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Gene: TMEM203 |
Gene summary for TMEM203 |
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Gene information | Species | Human | Gene symbol | TMEM203 | Gene ID | 94107 |
Gene name | transmembrane protein 203 | |
Gene Alias | HBEBP1 | |
Cytomap | 9q34.3 | |
Gene Type | protein-coding | GO ID | GO:0000003 | UniProtAcc | Q969S6 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
94107 | TMEM203 | LZE2T | Human | Esophagus | ESCC | 2.31e-03 | 4.95e-01 | 0.082 |
94107 | TMEM203 | LZE20T | Human | Esophagus | ESCC | 2.86e-06 | 2.82e-01 | 0.0662 |
94107 | TMEM203 | LZE24T | Human | Esophagus | ESCC | 1.86e-05 | 2.19e-01 | 0.0596 |
94107 | TMEM203 | P2T-E | Human | Esophagus | ESCC | 1.30e-45 | 7.22e-01 | 0.1177 |
94107 | TMEM203 | P4T-E | Human | Esophagus | ESCC | 2.42e-24 | 5.55e-01 | 0.1323 |
94107 | TMEM203 | P5T-E | Human | Esophagus | ESCC | 8.22e-21 | 4.21e-01 | 0.1327 |
94107 | TMEM203 | P8T-E | Human | Esophagus | ESCC | 2.85e-11 | 2.93e-01 | 0.0889 |
94107 | TMEM203 | P9T-E | Human | Esophagus | ESCC | 1.04e-09 | 2.58e-01 | 0.1131 |
94107 | TMEM203 | P10T-E | Human | Esophagus | ESCC | 1.55e-08 | 2.38e-01 | 0.116 |
94107 | TMEM203 | P11T-E | Human | Esophagus | ESCC | 3.46e-09 | 3.56e-01 | 0.1426 |
94107 | TMEM203 | P12T-E | Human | Esophagus | ESCC | 9.22e-15 | 1.66e-01 | 0.1122 |
94107 | TMEM203 | P15T-E | Human | Esophagus | ESCC | 1.56e-03 | 1.20e-01 | 0.1149 |
94107 | TMEM203 | P16T-E | Human | Esophagus | ESCC | 4.08e-08 | 1.48e-01 | 0.1153 |
94107 | TMEM203 | P20T-E | Human | Esophagus | ESCC | 1.91e-05 | 1.52e-01 | 0.1124 |
94107 | TMEM203 | P21T-E | Human | Esophagus | ESCC | 1.86e-21 | 4.30e-01 | 0.1617 |
94107 | TMEM203 | P22T-E | Human | Esophagus | ESCC | 2.30e-14 | 2.75e-01 | 0.1236 |
94107 | TMEM203 | P23T-E | Human | Esophagus | ESCC | 2.08e-12 | 2.90e-01 | 0.108 |
94107 | TMEM203 | P24T-E | Human | Esophagus | ESCC | 5.33e-09 | 2.95e-01 | 0.1287 |
94107 | TMEM203 | P26T-E | Human | Esophagus | ESCC | 2.20e-07 | 2.26e-01 | 0.1276 |
94107 | TMEM203 | P27T-E | Human | Esophagus | ESCC | 7.59e-05 | 1.59e-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 |
Cervix | N_HPV | ![]() |
Endometrium | AEH | ![]() |
Endometrium | EEC | ![]() |
Prostate | BPH | ![]() |
Prostate | Tumor | ![]() |
∗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 |
TMEM203 | SNV | Missense_Mutation | novel | c.309G>C | p.Gln103His | p.Q103H | Q969S6 | protein_coding | deleterious(0.05) | possibly_damaging(0.85) | TCGA-AJ-A2QM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Chemotherapy | carboplatin | CR |
TMEM203 | SNV | Missense_Mutation | c.370N>G | p.Leu124Val | p.L124V | Q969S6 | protein_coding | tolerated(0.07) | benign(0.217) | TCGA-49-AARE-01 | Lung | lung adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | PD | |
TMEM203 | SNV | Missense_Mutation | c.138N>T | p.Trp46Cys | p.W46C | Q969S6 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-BR-4257-01 | Stomach | stomach adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
TMEM203 | SNV | Missense_Mutation | c.172N>A | p.Gly58Arg | p.G58R | Q969S6 | protein_coding | tolerated(0.11) | probably_damaging(0.996) | TCGA-HU-A4GQ-01 | Stomach | stomach adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD | |
TMEM203 | SNV | Missense_Mutation | novel | c.113A>G | p.Asp38Gly | p.D38G | Q969S6 | protein_coding | deleterious(0.02) | probably_damaging(0.922) | TCGA-DJ-A3VK-01 | Thyroid | thyroid carcinoma | Male | <65 | III/IV | 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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