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Gene: VWA5A |
Gene summary for VWA5A |
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Gene information | Species | Human | Gene symbol | VWA5A | Gene ID | 4013 |
Gene name | von Willebrand factor A domain containing 5A | |
Gene Alias | BCSC-1 | |
Cytomap | 11q24.2 | |
Gene Type | protein-coding | GO ID | GO:0005575 | UniProtAcc | A0A024R3H3 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
4013 | VWA5A | P2T-E | Human | Esophagus | ESCC | 2.35e-04 | -3.10e-03 | 0.1177 |
4013 | VWA5A | P4T-E | Human | Esophagus | ESCC | 6.37e-06 | 7.86e-03 | 0.1323 |
4013 | VWA5A | P5T-E | Human | Esophagus | ESCC | 1.28e-02 | -5.15e-02 | 0.1327 |
4013 | VWA5A | P8T-E | Human | Esophagus | ESCC | 1.64e-06 | 5.22e-03 | 0.0889 |
4013 | VWA5A | P9T-E | Human | Esophagus | ESCC | 2.56e-03 | 3.46e-02 | 0.1131 |
4013 | VWA5A | P10T-E | Human | Esophagus | ESCC | 6.75e-03 | -4.89e-03 | 0.116 |
4013 | VWA5A | P16T-E | Human | Esophagus | ESCC | 1.32e-02 | -5.28e-02 | 0.1153 |
4013 | VWA5A | P21T-E | Human | Esophagus | ESCC | 9.90e-09 | 1.09e-01 | 0.1617 |
4013 | VWA5A | P22T-E | Human | Esophagus | ESCC | 4.57e-18 | 1.61e-01 | 0.1236 |
4013 | VWA5A | P24T-E | Human | Esophagus | ESCC | 1.88e-02 | -2.23e-02 | 0.1287 |
4013 | VWA5A | P26T-E | Human | Esophagus | ESCC | 4.08e-06 | 2.35e-01 | 0.1276 |
4013 | VWA5A | P27T-E | Human | Esophagus | ESCC | 6.28e-03 | -6.27e-02 | 0.1055 |
4013 | VWA5A | P30T-E | Human | Esophagus | ESCC | 5.23e-09 | 7.37e-01 | 0.137 |
4013 | VWA5A | P32T-E | Human | Esophagus | ESCC | 9.02e-05 | -1.64e-02 | 0.1666 |
4013 | VWA5A | P36T-E | Human | Esophagus | ESCC | 2.45e-03 | 1.04e-02 | 0.1187 |
4013 | VWA5A | P37T-E | Human | Esophagus | ESCC | 2.52e-08 | 7.16e-02 | 0.1371 |
4013 | VWA5A | P40T-E | Human | Esophagus | ESCC | 5.54e-03 | 7.50e-02 | 0.109 |
4013 | VWA5A | P42T-E | Human | Esophagus | ESCC | 8.19e-04 | 2.73e-02 | 0.1175 |
4013 | VWA5A | P44T-E | Human | Esophagus | ESCC | 2.49e-04 | 1.24e-01 | 0.1096 |
4013 | VWA5A | P47T-E | Human | Esophagus | ESCC | 8.87e-03 | 1.08e-01 | 0.1067 |
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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 |
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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 |
VWA5A | SNV | Missense_Mutation | rs763551541 | c.1886N>A | p.Arg629Gln | p.R629Q | O00534 | protein_coding | tolerated(0.6) | benign(0.048) | TCGA-A7-A5ZX-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | doxorubicin | CR |
VWA5A | SNV | Missense_Mutation | c.1813N>T | p.His605Tyr | p.H605Y | O00534 | protein_coding | tolerated(0.45) | benign(0.296) | TCGA-BH-A0B6-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
VWA5A | SNV | Missense_Mutation | novel | c.581A>G | p.Lys194Arg | p.K194R | O00534 | protein_coding | tolerated(0.89) | benign(0.015) | TCGA-S3-AA14-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | CR |
VWA5A | deletion | Frame_Shift_Del | novel | c.2083delG | p.Asp695IlefsTer2 | p.D695Ifs*2 | O00534 | protein_coding | TCGA-EW-A2FV-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | docetaxel | SD | ||
VWA5A | SNV | Missense_Mutation | c.827C>T | p.Ser276Leu | p.S276L | O00534 | protein_coding | tolerated(0.06) | benign(0.005) | TCGA-Q1-A6DW-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | SD | |
VWA5A | SNV | Missense_Mutation | rs533874979 | c.340G>T | p.Val114Leu | p.V114L | O00534 | protein_coding | tolerated(0.1) | possibly_damaging(0.856) | TCGA-ZJ-A8QR-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
VWA5A | SNV | Missense_Mutation | rs771497215 | c.2018N>A | p.Ser673Asn | p.S673N | O00534 | protein_coding | tolerated(0.48) | benign(0.046) | TCGA-AA-3672-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
VWA5A | SNV | Missense_Mutation | c.1294N>T | p.Gly432Cys | p.G432C | O00534 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR | |
VWA5A | SNV | Missense_Mutation | novel | c.374N>C | p.Val125Ala | p.V125A | O00534 | protein_coding | deleterious(0) | possibly_damaging(0.794) | TCGA-AM-5821-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
VWA5A | SNV | Missense_Mutation | c.1114N>T | p.Pro372Ser | p.P372S | O00534 | protein_coding | deleterious(0.01) | probably_damaging(0.982) | TCGA-AZ-6598-01 | Colorectum | colon adenocarcinoma | Female | >=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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