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Gene: VDAC3 |
Gene summary for VDAC3 |
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Gene information | Species | Human | Gene symbol | VDAC3 | Gene ID | 7419 |
Gene name | voltage dependent anion channel 3 | |
Gene Alias | HD-VDAC3 | |
Cytomap | 8p11.21 | |
Gene Type | protein-coding | GO ID | GO:0006810 | UniProtAcc | Q9Y277 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
7419 | VDAC3 | P1T-E | Human | Esophagus | ESCC | 2.93e-04 | 6.77e-01 | 0.0875 |
7419 | VDAC3 | P2T-E | Human | Esophagus | ESCC | 2.29e-41 | 1.04e+00 | 0.1177 |
7419 | VDAC3 | P4T-E | Human | Esophagus | ESCC | 3.66e-45 | 1.42e+00 | 0.1323 |
7419 | VDAC3 | P5T-E | Human | Esophagus | ESCC | 5.10e-15 | 5.11e-01 | 0.1327 |
7419 | VDAC3 | P8T-E | Human | Esophagus | ESCC | 1.96e-26 | 7.22e-01 | 0.0889 |
7419 | VDAC3 | P9T-E | Human | Esophagus | ESCC | 1.08e-13 | 5.05e-01 | 0.1131 |
7419 | VDAC3 | P10T-E | Human | Esophagus | ESCC | 1.50e-37 | 8.19e-01 | 0.116 |
7419 | VDAC3 | P11T-E | Human | Esophagus | ESCC | 1.34e-17 | 9.52e-01 | 0.1426 |
7419 | VDAC3 | P12T-E | Human | Esophagus | ESCC | 6.80e-59 | 1.42e+00 | 0.1122 |
7419 | VDAC3 | P15T-E | Human | Esophagus | ESCC | 2.27e-54 | 1.80e+00 | 0.1149 |
7419 | VDAC3 | P16T-E | Human | Esophagus | ESCC | 2.62e-60 | 1.47e+00 | 0.1153 |
7419 | VDAC3 | P17T-E | Human | Esophagus | ESCC | 2.38e-11 | 6.87e-01 | 0.1278 |
7419 | VDAC3 | P19T-E | Human | Esophagus | ESCC | 2.50e-09 | 1.15e+00 | 0.1662 |
7419 | VDAC3 | P20T-E | Human | Esophagus | ESCC | 1.12e-30 | 8.45e-01 | 0.1124 |
7419 | VDAC3 | P21T-E | Human | Esophagus | ESCC | 3.43e-42 | 1.10e+00 | 0.1617 |
7419 | VDAC3 | P22T-E | Human | Esophagus | ESCC | 3.66e-54 | 1.22e+00 | 0.1236 |
7419 | VDAC3 | P23T-E | Human | Esophagus | ESCC | 4.16e-55 | 1.90e+00 | 0.108 |
7419 | VDAC3 | P24T-E | Human | Esophagus | ESCC | 1.83e-28 | 8.22e-01 | 0.1287 |
7419 | VDAC3 | P26T-E | Human | Esophagus | ESCC | 2.30e-41 | 1.06e+00 | 0.1276 |
7419 | VDAC3 | P27T-E | Human | Esophagus | ESCC | 1.14e-25 | 7.54e-01 | 0.1055 |
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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). |
Page: 1 2 3 4 5 6 7 8 9 |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:0015698 | Colorectum | AD | inorganic anion transport | 52/3918 | 180/18723 | 6.83e-03 | 4.22e-02 | 52 |
GO:0120032 | Colorectum | AD | regulation of plasma membrane bounded cell projection assembly | 53/3918 | 186/18723 | 8.51e-03 | 4.97e-02 | 53 |
GO:01200321 | Colorectum | SER | regulation of plasma membrane bounded cell projection assembly | 43/2897 | 186/18723 | 3.82e-03 | 3.16e-02 | 43 |
GO:0060491 | Colorectum | SER | regulation of cell projection assembly | 43/2897 | 188/18723 | 4.68e-03 | 3.70e-02 | 43 |
GO:01200322 | Colorectum | MSS | regulation of plasma membrane bounded cell projection assembly | 51/3467 | 186/18723 | 1.78e-03 | 1.58e-02 | 51 |
GO:00604911 | Colorectum | MSS | regulation of cell projection assembly | 51/3467 | 188/18723 | 2.28e-03 | 1.87e-02 | 51 |
GO:00156981 | Colorectum | FAP | inorganic anion transport | 38/2622 | 180/18723 | 5.73e-03 | 3.67e-02 | 38 |
GO:01200323 | Colorectum | FAP | regulation of plasma membrane bounded cell projection assembly | 39/2622 | 186/18723 | 5.84e-03 | 3.73e-02 | 39 |
GO:00604912 | Colorectum | FAP | regulation of cell projection assembly | 39/2622 | 188/18723 | 7.01e-03 | 4.29e-02 | 39 |
GO:190211514 | Esophagus | ESCC | regulation of organelle assembly | 116/8552 | 186/18723 | 3.15e-06 | 3.53e-05 | 116 |
GO:006049118 | Esophagus | ESCC | regulation of cell projection assembly | 110/8552 | 188/18723 | 2.60e-04 | 1.58e-03 | 110 |
GO:012003218 | Esophagus | ESCC | regulation of plasma membrane bounded cell projection assembly | 108/8552 | 186/18723 | 4.37e-04 | 2.46e-03 | 108 |
GO:1902115 | Liver | Cirrhotic | regulation of organelle assembly | 66/4634 | 186/18723 | 6.66e-04 | 5.04e-03 | 66 |
GO:01200326 | Liver | Cirrhotic | regulation of plasma membrane bounded cell projection assembly | 63/4634 | 186/18723 | 3.16e-03 | 1.78e-02 | 63 |
GO:00604915 | Liver | Cirrhotic | regulation of cell projection assembly | 63/4634 | 188/18723 | 4.17e-03 | 2.22e-02 | 63 |
GO:19021151 | Liver | HCC | regulation of organelle assembly | 110/7958 | 186/18723 | 3.30e-06 | 4.34e-05 | 110 |
GO:006049112 | Liver | HCC | regulation of cell projection assembly | 101/7958 | 188/18723 | 1.20e-03 | 6.69e-03 | 101 |
GO:012003212 | Liver | HCC | regulation of plasma membrane bounded cell projection assembly | 100/7958 | 186/18723 | 1.23e-03 | 6.81e-03 | 100 |
GO:19021155 | Oral cavity | OSCC | regulation of organelle assembly | 109/7305 | 186/18723 | 4.54e-08 | 8.45e-07 | 109 |
GO:006049110 | Oral cavity | OSCC | regulation of cell projection assembly | 100/7305 | 188/18723 | 5.27e-05 | 4.38e-04 | 100 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa05012 | Colorectum | AD | Parkinson disease | 147/2092 | 266/8465 | 2.53e-27 | 8.48e-25 | 5.41e-25 | 147 |
hsa05208 | Colorectum | AD | Chemical carcinogenesis - reactive oxygen species | 126/2092 | 223/8465 | 1.01e-24 | 1.68e-22 | 1.07e-22 | 126 |
hsa05415 | Colorectum | AD | Diabetic cardiomyopathy | 114/2092 | 203/8465 | 3.65e-22 | 3.06e-20 | 1.95e-20 | 114 |
hsa05010 | Colorectum | AD | Alzheimer disease | 174/2092 | 384/8465 | 1.82e-19 | 9.26e-18 | 5.91e-18 | 174 |
hsa05016 | Colorectum | AD | Huntington disease | 147/2092 | 306/8465 | 1.93e-19 | 9.26e-18 | 5.91e-18 | 147 |
hsa05020 | Colorectum | AD | Prion disease | 133/2092 | 273/8465 | 2.47e-18 | 8.29e-17 | 5.29e-17 | 133 |
hsa05022 | Colorectum | AD | Pathways of neurodegeneration - multiple diseases | 201/2092 | 476/8465 | 4.54e-18 | 1.27e-16 | 8.09e-17 | 201 |
hsa05017 | Colorectum | AD | Spinocerebellar ataxia | 60/2092 | 143/8465 | 3.78e-06 | 4.35e-05 | 2.78e-05 | 60 |
hsa04216 | Colorectum | AD | Ferroptosis | 21/2092 | 41/8465 | 2.23e-04 | 1.78e-03 | 1.13e-03 | 21 |
hsa05166 | Colorectum | AD | Human T-cell leukemia virus 1 infection | 72/2092 | 222/8465 | 5.24e-03 | 2.44e-02 | 1.55e-02 | 72 |
hsa04218 | Colorectum | AD | Cellular senescence | 53/2092 | 156/8465 | 5.55e-03 | 2.48e-02 | 1.58e-02 | 53 |
hsa050121 | Colorectum | AD | Parkinson disease | 147/2092 | 266/8465 | 2.53e-27 | 8.48e-25 | 5.41e-25 | 147 |
hsa052081 | Colorectum | AD | Chemical carcinogenesis - reactive oxygen species | 126/2092 | 223/8465 | 1.01e-24 | 1.68e-22 | 1.07e-22 | 126 |
hsa054151 | Colorectum | AD | Diabetic cardiomyopathy | 114/2092 | 203/8465 | 3.65e-22 | 3.06e-20 | 1.95e-20 | 114 |
hsa050101 | Colorectum | AD | Alzheimer disease | 174/2092 | 384/8465 | 1.82e-19 | 9.26e-18 | 5.91e-18 | 174 |
hsa050161 | Colorectum | AD | Huntington disease | 147/2092 | 306/8465 | 1.93e-19 | 9.26e-18 | 5.91e-18 | 147 |
hsa050201 | Colorectum | AD | Prion disease | 133/2092 | 273/8465 | 2.47e-18 | 8.29e-17 | 5.29e-17 | 133 |
hsa050221 | Colorectum | AD | Pathways of neurodegeneration - multiple diseases | 201/2092 | 476/8465 | 4.54e-18 | 1.27e-16 | 8.09e-17 | 201 |
hsa050171 | Colorectum | AD | Spinocerebellar ataxia | 60/2092 | 143/8465 | 3.78e-06 | 4.35e-05 | 2.78e-05 | 60 |
hsa042161 | Colorectum | AD | Ferroptosis | 21/2092 | 41/8465 | 2.23e-04 | 1.78e-03 | 1.13e-03 | 21 |
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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 |
VDAC3 | SNV | Missense_Mutation | rs551923370 | c.353N>T | p.Ser118Phe | p.S118F | Q9Y277 | protein_coding | deleterious(0.01) | possibly_damaging(0.66) | TCGA-AR-A5QP-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD |
VDAC3 | SNV | Missense_Mutation | rs752791425 | c.511N>A | p.Ala171Thr | p.A171T | Q9Y277 | protein_coding | tolerated(0.07) | benign(0.02) | TCGA-A6-5665-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
VDAC3 | SNV | Missense_Mutation | c.673N>G | p.Lys225Glu | p.K225E | Q9Y277 | protein_coding | deleterious(0) | possibly_damaging(0.551) | TCGA-AA-3941-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
VDAC3 | SNV | Missense_Mutation | novel | c.104N>A | p.Ser35Tyr | p.S35Y | Q9Y277 | protein_coding | deleterious(0.03) | benign(0.015) | TCGA-A5-A0G1-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
VDAC3 | SNV | Missense_Mutation | novel | c.170N>A | p.Gly57Asp | p.G57D | Q9Y277 | protein_coding | deleterious(0.02) | probably_damaging(0.999) | TCGA-A5-A0G1-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
VDAC3 | SNV | Missense_Mutation | novel | c.104N>A | p.Ser35Tyr | p.S35Y | Q9Y277 | protein_coding | deleterious(0.03) | benign(0.015) | TCGA-A5-A0GG-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
VDAC3 | SNV | Missense_Mutation | novel | c.391N>A | p.Asp131Asn | p.D131N | Q9Y277 | protein_coding | tolerated(0.08) | possibly_damaging(0.635) | TCGA-A5-A2K7-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | taxol | SD |
VDAC3 | SNV | Missense_Mutation | rs775234791 | c.442N>A | p.Glu148Lys | p.E148K | Q9Y277 | protein_coding | tolerated(0.25) | benign(0.175) | TCGA-B5-A11N-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
VDAC3 | SNV | Missense_Mutation | novel | c.104C>A | p.Ser35Tyr | p.S35Y | Q9Y277 | protein_coding | deleterious(0.03) | benign(0.015) | TCGA-EO-A3AV-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatin | CR |
VDAC3 | SNV | Missense_Mutation | novel | c.485N>C | p.Lys162Thr | p.K162T | Q9Y277 | protein_coding | deleterious(0.01) | possibly_damaging(0.769) | TCGA-EO-A3AY-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | PD |
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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 |
7419 | VDAC3 | KINASE | OLESOXIME | OLESOXIME | ||
7419 | VDAC3 | KINASE | PRLX93936 |
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