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Gene: VRK2 |
Gene summary for VRK2 |
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Gene information | Species | Human | Gene symbol | VRK2 | Gene ID | 7444 |
Gene name | VRK serine/threonine kinase 2 | |
Gene Alias | VRK2 | |
Cytomap | 2p16.1 | |
Gene Type | protein-coding | GO ID | GO:0000165 | UniProtAcc | Q86Y07 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
7444 | VRK2 | CCI_1 | Human | Cervix | CC | 2.87e-06 | 7.52e-01 | 0.528 |
7444 | VRK2 | CCI_2 | Human | Cervix | CC | 1.61e-12 | 1.14e+00 | 0.5249 |
7444 | VRK2 | CCI_3 | Human | Cervix | CC | 5.30e-15 | 9.00e-01 | 0.516 |
7444 | VRK2 | LZE2T | Human | Esophagus | ESCC | 3.98e-05 | 4.20e-01 | 0.082 |
7444 | VRK2 | LZE4T | Human | Esophagus | ESCC | 1.11e-20 | 5.39e-01 | 0.0811 |
7444 | VRK2 | LZE7T | Human | Esophagus | ESCC | 5.92e-11 | 6.01e-01 | 0.0667 |
7444 | VRK2 | LZE8T | Human | Esophagus | ESCC | 1.52e-05 | 1.77e-01 | 0.067 |
7444 | VRK2 | LZE20T | Human | Esophagus | ESCC | 4.64e-04 | 1.94e-01 | 0.0662 |
7444 | VRK2 | LZE22T | Human | Esophagus | ESCC | 3.86e-03 | 2.90e-01 | 0.068 |
7444 | VRK2 | LZE24T | Human | Esophagus | ESCC | 2.32e-14 | 3.99e-01 | 0.0596 |
7444 | VRK2 | LZE21T | Human | Esophagus | ESCC | 1.23e-08 | 4.04e-01 | 0.0655 |
7444 | VRK2 | LZE6T | Human | Esophagus | ESCC | 3.97e-07 | 2.51e-01 | 0.0845 |
7444 | VRK2 | P1T-E | Human | Esophagus | ESCC | 1.57e-07 | 3.69e-01 | 0.0875 |
7444 | VRK2 | P2T-E | Human | Esophagus | ESCC | 3.39e-39 | 6.06e-01 | 0.1177 |
7444 | VRK2 | P4T-E | Human | Esophagus | ESCC | 4.55e-17 | 4.19e-01 | 0.1323 |
7444 | VRK2 | P5T-E | Human | Esophagus | ESCC | 1.71e-23 | 4.97e-01 | 0.1327 |
7444 | VRK2 | P8T-E | Human | Esophagus | ESCC | 2.44e-11 | 3.01e-01 | 0.0889 |
7444 | VRK2 | P9T-E | Human | Esophagus | ESCC | 5.63e-18 | 4.33e-01 | 0.1131 |
7444 | VRK2 | P10T-E | Human | Esophagus | ESCC | 1.49e-17 | 3.09e-01 | 0.116 |
7444 | VRK2 | P11T-E | Human | Esophagus | ESCC | 9.68e-11 | 4.69e-01 | 0.1426 |
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∗log2FC in expression of this searched gene in stem-like cells from each diseased tissue sample relative to stem-like cells in normal samples in each tissue plotted against the malignancy continuum. Samples are colored based on if they are from different disease stage. |
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Malignant transformation related pathway analysis |
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Tissue | Disease Stage | Enriched GO biological Processes |
Colorectum | AD | ![]() |
Colorectum | SER | ![]() |
Colorectum | MSS | ![]() |
Colorectum | MSI-H | ![]() |
Colorectum | FAP | ![]() |
∗Top 15 enriched GO BP terms are showed in the bar plot of each disease state in each tissue. Each row represents a significant GO biological process which is colored according to the -log10(p.adjust). |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:000697910 | Cervix | CC | response to oxidative stress | 102/2311 | 446/18723 | 2.99e-10 | 4.36e-08 | 102 |
GO:006219710 | Cervix | CC | cellular response to chemical stress | 76/2311 | 337/18723 | 1.01e-07 | 5.25e-06 | 76 |
GO:003459910 | Cervix | CC | cellular response to oxidative stress | 63/2311 | 288/18723 | 3.58e-06 | 9.50e-05 | 63 |
GO:00181057 | Cervix | CC | peptidyl-serine phosphorylation | 63/2311 | 315/18723 | 6.65e-05 | 9.47e-04 | 63 |
GO:00182096 | Cervix | CC | peptidyl-serine modification | 66/2311 | 338/18723 | 9.58e-05 | 1.25e-03 | 66 |
GO:00192213 | Cervix | CC | cytokine-mediated signaling pathway | 84/2311 | 472/18723 | 3.25e-04 | 3.44e-03 | 84 |
GO:0006979111 | Esophagus | ESCC | response to oxidative stress | 303/8552 | 446/18723 | 7.15e-22 | 1.30e-19 | 303 |
GO:0062197111 | Esophagus | ESCC | cellular response to chemical stress | 234/8552 | 337/18723 | 5.37e-19 | 5.97e-17 | 234 |
GO:0034599111 | Esophagus | ESCC | cellular response to oxidative stress | 197/8552 | 288/18723 | 3.76e-15 | 2.15e-13 | 197 |
GO:004677710 | Esophagus | ESCC | protein autophosphorylation | 138/8552 | 227/18723 | 2.98e-06 | 3.38e-05 | 138 |
GO:00182099 | Esophagus | ESCC | peptidyl-serine modification | 196/8552 | 338/18723 | 3.07e-06 | 3.47e-05 | 196 |
GO:00607595 | Esophagus | ESCC | regulation of response to cytokine stimulus | 103/8552 | 162/18723 | 3.14e-06 | 3.53e-05 | 103 |
GO:001810515 | Esophagus | ESCC | peptidyl-serine phosphorylation | 184/8552 | 315/18723 | 3.22e-06 | 3.61e-05 | 184 |
GO:00019595 | Esophagus | ESCC | regulation of cytokine-mediated signaling pathway | 95/8552 | 150/18723 | 9.48e-06 | 9.04e-05 | 95 |
GO:000697922 | Liver | HCC | response to oxidative stress | 281/7958 | 446/18723 | 9.75e-19 | 1.24e-16 | 281 |
GO:006219722 | Liver | HCC | cellular response to chemical stress | 216/7958 | 337/18723 | 6.86e-16 | 5.44e-14 | 216 |
GO:003459922 | Liver | HCC | cellular response to oxidative stress | 183/7958 | 288/18723 | 3.65e-13 | 1.93e-11 | 183 |
GO:001810511 | Liver | HCC | peptidyl-serine phosphorylation | 169/7958 | 315/18723 | 3.86e-05 | 3.81e-04 | 169 |
GO:001820911 | Liver | HCC | peptidyl-serine modification | 177/7958 | 338/18723 | 1.45e-04 | 1.17e-03 | 177 |
GO:00467775 | Liver | HCC | protein autophosphorylation | 123/7958 | 227/18723 | 2.40e-04 | 1.80e-03 | 123 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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Cell-cell communication analysis |
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Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
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TF | Cell Type | Tissue | Disease Stage | Target Gene | RSS | Regulon Activity |
∗The dot plots of a searched regulon are shown for all cell subpopulations in each disease state of each tissue based on the regulon specific score inferred using pySCENIC and by calculating the average expression. |
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Somatic mutation of malignant transformation related genes |
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Hugo Symbol | Variant Class | Variant Classification | dbSNP RS | HGVSc | HGVSp | HGVSp Short | SWISSPROT | BIOTYPE | SIFT | PolyPhen | Tumor Sample Barcode | Tissue | Histology | Sex | Age | Stage | Therapy Types | Drugs | Outcome |
VRK2 | SNV | Missense_Mutation | c.14G>T | p.Arg5Ile | p.R5I | Q86Y07 | protein_coding | deleterious(0.04) | possibly_damaging(0.68) | TCGA-AA-3510-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
VRK2 | SNV | Missense_Mutation | rs765840317 | c.275N>A | p.Arg92His | p.R92H | Q86Y07 | protein_coding | tolerated(0.16) | benign(0) | TCGA-AA-3672-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
VRK2 | SNV | Missense_Mutation | c.1337G>A | p.Arg446Lys | p.R446K | Q86Y07 | protein_coding | tolerated(0.14) | benign(0) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
VRK2 | SNV | Missense_Mutation | rs765840317 | c.275N>A | p.Arg92His | p.R92H | Q86Y07 | protein_coding | tolerated(0.16) | benign(0) | TCGA-AA-A02R-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
VRK2 | SNV | Missense_Mutation | c.14N>T | p.Arg5Ile | p.R5I | Q86Y07 | protein_coding | deleterious(0.04) | possibly_damaging(0.68) | TCGA-AZ-4315-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
VRK2 | SNV | Missense_Mutation | c.848G>A | p.Ser283Asn | p.S283N | Q86Y07 | protein_coding | tolerated(0.43) | benign(0.02) | TCGA-CM-6166-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
VRK2 | SNV | Missense_Mutation | c.166N>A | p.Ala56Thr | p.A56T | Q86Y07 | protein_coding | tolerated(0.08) | benign(0.181) | TCGA-D5-6930-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
VRK2 | SNV | Missense_Mutation | c.1516N>G | p.Phe506Val | p.F506V | Q86Y07 | protein_coding | deleterious_low_confidence(0.02) | benign(0) | TCGA-AG-3896-01 | Colorectum | rectum adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
VRK2 | SNV | Missense_Mutation | novel | c.1001N>C | p.Val334Ala | p.V334A | Q86Y07 | protein_coding | tolerated(0.82) | benign(0.001) | TCGA-F5-6814-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
VRK2 | SNV | Missense_Mutation | rs192754138 | c.1472N>A | p.Arg491His | p.R491H | Q86Y07 | protein_coding | deleterious_low_confidence(0) | benign(0) | TCGA-F5-6814-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
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Related drugs of malignant transformation related genes |
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(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
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