 | -2.15e-01 | 2.58e-01 |
| Cellular response to hypoxia | 60 | 4.16e-03 | -2.14e-01 | 2.69e-02 |
| AURKA Activation by TPX2 | 59 | 4.54e-03 | -2.14e-01 | 2.86e-02 |
| G1/S Transition | 115 | 7.82e-05 | -2.13e-01 | 1.92e-03 |
| Sema3A PAK dependent Axon repulsion | 11 | 2.21e-01 | -2.13e-01 | 4.21e-01 |
| Transcriptional Regulation by VENTX | 30 | 4.36e-02 | -2.13e-01 | 1.39e-01 |
| Sema4D in semaphorin signaling | 15 | 1.55e-01 | -2.12e-01 | 3.42e-01 |
| Elastic fibre formation | 17 | 1.30e-01 | 2.12e-01 | 3.03e-01 |
| Activated NOTCH1 Transmits Signal to the Nucleus | 19 | 1.10e-01 | -2.12e-01 | 2.67e-01 |
| Eukaryotic Translation Termination | 72 | 2.00e-03 | -2.11e-01 | 1.78e-02 |
| Selenocysteine synthesis | 70 | 2.39e-03 | -2.10e-01 | 2.02e-02 |
| Interleukin-6 family signaling | 13 | 1.90e-01 | 2.10e-01 | 3.84e-01 |
| Cap-dependent Translation Initiation | 95 | 4.20e-04 | -2.10e-01 | 5.43e-03 |
| Eukaryotic Translation Initiation | 95 | 4.20e-04 | -2.10e-01 | 5.43e-03 |
| TP53 Regulates Transcription of DNA Repair Genes | 52 | 8.98e-03 | -2.10e-01 | 4.55e-02 |
| Viral mRNA Translation | 69 | 2.65e-03 | -2.09e-01 | 2.06e-02 |
| Downregulation of ERBB2 signaling | 17 | 1.35e-01 | -2.09e-01 | 3.12e-01 |
| MAPK6/MAPK4 signaling | 69 | 2.69e-03 | -2.09e-01 | 2.06e-02 |
| Interleukin-10 signaling | 13 | 1.92e-01 | 2.09e-01 | 3.85e-01 |
| Branched-chain amino acid catabolism | 20 | 1.08e-01 | -2.08e-01 | 2.63e-01 |
| SUMOylation of SUMOylation proteins | 32 | 4.22e-02 | -2.08e-01 | 1.37e-01 |
| TICAM1-dependent activation of IRF3/IRF7 | 12 | 2.14e-01 | -2.07e-01 | 4.13e-01 |
| Negative regulation of MAPK pathway | 36 | 3.20e-02 | -2.07e-01 | 1.11e-01 |
| rRNA processing | 164 | 5.43e-06 | -2.06e-01 | 2.70e-04 |
| Nuclear Pore Complex (NPC) Disassembly | 34 | 3.76e-02 | -2.06e-01 | 1.27e-01 |
| ER-Phagosome pathway | 69 | 3.14e-03 | -2.06e-01 | 2.22e-02 |
| Termination of translesion DNA synthesis | 28 | 5.96e-02 | -2.06e-01 | 1.75e-01 |
| Termination of O-glycan biosynthesis | 10 | 2.61e-01 | -2.05e-01 | 4.63e-01 |
| Eukaryotic Translation Elongation | 72 | 2.64e-03 | -2.05e-01 | 2.06e-02 |
| ABC transporter disorders | 59 | 6.47e-03 | -2.05e-01 | 3.63e-02 |
| TP53 Regulates Transcription of Cell Cycle Genes | 43 | 2.04e-02 | -2.04e-01 | 8.08e-02 |
| Regulation of TP53 Activity | 136 | 3.97e-05 | -2.04e-01 | 1.49e-03 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | 78 | 1.83e-03 | -2.04e-01 | 1.70e-02 |
| Integrin cell surface interactions | 25 | 7.72e-02 | -2.04e-01 | 2.05e-01 |
| Resolution of Sister Chromatid Cohesion | 92 | 7.36e-04 | -2.04e-01 | 8.43e-03 |
| Downstream signaling events of B Cell Receptor (BCR) | 70 | 3.26e-03 | -2.03e-01 | 2.28e-02 |
| RHOBTB GTPase Cycle | 29 | 5.83e-02 | -2.03e-01 | 1.73e-01 |
| Mitochondrial translation termination | 83 | 1.43e-03 | -2.03e-01 | 1.40e-02 |
| UCH proteinases | 74 | 2.78e-03 | -2.01e-01 | 2.09e-02 |
| Activation of NF-kappaB in B cells | 57 | 8.64e-03 | -2.01e-01 | 4.42e-02 |
| InlB-mediated entry of Listeria monocytogenes into host cell | 11 | 2.48e-01 | -2.01e-01 | 4.52e-01 |
| Mitotic Prophase | 75 | 2.65e-03 | -2.01e-01 | 2.06e-02 |
| Antigen processing-Cross presentation | 76 | 2.54e-03 | -2.00e-01 | 2.06e-02 |
| Gap junction trafficking | 10 | 2.74e-01 | 2.00e-01 | 4.73e-01 |
| Apoptosis | 133 | 7.34e-05 | -1.99e-01 | 1.87e-03 |
| FLT3 Signaling | 32 | 5.14e-02 | -1.99e-01 | 1.58e-01 |
| Translation initiation complex formation | 47 | 1.86e-02 | -1.98e-01 | 7.56e-02 |
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | 16 | 1.70e-01 | -1.98e-01 | 3.60e-01 |
| Nucleotide Excision Repair | 99 | 6.91e-04 | -1.98e-01 | 7.99e-03 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | 35 | 4.35e-02 | 1.97e-01 | 1.39e-01 |
| Orc1 removal from chromatin | 62 | 7.27e-03 | -1.97e-01 | 3.95e-02 |
| Glucagon signaling in metabolic regulation | 18 | 1.48e-01 | 1.97e-01 | 3.35e-01 |
| Dual Incision in GG-NER | 35 | 4.40e-02 | -1.97e-01 | 1.40e-01 |
| LDL clearance | 12 | 2.38e-01 | -1.97e-01 | 4.41e-01 |
| SUMO E3 ligases SUMOylate target proteins | 132 | 1.00e-04 | -1.96e-01 | 2.15e-03 |
| Processing of SMDT1 | 13 | 2.21e-01 | -1.96e-01 | 4.21e-01 |
| Mitochondrial translation | 89 | 1.42e-03 | -1.96e-01 | 1.40e-02 |
| Mitotic Spindle Checkpoint | 98 | 8.76e-04 | -1.95e-01 | 9.75e-03 |
| M Phase | 297 | 9.25e-09 | -1.95e-01 | 1.24e-06 |
| Ribosomal scanning and start codon recognition | 47 | 2.12e-02 | -1.94e-01 | 8.17e-02 |
| Gap-filling DNA repair synthesis and ligation in TC-NER | 55 | 1.28e-02 | -1.94e-01 | 5.80e-02 |
| Downregulation of TGF-beta receptor signaling | 26 | 8.67e-02 | -1.94e-01 | 2.22e-01 |
| Base-Excision Repair, AP Site Formation | 15 | 1.94e-01 | -1.94e-01 | 3.86e-01 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 74 | 4.15e-03 | -1.93e-01 | 2.69e-02 |
| Hedgehog ligand biogenesis | 52 | 1.62e-02 | -1.93e-01 | 6.83e-02 |
| SUMOylation | 138 | 9.57e-05 | -1.93e-01 | 2.13e-03 |
| Transcription-Coupled Nucleotide Excision Repair (TC-NER) | 69 | 5.68e-03 | -1.93e-01 | 3.37e-02 |
| Formation of tubulin folding intermediates by CCT/TriC | 14 | 2.13e-01 | -1.92e-01 | 4.13e-01 |
| Formation of TC-NER Pre-Incision Complex | 46 | 2.42e-02 | -1.92e-01 | 9.04e-02 |
| Cell Cycle, Mitotic | 425 | 1.79e-11 | -1.91e-01 | 1.08e-08 |
| PTEN Regulation | 115 | 4.19e-04 | -1.91e-01 | 5.43e-03 |
| Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) | 28 | 8.08e-02 | -1.91e-01 | 2.12e-01 |
| Regulation of Glucokinase by Glucokinase Regulatory Protein | 28 | 8.08e-02 | -1.91e-01 | 2.12e-01 |
| NOTCH1 Intracellular Domain Regulates Transcription | 37 | 4.49e-02 | -1.90e-01 | 1.41e-01 |
| Mitochondrial translation elongation | 84 | 2.58e-03 | -1.90e-01 | 2.06e-02 |
| Programmed Cell Death | 155 | 4.47e-05 | -1.90e-01 | 1.52e-03 |
| Glutamate Neurotransmitter Release Cycle | 12 | 2.53e-01 | -1.90e-01 | 4.59e-01 |
| Signaling by TGF-beta Receptor Complex | 72 | 5.35e-03 | -1.90e-01 | 3.21e-02 |
| N-glycan trimming in the ER and Calnexin/Calreticulin cycle | 32 | 6.41e-02 | -1.89e-01 | 1.83e-01 |
| Regulation of expression of SLITs and ROBOs | 124 | 2.82e-04 | -1.89e-01 | 4.41e-03 |
| RHO GTPases activate CIT | 14 | 2.23e-01 | -1.88e-01 | 4.23e-01 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | 77 | 4.54e-03 | -1.87e-01 | 2.86e-02 |
| Loss of Nlp from mitotic centrosomes | 56 | 1.54e-02 | -1.87e-01 | 6.60e-02 |
| Loss of proteins required for interphase microtubule organization from the centrosome | 56 | 1.54e-02 | -1.87e-01 | 6.60e-02 |
| Cell Cycle | 530 | 2.75e-13 | -1.87e-01 | 3.30e-10 |
| SUMOylation of intracellular receptors | 19 | 1.59e-01 | -1.87e-01 | 3.47e-01 |
| Metal ion SLC transporters | 16 | 1.96e-01 | -1.87e-01 | 3.89e-01 |
| RHOQ GTPase cycle | 39 | 4.42e-02 | 1.86e-01 | 1.40e-01 |
| Sialic acid metabolism | 23 | 1.22e-01 | -1.86e-01 | 2.91e-01 |
| NOTCH4 Intracellular Domain Regulates Transcription | 14 | 2.29e-01 | -1.86e-01 | 4.28e-01 |
| Influenza Viral RNA Transcription and Replication | 113 | 6.62e-04 | -1.86e-01 | 7.72e-03 |
| Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon | 13 | 2.46e-01 | -1.86e-01 | 4.51e-01 |
| Signaling by ROBO receptors | 154 | 7.38e-05 | -1.85e-01 | 1.87e-03 |
| Maturation of nucleoprotein | 11 | 2.87e-01 | -1.85e-01 | 4.84e-01 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | 48 | 2.65e-02 | -1.85e-01 | 9.61e-02 |
| NoRC negatively regulates rRNA expression | 42 | 3.81e-02 | -1.85e-01 | 1.28e-01 |
| Anchoring of the basal body to the plasma membrane | 80 | 4.33e-03 | -1.85e-01 | 2.77e-02 |
| G2/M Transition | 156 | 7.13e-05 | -1.85e-01 | 1.87e-03 |
| ABC-family proteins mediated transport | 74 | 6.22e-03 | -1.84e-01 | 3.54e-02 |
| RNA Polymerase III Transcription Termination | 21 | 1.46e-01 | -1.83e-01 | 3.32e-01 |
| Vpr-mediated nuclear import of PICs | 32 | 7.31e-02 | -1.83e-01 | 1.99e-01 |
| Post-translational protein phosphorylation | 34 | 6.49e-02 | 1.83e-01 | 1.84e-01 |
| Processive synthesis on the lagging strand | 13 | 2.55e-01 | -1.82e-01 | 4.61e-01 |
| Mitochondrial translation initiation | 84 | 3.92e-03 | -1.82e-01 | 2.59e-02 |
| Prolonged ERK activation events | 13 | 2.57e-01 | -1.81e-01 | 4.61e-01 |
| Myogenesis | 13 | 2.57e-01 | -1.81e-01 | 4.61e-01 |
| Recycling pathway of L1 | 15 | 2.24e-01 | 1.81e-01 | 4.23e-01 |
| Mitotic G2-G2/M phases | 158 | 9.05e-05 | -1.81e-01 | 2.05e-03 |
| Nuclear events mediated by NFE2L2 | 67 | 1.09e-02 | -1.80e-01 | 5.16e-02 |
| Mitotic Prometaphase | 158 | 1.05e-04 | -1.79e-01 | 2.20e-03 |
| Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | 35 | 6.66e-02 | -1.79e-01 | 1.87e-01 |
| Nucleotide biosynthesis | 12 | 2.83e-01 | 1.79e-01 | 4.80e-01 |
| Resolution of D-loop Structures through Holliday Junction Intermediates | 28 | 1.01e-01 | -1.79e-01 | 2.51e-01 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | 83 | 4.86e-03 | -1.79e-01 | 2.99e-02 |
| Amplification of signal from the kinetochores | 83 | 4.86e-03 | -1.79e-01 | 2.99e-02 |
| TRAF6 mediated IRF7 activation | 16 | 2.17e-01 | -1.78e-01 | 4.16e-01 |
| Estrogen-dependent gene expression | 70 | 9.97e-03 | -1.78e-01 | 4.93e-02 |
| Sphingolipid de novo biosynthesis | 22 | 1.49e-01 | 1.78e-01 | 3.36e-01 |
| FCGR3A-mediated phagocytosis | 42 | 4.61e-02 | -1.78e-01 | 1.44e-01 |
| Leishmania phagocytosis | 42 | 4.61e-02 | -1.78e-01 | 1.44e-01 |
| Parasite infection | 42 | 4.61e-02 | -1.78e-01 | 1.44e-01 |
| CLEC7A (Dectin-1) induces NFAT activation | 11 | 3.07e-01 | -1.78e-01 | 5.10e-01 |
| Export of Viral Ribonucleoproteins from Nucleus | 31 | 8.79e-02 | -1.77e-01 | 2.23e-01 |
| DNA Repair | 248 | 1.80e-06 | -1.77e-01 | 1.20e-04 |
| Signaling by FGFR | 52 | 2.76e-02 | -1.77e-01 | 9.96e-02 |
| Protein folding | 63 | 1.56e-02 | -1.76e-01 | 6.67e-02 |
| RHOJ GTPase cycle | 37 | 6.44e-02 | 1.76e-01 | 1.83e-01 |
| Nuclear Envelope Breakdown | 49 | 3.34e-02 | -1.76e-01 | 1.15e-01 |
| Selenoamino acid metabolism | 78 | 7.36e-03 | -1.76e-01 | 3.95e-02 |
| Transcriptional regulation of white adipocyte differentiation | 56 | 2.35e-02 | -1.75e-01 | 8.87e-02 |
| Signaling by EGFR | 35 | 7.34e-02 | -1.75e-01 | 2.00e-01 |
| ER Quality Control Compartment (ERQC) | 18 | 1.99e-01 | -1.75e-01 | 3.94e-01 |
| Inflammasomes | 16 | 2.26e-01 | -1.75e-01 | 4.25e-01 |
| Activation of gene expression by SREBF (SREBP) | 36 | 6.97e-02 | -1.75e-01 | 1.92e-01 |
| Nuclear import of Rev protein | 31 | 9.26e-02 | -1.75e-01 | 2.34e-01 |
| Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein | 61 | 1.89e-02 | -1.74e-01 | 7.65e-02 |
| Signaling by FLT3 fusion proteins | 16 | 2.29e-01 | -1.74e-01 | 4.28e-01 |
| Regulation of IFNA/IFNB signaling | 12 | 2.99e-01 | 1.73e-01 | 5.01e-01 |
| Nuclear Envelope (NE) Reassembly | 60 | 2.06e-02 | -1.73e-01 | 8.09e-02 |
| DNA Damage Bypass | 42 | 5.26e-02 | -1.73e-01 | 1.59e-01 |
| Transcriptional regulation of granulopoiesis | 25 | 1.35e-01 | -1.73e-01 | 3.12e-01 |
| Signaling by ERBB2 TMD/JMD mutants | 10 | 3.46e-01 | -1.72e-01 | 5.45e-01 |
| Processive synthesis on the C-strand of the telomere | 17 | 2.20e-01 | -1.72e-01 | 4.20e-01 |
| SUMOylation of DNA damage response and repair proteins | 67 | 1.60e-02 | -1.70e-01 | 6.79e-02 |
| Regulation of PLK1 Activity at G2/M Transition | 74 | 1.15e-02 | -1.70e-01 | 5.37e-02 |
| SARS-CoV-2 targets host intracellular signalling and regulatory pathways | 11 | 3.29e-01 | 1.70e-01 | 5.29e-01 |
| Respiratory electron transport | 82 | 8.03e-03 | -1.69e-01 | 4.20e-02 |
| EML4 and NUDC in mitotic spindle formation | 87 | 6.53e-03 | -1.69e-01 | 3.63e-02 |
| Retinoid metabolism and transport | 11 | 3.33e-01 | -1.69e-01 | 5.32e-01 |
| Signaling by BMP | 15 | 2.59e-01 | 1.68e-01 | 4.62e-01 |
| Signaling by the B Cell Receptor (BCR) | 90 | 6.05e-03 | -1.68e-01 | 3.48e-02 |
| Signaling by NOTCH1 | 51 | 3.91e-02 | -1.67e-01 | 1.30e-01 |
| rRNA modification in the nucleus and cytosol | 49 | 4.36e-02 | -1.67e-01 | 1.39e-01 |
| Interleukin-15 signaling | 11 | 3.39e-01 | -1.67e-01 | 5.38e-01 |
| Negative epigenetic regulation of rRNA expression | 44 | 5.62e-02 | -1.66e-01 | 1.69e-01 |
| Nephrin family interactions | 14 | 2.83e-01 | 1.66e-01 | 4.81e-01 |
| Cellular Senescence | 106 | 3.41e-03 | -1.65e-01 | 2.34e-02 |
| IRS-mediated signalling | 21 | 1.91e-01 | 1.65e-01 | 3.84e-01 |
| FCERI mediated NF-kB activation | 64 | 2.29e-02 | -1.64e-01 | 8.73e-02 |
| GPVI-mediated activation cascade | 23 | 1.73e-01 | -1.64e-01 | 3.62e-01 |
| Hedgehog ‘on’ state | 63 | 2.44e-02 | -1.64e-01 | 9.05e-02 |
| Influenza Infection | 130 | 1.27e-03 | -1.64e-01 | 1.32e-02 |
| VxPx cargo-targeting to cilium | 16 | 2.58e-01 | 1.63e-01 | 4.61e-01 |
| Host Interactions of HIV factors | 106 | 3.75e-03 | -1.63e-01 | 2.54e-02 |
| Postmitotic nuclear pore complex (NPC) reformation | 26 | 1.50e-01 | -1.63e-01 | 3.37e-01 |
| Cell junction organization | 26 | 1.50e-01 | 1.63e-01 | 3.37e-01 |
| Deadenylation of mRNA | 23 | 1.76e-01 | -1.63e-01 | 3.68e-01 |
| Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. | 83 | 1.06e-02 | -1.62e-01 | 5.03e-02 |
| Transcriptional regulation by RUNX2 | 84 | 1.02e-02 | -1.62e-01 | 4.93e-02 |
| Formation of Incision Complex in GG-NER | 36 | 9.28e-02 | -1.62e-01 | 2.34e-01 |
| Transport of Ribonucleoproteins into the Host Nucleus | 30 | 1.27e-01 | -1.61e-01 | 2.99e-01 |
| ROS and RNS production in phagocytes | 23 | 1.83e-01 | 1.61e-01 | 3.76e-01 |
| Inwardly rectifying K+ channels | 13 | 3.18e-01 | 1.60e-01 | 5.19e-01 |
| Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) | 24 | 1.76e-01 | -1.60e-01 | 3.67e-01 |
| EPHB-mediated forward signaling | 25 | 1.67e-01 | -1.60e-01 | 3.60e-01 |
| Fc epsilon receptor (FCERI) signaling | 107 | 4.42e-03 | -1.59e-01 | 2.81e-02 |
| SUMOylation of DNA methylation proteins | 14 | 3.02e-01 | 1.59e-01 | 5.04e-01 |
| Condensation of Prophase Chromosomes | 12 | 3.41e-01 | -1.59e-01 | 5.38e-01 |
| Transferrin endocytosis and recycling | 19 | 2.32e-01 | 1.58e-01 | 4.32e-01 |
| Epigenetic regulation of gene expression | 76 | 1.73e-02 | -1.58e-01 | 7.14e-02 |
| Transcriptional regulation by RUNX1 | 137 | 1.46e-03 | -1.58e-01 | 1.40e-02 |
| SUMOylation of DNA replication proteins | 43 | 7.41e-02 | -1.57e-01 | 2.00e-01 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | 13 | 3.27e-01 | -1.57e-01 | 5.26e-01 |
| Metabolism of RNA | 553 | 3.99e-10 | -1.57e-01 | 9.58e-08 |
| Suppression of phagosomal maturation | 12 | 3.46e-01 | -1.57e-01 | 5.45e-01 |
| Collagen formation | 28 | 1.51e-01 | 1.57e-01 | 3.39e-01 |
| NEP/NS2 Interacts with the Cellular Export Machinery | 30 | 1.38e-01 | -1.57e-01 | 3.16e-01 |
| Signaling by FGFR2 | 48 | 6.12e-02 | -1.56e-01 | 1.78e-01 |
| Rev-mediated nuclear export of HIV RNA | 33 | 1.21e-01 | -1.56e-01 | 2.88e-01 |
| HCMV Early Events | 50 | 5.72e-02 | -1.56e-01 | 1.70e-01 |
| Pre-NOTCH Processing in Golgi | 16 | 2.82e-01 | 1.55e-01 | 4.79e-01 |
| CLEC7A (Dectin-1) signaling | 84 | 1.41e-02 | -1.55e-01 | 6.18e-02 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 88 | 1.20e-02 | -1.55e-01 | 5.55e-02 |
| Nonsense-Mediated Decay (NMD) | 88 | 1.20e-02 | -1.55e-01 | 5.55e-02 |
| Nuclear events stimulated by ALK signaling in cancer | 14 | 3.16e-01 | -1.55e-01 | 5.18e-01 |
| Collagen degradation | 14 | 3.17e-01 | 1.55e-01 | 5.18e-01 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | 58 | 4.20e-02 | -1.54e-01 | 1.37e-01 |
| Signaling by TGFB family members | 85 | 1.39e-02 | -1.54e-01 | 6.12e-02 |
| AKT phosphorylates targets in the cytosol | 13 | 3.35e-01 | 1.54e-01 | 5.36e-01 |
| Ephrin signaling | 12 | 3.55e-01 | 1.54e-01 | 5.55e-01 |
| Regulation of PTEN gene transcription | 48 | 6.69e-02 | -1.53e-01 | 1.87e-01 |
| alpha-linolenic (omega3) and linoleic (omega6) acid metabolism | 10 | 4.04e-01 | -1.52e-01 | 5.98e-01 |
| alpha-linolenic acid (ALA) metabolism | 10 | 4.04e-01 | -1.52e-01 | 5.98e-01 |
| Inhibition of replication initiation of damaged DNA by RB1/E2F1 | 10 | 4.06e-01 | -1.52e-01 | 6.00e-01 |
| Synaptic adhesion-like molecules | 10 | 4.06e-01 | 1.52e-01 | 6.00e-01 |
| Regulation of cholesterol biosynthesis by SREBP (SREBF) | 48 | 6.94e-02 | -1.51e-01 | 1.92e-01 |
| Interactions of Vpr with host cellular proteins | 33 | 1.32e-01 | -1.51e-01 | 3.07e-01 |
| EPH-Ephrin signaling | 55 | 5.25e-02 | -1.51e-01 | 1.59e-01 |
| NOTCH3 Intracellular Domain Regulates Transcription | 15 | 3.10e-01 | -1.51e-01 | 5.12e-01 |
| Negative regulation of NMDA receptor-mediated neuronal transmission | 12 | 3.65e-01 | 1.51e-01 | 5.63e-01 |
| Hedgehog ‘off’ state | 75 | 2.42e-02 | -1.51e-01 | 9.04e-02 |
| RHO GTPase Effectors | 188 | 3.91e-04 | -1.50e-01 | 5.26e-03 |
| Ub-specific processing proteases | 134 | 2.82e-03 | -1.50e-01 | 2.10e-02 |
| Nuclear Receptor transcription pathway | 27 | 1.79e-01 | -1.49e-01 | 3.70e-01 |
| KEAP1-NFE2L2 pathway | 86 | 1.69e-02 | -1.49e-01 | 7.07e-02 |
| Signaling by NOTCH | 135 | 2.85e-03 | -1.49e-01 | 2.10e-02 |
| RHO GTPases Activate Formins | 102 | 9.43e-03 | -1.49e-01 | 4.76e-02 |
| N-Glycan antennae elongation | 10 | 4.15e-01 | -1.49e-01 | 6.04e-01 |
| Aquaporin-mediated transport | 25 | 2.00e-01 | 1.48e-01 | 3.95e-01 |
| Cargo recognition for clathrin-mediated endocytosis | 63 | 4.25e-02 | -1.48e-01 | 1.37e-01 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | 29 | 1.71e-01 | -1.47e-01 | 3.60e-01 |
| Signaling by RAS mutants | 29 | 1.71e-01 | -1.47e-01 | 3.60e-01 |
| Signaling by moderate kinase activity BRAF mutants | 29 | 1.71e-01 | -1.47e-01 | 3.60e-01 |
| Signaling downstream of RAS mutants | 29 | 1.71e-01 | -1.47e-01 | 3.60e-01 |
| Telomere Extension By Telomerase | 20 | 2.55e-01 | -1.47e-01 | 4.61e-01 |
| PCP/CE pathway | 71 | 3.28e-02 | -1.47e-01 | 1.13e-01 |
| Collagen biosynthesis and modifying enzymes | 19 | 2.70e-01 | 1.46e-01 | 4.72e-01 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | 10 | 4.23e-01 | -1.46e-01 | 6.13e-01 |
| Dual incision in TC-NER | 56 | 5.87e-02 | -1.46e-01 | 1.73e-01 |
| Cellular response to heat stress | 80 | 2.44e-02 | -1.46e-01 | 9.05e-02 |
| B-WICH complex positively regulates rRNA expression | 27 | 1.90e-01 | -1.46e-01 | 3.84e-01 |
| Interleukin-1 signaling | 79 | 2.58e-02 | -1.45e-01 | 9.42e-02 |
| Metabolism of fat-soluble vitamins | 13 | 3.66e-01 | -1.45e-01 | 5.63e-01 |
| G1/S-Specific Transcription | 27 | 1.94e-01 | -1.45e-01 | 3.86e-01 |
| Activation of G protein gated Potassium channels | 12 | 3.86e-01 | 1.45e-01 | 5.82e-01 |
| G protein gated Potassium channels | 12 | 3.86e-01 | 1.45e-01 | 5.82e-01 |
| Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits | 12 | 3.86e-01 | 1.45e-01 | 5.82e-01 |
| Signalling to RAS | 12 | 3.86e-01 | -1.44e-01 | 5.82e-01 |
| Interactions of Rev with host cellular proteins | 34 | 1.46e-01 | -1.44e-01 | 3.32e-01 |
| RORA activates gene expression | 11 | 4.08e-01 | -1.44e-01 | 6.00e-01 |
| Signal transduction by L1 | 11 | 4.08e-01 | -1.44e-01 | 6.00e-01 |
| MicroRNA (miRNA) biogenesis | 21 | 2.53e-01 | 1.44e-01 | 4.59e-01 |
| Signaling by ERBB2 in Cancer | 13 | 3.69e-01 | -1.44e-01 | 5.66e-01 |
| RHO GTPases activate PKNs | 26 | 2.05e-01 | -1.44e-01 | 4.03e-01 |
| GPCR ligand binding | 80 | 2.66e-02 | 1.43e-01 | 9.64e-02 |
| TCF dependent signaling in response to WNT | 119 | 7.36e-03 | -1.42e-01 | 3.95e-02 |
| Disassembly of the destruction complex and recruitment of AXIN to the membrane | 26 | 2.09e-01 | -1.42e-01 | 4.09e-01 |
| Downstream TCR signaling | 71 | 3.84e-02 | -1.42e-01 | 1.28e-01 |
| FCERI mediated Ca+2 mobilization | 23 | 2.38e-01 | -1.42e-01 | 4.41e-01 |
| KSRP (KHSRP) binds and destabilizes mRNA | 15 | 3.41e-01 | -1.42e-01 | 5.38e-01 |
| Mitochondrial calcium ion transport | 19 | 2.84e-01 | -1.42e-01 | 4.81e-01 |
| Glutathione conjugation | 21 | 2.60e-01 | -1.42e-01 | 4.62e-01 |
| Metalloprotease DUBs | 17 | 3.12e-01 | -1.42e-01 | 5.15e-01 |
| ABC transporters in lipid homeostasis | 10 | 4.39e-01 | -1.41e-01 | 6.25e-01 |
| RNA Polymerase III Abortive And Retractive Initiation | 39 | 1.27e-01 | -1.41e-01 | 2.99e-01 |
| RNA Polymerase III Transcription | 39 | 1.27e-01 | -1.41e-01 | 2.99e-01 |
| Assembly Of The HIV Virion | 14 | 3.61e-01 | 1.41e-01 | 5.60e-01 |
| RHOU GTPase cycle | 32 | 1.68e-01 | 1.41e-01 | 3.60e-01 |
| mTORC1-mediated signalling | 21 | 2.65e-01 | 1.40e-01 | 4.68e-01 |
| Viral Messenger RNA Synthesis | 41 | 1.20e-01 | -1.40e-01 | 2.87e-01 |
| SUMOylation of chromatin organization proteins | 49 | 8.95e-02 | -1.40e-01 | 2.27e-01 |
| Resolution of D-Loop Structures | 29 | 1.92e-01 | -1.40e-01 | 3.85e-01 |
| Regulation of HSF1-mediated heat shock response | 67 | 4.96e-02 | -1.39e-01 | 1.53e-01 |
| NGF-stimulated transcription | 25 | 2.31e-01 | -1.39e-01 | 4.30e-01 |
| Regulation of TNFR1 signaling | 31 | 1.83e-01 | -1.38e-01 | 3.76e-01 |
| RUNX2 regulates osteoblast differentiation | 13 | 3.89e-01 | -1.38e-01 | 5.83e-01 |
| Diseases associated with glycosylation precursor biosynthesis | 15 | 3.57e-01 | -1.37e-01 | 5.57e-01 |
| Transcriptional Regulation by TP53 | 302 | 4.55e-05 | -1.37e-01 | 1.52e-03 |
| MTOR signalling | 36 | 1.55e-01 | 1.37e-01 | 3.42e-01 |
| C-type lectin receptors (CLRs) | 100 | 1.80e-02 | -1.37e-01 | 7.40e-02 |
| PERK regulates gene expression | 26 | 2.29e-01 | -1.36e-01 | 4.28e-01 |
| TNFR2 non-canonical NF-kB pathway | 68 | 5.20e-02 | -1.36e-01 | 1.58e-01 |
| Downregulation of SMAD2/3:SMAD4 transcriptional activity | 24 | 2.50e-01 | -1.36e-01 | 4.54e-01 |
| Transcriptional Regulation by E2F6 | 29 | 2.06e-01 | -1.36e-01 | 4.05e-01 |
| ATF4 activates genes in response to endoplasmic reticulum stress | 23 | 2.60e-01 | -1.36e-01 | 4.62e-01 |
| SARS-CoV-2 modulates host translation machinery | 39 | 1.44e-01 | -1.35e-01 | 3.29e-01 |
| RAS processing | 15 | 3.65e-01 | -1.35e-01 | 5.63e-01 |
| Signaling by ALK | 18 | 3.21e-01 | -1.35e-01 | 5.22e-01 |
| Signalling to ERKs | 25 | 2.43e-01 | -1.35e-01 | 4.48e-01 |
| RUNX3 regulates NOTCH signaling | 11 | 4.40e-01 | -1.34e-01 | 6.25e-01 |
| Signaling by cytosolic FGFR1 fusion mutants | 16 | 3.56e-01 | -1.33e-01 | 5.55e-01 |
| Recruitment of NuMA to mitotic centrosomes | 65 | 6.35e-02 | -1.33e-01 | 1.81e-01 |
| Activation of the pre-replicative complex | 30 | 2.07e-01 | -1.33e-01 | 4.07e-01 |
| NS1 Mediated Effects on Host Pathways | 38 | 1.57e-01 | -1.33e-01 | 3.44e-01 |
| Disorders of transmembrane transporters | 111 | 1.62e-02 | -1.32e-01 | 6.83e-02 |
| Citric acid cycle (TCA cycle) | 19 | 3.18e-01 | 1.32e-01 | 5.19e-01 |
| Class A/1 (Rhodopsin-like receptors) | 49 | 1.10e-01 | 1.32e-01 | 2.66e-01 |
| NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux | 23 | 2.73e-01 | 1.32e-01 | 4.73e-01 |
| Generic Transcription Pathway | 826 | 2.61e-10 | -1.31e-01 | 7.85e-08 |
| Pausing and recovery of Tat-mediated HIV elongation | 26 | 2.47e-01 | -1.31e-01 | 4.51e-01 |
| Tat-mediated HIV elongation arrest and recovery | 26 | 2.47e-01 | -1.31e-01 | 4.51e-01 |
| ESR-mediated signaling | 115 | 1.54e-02 | -1.31e-01 | 6.60e-02 |
| NRAGE signals death through JNK | 30 | 2.15e-01 | 1.31e-01 | 4.15e-01 |
| Fcgamma receptor (FCGR) dependent phagocytosis | 62 | 7.56e-02 | -1.31e-01 | 2.02e-01 |
| RET signaling | 23 | 2.79e-01 | 1.30e-01 | 4.76e-01 |
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | 11 | 4.55e-01 | -1.30e-01 | 6.34e-01 |
| Inhibition of DNA recombination at telomere | 18 | 3.39e-01 | -1.30e-01 | 5.38e-01 |
| Signaling by Non-Receptor Tyrosine Kinases | 36 | 1.78e-01 | -1.30e-01 | 3.69e-01 |
| Signaling by PTK6 | 36 | 1.78e-01 | -1.30e-01 | 3.69e-01 |
| IRS-related events triggered by IGF1R | 22 | 2.92e-01 | 1.30e-01 | 4.91e-01 |
| Gastrin-CREB signalling pathway via PKC and MAPK | 11 | 4.57e-01 | -1.29e-01 | 6.34e-01 |
| tRNA processing | 93 | 3.13e-02 | -1.29e-01 | 1.09e-01 |
| TCR signaling | 87 | 3.78e-02 | -1.29e-01 | 1.27e-01 |
| tRNA modification in the nucleus and cytosol | 34 | 1.93e-01 | -1.29e-01 | 3.86e-01 |
| Activation of BH3-only proteins | 27 | 2.47e-01 | 1.29e-01 | 4.51e-01 |
| Mitophagy | 25 | 2.66e-01 | -1.29e-01 | 4.69e-01 |
| Nonhomologous End-Joining (NHEJ) | 29 | 2.33e-01 | -1.28e-01 | 4.33e-01 |
| SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs | 10 | 4.85e-01 | 1.28e-01 | 6.61e-01 |
| G alpha (s) signalling events | 48 | 1.27e-01 | 1.27e-01 | 2.99e-01 |
| PINK1-PRKN Mediated Mitophagy | 20 | 3.24e-01 | -1.27e-01 | 5.24e-01 |
| Netrin-1 signaling | 25 | 2.71e-01 | 1.27e-01 | 4.73e-01 |
| Activation of BAD and translocation to mitochondria | 14 | 4.10e-01 | 1.27e-01 | 6.01e-01 |
| Cilium Assembly | 150 | 7.49e-03 | -1.27e-01 | 4.00e-02 |
| Diseases associated with glycosaminoglycan metabolism | 16 | 3.81e-01 | -1.27e-01 | 5.77e-01 |
| Vasopressin regulates renal water homeostasis via Aquaporins | 23 | 2.94e-01 | 1.26e-01 | 4.94e-01 |
| Metabolism of amino acids and derivatives | 225 | 1.14e-03 | -1.26e-01 | 1.23e-02 |
| MAP3K8 (TPL2)-dependent MAPK1/3 activation | 14 | 4.13e-01 | -1.26e-01 | 6.04e-01 |
| RNA Polymerase III Transcription Initiation From Type 1 Promoter | 27 | 2.57e-01 | -1.26e-01 | 4.61e-01 |
| G alpha (z) signalling events | 25 | 2.76e-01 | 1.26e-01 | 4.73e-01 |
| COPI-dependent Golgi-to-ER retrograde traffic | 66 | 7.85e-02 | -1.25e-01 | 2.07e-01 |
| Signaling by WNT in cancer | 23 | 2.99e-01 | -1.25e-01 | 5.01e-01 |
| Axon guidance | 300 | 2.10e-04 | -1.25e-01 | 3.66e-03 |
| Cellular response to starvation | 120 | 1.82e-02 | -1.25e-01 | 7.43e-02 |
| RNA Polymerase III Transcription Initiation From Type 3 Promoter | 27 | 2.61e-01 | -1.25e-01 | 4.63e-01 |
| Integrin signaling | 16 | 3.87e-01 | 1.25e-01 | 5.82e-01 |
| Platelet Aggregation (Plug Formation) | 16 | 3.87e-01 | 1.25e-01 | 5.82e-01 |
| tRNA Aminoacylation | 23 | 3.00e-01 | -1.25e-01 | 5.01e-01 |
| Transcriptional Regulation by MECP2 | 31 | 2.31e-01 | -1.24e-01 | 4.31e-01 |
| Polymerase switching on the C-strand of the telomere | 22 | 3.14e-01 | -1.24e-01 | 5.17e-01 |
| Extracellular matrix organization | 93 | 4.00e-02 | 1.23e-01 | 1.32e-01 |
| Sensory processing of sound | 27 | 2.68e-01 | 1.23e-01 | 4.69e-01 |
| Sensory processing of sound by inner hair cells of the cochlea | 27 | 2.68e-01 | 1.23e-01 | 4.69e-01 |
| Deubiquitination | 198 | 2.90e-03 | -1.23e-01 | 2.10e-02 |
| Cell-Cell communication | 48 | 1.40e-01 | 1.23e-01 | 3.22e-01 |
| RND2 GTPase cycle | 34 | 2.15e-01 | 1.23e-01 | 4.15e-01 |
| Nuclear Events (kinase and transcription factor activation) | 42 | 1.69e-01 | -1.23e-01 | 3.60e-01 |
| Telomere C-strand synthesis initiation | 10 | 5.02e-01 | -1.23e-01 | 6.76e-01 |
| mRNA Splicing | 158 | 7.95e-03 | -1.23e-01 | 4.17e-02 |
| Gene expression (Transcription) | 1040 | 5.74e-11 | -1.23e-01 | 2.30e-08 |
| Cytosolic sulfonation of small molecules | 10 | 5.03e-01 | -1.22e-01 | 6.77e-01 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | 10 | 5.03e-01 | 1.22e-01 | 6.77e-01 |
| Other semaphorin interactions | 10 | 5.05e-01 | 1.22e-01 | 6.77e-01 |
| The NLRP3 inflammasome | 12 | 4.67e-01 | -1.21e-01 | 6.46e-01 |
| ADP signalling through P2Y purinoceptor 1 | 16 | 4.04e-01 | 1.20e-01 | 5.98e-01 |
| HSF1 activation | 21 | 3.40e-01 | -1.20e-01 | 5.38e-01 |
| Neurotransmitter release cycle | 20 | 3.52e-01 | -1.20e-01 | 5.52e-01 |
| Anti-inflammatory response favouring Leishmania parasite infection | 54 | 1.27e-01 | 1.20e-01 | 2.99e-01 |
| Leishmania parasite growth and survival | 54 | 1.27e-01 | 1.20e-01 | 2.99e-01 |
| activated TAK1 mediates p38 MAPK activation | 13 | 4.56e-01 | 1.19e-01 | 6.34e-01 |
| Golgi-to-ER retrograde transport | 95 | 4.48e-02 | -1.19e-01 | 1.41e-01 |
| Class B/2 (Secretin family receptors) | 29 | 2.67e-01 | 1.19e-01 | 4.69e-01 |
| Cytoprotection by HMOX1 | 44 | 1.72e-01 | -1.19e-01 | 3.62e-01 |
| MAPK1/MAPK3 signaling | 164 | 8.79e-03 | -1.19e-01 | 4.48e-02 |
| Nervous system development | 313 | 3.25e-04 | -1.19e-01 | 4.82e-03 |
| CD209 (DC-SIGN) signaling | 15 | 4.28e-01 | -1.18e-01 | 6.18e-01 |
| Glycosphingolipid metabolism | 27 | 2.89e-01 | -1.18e-01 | 4.87e-01 |
| Signaling by Retinoic Acid | 17 | 4.00e-01 | -1.18e-01 | 5.96e-01 |
| Generation of second messenger molecules | 15 | 4.29e-01 | -1.18e-01 | 6.18e-01 |
| Signaling by CSF3 (G-CSF) | 24 | 3.18e-01 | -1.18e-01 | 5.19e-01 |
| RNA Polymerase II Transcription | 927 | 2.31e-09 | -1.18e-01 | 4.62e-07 |
| HSF1-dependent transactivation | 25 | 3.09e-01 | -1.18e-01 | 5.11e-01 |
| Assembly of the ORC complex at the origin of replication | 10 | 5.21e-01 | 1.17e-01 | 6.90e-01 |
| RAF/MAP kinase cascade | 159 | 1.12e-02 | -1.17e-01 | 5.28e-02 |
| Regulation of MECP2 expression and activity | 23 | 3.32e-01 | -1.17e-01 | 5.32e-01 |
| Diseases of metabolism | 126 | 2.38e-02 | -1.17e-01 | 8.95e-02 |
| Attenuation phase | 19 | 3.79e-01 | -1.16e-01 | 5.77e-01 |
| mRNA Splicing - Minor Pathway | 49 | 1.59e-01 | -1.16e-01 | 3.47e-01 |
| Centrosome maturation | 66 | 1.03e-01 | -1.16e-01 | 2.54e-01 |
| Recruitment of mitotic centrosome proteins and complexes | 66 | 1.03e-01 | -1.16e-01 | 2.54e-01 |
| Processing of Capped Intron-Containing Pre-mRNA | 199 | 5.00e-03 | -1.16e-01 | 3.05e-02 |
| Signaling by WNT | 177 | 8.19e-03 | -1.16e-01 | 4.22e-02 |
| ADORA2B mediated anti-inflammatory cytokines production | 33 | 2.51e-01 | 1.15e-01 | 4.57e-01 |
| Translation of Replicase and Assembly of the Replication Transcription Complex | 11 | 5.08e-01 | -1.15e-01 | 6.80e-01 |
| PIP3 activates AKT signaling | 185 | 7.08e-03 | -1.15e-01 | 3.87e-02 |
| Metabolism of vitamins and cofactors | 111 | 3.68e-02 | -1.15e-01 | 1.25e-01 |
| Metabolism of non-coding RNA | 48 | 1.69e-01 | -1.15e-01 | 3.60e-01 |
| snRNP Assembly | 48 | 1.69e-01 | -1.15e-01 | 3.60e-01 |
| Plasma lipoprotein assembly, remodeling, and clearance | 39 | 2.16e-01 | -1.15e-01 | 4.16e-01 |
| Semaphorin interactions | 39 | 2.17e-01 | -1.14e-01 | 4.16e-01 |
| Phase II - Conjugation of compounds | 46 | 1.81e-01 | -1.14e-01 | 3.73e-01 |
| Metabolism of water-soluble vitamins and cofactors | 82 | 7.44e-02 | -1.14e-01 | 2.00e-01 |
| N-glycan antennae elongation in the medial/trans-Golgi | 17 | 4.15e-01 | 1.14e-01 | 6.04e-01 |
| Synthesis of substrates in N-glycan biosythesis | 48 | 1.72e-01 | -1.14e-01 | 3.62e-01 |
| mRNA Splicing - Major Pathway | 148 | 1.71e-02 | -1.14e-01 | 7.10e-02 |
| Asparagine N-linked glycosylation | 225 | 3.42e-03 | -1.14e-01 | 2.34e-02 |
| Purine ribonucleoside monophosphate biosynthesis | 10 | 5.35e-01 | 1.13e-01 | 7.00e-01 |
| RHOB GTPase cycle | 44 | 1.95e-01 | 1.13e-01 | 3.87e-01 |
| Oxidative Stress Induced Senescence | 55 | 1.48e-01 | -1.13e-01 | 3.35e-01 |
| Cytosolic sensors of pathogen-associated DNA | 53 | 1.57e-01 | -1.12e-01 | 3.44e-01 |
| Role of phospholipids in phagocytosis | 16 | 4.40e-01 | 1.12e-01 | 6.25e-01 |
| Signaling by Nuclear Receptors | 151 | 1.91e-02 | -1.11e-01 | 7.68e-02 |
| MAPK targets/ Nuclear events mediated by MAP kinases | 23 | 3.59e-01 | -1.11e-01 | 5.57e-01 |
| RNA Polymerase II Pre-transcription Events | 68 | 1.16e-01 | -1.10e-01 | 2.79e-01 |
| Signaling by FGFR1 in disease | 24 | 3.50e-01 | -1.10e-01 | 5.49e-01 |
| Cargo concentration in the ER | 20 | 3.95e-01 | -1.10e-01 | 5.90e-01 |
| HIV elongation arrest and recovery | 27 | 3.24e-01 | -1.10e-01 | 5.24e-01 |
| Pausing and recovery of HIV elongation | 27 | 3.24e-01 | -1.10e-01 | 5.24e-01 |
| The citric acid (TCA) cycle and respiratory electron transport | 121 | 3.77e-02 | -1.10e-01 | 1.27e-01 |
| Prostacyclin signalling through prostacyclin receptor | 12 | 5.12e-01 | 1.09e-01 | 6.81e-01 |
| Signaling by ERBB2 | 33 | 2.77e-01 | -1.09e-01 | 4.73e-01 |
| Detoxification of Reactive Oxygen Species | 23 | 3.65e-01 | 1.09e-01 | 5.63e-01 |
| Bile acid and bile salt metabolism | 15 | 4.65e-01 | 1.09e-01 | 6.44e-01 |
| NCAM signaling for neurite out-growth | 24 | 3.58e-01 | -1.08e-01 | 5.57e-01 |
| Inactivation of CSF3 (G-CSF) signaling | 19 | 4.14e-01 | -1.08e-01 | 6.04e-01 |
| MAPK family signaling cascades | 191 | 1.03e-02 | -1.08e-01 | 4.93e-02 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | 158 | 1.95e-02 | -1.08e-01 | 7.84e-02 |
| TRAF6-mediated induction of TAK1 complex within TLR4 complex | 10 | 5.55e-01 | -1.08e-01 | 7.17e-01 |
| Beta-catenin independent WNT signaling | 106 | 5.65e-02 | -1.07e-01 | 1.69e-01 |
| Organelle biogenesis and maintenance | 204 | 8.48e-03 | -1.07e-01 | 4.35e-02 |
| Other interleukin signaling | 15 | 4.73e-01 | -1.07e-01 | 6.52e-01 |
| Inactivation, recovery and regulation of the phototransduction cascade | 17 | 4.45e-01 | -1.07e-01 | 6.31e-01 |
| Interferon alpha/beta signaling | 51 | 1.87e-01 | 1.07e-01 | 3.82e-01 |
| Josephin domain DUBs | 11 | 5.41e-01 | -1.06e-01 | 7.05e-01 |
| Transcription of the HIV genome | 57 | 1.66e-01 | -1.06e-01 | 3.58e-01 |
| Peroxisomal lipid metabolism | 22 | 3.89e-01 | 1.06e-01 | 5.83e-01 |
| Activation of GABAB receptors | 18 | 4.37e-01 | 1.06e-01 | 6.25e-01 |
| GABA B receptor activation | 18 | 4.37e-01 | 1.06e-01 | 6.25e-01 |
| tRNA processing in the nucleus | 55 | 1.75e-01 | -1.06e-01 | 3.67e-01 |
| RNA Polymerase III Chain Elongation | 17 | 4.51e-01 | -1.06e-01 | 6.34e-01 |
| Interleukin-1 family signaling | 99 | 7.00e-02 | -1.06e-01 | 1.92e-01 |
| Signaling by Rho GTPases, Miro GTPases and RHOBTB3 | 449 | 1.51e-04 | -1.05e-01 | 2.83e-03 |
| p75 NTR receptor-mediated signalling | 59 | 1.63e-01 | -1.05e-01 | 3.53e-01 |
| Uptake and actions of bacterial toxins | 18 | 4.40e-01 | -1.05e-01 | 6.25e-01 |
| Developmental Biology | 468 | 1.12e-04 | -1.05e-01 | 2.24e-03 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | 33 | 2.97e-01 | -1.05e-01 | 4.97e-01 |
| Cellular response to chemical stress | 145 | 3.00e-02 | -1.05e-01 | 1.07e-01 |
| E2F mediated regulation of DNA replication | 19 | 4.30e-01 | -1.05e-01 | 6.18e-01 |
| COPI-independent Golgi-to-ER retrograde traffic | 29 | 3.31e-01 | -1.04e-01 | 5.31e-01 |
| Endosomal Sorting Complex Required For Transport (ESCRT) | 27 | 3.49e-01 | 1.04e-01 | 5.48e-01 |
| RNA Polymerase III Transcription Initiation From Type 2 Promoter | 26 | 3.59e-01 | -1.04e-01 | 5.57e-01 |
| Synthesis of very long-chain fatty acyl-CoAs | 16 | 4.72e-01 | 1.04e-01 | 6.51e-01 |
| Regulation of lipid metabolism by PPARalpha | 84 | 1.01e-01 | -1.04e-01 | 2.51e-01 |
| Energy dependent regulation of mTOR by LKB1-AMPK | 25 | 3.74e-01 | 1.03e-01 | 5.72e-01 |
| Metabolism of proteins | 1246 | 2.76e-09 | -1.03e-01 | 4.74e-07 |
| Signaling by NODAL | 12 | 5.40e-01 | 1.02e-01 | 7.05e-01 |
| FOXO-mediated transcription of cell cycle genes | 13 | 5.24e-01 | -1.02e-01 | 6.93e-01 |
| Cell-cell junction organization | 13 | 5.24e-01 | 1.02e-01 | 6.93e-01 |
| A tetrasaccharide linker sequence is required for GAG synthesis | 10 | 5.77e-01 | 1.02e-01 | 7.35e-01 |
| TGF-beta receptor signaling activates SMADs | 39 | 2.72e-01 | -1.02e-01 | 4.73e-01 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | 23 | 3.99e-01 | -1.02e-01 | 5.95e-01 |
| TRAF3-dependent IRF activation pathway | 14 | 5.10e-01 | -1.02e-01 | 6.81e-01 |
| Glucose metabolism | 72 | 1.37e-01 | -1.01e-01 | 3.16e-01 |
| GPER1 signaling | 25 | 3.81e-01 | 1.01e-01 | 5.77e-01 |
| Diseases of signal transduction by growth factor receptors and second messengers | 299 | 2.75e-03 | -1.01e-01 | 2.08e-02 |
| GABA receptor activation | 19 | 4.45e-01 | 1.01e-01 | 6.31e-01 |
| Synthesis of PIPs at the Golgi membrane | 12 | 5.45e-01 | -1.01e-01 | 7.08e-01 |
| Retrograde transport at the Trans-Golgi-Network | 45 | 2.43e-01 | -1.01e-01 | 4.48e-01 |
| HIV Transcription Initiation | 39 | 2.77e-01 | -1.01e-01 | 4.73e-01 |
| RNA Polymerase II HIV Promoter Escape | 39 | 2.77e-01 | -1.01e-01 | 4.73e-01 |
| RNA Polymerase II Promoter Escape | 39 | 2.77e-01 | -1.01e-01 | 4.73e-01 |
| RNA Polymerase II Transcription Initiation | 39 | 2.77e-01 | -1.01e-01 | 4.73e-01 |
| RNA Polymerase II Transcription Initiation And Promoter Clearance | 39 | 2.77e-01 | -1.01e-01 | 4.73e-01 |
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | 39 | 2.77e-01 | -1.01e-01 | 4.73e-01 |
| Signaling by ERBB2 KD Mutants | 12 | 5.46e-01 | -1.01e-01 | 7.08e-01 |
| Cellular responses to stress | 546 | 6.87e-05 | -1.01e-01 | 1.87e-03 |
| Signaling by Rho GTPases | 437 | 3.71e-04 | -1.00e-01 | 5.07e-03 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | 38 | 2.86e-01 | -9.99e-02 | 4.84e-01 |
| Ras activation upon Ca2+ influx through NMDA receptor | 10 | 5.84e-01 | -9.99e-02 | 7.42e-01 |
| Diseases of glycosylation | 69 | 1.52e-01 | -9.98e-02 | 3.40e-01 |
| RAF activation | 28 | 3.61e-01 | -9.97e-02 | 5.60e-01 |
| Regulation of IFNG signaling | 13 | 5.34e-01 | 9.95e-02 | 7.00e-01 |
| RNA Polymerase III Transcription Initiation | 35 | 3.13e-01 | -9.85e-02 | 5.16e-01 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat | 36 | 3.08e-01 | -9.82e-02 | 5.10e-01 |
| HIV Transcription Elongation | 36 | 3.08e-01 | -9.82e-02 | 5.10e-01 |
| Tat-mediated elongation of the HIV-1 transcript | 36 | 3.08e-01 | -9.82e-02 | 5.10e-01 |
| HIV Infection | 190 | 2.00e-02 | -9.81e-02 | 7.98e-02 |
| Disease | 1086 | 9.51e-08 | -9.79e-02 | 9.53e-06 |
| Syndecan interactions | 10 | 5.93e-01 | -9.77e-02 | 7.49e-01 |
| RHOBTB2 GTPase cycle | 20 | 4.49e-01 | -9.77e-02 | 6.34e-01 |
| Synthesis of PC | 22 | 4.29e-01 | -9.74e-02 | 6.18e-01 |
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes | 27 | 3.83e-01 | -9.70e-02 | 5.80e-01 |
| The phototransduction cascade | 18 | 4.77e-01 | -9.69e-02 | 6.55e-01 |
| Cellular responses to stimuli | 551 | 1.25e-04 | -9.65e-02 | 2.42e-03 |
| Transport of the SLBP independent Mature mRNA | 33 | 3.38e-01 | -9.64e-02 | 5.38e-01 |
| Protein localization | 123 | 6.70e-02 | -9.58e-02 | 1.87e-01 |
| Negative regulation of MET activity | 16 | 5.08e-01 | -9.55e-02 | 6.80e-01 |
| FCGR3A-mediated IL10 synthesis | 22 | 4.38e-01 | 9.55e-02 | 6.25e-01 |
| RNA polymerase II transcribes snRNA genes | 71 | 1.66e-01 | -9.52e-02 | 3.57e-01 |
| Phase I - Functionalization of compounds | 30 | 3.68e-01 | 9.50e-02 | 5.65e-01 |
| Neddylation | 188 | 2.59e-02 | -9.45e-02 | 9.42e-02 |
| Intracellular signaling by second messengers | 210 | 2.01e-02 | -9.34e-02 | 7.98e-02 |
| Diseases of programmed cell death | 37 | 3.26e-01 | -9.34e-02 | 5.25e-01 |
| ISG15 antiviral mechanism | 70 | 1.78e-01 | -9.32e-02 | 3.69e-01 |
| Cytochrome P450 - arranged by substrate type | 14 | 5.47e-01 | 9.29e-02 | 7.09e-01 |
| Formation of RNA Pol II elongation complex | 50 | 2.56e-01 | -9.28e-02 | 4.61e-01 |
| RNA Polymerase II Transcription Elongation | 50 | 2.56e-01 | -9.28e-02 | 4.61e-01 |
| Signaling by high-kinase activity BRAF mutants | 22 | 4.52e-01 | -9.27e-02 | 6.34e-01 |
| COPII-mediated vesicle transport | 51 | 2.58e-01 | -9.15e-02 | 4.61e-01 |
| Cargo trafficking to the periciliary membrane | 40 | 3.17e-01 | -9.14e-02 | 5.18e-01 |
| EGR2 and SOX10-mediated initiation of Schwann cell myelination | 14 | 5.54e-01 | 9.13e-02 | 7.17e-01 |
| COPI-mediated anterograde transport | 71 | 1.85e-01 | -9.10e-02 | 3.79e-01 |
| TAK1-dependent IKK and NF-kappa-B activation | 18 | 5.05e-01 | 9.08e-02 | 6.77e-01 |
| Basigin interactions | 14 | 5.59e-01 | 9.03e-02 | 7.19e-01 |
| SUMOylation of transcription cofactors | 35 | 3.56e-01 | -9.02e-02 | 5.55e-01 |
| Amino acid transport across the plasma membrane | 16 | 5.33e-01 | -9.01e-02 | 7.00e-01 |
| Metabolic disorders of biological oxidation enzymes | 14 | 5.60e-01 | -9.00e-02 | 7.20e-01 |
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 16 | 5.34e-01 | -8.98e-02 | 7.00e-01 |
| IGF1R signaling cascade | 23 | 4.56e-01 | 8.98e-02 | 6.34e-01 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | 23 | 4.56e-01 | 8.98e-02 | 6.34e-01 |
| Telomere C-strand (Lagging Strand) Synthesis | 29 | 4.04e-01 | -8.96e-02 | 5.98e-01 |
| Defective Intrinsic Pathway for Apoptosis | 23 | 4.57e-01 | -8.95e-02 | 6.34e-01 |
| O-linked glycosylation of mucins | 26 | 4.31e-01 | -8.93e-02 | 6.18e-01 |
| Response to elevated platelet cytosolic Ca2+ | 53 | 2.62e-01 | -8.92e-02 | 4.63e-01 |
| Transport of Mature mRNA Derived from an Intronless Transcript | 40 | 3.29e-01 | -8.91e-02 | 5.29e-01 |
| Toll Like Receptor 3 (TLR3) Cascade | 74 | 1.87e-01 | -8.88e-02 | 3.82e-01 |
| FGFR2 mutant receptor activation | 17 | 5.28e-01 | 8.84e-02 | 6.96e-01 |
| Signaling by Receptor Tyrosine Kinases | 293 | 9.64e-03 | -8.83e-02 | 4.83e-02 |
| PPARA activates gene expression | 82 | 1.68e-01 | -8.81e-02 | 3.60e-01 |
| MET promotes cell motility | 13 | 5.82e-01 | 8.81e-02 | 7.41e-01 |
| Regulation of RUNX1 Expression and Activity | 17 | 5.30e-01 | -8.80e-02 | 6.97e-01 |
| MyD88-independent TLR4 cascade | 74 | 1.91e-01 | -8.79e-02 | 3.84e-01 |
| TRIF(TICAM1)-mediated TLR4 signaling | 74 | 1.91e-01 | -8.79e-02 | 3.84e-01 |
| RNA Pol II CTD phosphorylation and interaction with CE | 24 | 4.57e-01 | -8.77e-02 | 6.34e-01 |
| RNA Pol II CTD phosphorylation and interaction with CE during HIV infection | 24 | 4.57e-01 | -8.77e-02 | 6.34e-01 |
| Antigen Presentation: Folding, assembly and peptide loading of class I MHC | 26 | 4.40e-01 | 8.74e-02 | 6.25e-01 |
| Aggrephagy | 19 | 5.12e-01 | -8.68e-02 | 6.81e-01 |
| Death Receptor Signalling | 96 | 1.44e-01 | -8.63e-02 | 3.30e-01 |
| Muscle contraction | 67 | 2.24e-01 | -8.60e-02 | 4.23e-01 |
| Late Phase of HIV Life Cycle | 117 | 1.09e-01 | -8.60e-02 | 2.64e-01 |
| Cell surface interactions at the vascular wall | 56 | 2.66e-01 | -8.59e-02 | 4.69e-01 |
| VEGFA-VEGFR2 Pathway | 71 | 2.11e-01 | -8.59e-02 | 4.11e-01 |
| Antigen processing: Ubiquitination & Proteasome degradation | 241 | 2.32e-02 | -8.52e-02 | 8.81e-02 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | 55 | 2.75e-01 | -8.51e-02 | 4.73e-01 |
| Molecules associated with elastic fibres | 12 | 6.10e-01 | 8.49e-02 | 7.63e-01 |
| Glycolysis | 57 | 2.70e-01 | -8.45e-02 | 4.72e-01 |
| MAP2K and MAPK activation | 25 | 4.68e-01 | -8.39e-02 | 6.46e-01 |
| Formation of HIV elongation complex in the absence of HIV Tat | 37 | 3.80e-01 | -8.34e-02 | 5.77e-01 |
| Signaling by FLT3 ITD and TKD mutants | 12 | 6.17e-01 | -8.34e-02 | 7.69e-01 |
| Hemostasis | 304 | 1.30e-02 | -8.33e-02 | 5.86e-02 |
| PI Metabolism | 60 | 2.66e-01 | -8.31e-02 | 4.69e-01 |
| Response of EIF2AK1 (HRI) to heme deficiency | 14 | 5.90e-01 | -8.31e-02 | 7.47e-01 |
| TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway | 10 | 6.50e-01 | 8.29e-02 | 7.88e-01 |
| Platelet degranulation | 49 | 3.17e-01 | -8.27e-02 | 5.18e-01 |
| Antiviral mechanism by IFN-stimulated genes | 77 | 2.11e-01 | -8.26e-02 | 4.11e-01 |
| Chromatin modifying enzymes | 158 | 7.45e-02 | -8.24e-02 | 2.00e-01 |
| Chromatin organization | 158 | 7.45e-02 | -8.24e-02 | 2.00e-01 |
| Transcriptional regulation by small RNAs | 45 | 3.41e-01 | -8.20e-02 | 5.38e-01 |
| Competing endogenous RNAs (ceRNAs) regulate PTEN translation | 10 | 6.53e-01 | 8.20e-02 | 7.89e-01 |
| Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | 16 | 5.71e-01 | -8.19e-02 | 7.31e-01 |
| Intrinsic Pathway for Apoptosis | 47 | 3.33e-01 | -8.17e-02 | 5.32e-01 |
| Visual phototransduction | 34 | 4.11e-01 | -8.14e-02 | 6.02e-01 |
| ZBP1(DAI) mediated induction of type I IFNs | 17 | 5.65e-01 | -8.07e-02 | 7.25e-01 |
| G-protein mediated events | 32 | 4.33e-01 | -8.02e-02 | 6.20e-01 |
| Transcriptional activation of mitochondrial biogenesis | 40 | 3.81e-01 | -8.01e-02 | 5.77e-01 |
| Listeria monocytogenes entry into host cells | 14 | 6.04e-01 | -8.01e-02 | 7.57e-01 |
| HIV Life Cycle | 129 | 1.18e-01 | -7.98e-02 | 2.84e-01 |
| ER to Golgi Anterograde Transport | 108 | 1.54e-01 | -7.95e-02 | 3.42e-01 |
| G alpha (q) signalling events | 78 | 2.26e-01 | 7.94e-02 | 4.25e-01 |
| Platelet calcium homeostasis | 17 | 5.73e-01 | 7.90e-02 | 7.33e-01 |
| Signal Transduction | 1356 | 2.11e-06 | -7.89e-02 | 1.33e-04 |
| SARS-CoV-2 Infection | 213 | 4.82e-02 | -7.88e-02 | 1.49e-01 |
| SLC-mediated transmembrane transport | 105 | 1.65e-01 | 7.85e-02 | 3.57e-01 |
| Regulation of FZD by ubiquitination | 12 | 6.38e-01 | -7.83e-02 | 7.86e-01 |
| Selective autophagy | 50 | 3.41e-01 | -7.78e-02 | 5.38e-01 |
| Azathioprine ADME | 15 | 6.03e-01 | 7.74e-02 | 7.57e-01 |
| Neurotransmitter receptors and postsynaptic signal transmission | 77 | 2.42e-01 | 7.72e-02 | 4.47e-01 |
| Interleukin-6 signaling | 10 | 6.73e-01 | 7.70e-02 | 8.02e-01 |
| MyD88 dependent cascade initiated on endosome | 67 | 2.76e-01 | -7.70e-02 | 4.73e-01 |
| Toll Like Receptor 7/8 (TLR7/8) Cascade | 67 | 2.76e-01 | -7.70e-02 | 4.73e-01 |
| Activation of kainate receptors upon glutamate binding | 17 | 5.83e-01 | 7.69e-02 | 7.41e-01 |
| TNF signaling | 38 | 4.15e-01 | -7.65e-02 | 6.04e-01 |
| Protein methylation | 14 | 6.21e-01 | 7.63e-02 | 7.73e-01 |
| RHO GTPases Activate NADPH Oxidases | 14 | 6.22e-01 | 7.61e-02 | 7.73e-01 |
| Signaling by RAF1 mutants | 25 | 5.12e-01 | -7.58e-02 | 6.81e-01 |
| Infectious disease | 627 | 1.42e-03 | -7.55e-02 | 1.40e-02 |
| Toll Like Receptor 9 (TLR9) Cascade | 70 | 2.76e-01 | -7.54e-02 | 4.73e-01 |
| Metabolism of nitric oxide: NOS3 activation and regulation | 12 | 6.52e-01 | 7.51e-02 | 7.89e-01 |
| PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases | 10 | 6.81e-01 | -7.50e-02 | 8.07e-01 |
| Clathrin-mediated endocytosis | 89 | 2.22e-01 | -7.50e-02 | 4.23e-01 |
| SUMOylation of RNA binding proteins | 42 | 4.02e-01 | -7.48e-02 | 5.98e-01 |
| Neuronal System | 139 | 1.30e-01 | 7.45e-02 | 3.03e-01 |
| Constitutive Signaling by Aberrant PI3K in Cancer | 28 | 4.96e-01 | 7.44e-02 | 6.71e-01 |
| Synthesis of bile acids and bile salts | 13 | 6.43e-01 | 7.42e-02 | 7.86e-01 |
| HDACs deacetylate histones | 28 | 4.97e-01 | -7.42e-02 | 6.72e-01 |
| Class I MHC mediated antigen processing & presentation | 289 | 3.09e-02 | -7.41e-02 | 1.08e-01 |
| Toll Like Receptor 4 (TLR4) Cascade | 94 | 2.16e-01 | -7.39e-02 | 4.16e-01 |
| Role of LAT2/NTAL/LAB on calcium mobilization | 10 | 6.88e-01 | 7.33e-02 | 8.12e-01 |
| Signaling by Hedgehog | 99 | 2.12e-01 | -7.27e-02 | 4.12e-01 |
| Signaling by VEGF | 73 | 2.86e-01 | -7.22e-02 | 4.84e-01 |
| Signaling by Insulin receptor | 42 | 4.18e-01 | 7.22e-02 | 6.08e-01 |
| Pre-NOTCH Transcription and Translation | 31 | 4.87e-01 | -7.20e-02 | 6.64e-01 |
| The role of Nef in HIV-1 replication and disease pathogenesis | 19 | 5.87e-01 | -7.20e-02 | 7.43e-01 |
| SARS-CoV Infections | 270 | 4.25e-02 | -7.20e-02 | 1.37e-01 |
| Signaling by SCF-KIT | 32 | 4.81e-01 | -7.20e-02 | 6.58e-01 |
| Signaling by ERBB4 | 31 | 4.95e-01 | -7.08e-02 | 6.71e-01 |
| Interleukin-2 family signaling | 28 | 5.17e-01 | -7.08e-02 | 6.86e-01 |
| Intra-Golgi traffic | 39 | 4.47e-01 | -7.03e-02 | 6.32e-01 |
| Extension of Telomeres | 44 | 4.22e-01 | -6.99e-02 | 6.12e-01 |
| Post-translational protein modification | 917 | 4.38e-04 | -6.97e-02 | 5.49e-03 |
| Metabolism of porphyrins | 15 | 6.42e-01 | -6.92e-02 | 7.86e-01 |
| Chondroitin sulfate/dermatan sulfate metabolism | 27 | 5.34e-01 | 6.92e-02 | 7.00e-01 |
| G beta:gamma signalling through BTK | 11 | 6.91e-01 | 6.91e-02 | 8.12e-01 |
| Synthesis of PA | 18 | 6.13e-01 | -6.88e-02 | 7.66e-01 |
| Adaptive Immune System | 481 | 1.05e-02 | -6.87e-02 | 5.02e-02 |
| Signaling by NTRK1 (TRKA) | 79 | 2.92e-01 | -6.86e-02 | 4.91e-01 |
| Signaling by BRAF and RAF1 fusions | 42 | 4.42e-01 | -6.85e-02 | 6.28e-01 |
| DAP12 signaling | 19 | 6.06e-01 | -6.83e-02 | 7.59e-01 |
| GPCR downstream signalling | 197 | 1.00e-01 | 6.82e-02 | 2.49e-01 |
| Formation of the beta-catenin:TCF transactivating complex | 25 | 5.55e-01 | -6.81e-02 | 7.17e-01 |
| Synthesis of IP3 and IP4 in the cytosol | 16 | 6.37e-01 | -6.81e-02 | 7.86e-01 |
| Platelet activation, signaling and aggregation | 132 | 1.86e-01 | -6.69e-02 | 3.80e-01 |
| Transmission across Chemical Synapses | 101 | 2.46e-01 | 6.68e-02 | 4.51e-01 |
| Transport of the SLBP Dependant Mature mRNA | 34 | 5.01e-01 | -6.67e-02 | 6.76e-01 |
| Membrane binding and targetting of GAG proteins | 12 | 6.89e-01 | 6.67e-02 | 8.12e-01 |
| Synthesis And Processing Of GAG, GAGPOL Polyproteins | 12 | 6.89e-01 | 6.67e-02 | 8.12e-01 |
| ECM proteoglycans | 13 | 6.78e-01 | 6.66e-02 | 8.04e-01 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | 29 | 5.36e-01 | -6.63e-02 | 7.01e-01 |
| Lysosome Vesicle Biogenesis | 24 | 5.75e-01 | -6.61e-02 | 7.35e-01 |
| Pyruvate metabolism | 20 | 6.10e-01 | -6.59e-02 | 7.63e-01 |
| Negative regulators of DDX58/IFIH1 signaling | 34 | 5.12e-01 | -6.49e-02 | 6.81e-01 |
| Plasma lipoprotein remodeling | 11 | 7.09e-01 | 6.49e-02 | 8.26e-01 |
| Transport of Mature mRNAs Derived from Intronless Transcripts | 41 | 4.74e-01 | -6.47e-02 | 6.52e-01 |
| Synthesis of glycosylphosphatidylinositol (GPI) | 14 | 6.75e-01 | -6.46e-02 | 8.03e-01 |
| Diseases associated with the TLR signaling cascade | 17 | 6.45e-01 | 6.45e-02 | 7.86e-01 |
| Diseases of Immune System | 17 | 6.45e-01 | 6.45e-02 | 7.86e-01 |
| Signaling by FGFR in disease | 39 | 4.87e-01 | -6.43e-02 | 6.64e-01 |
| Signaling by GPCR | 216 | 1.05e-01 | 6.43e-02 | 2.58e-01 |
| Triglyceride metabolism | 16 | 6.56e-01 | -6.42e-02 | 7.92e-01 |
| Transport to the Golgi and subsequent modification | 130 | 2.10e-01 | -6.38e-02 | 4.10e-01 |
| TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 66 | 3.72e-01 | -6.36e-02 | 5.70e-01 |
| Gene Silencing by RNA | 62 | 3.89e-01 | -6.33e-02 | 5.83e-01 |
| Signaling by MET | 41 | 4.84e-01 | -6.32e-02 | 6.61e-01 |
| Cell recruitment (pro-inflammatory response) | 15 | 6.73e-01 | -6.29e-02 | 8.02e-01 |
| Purinergic signaling in leishmaniasis infection | 15 | 6.73e-01 | -6.29e-02 | 8.02e-01 |
| Glucagon-type ligand receptors | 14 | 6.85e-01 | 6.26e-02 | 8.11e-01 |
| NR1H2 and NR1H3-mediated signaling | 27 | 5.77e-01 | 6.21e-02 | 7.35e-01 |
| Cytokine Signaling in Immune system | 427 | 2.92e-02 | -6.20e-02 | 1.05e-01 |
| Neurexins and neuroligins | 21 | 6.23e-01 | 6.20e-02 | 7.73e-01 |
| Estrogen-dependent nuclear events downstream of ESR-membrane signaling | 16 | 6.69e-01 | -6.18e-02 | 8.01e-01 |
| trans-Golgi Network Vesicle Budding | 51 | 4.47e-01 | -6.16e-02 | 6.32e-01 |
| Signaling by NTRKs | 87 | 3.22e-01 | -6.16e-02 | 5.22e-01 |
| Factors involved in megakaryocyte development and platelet production | 87 | 3.22e-01 | -6.15e-02 | 5.22e-01 |
| Interleukin-7 signaling | 14 | 6.92e-01 | 6.11e-02 | 8.12e-01 |
| RHO GTPase cycle | 294 | 7.69e-02 | -6.03e-02 | 2.05e-01 |
| ERK/MAPK targets | 16 | 6.76e-01 | -6.02e-02 | 8.03e-01 |
| Macroautophagy | 97 | 3.08e-01 | -6.00e-02 | 5.10e-01 |
| Diseases associated with O-glycosylation of proteins | 21 | 6.35e-01 | 5.98e-02 | 7.86e-01 |
| mRNA Capping | 26 | 5.97e-01 | -5.98e-02 | 7.52e-01 |
| Signal amplification | 20 | 6.45e-01 | 5.95e-02 | 7.86e-01 |
| MyD88 cascade initiated on plasma membrane | 65 | 4.09e-01 | -5.93e-02 | 6.00e-01 |
| Toll Like Receptor 10 (TLR10) Cascade | 65 | 4.09e-01 | -5.93e-02 | 6.00e-01 |
| Toll Like Receptor 5 (TLR5) Cascade | 65 | 4.09e-01 | -5.93e-02 | 6.00e-01 |
| Unfolded Protein Response (UPR) | 76 | 3.76e-01 | -5.87e-02 | 5.76e-01 |
| Signaling by ALK fusions and activated point mutants | 46 | 4.94e-01 | -5.83e-02 | 6.70e-01 |
| Signaling by ALK in cancer | 46 | 4.94e-01 | -5.83e-02 | 6.70e-01 |
| BMAL1:CLOCK,NPAS2 activates circadian gene expression | 16 | 6.87e-01 | 5.82e-02 | 8.12e-01 |
| Immune System | 1156 | 1.26e-03 | -5.76e-02 | 1.32e-02 |
| Activation of HOX genes during differentiation | 41 | 5.28e-01 | -5.70e-02 | 6.96e-01 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | 41 | 5.28e-01 | -5.70e-02 | 6.96e-01 |
| TP53 Regulates Transcription of Cell Death Genes | 31 | 5.83e-01 | -5.69e-02 | 7.41e-01 |
| Metabolism of nucleotides | 73 | 4.01e-01 | 5.69e-02 | 5.98e-01 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | 29 | 5.97e-01 | -5.66e-02 | 7.52e-01 |
| Circadian Clock | 52 | 4.81e-01 | -5.65e-02 | 6.58e-01 |
| FGFR1 mutant receptor activation | 20 | 6.62e-01 | -5.64e-02 | 7.98e-01 |
| Interferon Signaling | 142 | 2.47e-01 | -5.64e-02 | 4.51e-01 |
| Signaling by Interleukins | 265 | 1.16e-01 | -5.64e-02 | 2.79e-01 |
| Glucagon-like Peptide-1 (GLP1) regulates insulin secretion | 22 | 6.47e-01 | 5.64e-02 | 7.87e-01 |
| XBP1(S) activates chaperone genes | 42 | 5.31e-01 | 5.58e-02 | 6.99e-01 |
| CaM pathway | 20 | 6.66e-01 | 5.58e-02 | 8.00e-01 |
| Calmodulin induced events | 20 | 6.66e-01 | 5.58e-02 | 8.00e-01 |
| MHC class II antigen presentation | 69 | 4.25e-01 | -5.56e-02 | 6.15e-01 |
| Insulin receptor recycling | 17 | 6.92e-01 | 5.54e-02 | 8.12e-01 |
| Kinesins | 32 | 5.93e-01 | -5.45e-02 | 7.49e-01 |
| Signaling by PDGF | 25 | 6.37e-01 | -5.45e-02 | 7.86e-01 |
| Disorders of Developmental Biology | 10 | 7.67e-01 | -5.42e-02 | 8.71e-01 |
| Disorders of Nervous System Development | 10 | 7.67e-01 | -5.42e-02 | 8.71e-01 |
| Loss of function of MECP2 in Rett syndrome | 10 | 7.67e-01 | -5.42e-02 | 8.71e-01 |
| Pervasive developmental disorders | 10 | 7.67e-01 | -5.42e-02 | 8.71e-01 |
| PLC beta mediated events | 29 | 6.18e-01 | -5.35e-02 | 7.70e-01 |
| Metabolism | 1253 | 1.94e-03 | -5.34e-02 | 1.74e-02 |
| Insulin receptor signalling cascade | 26 | 6.38e-01 | 5.33e-02 | 7.86e-01 |
| Stimuli-sensing channels | 39 | 5.70e-01 | 5.26e-02 | 7.31e-01 |
| RAC1 GTPase cycle | 110 | 3.41e-01 | -5.26e-02 | 5.38e-01 |
| Interleukin-20 family signaling | 13 | 7.43e-01 | -5.25e-02 | 8.58e-01 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 20 | 6.85e-01 | -5.23e-02 | 8.11e-01 |
| Transport of inorganic cations/anions and amino acids/oligopeptides | 45 | 5.45e-01 | 5.21e-02 | 7.08e-01 |
| SHC1 events in ERBB2 signaling | 11 | 7.65e-01 | -5.21e-02 | 8.71e-01 |
| Telomere Maintenance | 57 | 4.98e-01 | -5.19e-02 | 6.73e-01 |
| CDC42 GTPase cycle | 97 | 3.79e-01 | 5.17e-02 | 5.77e-01 |
| DAG and IP3 signaling | 26 | 6.48e-01 | 5.17e-02 | 7.87e-01 |
| Integration of energy metabolism | 60 | 4.89e-01 | -5.17e-02 | 6.65e-01 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 71 | 4.53e-01 | -5.15e-02 | 6.34e-01 |
| Toll Like Receptor 2 (TLR2) Cascade | 71 | 4.53e-01 | -5.15e-02 | 6.34e-01 |
| Toll Like Receptor TLR1:TLR2 Cascade | 71 | 4.53e-01 | -5.15e-02 | 6.34e-01 |
| Toll Like Receptor TLR6:TLR2 Cascade | 71 | 4.53e-01 | -5.15e-02 | 6.34e-01 |
| Toll-like Receptor Cascades | 108 | 3.62e-01 | -5.08e-02 | 5.60e-01 |
| Mitochondrial biogenesis | 54 | 5.19e-01 | -5.08e-02 | 6.88e-01 |
| Transport of Mature Transcript to Cytoplasm | 64 | 4.84e-01 | -5.06e-02 | 6.61e-01 |
| Metabolism of carbohydrates | 181 | 2.43e-01 | -5.05e-02 | 4.48e-01 |
| Interconversion of nucleotide di- and triphosphates | 25 | 6.64e-01 | 5.02e-02 | 8.00e-01 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | 29 | 6.44e-01 | -4.96e-02 | 7.86e-01 |
| Arachidonic acid metabolism | 21 | 6.99e-01 | 4.87e-02 | 8.18e-01 |
| SLC transporter disorders | 52 | 5.45e-01 | -4.85e-02 | 7.08e-01 |
| Regulation of signaling by CBL | 14 | 7.54e-01 | 4.84e-02 | 8.63e-01 |
| PRC2 methylates histones and DNA | 12 | 7.73e-01 | -4.81e-02 | 8.74e-01 |
| Peptide hormone metabolism | 31 | 6.45e-01 | -4.78e-02 | 7.86e-01 |
| Glutamate binding, activation of AMPA receptors and synaptic plasticity | 12 | 7.75e-01 | -4.77e-02 | 8.74e-01 |
| Trafficking of AMPA receptors | 12 | 7.75e-01 | -4.77e-02 | 8.74e-01 |
| Intraflagellar transport | 33 | 6.36e-01 | -4.76e-02 | 7.86e-01 |
| TNFR1-induced NFkappaB signaling pathway | 20 | 7.13e-01 | 4.75e-02 | 8.28e-01 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | 31 | 6.50e-01 | 4.71e-02 | 7.88e-01 |
| Vitamin B5 (pantothenate) metabolism | 11 | 7.87e-01 | -4.70e-02 | 8.83e-01 |
| Metabolism of steroids | 86 | 4.56e-01 | -4.65e-02 | 6.34e-01 |
| Processing of Capped Intronless Pre-mRNA | 23 | 7.01e-01 | 4.62e-02 | 8.20e-01 |
| Signaling by NTRK3 (TRKC) | 11 | 7.91e-01 | -4.62e-02 | 8.84e-01 |
| Membrane Trafficking | 446 | 9.93e-02 | -4.59e-02 | 2.48e-01 |
| Interferon gamma signaling | 55 | 5.57e-01 | 4.58e-02 | 7.17e-01 |
| Signaling by KIT in disease | 16 | 7.51e-01 | -4.57e-02 | 8.63e-01 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | 16 | 7.51e-01 | -4.57e-02 | 8.63e-01 |
| Activation of NMDA receptors and postsynaptic events | 44 | 6.00e-01 | 4.57e-02 | 7.54e-01 |
| Heparan sulfate/heparin (HS-GAG) metabolism | 22 | 7.12e-01 | 4.54e-02 | 8.28e-01 |
| G beta:gamma signalling through PI3Kgamma | 17 | 7.46e-01 | 4.54e-02 | 8.58e-01 |
| Deposition of new CENPA-containing nucleosomes at the centromere | 23 | 7.09e-01 | 4.50e-02 | 8.26e-01 |
| Nucleosome assembly | 23 | 7.09e-01 | 4.50e-02 | 8.26e-01 |
| Dopamine Neurotransmitter Release Cycle | 12 | 7.88e-01 | -4.48e-02 | 8.83e-01 |
| Vesicle-mediated transport | 454 | 1.05e-01 | -4.48e-02 | 2.58e-01 |
| G-protein beta:gamma signalling | 21 | 7.23e-01 | -4.47e-02 | 8.37e-01 |
| RAC3 GTPase cycle | 59 | 5.56e-01 | -4.43e-02 | 7.17e-01 |
| Growth hormone receptor signaling | 17 | 7.59e-01 | -4.29e-02 | 8.68e-01 |
| RHOA GTPase cycle | 93 | 4.80e-01 | -4.24e-02 | 6.58e-01 |
| L1CAM interactions | 41 | 6.40e-01 | 4.23e-02 | 7.86e-01 |
| SARS-CoV-2-host interactions | 150 | 3.79e-01 | -4.17e-02 | 5.77e-01 |
| HCMV Infection | 71 | 5.44e-01 | -4.16e-02 | 7.08e-01 |
| Inositol phosphate metabolism | 30 | 6.95e-01 | -4.13e-02 | 8.15e-01 |
| Innate Immune System | 620 | 8.78e-02 | -4.06e-02 | 2.23e-01 |
| Autophagy | 106 | 4.74e-01 | -4.03e-02 | 6.52e-01 |
| Nucleotide salvage | 18 | 7.69e-01 | 3.99e-02 | 8.73e-01 |
| Phospholipid metabolism | 133 | 4.27e-01 | -3.99e-02 | 6.18e-01 |
| HATs acetylate histones | 63 | 5.87e-01 | -3.96e-02 | 7.43e-01 |
| DARPP-32 events | 21 | 7.54e-01 | 3.95e-02 | 8.63e-01 |
| Post NMDA receptor activation events | 38 | 6.74e-01 | 3.95e-02 | 8.02e-01 |
| Ca2+ pathway | 40 | 6.68e-01 | -3.92e-02 | 8.01e-01 |
| Metabolism of cofactors | 17 | 7.80e-01 | -3.91e-02 | 8.78e-01 |
| Late endosomal microautophagy | 23 | 7.46e-01 | 3.90e-02 | 8.58e-01 |
| Sulfur amino acid metabolism | 17 | 7.82e-01 | -3.88e-02 | 8.79e-01 |
| Downstream signal transduction | 20 | 7.64e-01 | -3.87e-02 | 8.71e-01 |
| Mitochondrial Fatty Acid Beta-Oxidation | 26 | 7.35e-01 | -3.84e-02 | 8.49e-01 |
| Regulation of pyruvate dehydrogenase (PDH) complex | 11 | 8.26e-01 | -3.83e-02 | 9.07e-01 |
| Extra-nuclear estrogen signaling | 49 | 6.45e-01 | -3.81e-02 | 7.86e-01 |
| Downstream signaling of activated FGFR1 | 12 | 8.19e-01 | -3.80e-02 | 9.06e-01 |
| Downstream signaling of activated FGFR2 | 12 | 8.19e-01 | -3.80e-02 | 9.06e-01 |
| Downstream signaling of activated FGFR3 | 12 | 8.19e-01 | -3.80e-02 | 9.06e-01 |
| Downstream signaling of activated FGFR4 | 12 | 8.19e-01 | -3.80e-02 | 9.06e-01 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | 33 | 7.06e-01 | -3.80e-02 | 8.24e-01 |
| Oncogenic MAPK signaling | 56 | 6.23e-01 | -3.80e-02 | 7.73e-01 |
| MAP kinase activation | 49 | 6.48e-01 | -3.77e-02 | 7.87e-01 |
| PI3K/AKT Signaling in Cancer | 52 | 6.40e-01 | 3.75e-02 | 7.86e-01 |
| Budding and maturation of HIV virion | 24 | 7.53e-01 | 3.71e-02 | 8.63e-01 |
| IRE1alpha activates chaperones | 43 | 6.75e-01 | 3.69e-02 | 8.03e-01 |
| Binding and Uptake of Ligands by Scavenger Receptors | 10 | 8.41e-01 | 3.67e-02 | 9.14e-01 |
| Hyaluronan metabolism | 11 | 8.35e-01 | -3.64e-02 | 9.10e-01 |
| Signaling by Activin | 12 | 8.28e-01 | 3.62e-02 | 9.07e-01 |
| Mismatch Repair | 13 | 8.22e-01 | 3.61e-02 | 9.07e-01 |
| Assembly and cell surface presentation of NMDA receptors | 13 | 8.24e-01 | 3.57e-02 | 9.07e-01 |
| Mitochondrial protein import | 48 | 6.71e-01 | -3.54e-02 | 8.02e-01 |
| Glycosaminoglycan metabolism | 64 | 6.25e-01 | 3.54e-02 | 7.74e-01 |
| Pyruvate metabolism and Citric Acid (TCA) cycle | 41 | 6.96e-01 | 3.53e-02 | 8.15e-01 |
| Transport of bile salts and organic acids, metal ions and amine compounds | 34 | 7.23e-01 | -3.51e-02 | 8.37e-01 |
| Chromosome Maintenance | 78 | 5.97e-01 | -3.47e-02 | 7.52e-01 |
| Opioid Signalling | 58 | 6.53e-01 | -3.42e-02 | 7.89e-01 |
| Signaling by FGFR2 in disease | 24 | 7.74e-01 | 3.38e-02 | 8.74e-01 |
| Ion homeostasis | 26 | 7.66e-01 | -3.36e-02 | 8.71e-01 |
| Hyaluronan uptake and degradation | 10 | 8.54e-01 | -3.36e-02 | 9.19e-01 |
| Rab regulation of trafficking | 94 | 5.77e-01 | -3.33e-02 | 7.35e-01 |
| Cholesterol biosynthesis | 22 | 7.89e-01 | 3.29e-02 | 8.83e-01 |
| DAP12 interactions | 21 | 7.95e-01 | 3.27e-02 | 8.86e-01 |
| Rap1 signalling | 11 | 8.51e-01 | -3.27e-02 | 9.18e-01 |
| FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | 15 | 8.27e-01 | -3.27e-02 | 9.07e-01 |
| Potential therapeutics for SARS | 66 | 6.47e-01 | -3.26e-02 | 7.87e-01 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 50 | 6.90e-01 | -3.26e-02 | 8.12e-01 |
| CD28 co-stimulation | 27 | 7.70e-01 | -3.25e-02 | 8.73e-01 |
| FOXO-mediated transcription of cell death genes | 14 | 8.35e-01 | -3.21e-02 | 9.10e-01 |
| Nuclear signaling by ERBB4 | 16 | 8.26e-01 | 3.18e-02 | 9.07e-01 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | 21 | 8.01e-01 | -3.18e-02 | 8.91e-01 |
| Peroxisomal protein import | 48 | 7.11e-01 | -3.09e-02 | 8.27e-01 |
| RNA Polymerase II Transcription Termination | 45 | 7.23e-01 | 3.06e-02 | 8.37e-01 |
| Signaling by Hippo | 12 | 8.55e-01 | -3.05e-02 | 9.19e-01 |
| PKMTs methylate histone lysines | 31 | 7.74e-01 | -2.99e-02 | 8.74e-01 |
| Fatty acid metabolism | 104 | 6.02e-01 | 2.97e-02 | 7.56e-01 |
| Constitutive Signaling by AKT1 E17K in Cancer | 23 | 8.09e-01 | 2.91e-02 | 8.99e-01 |
| RND3 GTPase cycle | 29 | 7.88e-01 | -2.89e-02 | 8.83e-01 |
| RND1 GTPase cycle | 29 | 7.96e-01 | -2.78e-02 | 8.86e-01 |
| Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | 12 | 8.68e-01 | -2.78e-02 | 9.29e-01 |
| RHOC GTPase cycle | 49 | 7.46e-01 | 2.68e-02 | 8.58e-01 |
| Interleukin-37 signaling | 17 | 8.49e-01 | 2.66e-02 | 9.18e-01 |
| Carboxyterminal post-translational modifications of tubulin | 24 | 8.22e-01 | -2.65e-02 | 9.07e-01 |
| G alpha (12/13) signalling events | 40 | 7.75e-01 | 2.61e-02 | 8.74e-01 |
| Ca-dependent events | 21 | 8.36e-01 | 2.61e-02 | 9.10e-01 |
| Adrenaline,noradrenaline inhibits insulin secretion | 15 | 8.64e-01 | -2.56e-02 | 9.26e-01 |
| Effects of PIP2 hydrolysis | 19 | 8.47e-01 | -2.55e-02 | 9.18e-01 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | 19 | 8.48e-01 | -2.54e-02 | 9.18e-01 |
| G alpha (i) signalling events | 93 | 6.73e-01 | 2.53e-02 | 8.02e-01 |
| EPH-ephrin mediated repulsion of cells | 25 | 8.28e-01 | -2.51e-02 | 9.07e-01 |
| Peptide ligand-binding receptors | 20 | 8.47e-01 | 2.50e-02 | 9.18e-01 |
| Transport of small molecules | 359 | 4.20e-01 | -2.49e-02 | 6.10e-01 |
| Iron uptake and transport | 38 | 7.92e-01 | 2.47e-02 | 8.85e-01 |
| Metabolism of folate and pterines | 11 | 8.89e-01 | 2.42e-02 | 9.43e-01 |
| Leishmania infection | 112 | 6.67e-01 | -2.36e-02 | 8.01e-01 |
| Amino acids regulate mTORC1 | 42 | 7.94e-01 | 2.33e-02 | 8.86e-01 |
| TNFR1-induced proapoptotic signaling | 12 | 8.90e-01 | -2.30e-02 | 9.44e-01 |
| Biological oxidations | 79 | 7.28e-01 | -2.26e-02 | 8.42e-01 |
| Processing of Intronless Pre-mRNAs | 15 | 8.81e-01 | 2.24e-02 | 9.37e-01 |
| FOXO-mediated transcription | 46 | 7.95e-01 | -2.21e-02 | 8.86e-01 |
| Early Phase of HIV Life Cycle | 13 | 8.93e-01 | 2.15e-02 | 9.46e-01 |
| Protein-protein interactions at synapses | 33 | 8.31e-01 | -2.14e-02 | 9.08e-01 |
| G beta:gamma signalling through CDC42 | 13 | 8.94e-01 | -2.13e-02 | 9.46e-01 |
| Regulation of insulin secretion | 40 | 8.16e-01 | -2.12e-02 | 9.06e-01 |
| Ion channel transport | 80 | 7.45e-01 | -2.10e-02 | 8.58e-01 |
| Negative regulation of the PI3K/AKT network | 56 | 7.86e-01 | -2.10e-02 | 8.83e-01 |
| CD28 dependent PI3K/Akt signaling | 18 | 8.82e-01 | -2.03e-02 | 9.37e-01 |
| Interleukin-35 Signalling | 11 | 9.08e-01 | 2.01e-02 | 9.57e-01 |
| Cardiac conduction | 43 | 8.24e-01 | 1.96e-02 | 9.07e-01 |
| RAB geranylgeranylation | 40 | 8.31e-01 | 1.95e-02 | 9.08e-01 |
| Post-translational modification: synthesis of GPI-anchored proteins | 31 | 8.54e-01 | -1.91e-02 | 9.19e-01 |
| Golgi Associated Vesicle Biogenesis | 38 | 8.39e-01 | -1.91e-02 | 9.12e-01 |
| Platelet homeostasis | 49 | 8.20e-01 | -1.88e-02 | 9.06e-01 |
| Interleukin receptor SHC signaling | 15 | 9.01e-01 | 1.85e-02 | 9.52e-01 |
| Metabolism of lipids | 439 | 5.12e-01 | -1.84e-02 | 6.81e-01 |
| RHOV GTPase cycle | 28 | 8.66e-01 | -1.84e-02 | 9.28e-01 |
| Interleukin-12 signaling | 36 | 8.50e-01 | -1.82e-02 | 9.18e-01 |
| HCMV Late Events | 51 | 8.28e-01 | -1.76e-02 | 9.07e-01 |
| Metabolism of steroid hormones | 13 | 9.13e-01 | -1.75e-02 | 9.59e-01 |
| mRNA 3’-end processing | 37 | 8.54e-01 | 1.75e-02 | 9.19e-01 |
| TBC/RABGAPs | 40 | 8.49e-01 | -1.74e-02 | 9.18e-01 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | 88 | 7.78e-01 | 1.74e-02 | 8.77e-01 |
| Purine catabolism | 10 | 9.25e-01 | 1.72e-02 | 9.65e-01 |
| Post-chaperonin tubulin folding pathway | 13 | 9.17e-01 | 1.68e-02 | 9.60e-01 |
| O-linked glycosylation | 42 | 8.51e-01 | -1.67e-02 | 9.18e-01 |
| Keratan sulfate biosynthesis | 14 | 9.15e-01 | -1.65e-02 | 9.60e-01 |
| Regulation of BACH1 activity | 11 | 9.26e-01 | -1.61e-02 | 9.65e-01 |
| Formation of the Early Elongation Complex | 30 | 8.79e-01 | -1.60e-02 | 9.37e-01 |
| Formation of the HIV-1 Early Elongation Complex | 30 | 8.79e-01 | -1.60e-02 | 9.37e-01 |
| Signaling by PDGFR in disease | 15 | 9.15e-01 | 1.59e-02 | 9.60e-01 |
| Costimulation by the CD28 family | 44 | 8.62e-01 | -1.52e-02 | 9.25e-01 |
| Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | 12 | 9.28e-01 | 1.51e-02 | 9.65e-01 |
| Sphingolipid metabolism | 49 | 8.56e-01 | 1.50e-02 | 9.20e-01 |
| Depolymerisation of the Nuclear Lamina | 13 | 9.26e-01 | -1.48e-02 | 9.65e-01 |
| TP53 Regulates Metabolic Genes | 71 | 8.33e-01 | -1.44e-02 | 9.10e-01 |
| RHOF GTPase cycle | 25 | 9.01e-01 | 1.44e-02 | 9.52e-01 |
| Nicotinamide salvaging | 11 | 9.35e-01 | 1.42e-02 | 9.68e-01 |
| Cell death signalling via NRAGE, NRIF and NADE | 45 | 8.70e-01 | -1.41e-02 | 9.30e-01 |
| TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 14 | 9.27e-01 | 1.41e-02 | 9.65e-01 |
| Signaling by NTRK2 (TRKB) | 15 | 9.26e-01 | 1.39e-02 | 9.65e-01 |
| Nicotinate metabolism | 19 | 9.17e-01 | 1.39e-02 | 9.60e-01 |
| NOD1/2 Signaling Pathway | 23 | 9.10e-01 | -1.37e-02 | 9.58e-01 |
| FGFR2 alternative splicing | 22 | 9.12e-01 | -1.35e-02 | 9.59e-01 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | 45 | 8.82e-01 | 1.28e-02 | 9.37e-01 |
| Heme signaling | 26 | 9.10e-01 | 1.28e-02 | 9.58e-01 |
| RAC2 GTPase cycle | 56 | 8.73e-01 | -1.23e-02 | 9.32e-01 |
| Sensory Perception | 68 | 8.70e-01 | 1.15e-02 | 9.30e-01 |
| Thrombin signalling through proteinase activated receptors (PARs) | 20 | 9.31e-01 | -1.12e-02 | 9.67e-01 |
| E3 ubiquitin ligases ubiquitinate target proteins | 41 | 9.06e-01 | -1.06e-02 | 9.56e-01 |
| Regulation of innate immune responses to cytosolic DNA | 12 | 9.52e-01 | -9.99e-03 | 9.76e-01 |
| Nucleotide catabolism | 21 | 9.37e-01 | 9.99e-03 | 9.69e-01 |
| RHOD GTPase cycle | 36 | 9.21e-01 | -9.54e-03 | 9.64e-01 |
| Regulation of TP53 Activity through Acetylation | 27 | 9.32e-01 | -9.45e-03 | 9.68e-01 |
| Signaling by FGFR2 IIIa TM | 15 | 9.50e-01 | 9.40e-03 | 9.75e-01 |
| Drug ADME | 27 | 9.33e-01 | -9.30e-03 | 9.68e-01 |
| Abortive elongation of HIV-1 transcript in the absence of Tat | 22 | 9.44e-01 | 8.67e-03 | 9.75e-01 |
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | 14 | 9.56e-01 | -8.54e-03 | 9.79e-01 |
| RAF-independent MAPK1/3 activation | 20 | 9.49e-01 | -8.33e-03 | 9.75e-01 |
| Gamma carboxylation, hypusine formation and arylsulfatase activation | 23 | 9.49e-01 | -7.77e-03 | 9.75e-01 |
| Degradation of cysteine and homocysteine | 10 | 9.67e-01 | -7.57e-03 | 9.87e-01 |
| RHOG GTPase cycle | 49 | 9.28e-01 | 7.44e-03 | 9.65e-01 |
| Fatty acyl-CoA biosynthesis | 26 | 9.50e-01 | 7.14e-03 | 9.75e-01 |
| G beta:gamma signalling through PLC beta | 13 | 9.66e-01 | 6.81e-03 | 9.87e-01 |
| Presynaptic function of Kainate receptors | 13 | 9.66e-01 | 6.81e-03 | 9.87e-01 |
| Regulation of KIT signaling | 10 | 9.72e-01 | -6.35e-03 | 9.88e-01 |
| RAB GEFs exchange GTP for GDP on RABs | 64 | 9.34e-01 | 5.97e-03 | 9.68e-01 |
| Interleukin-12 family signaling | 42 | 9.48e-01 | -5.81e-03 | 9.75e-01 |
| Defective pyroptosis | 10 | 9.76e-01 | -5.54e-03 | 9.88e-01 |
| Interleukin-17 signaling | 52 | 9.45e-01 | -5.53e-03 | 9.75e-01 |
| PIWI-interacting RNA (piRNA) biogenesis | 16 | 9.70e-01 | 5.50e-03 | 9.88e-01 |
| Protein ubiquitination | 59 | 9.45e-01 | 5.24e-03 | 9.75e-01 |
| Interleukin-4 and Interleukin-13 signaling | 49 | 9.50e-01 | 5.19e-03 | 9.75e-01 |
| RHOH GTPase cycle | 29 | 9.62e-01 | 5.16e-03 | 9.84e-01 |
| Neutrophil degranulation | 307 | 8.81e-01 | -5.01e-03 | 9.37e-01 |
| Thromboxane signalling through TP receptor | 15 | 9.74e-01 | 4.81e-03 | 9.88e-01 |
| G-protein activation | 13 | 9.76e-01 | 4.72e-03 | 9.88e-01 |
| CTLA4 inhibitory signaling | 16 | 9.74e-01 | -4.70e-03 | 9.88e-01 |
| VEGFR2 mediated vascular permeability | 21 | 9.70e-01 | 4.69e-03 | 9.88e-01 |
| RUNX2 regulates bone development | 18 | 9.73e-01 | 4.68e-03 | 9.88e-01 |
| Non-integrin membrane-ECM interactions | 14 | 9.76e-01 | -4.57e-03 | 9.88e-01 |
| Gluconeogenesis | 24 | 9.72e-01 | -4.10e-03 | 9.88e-01 |
| Glycerophospholipid biosynthesis | 74 | 9.53e-01 | -3.97e-03 | 9.76e-01 |
| VEGFR2 mediated cell proliferation | 16 | 9.81e-01 | -3.38e-03 | 9.92e-01 |
| Regulation of beta-cell development | 16 | 9.88e-01 | -2.24e-03 | 9.98e-01 |
| Triglyceride catabolism | 11 | 9.90e-01 | 2.17e-03 | 9.98e-01 |
| Insulin processing | 17 | 9.90e-01 | -1.84e-03 | 9.98e-01 |
| Regulation of PTEN mRNA translation | 11 | 9.93e-01 | 1.46e-03 | 9.98e-01 |
| Keratan sulfate/keratin metabolism | 18 | 9.93e-01 | -1.19e-03 | 9.98e-01 |
| Diseases of carbohydrate metabolism | 23 | 9.94e-01 | -9.76e-04 | 9.98e-01 |
| ADP signalling through P2Y purinoceptor 12 | 13 | 9.95e-01 | 9.74e-04 | 9.98e-01 |
| Pyroptosis | 18 | 9.95e-01 | -8.71e-04 | 9.98e-01 |
| Synthesis of PIPs at the early endosome membrane | 12 | 9.97e-01 | -7.08e-04 | 9.98e-01 |
| Synthesis of PIPs at the plasma membrane | 36 | 9.94e-01 | 6.77e-04 | 9.98e-01 |
| Pre-NOTCH Expression and Processing | 46 | 9.95e-01 | -4.92e-04 | 9.98e-01 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer’s disease models | 20 | 1.00e+00 | 5.84e-05 | 1.00e+00 |
| Neurodegenerative Diseases | 20 | 1.00e+00 | 5.84e-05 | 1.00e+00 |
Condensation of Prometaphase Chromosomes
| 164 | |
|---|---|
| set | Condensation of Prometaphase Chromosomes |
| setSize | 10 |
| pANOVA | 0.00289 |
| s.dist | -0.544 |
| p.adjustANOVA | 0.021 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NCAPD2 | -10032.5 |
| CSNK2B | -9702.5 |
| CCNB2 | -9599.5 |
| SMC2 | -9536.5 |
| CDK1 | -9335.5 |
| SMC4 | -8209.5 |
| NCAPG | -7088.0 |
| CSNK2A2 | -6990.5 |
| CCNB1 | -1966.5 |
| NCAPH | -1008.5 |
| GeneID | Gene Rank |
|---|---|
| NCAPD2 | -10032.5 |
| CSNK2B | -9702.5 |
| CCNB2 | -9599.5 |
| SMC2 | -9536.5 |
| CDK1 | -9335.5 |
| SMC4 | -8209.5 |
| NCAPG | -7088.0 |
| CSNK2A2 | -6990.5 |
| CCNB1 | -1966.5 |
| NCAPH | -1008.5 |
HDR through MMEJ (alt-NHEJ)
| 405 | |
|---|---|
| set | HDR through MMEJ (alt-NHEJ) |
| setSize | 11 |
| pANOVA | 0.00204 |
| s.dist | -0.537 |
| p.adjustANOVA | 0.0181 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| POLQ | -9768.5 |
| PARP2 | -9231.5 |
| RAD52 | -8910.5 |
| XRCC1 | -8524.5 |
| RBBP8 | -8435.5 |
| FEN1 | -7907.5 |
| LIG3 | -6824.5 |
| BRCA2 | -5847.5 |
| PARP1 | -5803.5 |
| NBN | -5346.5 |
| RAD50 | -3747.5 |
| GeneID | Gene Rank |
|---|---|
| POLQ | -9768.5 |
| PARP2 | -9231.5 |
| RAD52 | -8910.5 |
| XRCC1 | -8524.5 |
| RBBP8 | -8435.5 |
| FEN1 | -7907.5 |
| LIG3 | -6824.5 |
| BRCA2 | -5847.5 |
| PARP1 | -5803.5 |
| NBN | -5346.5 |
| RAD50 | -3747.5 |
NOTCH2 Activation and Transmission of Signal to the Nucleus
| 600 | |
|---|---|
| set | NOTCH2 Activation and Transmission of Signal to the Nucleus |
| setSize | 12 |
| pANOVA | 0.0014 |
| s.dist | -0.532 |
| p.adjustANOVA | 0.014 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| PSENEN | -9683.0 |
| APH1A | -9523.5 |
| APH1B | -9044.5 |
| UBC | -8335.5 |
| ADAM10 | -8323.5 |
| UBA52 | -7829.5 |
| MIB1 | -6705.5 |
| UBB | -5890.5 |
| NCSTN | -4981.0 |
| PSEN1 | -4874.5 |
| PSEN2 | -2301.5 |
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| PSENEN | -9683.0 |
| APH1A | -9523.5 |
| APH1B | -9044.5 |
| UBC | -8335.5 |
| ADAM10 | -8323.5 |
| UBA52 | -7829.5 |
| MIB1 | -6705.5 |
| UBB | -5890.5 |
| NCSTN | -4981.0 |
| PSEN1 | -4874.5 |
| PSEN2 | -2301.5 |
p75NTR signals via NF-kB
| 1193 | |
|---|---|
| set | p75NTR signals via NF-kB |
| setSize | 11 |
| pANOVA | 0.00389 |
| s.dist | -0.502 |
| p.adjustANOVA | 0.0258 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| IKBKB | -9462.5 |
| PRKCI | -9244.5 |
| MYD88 | -8834.5 |
| UBC | -8335.5 |
| UBA52 | -7829.5 |
| SQSTM1 | -7107.5 |
| NFKBIA | -6897.5 |
| UBB | -5890.5 |
| RELA | -5735.5 |
| TRAF6 | 1097.5 |
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| IKBKB | -9462.5 |
| PRKCI | -9244.5 |
| MYD88 | -8834.5 |
| UBC | -8335.5 |
| UBA52 | -7829.5 |
| SQSTM1 | -7107.5 |
| NFKBIA | -6897.5 |
| UBB | -5890.5 |
| RELA | -5735.5 |
| TRAF6 | 1097.5 |
VLDLR internalisation and degradation
| 1162 | |
|---|---|
| set | VLDLR internalisation and degradation |
| setSize | 11 |
| pANOVA | 0.0057 |
| s.dist | -0.481 |
| p.adjustANOVA | 0.0337 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| NR1H3 | -9568.5 |
| MYLIP | -8917.5 |
| UBC | -8335.5 |
| CLTA | -8299.5 |
| AP2A1 | -8060.5 |
| UBA52 | -7829.5 |
| NR1H2 | -6679.5 |
| UBB | -5890.5 |
| AP2S1 | -4086.5 |
| AP2M1 | 829.5 |
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| NR1H3 | -9568.5 |
| MYLIP | -8917.5 |
| UBC | -8335.5 |
| CLTA | -8299.5 |
| AP2A1 | -8060.5 |
| UBA52 | -7829.5 |
| NR1H2 | -6679.5 |
| UBB | -5890.5 |
| AP2S1 | -4086.5 |
| AP2M1 | 829.5 |
SARS-CoV-2 modulates autophagy
| 900 | |
|---|---|
| set | SARS-CoV-2 modulates autophagy |
| setSize | 11 |
| pANOVA | 0.00655 |
| s.dist | -0.473 |
| p.adjustANOVA | 0.0363 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| VPS45 | -9955.5 |
| VPS33B | -8498.5 |
| UVRAG | -8193.5 |
| VPS18 | -7791.5 |
| VPS11 | -7554.5 |
| VPS39 | -7205.5 |
| TUFM | -6919.5 |
| VPS41 | -6475.5 |
| VPS33A | -6251.5 |
| MAP1LC3B | -4494.5 |
| VPS16 | -2817.5 |
| GeneID | Gene Rank |
|---|---|
| VPS45 | -9955.5 |
| VPS33B | -8498.5 |
| UVRAG | -8193.5 |
| VPS18 | -7791.5 |
| VPS11 | -7554.5 |
| VPS39 | -7205.5 |
| TUFM | -6919.5 |
| VPS41 | -6475.5 |
| VPS33A | -6251.5 |
| MAP1LC3B | -4494.5 |
| VPS16 | -2817.5 |
RHO GTPases Activate ROCKs
| 764 | |
|---|---|
| set | RHO GTPases Activate ROCKs |
| setSize | 13 |
| pANOVA | 0.00408 |
| s.dist | -0.46 |
| p.adjustANOVA | 0.0267 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RHOA | -9322.0 |
| CFL1 | -9205.5 |
| MYL6 | -9081.5 |
| MYH10 | -9072.5 |
| MYH9 | -7785.5 |
| RHOB | -7665.5 |
| PPP1CB | -7568.5 |
| ROCK1 | -6350.5 |
| PAK1 | -5418.5 |
| PPP1R12A | -5139.5 |
| PPP1R12B | -4449.5 |
| LIMK2 | -4096.5 |
| LIMK1 | -3795.5 |
| GeneID | Gene Rank |
|---|---|
| RHOA | -9322.0 |
| CFL1 | -9205.5 |
| MYL6 | -9081.5 |
| MYH10 | -9072.5 |
| MYH9 | -7785.5 |
| RHOB | -7665.5 |
| PPP1CB | -7568.5 |
| ROCK1 | -6350.5 |
| PAK1 | -5418.5 |
| PPP1R12A | -5139.5 |
| PPP1R12B | -4449.5 |
| LIMK2 | -4096.5 |
| LIMK1 | -3795.5 |
RIPK1-mediated regulated necrosis
| 784 | |
|---|---|
| set | RIPK1-mediated regulated necrosis |
| setSize | 25 |
| pANOVA | 8.38e-05 |
| s.dist | -0.454 |
| p.adjustANOVA | 0.00198 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CFLAR | -10082.5 |
| CASP8 | -10073.5 |
| PDCD6IP | -9993.5 |
| RPS27A | -9845.5 |
| RIPK3 | -9785.5 |
| TNFRSF10B | -9339.5 |
| PELI1 | -9120.5 |
| UBC | -8335.5 |
| FAS | -8198.0 |
| TRAF2 | -8182.5 |
| UBA52 | -7829.5 |
| CDC37 | -7681.0 |
| HSP90AA1 | -7192.5 |
| FLOT1 | -7039.5 |
| BIRC3 | -6746.5 |
| FLOT2 | -6165.5 |
| BIRC2 | -6098.5 |
| STUB1 | -6073.5 |
| UBB | -5890.5 |
| TNFSF10 | -5850.5 |
| GeneID | Gene Rank |
|---|---|
| CFLAR | -10082.5 |
| CASP8 | -10073.5 |
| PDCD6IP | -9993.5 |
| RPS27A | -9845.5 |
| RIPK3 | -9785.5 |
| TNFRSF10B | -9339.5 |
| PELI1 | -9120.5 |
| UBC | -8335.5 |
| FAS | -8198.0 |
| TRAF2 | -8182.5 |
| UBA52 | -7829.5 |
| CDC37 | -7681.0 |
| HSP90AA1 | -7192.5 |
| FLOT1 | -7039.5 |
| BIRC3 | -6746.5 |
| FLOT2 | -6165.5 |
| BIRC2 | -6098.5 |
| STUB1 | -6073.5 |
| UBB | -5890.5 |
| TNFSF10 | -5850.5 |
| TRADD | -5100.0 |
| MLKL | -3839.5 |
| TNFRSF10A | -2126.5 |
| FADD | -994.5 |
| SDCBP | 1421.5 |
Regulation of necroptotic cell death
| 870 | |
|---|---|
| set | Regulation of necroptotic cell death |
| setSize | 25 |
| pANOVA | 8.38e-05 |
| s.dist | -0.454 |
| p.adjustANOVA | 0.00198 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CFLAR | -10082.5 |
| CASP8 | -10073.5 |
| PDCD6IP | -9993.5 |
| RPS27A | -9845.5 |
| RIPK3 | -9785.5 |
| TNFRSF10B | -9339.5 |
| PELI1 | -9120.5 |
| UBC | -8335.5 |
| FAS | -8198.0 |
| TRAF2 | -8182.5 |
| UBA52 | -7829.5 |
| CDC37 | -7681.0 |
| HSP90AA1 | -7192.5 |
| FLOT1 | -7039.5 |
| BIRC3 | -6746.5 |
| FLOT2 | -6165.5 |
| BIRC2 | -6098.5 |
| STUB1 | -6073.5 |
| UBB | -5890.5 |
| TNFSF10 | -5850.5 |
| GeneID | Gene Rank |
|---|---|
| CFLAR | -10082.5 |
| CASP8 | -10073.5 |
| PDCD6IP | -9993.5 |
| RPS27A | -9845.5 |
| RIPK3 | -9785.5 |
| TNFRSF10B | -9339.5 |
| PELI1 | -9120.5 |
| UBC | -8335.5 |
| FAS | -8198.0 |
| TRAF2 | -8182.5 |
| UBA52 | -7829.5 |
| CDC37 | -7681.0 |
| HSP90AA1 | -7192.5 |
| FLOT1 | -7039.5 |
| BIRC3 | -6746.5 |
| FLOT2 | -6165.5 |
| BIRC2 | -6098.5 |
| STUB1 | -6073.5 |
| UBB | -5890.5 |
| TNFSF10 | -5850.5 |
| TRADD | -5100.0 |
| MLKL | -3839.5 |
| TNFRSF10A | -2126.5 |
| FADD | -994.5 |
| SDCBP | 1421.5 |
Voltage gated Potassium channels
| 1170 | |
|---|---|
| set | Voltage gated Potassium channels |
| setSize | 13 |
| pANOVA | 0.0059 |
| s.dist | 0.441 |
| p.adjustANOVA | 0.0346 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| KCNC3 | 1650.5 |
| KCNQ5 | 979.5 |
| KCNA6 | 0.5 |
| KCNH2 | 0.5 |
| KCNQ4 | -857.5 |
| KCNQ1 | -1019.0 |
| KCNG3 | -1287.5 |
| KCNAB2 | -1673.5 |
| KCNC4 | -1845.5 |
| KCNA3 | -2005.5 |
| KCNS1 | -2406.5 |
| KCNH4 | -5017.5 |
| KCNA2 | -5228.5 |
| GeneID | Gene Rank |
|---|---|
| KCNC3 | 1650.5 |
| KCNQ5 | 979.5 |
| KCNA6 | 0.5 |
| KCNH2 | 0.5 |
| KCNQ4 | -857.5 |
| KCNQ1 | -1019.0 |
| KCNG3 | -1287.5 |
| KCNAB2 | -1673.5 |
| KCNC4 | -1845.5 |
| KCNA3 | -2005.5 |
| KCNS1 | -2406.5 |
| KCNH4 | -5017.5 |
| KCNA2 | -5228.5 |
Negative regulation of FLT3
| 616 | |
|---|---|
| set | Negative regulation of FLT3 |
| setSize | 13 |
| pANOVA | 0.00651 |
| s.dist | -0.436 |
| p.adjustANOVA | 0.0363 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| SLA2 | -9770.5 |
| SLA | -9754.0 |
| SH2B3 | -9084.5 |
| UBC | -8335.5 |
| CSK | -8254.5 |
| UBA52 | -7829.5 |
| UBB | -5890.5 |
| FLT3LG | -5813.5 |
| ABL2 | -5439.5 |
| CBL | -4657.5 |
| SOCS2 | -2391.5 |
| PTPRJ | 0.5 |
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| SLA2 | -9770.5 |
| SLA | -9754.0 |
| SH2B3 | -9084.5 |
| UBC | -8335.5 |
| CSK | -8254.5 |
| UBA52 | -7829.5 |
| UBB | -5890.5 |
| FLT3LG | -5813.5 |
| ABL2 | -5439.5 |
| CBL | -4657.5 |
| SOCS2 | -2391.5 |
| PTPRJ | 0.5 |
Signaling by NOTCH2
| 993 | |
|---|---|
| set | Signaling by NOTCH2 |
| setSize | 18 |
| pANOVA | 0.00144 |
| s.dist | -0.433 |
| p.adjustANOVA | 0.014 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RBPJ | -10048.5 |
| RPS27A | -9845.5 |
| PSENEN | -9683.0 |
| APH1A | -9523.5 |
| MAML2 | -9152.5 |
| APH1B | -9044.5 |
| UBC | -8335.5 |
| ADAM10 | -8323.5 |
| UBA52 | -7829.5 |
| MIB1 | -6705.5 |
| CREB1 | -6241.5 |
| UBB | -5890.5 |
| MAML1 | -5408.5 |
| NCSTN | -4981.0 |
| PSEN1 | -4874.5 |
| PSEN2 | -2301.5 |
| EP300 | -1424.5 |
| MAML3 | -691.5 |
| GeneID | Gene Rank |
|---|---|
| RBPJ | -10048.5 |
| RPS27A | -9845.5 |
| PSENEN | -9683.0 |
| APH1A | -9523.5 |
| MAML2 | -9152.5 |
| APH1B | -9044.5 |
| UBC | -8335.5 |
| ADAM10 | -8323.5 |
| UBA52 | -7829.5 |
| MIB1 | -6705.5 |
| CREB1 | -6241.5 |
| UBB | -5890.5 |
| MAML1 | -5408.5 |
| NCSTN | -4981.0 |
| PSEN1 | -4874.5 |
| PSEN2 | -2301.5 |
| EP300 | -1424.5 |
| MAML3 | -691.5 |
Meiotic recombination
| 533 | |
|---|---|
| set | Meiotic recombination |
| setSize | 19 |
| pANOVA | 0.00112 |
| s.dist | -0.432 |
| p.adjustANOVA | 0.0121 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ATM | -10077.0 |
| PSMC3IP | -9776.5 |
| BRCA1 | -9585.0 |
| DMC1 | -9489.5 |
| MLH3 | -8914.5 |
| RBBP8 | -8435.5 |
| TOP3A | -8205.0 |
| CDK4 | -7355.5 |
| RPA1 | -7258.0 |
| RAD51 | -6975.5 |
| MND1 | -6910.5 |
| RPA3 | -6476.5 |
| BRCA2 | -5847.5 |
| MSH5 | -5697.5 |
| NBN | -5346.5 |
| RAD50 | -3747.5 |
| CDK2 | -2911.5 |
| BLM | -2156.5 |
| H2AFX | -1621.5 |
| GeneID | Gene Rank |
|---|---|
| ATM | -10077.0 |
| PSMC3IP | -9776.5 |
| BRCA1 | -9585.0 |
| DMC1 | -9489.5 |
| MLH3 | -8914.5 |
| RBBP8 | -8435.5 |
| TOP3A | -8205.0 |
| CDK4 | -7355.5 |
| RPA1 | -7258.0 |
| RAD51 | -6975.5 |
| MND1 | -6910.5 |
| RPA3 | -6476.5 |
| BRCA2 | -5847.5 |
| MSH5 | -5697.5 |
| NBN | -5346.5 |
| RAD50 | -3747.5 |
| CDK2 | -2911.5 |
| BLM | -2156.5 |
| H2AFX | -1621.5 |
Caspase activation via Death Receptors in the presence of ligand
| 120 | |
|---|---|
| set | Caspase activation via Death Receptors in the presence of ligand |
| setSize | 10 |
| pANOVA | 0.0181 |
| s.dist | -0.431 |
| p.adjustANOVA | 0.074 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CFLAR | -10082.5 |
| CASP8 | -10073.5 |
| TNFRSF10B | -9339.5 |
| FAS | -8198.0 |
| TRAF2 | -8182.5 |
| TICAM1 | -6782.5 |
| TNFSF10 | -5850.5 |
| TRADD | -5100.0 |
| TNFRSF10A | -2126.5 |
| FADD | -994.5 |
| GeneID | Gene Rank |
|---|---|
| CFLAR | -10082.5 |
| CASP8 | -10073.5 |
| TNFRSF10B | -9339.5 |
| FAS | -8198.0 |
| TRAF2 | -8182.5 |
| TICAM1 | -6782.5 |
| TNFSF10 | -5850.5 |
| TRADD | -5100.0 |
| TNFRSF10A | -2126.5 |
| FADD | -994.5 |
Glyoxylate metabolism and glycine degradation
| 392 | |
|---|---|
| set | Glyoxylate metabolism and glycine degradation |
| setSize | 19 |
| pANOVA | 0.00139 |
| s.dist | -0.423 |
| p.adjustANOVA | 0.014 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| LIAS | -9871.0 |
| OGDH | -9729.5 |
| ALDH4A1 | -9531.5 |
| DBT | -9474.5 |
| DHTKD1 | -9285.5 |
| NDUFAB1 | -9153.5 |
| BCKDHA | -8898.0 |
| PDHB | -8582.5 |
| DLST | -8391.5 |
| BCKDHB | -8369.5 |
| LIPT1 | -6558.5 |
| GOT2 | -5789.5 |
| DLD | -5416.5 |
| PXMP2 | -4994.0 |
| LIPT2 | -4509.5 |
| DLAT | -4470.5 |
| PDHX | -1946.0 |
| GRHPR | -1619.5 |
| GCSH | 749.0 |
| GeneID | Gene Rank |
|---|---|
| LIAS | -9871.0 |
| OGDH | -9729.5 |
| ALDH4A1 | -9531.5 |
| DBT | -9474.5 |
| DHTKD1 | -9285.5 |
| NDUFAB1 | -9153.5 |
| BCKDHA | -8898.0 |
| PDHB | -8582.5 |
| DLST | -8391.5 |
| BCKDHB | -8369.5 |
| LIPT1 | -6558.5 |
| GOT2 | -5789.5 |
| DLD | -5416.5 |
| PXMP2 | -4994.0 |
| LIPT2 | -4509.5 |
| DLAT | -4470.5 |
| PDHX | -1946.0 |
| GRHPR | -1619.5 |
| GCSH | 749.0 |
NOTCH3 Activation and Transmission of Signal to the Nucleus
| 601 | |
|---|---|
| set | NOTCH3 Activation and Transmission of Signal to the Nucleus |
| setSize | 15 |
| pANOVA | 0.00519 |
| s.dist | -0.417 |
| p.adjustANOVA | 0.0315 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| PSENEN | -9683.0 |
| APH1A | -9523.5 |
| APH1B | -9044.5 |
| UBC | -8335.5 |
| ADAM10 | -8323.5 |
| UBA52 | -7829.5 |
| MIB1 | -6705.5 |
| UBB | -5890.5 |
| YBX1 | -5801.5 |
| NCSTN | -4981.0 |
| PSEN1 | -4874.5 |
| WWP2 | -4004.5 |
| PSEN2 | -2301.5 |
| TACC3 | -1598.5 |
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| PSENEN | -9683.0 |
| APH1A | -9523.5 |
| APH1B | -9044.5 |
| UBC | -8335.5 |
| ADAM10 | -8323.5 |
| UBA52 | -7829.5 |
| MIB1 | -6705.5 |
| UBB | -5890.5 |
| YBX1 | -5801.5 |
| NCSTN | -4981.0 |
| PSEN1 | -4874.5 |
| WWP2 | -4004.5 |
| PSEN2 | -2301.5 |
| TACC3 | -1598.5 |
CTNNB1 S33 mutants aren’t phosphorylated
| 105 | |
|---|---|
| set | CTNNB1 S33 mutants aren’t phosphorylated |
| setSize | 13 |
| pANOVA | 0.0103 |
| s.dist | -0.411 |
| p.adjustANOVA | 0.0493 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| CTNNB1 | -8407.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| CTNNB1 | -8407.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
CTNNB1 S37 mutants aren’t phosphorylated
| 106 | |
|---|---|
| set | CTNNB1 S37 mutants aren’t phosphorylated |
| setSize | 13 |
| pANOVA | 0.0103 |
| s.dist | -0.411 |
| p.adjustANOVA | 0.0493 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| CTNNB1 | -8407.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| CTNNB1 | -8407.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
CTNNB1 S45 mutants aren’t phosphorylated
| 107 | |
|---|---|
| set | CTNNB1 S45 mutants aren’t phosphorylated |
| setSize | 13 |
| pANOVA | 0.0103 |
| s.dist | -0.411 |
| p.adjustANOVA | 0.0493 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| CTNNB1 | -8407.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| CTNNB1 | -8407.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
CTNNB1 T41 mutants aren’t phosphorylated
| 108 | |
|---|---|
| set | CTNNB1 T41 mutants aren’t phosphorylated |
| setSize | 13 |
| pANOVA | 0.0103 |
| s.dist | -0.411 |
| p.adjustANOVA | 0.0493 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| CTNNB1 | -8407.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| CTNNB1 | -8407.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
Signaling by CTNNB1 phospho-site mutants
| 955 | |
|---|---|
| set | Signaling by CTNNB1 phospho-site mutants |
| setSize | 13 |
| pANOVA | 0.0103 |
| s.dist | -0.411 |
| p.adjustANOVA | 0.0493 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| CTNNB1 | -8407.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| CTNNB1 | -8407.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
Signaling by GSK3beta mutants
| 978 | |
|---|---|
| set | Signaling by GSK3beta mutants |
| setSize | 13 |
| pANOVA | 0.0103 |
| s.dist | -0.411 |
| p.adjustANOVA | 0.0493 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| CTNNB1 | -8407.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| CTNNB1 | -8407.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
Golgi Cisternae Pericentriolar Stack Reorganization
| 394 | |
|---|---|
| set | Golgi Cisternae Pericentriolar Stack Reorganization |
| setSize | 14 |
| pANOVA | 0.00795 |
| s.dist | -0.41 |
| p.adjustANOVA | 0.0417 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RAB1B | -9981.5 |
| CCNB2 | -9599.5 |
| MAPK3 | -9428.5 |
| CDK1 | -9335.5 |
| BLZF1 | -9271.0 |
| USO1 | -9015.5 |
| RAB1A | -8106.5 |
| PLK1 | -7634.5 |
| MAPK1 | -7492.5 |
| GOLGA2 | -4678.5 |
| GORASP2 | -3470.5 |
| RAB2A | -2452.5 |
| CCNB1 | -1966.5 |
| GORASP1 | 863.0 |
| GeneID | Gene Rank |
|---|---|
| RAB1B | -9981.5 |
| CCNB2 | -9599.5 |
| MAPK3 | -9428.5 |
| CDK1 | -9335.5 |
| BLZF1 | -9271.0 |
| USO1 | -9015.5 |
| RAB1A | -8106.5 |
| PLK1 | -7634.5 |
| MAPK1 | -7492.5 |
| GOLGA2 | -4678.5 |
| GORASP2 | -3470.5 |
| RAB2A | -2452.5 |
| CCNB1 | -1966.5 |
| GORASP1 | 863.0 |
Defects in vitamin and cofactor metabolism
| 217 | |
|---|---|
| set | Defects in vitamin and cofactor metabolism |
| setSize | 16 |
| pANOVA | 0.00594 |
| s.dist | -0.397 |
| p.adjustANOVA | 0.0346 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| MCCC1 | -9827.5 |
| LMBRD1 | -9329.5 |
| CD320 | -8481.5 |
| BTD | -8120.0 |
| MMAA | -7852.5 |
| MMACHC | -7488.0 |
| MMADHC | -7119.5 |
| MTRR | -7118.5 |
| ACACA | -7071.5 |
| MTR | -6157.5 |
| HLCS | -5516.5 |
| MMAB | -5184.0 |
| PC | -4793.5 |
| ABCD4 | -3833.5 |
| MCCC2 | -3832.5 |
| PCCB | -1725.5 |
| GeneID | Gene Rank |
|---|---|
| MCCC1 | -9827.5 |
| LMBRD1 | -9329.5 |
| CD320 | -8481.5 |
| BTD | -8120.0 |
| MMAA | -7852.5 |
| MMACHC | -7488.0 |
| MMADHC | -7119.5 |
| MTRR | -7118.5 |
| ACACA | -7071.5 |
| MTR | -6157.5 |
| HLCS | -5516.5 |
| MMAB | -5184.0 |
| PC | -4793.5 |
| ABCD4 | -3833.5 |
| MCCC2 | -3832.5 |
| PCCB | -1725.5 |
APC truncation mutants have impaired AXIN binding
| 9 | |
|---|---|
| set | APC truncation mutants have impaired AXIN binding |
| setSize | 12 |
| pANOVA | 0.0209 |
| s.dist | -0.385 |
| p.adjustANOVA | 0.0809 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
AXIN missense mutants destabilize the destruction complex
| 20 | |
|---|---|
| set | AXIN missense mutants destabilize the destruction complex |
| setSize | 12 |
| pANOVA | 0.0209 |
| s.dist | -0.385 |
| p.adjustANOVA | 0.0809 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
Signaling by AMER1 mutants
| 948 | |
|---|---|
| set | Signaling by AMER1 mutants |
| setSize | 12 |
| pANOVA | 0.0209 |
| s.dist | -0.385 |
| p.adjustANOVA | 0.0809 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
Signaling by APC mutants
| 949 | |
|---|---|
| set | Signaling by APC mutants |
| setSize | 12 |
| pANOVA | 0.0209 |
| s.dist | -0.385 |
| p.adjustANOVA | 0.0809 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
Signaling by AXIN mutants
| 950 | |
|---|---|
| set | Signaling by AXIN mutants |
| setSize | 12 |
| pANOVA | 0.0209 |
| s.dist | -0.385 |
| p.adjustANOVA | 0.0809 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
Truncations of AMER1 destabilize the destruction complex
| 1151 | |
|---|---|
| set | Truncations of AMER1 destabilize the destruction complex |
| setSize | 12 |
| pANOVA | 0.0209 |
| s.dist | -0.385 |
| p.adjustANOVA | 0.0809 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
NRIF signals cell death from the nucleus
| 607 | |
|---|---|
| set | NRIF signals cell death from the nucleus |
| setSize | 14 |
| pANOVA | 0.0128 |
| s.dist | -0.384 |
| p.adjustANOVA | 0.058 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| PSENEN | -9683.0 |
| APH1A | -9523.5 |
| APH1B | -9044.5 |
| ITGB3BP | -8926.0 |
| UBC | -8335.5 |
| UBA52 | -7829.5 |
| SQSTM1 | -7107.5 |
| UBB | -5890.5 |
| NCSTN | -4981.0 |
| PSEN1 | -4874.5 |
| PSEN2 | -2301.5 |
| MAPK8 | -2204.5 |
| TRAF6 | 1097.5 |
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| PSENEN | -9683.0 |
| APH1A | -9523.5 |
| APH1B | -9044.5 |
| ITGB3BP | -8926.0 |
| UBC | -8335.5 |
| UBA52 | -7829.5 |
| SQSTM1 | -7107.5 |
| UBB | -5890.5 |
| NCSTN | -4981.0 |
| PSEN1 | -4874.5 |
| PSEN2 | -2301.5 |
| MAPK8 | -2204.5 |
| TRAF6 | 1097.5 |
Glycogen storage diseases
| 387 | |
|---|---|
| set | Glycogen storage diseases |
| setSize | 10 |
| pANOVA | 0.0364 |
| s.dist | -0.382 |
| p.adjustANOVA | 0.124 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| G6PC3 | -9701.5 |
| UBC | -8335.5 |
| GYG1 | -8027.5 |
| UBA52 | -7829.5 |
| GAA | -7392.5 |
| UBB | -5890.5 |
| SLC37A4 | -5112.5 |
| NHLRC1 | -927.5 |
| GYS1 | -696.0 |
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| G6PC3 | -9701.5 |
| UBC | -8335.5 |
| GYG1 | -8027.5 |
| UBA52 | -7829.5 |
| GAA | -7392.5 |
| UBB | -5890.5 |
| SLC37A4 | -5112.5 |
| NHLRC1 | -927.5 |
| GYS1 | -696.0 |
SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription
| 911 | |
|---|---|
| set | SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription |
| setSize | 27 |
| pANOVA | 0.000633 |
| s.dist | -0.38 |
| p.adjustANOVA | 0.00746 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TGIF1 | -10051.5 |
| RPS27A | -9845.5 |
| MAPK3 | -9428.5 |
| SP1 | -9348.5 |
| CDK9 | -8955.5 |
| E2F5 | -8756.5 |
| SMAD3 | -8709.5 |
| RNF111 | -8523.5 |
| UBC | -8335.5 |
| CCNT1 | -8326.5 |
| HDAC1 | -8140.5 |
| RBL1 | -7894.5 |
| CDK8 | -7873.5 |
| UBA52 | -7829.5 |
| MAPK1 | -7492.5 |
| TFDP1 | -7186.5 |
| MEN1 | -7106.5 |
| JUNB | -6862.5 |
| CCNC | -6793.5 |
| UBB | -5890.5 |
| GeneID | Gene Rank |
|---|---|
| TGIF1 | -10051.5 |
| RPS27A | -9845.5 |
| MAPK3 | -9428.5 |
| SP1 | -9348.5 |
| CDK9 | -8955.5 |
| E2F5 | -8756.5 |
| SMAD3 | -8709.5 |
| RNF111 | -8523.5 |
| UBC | -8335.5 |
| CCNT1 | -8326.5 |
| HDAC1 | -8140.5 |
| RBL1 | -7894.5 |
| CDK8 | -7873.5 |
| UBA52 | -7829.5 |
| MAPK1 | -7492.5 |
| TFDP1 | -7186.5 |
| MEN1 | -7106.5 |
| JUNB | -6862.5 |
| CCNC | -6793.5 |
| UBB | -5890.5 |
| TFDP2 | -5086.5 |
| SMAD7 | -3220.5 |
| CCNK | -1393.0 |
| E2F4 | -1094.5 |
| SMAD4 | 0.5 |
| TGIF2 | 1048.5 |
| SMAD2 | 1377.5 |
Gap-filling DNA repair synthesis and ligation in GG-NER
| 368 | |
|---|---|
| set | Gap-filling DNA repair synthesis and ligation in GG-NER |
| setSize | 23 |
| pANOVA | 0.00165 |
| s.dist | -0.379 |
| p.adjustANOVA | 0.0154 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| POLK | -9952.0 |
| RPS27A | -9845.5 |
| RFC5 | -9018.5 |
| XRCC1 | -8524.5 |
| UBC | -8335.5 |
| POLE2 | -8076.5 |
| POLD3 | -7834.5 |
| UBA52 | -7829.5 |
| RFC3 | -7644.5 |
| POLD4 | -7616.5 |
| POLE3 | -7383.0 |
| RPA1 | -7258.0 |
| LIG3 | -6824.5 |
| RFC4 | -6563.5 |
| RPA3 | -6476.5 |
| POLD2 | -6072.5 |
| UBB | -5890.5 |
| POLE | -4994.0 |
| RFC2 | -4130.5 |
| PCNA | -3925.5 |
| GeneID | Gene Rank |
|---|---|
| POLK | -9952.0 |
| RPS27A | -9845.5 |
| RFC5 | -9018.5 |
| XRCC1 | -8524.5 |
| UBC | -8335.5 |
| POLE2 | -8076.5 |
| POLD3 | -7834.5 |
| UBA52 | -7829.5 |
| RFC3 | -7644.5 |
| POLD4 | -7616.5 |
| POLE3 | -7383.0 |
| RPA1 | -7258.0 |
| LIG3 | -6824.5 |
| RFC4 | -6563.5 |
| RPA3 | -6476.5 |
| POLD2 | -6072.5 |
| UBB | -5890.5 |
| POLE | -4994.0 |
| RFC2 | -4130.5 |
| PCNA | -3925.5 |
| POLE4 | -3471.5 |
| LIG1 | 0.5 |
| POLD1 | 1492.5 |
Translesion synthesis by POLK
| 1131 | |
|---|---|
| set | Translesion synthesis by POLK |
| setSize | 15 |
| pANOVA | 0.012 |
| s.dist | -0.374 |
| p.adjustANOVA | 0.0555 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| POLK | -9952.0 |
| RPS27A | -9845.5 |
| RFC5 | -9018.5 |
| UBC | -8335.5 |
| UBA52 | -7829.5 |
| RFC3 | -7644.5 |
| RPA1 | -7258.0 |
| RFC4 | -6563.5 |
| RPA3 | -6476.5 |
| MAD2L2 | -6213.5 |
| UBB | -5890.5 |
| RFC2 | -4130.5 |
| PCNA | -3925.5 |
| REV3L | -1860.5 |
| REV1 | 0.5 |
| GeneID | Gene Rank |
|---|---|
| POLK | -9952.0 |
| RPS27A | -9845.5 |
| RFC5 | -9018.5 |
| UBC | -8335.5 |
| UBA52 | -7829.5 |
| RFC3 | -7644.5 |
| RPA1 | -7258.0 |
| RFC4 | -6563.5 |
| RPA3 | -6476.5 |
| MAD2L2 | -6213.5 |
| UBB | -5890.5 |
| RFC2 | -4130.5 |
| PCNA | -3925.5 |
| REV3L | -1860.5 |
| REV1 | 0.5 |
Impaired BRCA2 binding to RAD51
| 438 | |
|---|---|
| set | Impaired BRCA2 binding to RAD51 |
| setSize | 32 |
| pANOVA | 0.000265 |
| s.dist | -0.372 |
| p.adjustANOVA | 0.00426 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ATM | -10077.0 |
| RAD9B | -9886.0 |
| TOPBP1 | -9636.5 |
| BRCA1 | -9585.0 |
| RAD17 | -9213.0 |
| RFC5 | -9018.5 |
| RMI1 | -8664.0 |
| RBBP8 | -8435.5 |
| TOP3A | -8205.0 |
| ATRIP | -7955.5 |
| ATR | -7840.5 |
| RAD9A | -7827.5 |
| RFC3 | -7644.5 |
| BRIP1 | -7547.5 |
| RPA1 | -7258.0 |
| RAD51 | -6975.5 |
| RAD1 | -6858.0 |
| RFC4 | -6563.5 |
| RPA3 | -6476.5 |
| BRCA2 | -5847.5 |
| GeneID | Gene Rank |
|---|---|
| ATM | -10077.0 |
| RAD9B | -9886.0 |
| TOPBP1 | -9636.5 |
| BRCA1 | -9585.0 |
| RAD17 | -9213.0 |
| RFC5 | -9018.5 |
| RMI1 | -8664.0 |
| RBBP8 | -8435.5 |
| TOP3A | -8205.0 |
| ATRIP | -7955.5 |
| ATR | -7840.5 |
| RAD9A | -7827.5 |
| RFC3 | -7644.5 |
| BRIP1 | -7547.5 |
| RPA1 | -7258.0 |
| RAD51 | -6975.5 |
| RAD1 | -6858.0 |
| RFC4 | -6563.5 |
| RPA3 | -6476.5 |
| BRCA2 | -5847.5 |
| DNA2 | -5765.5 |
| KAT5 | -5567.5 |
| NBN | -5346.5 |
| EXO1 | -4768.5 |
| RMI2 | -4253.5 |
| RFC2 | -4130.5 |
| RAD50 | -3747.5 |
| RHNO1 | -3722.5 |
| HUS1 | -2189.5 |
| BLM | -2156.5 |
| BARD1 | -670.5 |
| WRN | 1750.0 |
HDR through Single Strand Annealing (SSA)
| 406 | |
|---|---|
| set | HDR through Single Strand Annealing (SSA) |
| setSize | 35 |
| pANOVA | 0.000248 |
| s.dist | -0.358 |
| p.adjustANOVA | 0.0042 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ATM | -10077.0 |
| RAD9B | -9886.0 |
| TOPBP1 | -9636.5 |
| BRCA1 | -9585.0 |
| ABL1 | -9490.5 |
| RAD17 | -9213.0 |
| RFC5 | -9018.5 |
| RAD52 | -8910.5 |
| RMI1 | -8664.0 |
| RBBP8 | -8435.5 |
| TOP3A | -8205.0 |
| ATRIP | -7955.5 |
| ATR | -7840.5 |
| RAD9A | -7827.5 |
| RFC3 | -7644.5 |
| BRIP1 | -7547.5 |
| RPA1 | -7258.0 |
| RAD51 | -6975.5 |
| RAD1 | -6858.0 |
| RFC4 | -6563.5 |
| GeneID | Gene Rank |
|---|---|
| ATM | -10077.0 |
| RAD9B | -9886.0 |
| TOPBP1 | -9636.5 |
| BRCA1 | -9585.0 |
| ABL1 | -9490.5 |
| RAD17 | -9213.0 |
| RFC5 | -9018.5 |
| RAD52 | -8910.5 |
| RMI1 | -8664.0 |
| RBBP8 | -8435.5 |
| TOP3A | -8205.0 |
| ATRIP | -7955.5 |
| ATR | -7840.5 |
| RAD9A | -7827.5 |
| RFC3 | -7644.5 |
| BRIP1 | -7547.5 |
| RPA1 | -7258.0 |
| RAD51 | -6975.5 |
| RAD1 | -6858.0 |
| RFC4 | -6563.5 |
| RPA3 | -6476.5 |
| DNA2 | -5765.5 |
| KAT5 | -5567.5 |
| NBN | -5346.5 |
| EXO1 | -4768.5 |
| RMI2 | -4253.5 |
| RFC2 | -4130.5 |
| RAD50 | -3747.5 |
| RHNO1 | -3722.5 |
| HUS1 | -2189.5 |
| BLM | -2156.5 |
| ERCC4 | -2116.5 |
| ERCC1 | -1185.5 |
| BARD1 | -670.5 |
| WRN | 1750.0 |
Beta-catenin phosphorylation cascade
| 83 | |
|---|---|
| set | Beta-catenin phosphorylation cascade |
| setSize | 15 |
| pANOVA | 0.0166 |
| s.dist | -0.357 |
| p.adjustANOVA | 0.0694 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| CTNNB1 | -8407.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| FRAT1 | -6545.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| FRAT2 | -1720.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
| GeneID | Gene Rank |
|---|---|
| APC | -9654.5 |
| PPP2R5D | -9476.5 |
| PPP2CA | -8895.5 |
| PPP2R5E | -8889.5 |
| CTNNB1 | -8407.5 |
| AXIN1 | -8087.5 |
| PPP2R5A | -7872.5 |
| CSNK1A1 | -7759.5 |
| FRAT1 | -6545.5 |
| PPP2R5B | -6134.5 |
| PPP2CB | -5145.5 |
| GSK3B | -3166.5 |
| FRAT2 | -1720.5 |
| PPP2R1B | -876.5 |
| PPP2R5C | -768.5 |
Cobalamin (Cbl, vitamin B12) transport and metabolism
| 158 | |
|---|---|
| set | Cobalamin (Cbl, vitamin B12) transport and metabolism |
| setSize | 11 |
| pANOVA | 0.0413 |
| s.dist | -0.355 |
| p.adjustANOVA | 0.135 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| LMBRD1 | -9329.5 |
| CD320 | -8481.5 |
| MMAA | -7852.5 |
| MMACHC | -7488.0 |
| MMADHC | -7119.5 |
| MTRR | -7118.5 |
| MTR | -6157.5 |
| ABCC1 | -5800.5 |
| MMAB | -5184.0 |
| ABCD4 | -3833.5 |
| LDLRAP1 | 0.5 |
| GeneID | Gene Rank |
|---|---|
| LMBRD1 | -9329.5 |
| CD320 | -8481.5 |
| MMAA | -7852.5 |
| MMACHC | -7488.0 |
| MMADHC | -7119.5 |
| MTRR | -7118.5 |
| MTR | -6157.5 |
| ABCC1 | -5800.5 |
| MMAB | -5184.0 |
| ABCD4 | -3833.5 |
| LDLRAP1 | 0.5 |
mRNA decay by 3’ to 5’ exoribonuclease
| 1185 | |
|---|---|
| set | mRNA decay by 3’ to 5’ exoribonuclease |
| setSize | 14 |
| pANOVA | 0.022 |
| s.dist | -0.353 |
| p.adjustANOVA | 0.0841 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| DIS3 | -9204.0 |
| EXOSC8 | -9127.5 |
| EXOSC2 | -9064.5 |
| EXOSC5 | -8898.0 |
| HBS1L | -8652.5 |
| EXOSC3 | -7414.5 |
| EXOSC1 | -7176.0 |
| WDR61 | -6043.5 |
| TTC37 | -5723.0 |
| SKIV2L | -5159.5 |
| EXOSC4 | -4159.5 |
| DCPS | -3344.5 |
| EXOSC7 | -1547.5 |
| EXOSC6 | -1345.5 |
| GeneID | Gene Rank |
|---|---|
| DIS3 | -9204.0 |
| EXOSC8 | -9127.5 |
| EXOSC2 | -9064.5 |
| EXOSC5 | -8898.0 |
| HBS1L | -8652.5 |
| EXOSC3 | -7414.5 |
| EXOSC1 | -7176.0 |
| WDR61 | -6043.5 |
| TTC37 | -5723.0 |
| SKIV2L | -5159.5 |
| EXOSC4 | -4159.5 |
| DCPS | -3344.5 |
| EXOSC7 | -1547.5 |
| EXOSC6 | -1345.5 |
Glycogen synthesis
| 388 | |
|---|---|
| set | Glycogen synthesis |
| setSize | 11 |
| pANOVA | 0.0425 |
| s.dist | -0.353 |
| p.adjustANOVA | 0.137 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| UGP2 | -10040.5 |
| RPS27A | -9845.5 |
| UBC | -8335.5 |
| GYG1 | -8027.5 |
| UBA52 | -7829.5 |
| PGM2L1 | -7014.5 |
| PGM2 | -6129.5 |
| UBB | -5890.5 |
| PGM1 | -3490.5 |
| NHLRC1 | -927.5 |
| GYS1 | -696.0 |
| GeneID | Gene Rank |
|---|---|
| UGP2 | -10040.5 |
| RPS27A | -9845.5 |
| UBC | -8335.5 |
| GYG1 | -8027.5 |
| UBA52 | -7829.5 |
| PGM2L1 | -7014.5 |
| PGM2 | -6129.5 |
| UBB | -5890.5 |
| PGM1 | -3490.5 |
| NHLRC1 | -927.5 |
| GYS1 | -696.0 |
APC/C:Cdc20 mediated degradation of Cyclin B
| 12 | |
|---|---|
| set | APC/C:Cdc20 mediated degradation of Cyclin B |
| setSize | 22 |
| pANOVA | 0.00481 |
| s.dist | -0.347 |
| p.adjustANOVA | 0.0299 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ANAPC7 | -10044.5 |
| RPS27A | -9845.5 |
| ANAPC10 | -9790.0 |
| CDK1 | -9335.5 |
| CDC23 | -9279.5 |
| ANAPC15 | -8853.5 |
| ANAPC1 | -8623.5 |
| UBC | -8335.5 |
| UBE2E1 | -8329.5 |
| ANAPC16 | -8113.5 |
| UBA52 | -7829.5 |
| CDC20 | -6092.5 |
| ANAPC5 | -5955.5 |
| UBB | -5890.5 |
| ANAPC4 | -5676.5 |
| ANAPC2 | -4120.0 |
| UBE2D1 | -3813.5 |
| ANAPC11 | -2966.5 |
| CCNB1 | -1966.5 |
| UBE2C | -1905.5 |
| GeneID | Gene Rank |
|---|---|
| ANAPC7 | -10044.5 |
| RPS27A | -9845.5 |
| ANAPC10 | -9790.0 |
| CDK1 | -9335.5 |
| CDC23 | -9279.5 |
| ANAPC15 | -8853.5 |
| ANAPC1 | -8623.5 |
| UBC | -8335.5 |
| UBE2E1 | -8329.5 |
| ANAPC16 | -8113.5 |
| UBA52 | -7829.5 |
| CDC20 | -6092.5 |
| ANAPC5 | -5955.5 |
| UBB | -5890.5 |
| ANAPC4 | -5676.5 |
| ANAPC2 | -4120.0 |
| UBE2D1 | -3813.5 |
| ANAPC11 | -2966.5 |
| CCNB1 | -1966.5 |
| UBE2C | -1905.5 |
| UBE2S | 0.5 |
| CDC16 | 1131.5 |
Chaperone Mediated Autophagy
| 141 | |
|---|---|
| set | Chaperone Mediated Autophagy |
| setSize | 12 |
| pANOVA | 0.0383 |
| s.dist | -0.345 |
| p.adjustANOVA | 0.128 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| EEF1A1 | -9269.5 |
| HSP90AB1 | -8459.5 |
| UBC | -8335.5 |
| UBA52 | -7829.5 |
| HSP90AA1 | -7192.5 |
| PLIN3 | -5913.5 |
| UBB | -5890.5 |
| PARK7 | -4903.5 |
| ARL13B | -3530.5 |
| PCNT | -1365.0 |
| PLIN2 | -1326.5 |
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| EEF1A1 | -9269.5 |
| HSP90AB1 | -8459.5 |
| UBC | -8335.5 |
| UBA52 | -7829.5 |
| HSP90AA1 | -7192.5 |
| PLIN3 | -5913.5 |
| UBB | -5890.5 |
| PARK7 | -4903.5 |
| ARL13B | -3530.5 |
| PCNT | -1365.0 |
| PLIN2 | -1326.5 |
Translation of Structural Proteins
| 1128 | |
|---|---|
| set | Translation of Structural Proteins |
| setSize | 27 |
| pANOVA | 0.00193 |
| s.dist | -0.345 |
| p.adjustANOVA | 0.0174 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PARP9 | -9901.0 |
| RPS27A | -9845.5 |
| GSK3A | -9586.5 |
| PRKCSH | -9243.0 |
| MGAT1 | -9151.5 |
| ST3GAL1 | -9131.5 |
| ST3GAL3 | -8855.5 |
| UBC | -8335.5 |
| GANAB | -8154.5 |
| ST6GAL1 | -8058.5 |
| UBA52 | -7829.5 |
| ST3GAL2 | -7454.5 |
| PARP14 | -7137.5 |
| ST6GALNAC3 | -6674.5 |
| UBB | -5890.5 |
| MOGS | -5695.5 |
| SUMO1 | -5641.5 |
| PARP4 | -5381.5 |
| UBE2I | -5253.5 |
| PARP10 | -4659.5 |
| GeneID | Gene Rank |
|---|---|
| PARP9 | -9901.0 |
| RPS27A | -9845.5 |
| GSK3A | -9586.5 |
| PRKCSH | -9243.0 |
| MGAT1 | -9151.5 |
| ST3GAL1 | -9131.5 |
| ST3GAL3 | -8855.5 |
| UBC | -8335.5 |
| GANAB | -8154.5 |
| ST6GAL1 | -8058.5 |
| UBA52 | -7829.5 |
| ST3GAL2 | -7454.5 |
| PARP14 | -7137.5 |
| ST6GALNAC3 | -6674.5 |
| UBB | -5890.5 |
| MOGS | -5695.5 |
| SUMO1 | -5641.5 |
| PARP4 | -5381.5 |
| UBE2I | -5253.5 |
| PARP10 | -4659.5 |
| PARP16 | -4577.5 |
| ST3GAL4 | -3816.5 |
| PARP8 | -3573.5 |
| GSK3B | -3166.5 |
| ST6GALNAC4 | -751.5 |
| CANX | 0.5 |
| PARP6 | 1721.5 |
Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants
| 169 | |
|---|---|
| set | Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants |
| setSize | 14 |
| pANOVA | 0.0257 |
| s.dist | -0.344 |
| p.adjustANOVA | 0.0942 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| KRAS | -8859.5 |
| SHC1 | -8813.0 |
| UBC | -8335.5 |
| UBA52 | -7829.5 |
| CDC37 | -7681.0 |
| HRAS | -7209.5 |
| HSP90AA1 | -7192.5 |
| UBB | -5890.5 |
| PIK3CA | -5753.5 |
| CBL | -4657.5 |
| PLCG1 | -2462.5 |
| GRB2 | -2220.5 |
| PIK3R1 | 668.5 |
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| KRAS | -8859.5 |
| SHC1 | -8813.0 |
| UBC | -8335.5 |
| UBA52 | -7829.5 |
| CDC37 | -7681.0 |
| HRAS | -7209.5 |
| HSP90AA1 | -7192.5 |
| UBB | -5890.5 |
| PIK3CA | -5753.5 |
| CBL | -4657.5 |
| PLCG1 | -2462.5 |
| GRB2 | -2220.5 |
| PIK3R1 | 668.5 |
Signaling by Ligand-Responsive EGFR Variants in Cancer
| 985 | |
|---|---|
| set | Signaling by Ligand-Responsive EGFR Variants in Cancer |
| setSize | 14 |
| pANOVA | 0.0257 |
| s.dist | -0.344 |
| p.adjustANOVA | 0.0942 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| KRAS | -8859.5 |
| SHC1 | -8813.0 |
| UBC | -8335.5 |
| UBA52 | -7829.5 |
| CDC37 | -7681.0 |
| HRAS | -7209.5 |
| HSP90AA1 | -7192.5 |
| UBB | -5890.5 |
| PIK3CA | -5753.5 |
| CBL | -4657.5 |
| PLCG1 | -2462.5 |
| GRB2 | -2220.5 |
| PIK3R1 | 668.5 |
| GeneID | Gene Rank |
|---|---|
| RPS27A | -9845.5 |
| KRAS | -8859.5 |
| SHC1 | -8813.0 |
| UBC | -8335.5 |
| UBA52 | -7829.5 |
| CDC37 | -7681.0 |
| HRAS | -7209.5 |
| HSP90AA1 | -7192.5 |
| UBB | -5890.5 |
| PIK3CA | -5753.5 |
| CBL | -4657.5 |
| PLCG1 | -2462.5 |
| GRB2 | -2220.5 |
| PIK3R1 | 668.5 |
Spry regulation of FGF signaling
| 1030 | |
|---|---|
| set | Spry regulation of FGF signaling |
| setSize | 15 |
| pANOVA | 0.0217 |
| s.dist | -0.342 |
| p.adjustANOVA | 0.0835 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| SPRY2 | -9909.5 |
| RPS27A | -9845.5 |
| MAPK3 | -9428.5 |
| PPP2CA | -8895.5 |
| UBC | -8335.5 |
| UBA52 | -7829.5 |
| MAPK1 | -7492.5 |
| MKNK1 | -7474.5 |
| UBB | -5890.5 |
| PPP2CB | -5145.5 |
| BRAF | -4674.5 |
| CBL | -4657.5 |
| GRB2 | -2220.5 |
| PTPN11 | -1453.5 |
| SRC | 1212.5 |
| GeneID | Gene Rank |
|---|---|
| SPRY2 | -9909.5 |
| RPS27A | -9845.5 |
| MAPK3 | -9428.5 |
| PPP2CA | -8895.5 |
| UBC | -8335.5 |
| UBA52 | -7829.5 |
| MAPK1 | -7492.5 |
| MKNK1 | -7474.5 |
| UBB | -5890.5 |
| PPP2CB | -5145.5 |
| BRAF | -4674.5 |
| CBL | -4657.5 |
| GRB2 | -2220.5 |
| PTPN11 | -1453.5 |
| SRC | 1212.5 |
Aberrant regulation of mitotic exit in cancer due to RB1 defects
| 23 | |
|---|---|
| set | Aberrant regulation of mitotic exit in cancer due to RB1 defects |
| setSize | 18 |
| pANOVA | 0.0124 |
| s.dist | -0.34 |
| p.adjustANOVA | 0.0565 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ANAPC7 | -10044.5 |
| ANAPC10 | -9790.0 |
| CDC23 | -9279.5 |
| ANAPC15 | -8853.5 |
| ANAPC1 | -8623.5 |
| FZR1 | -8519.5 |
| RB1 | -8397.5 |
| UBE2E1 | -8329.5 |
| ANAPC16 | -8113.5 |
| SKP2 | -7001.0 |
| ANAPC5 | -5955.5 |
| ANAPC4 | -5676.5 |
| ANAPC2 | -4120.0 |
| UBE2D1 | -3813.5 |
| ANAPC11 | -2966.5 |
| UBE2C | -1905.5 |
| UBE2S | 0.5 |
| CDC16 | 1131.5 |
| GeneID | Gene Rank |
|---|---|
| ANAPC7 | -10044.5 |
| ANAPC10 | -9790.0 |
| CDC23 | -9279.5 |
| ANAPC15 | -8853.5 |
| ANAPC1 | -8623.5 |
| FZR1 | -8519.5 |
| RB1 | -8397.5 |
| UBE2E1 | -8329.5 |
| ANAPC16 | -8113.5 |
| SKP2 | -7001.0 |
| ANAPC5 | -5955.5 |
| ANAPC4 | -5676.5 |
| ANAPC2 | -4120.0 |
| UBE2D1 | -3813.5 |
| ANAPC11 | -2966.5 |
| UBE2C | -1905.5 |
| UBE2S | 0.5 |
| CDC16 | 1131.5 |
ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression
| 278 | |
|---|---|
| set | ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression |
| setSize | 15 |
| pANOVA | 0.0228 |
| s.dist | -0.339 |
| p.adjustANOVA | 0.0869 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| EHMT2 | -10089.5 |
| GATAD2B | -9675.5 |
| CHD4 | -9435.5 |
| CHD3 | -9405.5 |
| ERCC6 | -8488.5 |
| MTA3 | -8385.5 |
| HDAC2 | -8146.5 |
| HDAC1 | -8140.5 |
| GATAD2A | -7786.5 |
| CBX3 | -7261.5 |
| MBD3 | -2721.5 |
| H2AFX | -1621.5 |
| TTF1 | -1139.5 |
| RBBP4 | -809.0 |
| MTA2 | 1300.5 |
| GeneID | Gene Rank |
|---|---|
| EHMT2 | -10089.5 |
| GATAD2B | -9675.5 |
| CHD4 | -9435.5 |
| CHD3 | -9405.5 |
| ERCC6 | -8488.5 |
| MTA3 | -8385.5 |
| HDAC2 | -8146.5 |
| HDAC1 | -8140.5 |
| GATAD2A | -7786.5 |
| CBX3 | -7261.5 |
| MBD3 | -2721.5 |
| H2AFX | -1621.5 |
| TTF1 | -1139.5 |
| RBBP4 | -809.0 |
| MTA2 | 1300.5 |
Defective homologous recombination repair (HRR) due to BRCA2 loss of function
| 215 | |
|---|---|
| set | Defective homologous recombination repair (HRR) due to BRCA2 loss of function |
| setSize | 37 |
| pANOVA | 0.000352 |
| s.dist | -0.339 |
| p.adjustANOVA | 0.00492 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ATM | -10077.0 |
| RAD9B | -9886.0 |
| TOPBP1 | -9636.5 |
| BRCA1 | -9585.0 |
| RAD17 | -9213.0 |
| RFC5 | -9018.5 |
| RAD51AP1 | -8997.0 |
| RMI1 | -8664.0 |
| RBBP8 | -8435.5 |
| TOP3A | -8205.0 |
| ATRIP | -7955.5 |
| ATR | -7840.5 |
| RAD9A | -7827.5 |
| RFC3 | -7644.5 |
| BRIP1 | -7547.5 |
| RPA1 | -7258.0 |
| RAD51 | -6975.5 |
| RAD1 | -6858.0 |
| RAD51B | -6749.5 |
| RFC4 | -6563.5 |
| GeneID | Gene Rank |
|---|---|
| ATM | -10077.0 |
| RAD9B | -9886.0 |
| TOPBP1 | -9636.5 |
| BRCA1 | -9585.0 |
| RAD17 | -9213.0 |
| RFC5 | -9018.5 |
| RAD51AP1 | -8997.0 |
| RMI1 | -8664.0 |
| RBBP8 | -8435.5 |
| TOP3A | -8205.0 |
| ATRIP | -7955.5 |
| ATR | -7840.5 |
| RAD9A | -7827.5 |
| RFC3 | -7644.5 |
| BRIP1 | -7547.5 |
| RPA1 | -7258.0 |
| RAD51 | -6975.5 |
| RAD1 | -6858.0 |
| RAD51B | -6749.5 |
| RFC4 | -6563.5 |
| RPA3 | -6476.5 |
| BRCA2 | -5847.5 |
| DNA2 | -5765.5 |
| PALB2 | -5578.0 |
| KAT5 | -5567.5 |
| NBN | -5346.5 |
| EXO1 | -4768.5 |
| RMI2 | -4253.5 |
| RFC2 | -4130.5 |
| RAD50 | -3747.5 |
| RHNO1 | -3722.5 |
| XRCC2 | -2900.5 |
| HUS1 | -2189.5 |
| BLM | -2156.5 |
| BARD1 | -670.5 |
| RAD51D | 0.5 |
| WRN | 1750.0 |
Here is the session info with all the versions of packages used.
sessionInfo()
## R version 4.2.0 (2022-04-22)
## Platform: x86_64-pc-linux-gnu (64-bit)
## Running under: Ubuntu 20.04.4 LTS
##
## Matrix products: default
## BLAS: /usr/lib/x86_64-linux-gnu/blas/libblas.so.3.9.0
## LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.9.0
##
## 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] grid stats4 parallel stats graphics grDevices utils
## [8] datasets methods base
##
## other attached packages:
## [1] pkgload_1.2.4
## [2] GGally_2.1.2
## [3] ggplot2_3.3.6
## [4] gtools_3.9.2
## [5] tibble_3.1.7
## [6] echarts4r_0.4.3
## [7] ENmix_1.32.0
## [8] doParallel_1.0.17
## [9] qqman_0.1.8
## [10] RCircos_1.2.2
## [11] beeswarm_0.4.0
## [12] forestplot_2.0.1
## [13] checkmate_2.1.0
## [14] magrittr_2.0.3
## [15] reshape2_1.4.4
## [16] gplots_3.1.3
## [17] GEOquery_2.64.2
## [18] RColorBrewer_1.1-3
## [19] IlluminaHumanMethylation450kmanifest_0.4.0
## [20] topconfects_1.12.0
## [21] DMRcatedata_2.14.0
## [22] ExperimentHub_2.4.0
## [23] AnnotationHub_3.4.0
## [24] BiocFileCache_2.4.0
## [25] dbplyr_2.1.1
## [26] DMRcate_2.10.0
## [27] limma_3.52.1
## [28] missMethyl_1.30.0
## [29] IlluminaHumanMethylationEPICanno.ilm10b4.hg19_0.6.0
## [30] IlluminaHumanMethylation450kanno.ilmn12.hg19_0.6.1
## [31] minfi_1.42.0
## [32] bumphunter_1.38.0
## [33] locfit_1.5-9.5
## [34] iterators_1.0.14
## [35] foreach_1.5.2
## [36] Biostrings_2.64.0
## [37] XVector_0.36.0
## [38] SummarizedExperiment_1.26.1
## [39] Biobase_2.56.0
## [40] MatrixGenerics_1.8.0
## [41] matrixStats_0.62.0
## [42] GenomicRanges_1.48.0
## [43] GenomeInfoDb_1.32.2
## [44] IRanges_2.30.0
## [45] S4Vectors_0.34.0
## [46] BiocGenerics_0.42.0
## [47] R.utils_2.11.0
## [48] R.oo_1.24.0
## [49] R.methodsS3_1.8.1
## [50] plyr_1.8.7
## [51] tictoc_1.0.1
## [52] mitch_1.8.0
## [53] eulerr_6.1.1
## [54] kableExtra_1.3.4
## [55] dplyr_1.0.9
##
## loaded via a namespace (and not attached):
## [1] rappdirs_0.3.3 rtracklayer_1.56.0
## [3] tidyr_1.2.0 bit64_4.0.5
## [5] knitr_1.39 DelayedArray_0.22.0
## [7] data.table_1.14.2 rpart_4.1.16
## [9] KEGGREST_1.36.0 RCurl_1.98-1.6
## [11] AnnotationFilter_1.20.0 generics_0.1.2
## [13] GenomicFeatures_1.48.1 preprocessCore_1.58.0
## [15] RSQLite_2.2.14 bit_4.0.4
## [17] tzdb_0.3.0 webshot_0.5.3
## [19] xml2_1.3.3 httpuv_1.6.5
## [21] assertthat_0.2.1 xfun_0.31
## [23] hms_1.1.1 jquerylib_0.1.4
## [25] evaluate_0.15 promises_1.2.0.1
## [27] fansi_1.0.3 restfulr_0.0.13
## [29] scrime_1.3.5 progress_1.2.2
## [31] caTools_1.18.2 readxl_1.4.0
## [33] DBI_1.1.2 geneplotter_1.74.0
## [35] htmlwidgets_1.5.4 reshape_0.8.9
## [37] purrr_0.3.4 ellipsis_0.3.2
## [39] backports_1.4.1 permute_0.9-7
## [41] calibrate_1.7.7 annotate_1.74.0
## [43] biomaRt_2.52.0 sparseMatrixStats_1.8.0
## [45] vctrs_0.4.1 ensembldb_2.20.1
## [47] withr_2.5.0 cachem_1.0.6
## [49] Gviz_1.40.1 BSgenome_1.64.0
## [51] GenomicAlignments_1.32.0 prettyunits_1.1.1
## [53] mclust_5.4.9 svglite_2.1.0
## [55] cluster_2.1.3 RPMM_1.25
## [57] lazyeval_0.2.2 crayon_1.5.1
## [59] genefilter_1.78.0 edgeR_3.38.1
## [61] pkgconfig_2.0.3 nlme_3.1-157
## [63] ProtGenerics_1.28.0 nnet_7.3-17
## [65] rlang_1.0.2 lifecycle_1.0.1
## [67] filelock_1.0.2 dichromat_2.0-0.1
## [69] rprojroot_2.0.3 cellranger_1.1.0
## [71] rngtools_1.5.2 base64_2.0
## [73] Matrix_1.4-1 Rhdf5lib_1.18.2
## [75] base64enc_0.1-3 png_0.1-7
## [77] viridisLite_0.4.0 rjson_0.2.21
## [79] bitops_1.0-7 KernSmooth_2.23-20
## [81] rhdf5filters_1.8.0 blob_1.2.3
## [83] DelayedMatrixStats_1.18.0 doRNG_1.8.2
## [85] stringr_1.4.0 nor1mix_1.3-0
## [87] readr_2.1.2 jpeg_0.1-9
## [89] scales_1.2.0 memoise_2.0.1
## [91] zlibbioc_1.42.0 compiler_4.2.0
## [93] BiocIO_1.6.0 illuminaio_0.38.0
## [95] Rsamtools_2.12.0 cli_3.3.0
## [97] DSS_2.44.0 htmlTable_2.4.0
## [99] Formula_1.2-4 MASS_7.3-57
## [101] tidyselect_1.1.2 stringi_1.7.6
## [103] highr_0.9 yaml_2.3.5
## [105] askpass_1.1 latticeExtra_0.6-29
## [107] sass_0.4.1 VariantAnnotation_1.42.1
## [109] tools_4.2.0 rstudioapi_0.13
## [111] foreign_0.8-82 bsseq_1.32.0
## [113] gridExtra_2.3 digest_0.6.29
## [115] BiocManager_1.30.17 shiny_1.7.1
## [117] quadprog_1.5-8 Rcpp_1.0.8.3
## [119] siggenes_1.70.0 BiocVersion_3.15.2
## [121] later_1.3.0 org.Hs.eg.db_3.15.0
## [123] httr_1.4.3 AnnotationDbi_1.58.0
## [125] biovizBase_1.44.0 colorspace_2.0-3
## [127] brio_1.1.3 rvest_1.0.2
## [129] XML_3.99-0.9 splines_4.2.0
## [131] statmod_1.4.36 multtest_2.52.0
## [133] systemfonts_1.0.4 xtable_1.8-4
## [135] jsonlite_1.8.0 dynamicTreeCut_1.63-1
## [137] testthat_3.1.4 R6_2.5.1
## [139] Hmisc_4.7-0 pillar_1.7.0
## [141] htmltools_0.5.2 mime_0.12
## [143] glue_1.6.2 fastmap_1.1.0
## [145] BiocParallel_1.30.2 interactiveDisplayBase_1.34.0
## [147] beanplot_1.3.1 codetools_0.2-18
## [149] utf8_1.2.2 bslib_0.3.1
## [151] lattice_0.20-45 curl_4.3.2
## [153] openssl_2.0.1 survival_3.3-1
## [155] rmarkdown_2.14 desc_1.4.1
## [157] munsell_0.5.0 rhdf5_2.40.0
## [159] GenomeInfoDbData_1.2.8 HDF5Array_1.24.0
## [161] impute_1.70.0 gtable_0.3.0
END of report