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Gene: TSPAN13 |
Gene summary for TSPAN13 |
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Gene information | Species | Human | Gene symbol | TSPAN13 | Gene ID | 27075 |
Gene name | tetraspanin 13 | |
Gene Alias | NET-6 | |
Cytomap | 7p21.1 | |
Gene Type | protein-coding | GO ID | GO:0006810 | UniProtAcc | O95857 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
27075 | TSPAN13 | P37T-E | Human | Esophagus | ESCC | 8.96e-53 | 1.58e+00 | 0.1371 |
27075 | TSPAN13 | P38T-E | Human | Esophagus | ESCC | 2.01e-02 | 8.63e-02 | 0.127 |
27075 | TSPAN13 | P39T-E | Human | Esophagus | ESCC | 1.22e-41 | 9.61e-01 | 0.0894 |
27075 | TSPAN13 | P40T-E | Human | Esophagus | ESCC | 1.62e-12 | 5.51e-01 | 0.109 |
27075 | TSPAN13 | P42T-E | Human | Esophagus | ESCC | 7.50e-06 | 5.09e-01 | 0.1175 |
27075 | TSPAN13 | P44T-E | Human | Esophagus | ESCC | 8.15e-09 | 4.97e-01 | 0.1096 |
27075 | TSPAN13 | P47T-E | Human | Esophagus | ESCC | 5.96e-11 | 2.84e-01 | 0.1067 |
27075 | TSPAN13 | P48T-E | Human | Esophagus | ESCC | 1.11e-22 | 7.02e-01 | 0.0959 |
27075 | TSPAN13 | P49T-E | Human | Esophagus | ESCC | 2.00e-15 | 2.13e+00 | 0.1768 |
27075 | TSPAN13 | P52T-E | Human | Esophagus | ESCC | 1.59e-20 | 6.49e-01 | 0.1555 |
27075 | TSPAN13 | P54T-E | Human | Esophagus | ESCC | 1.58e-32 | 9.96e-01 | 0.0975 |
27075 | TSPAN13 | P56T-E | Human | Esophagus | ESCC | 2.85e-05 | 1.63e+00 | 0.1613 |
27075 | TSPAN13 | P57T-E | Human | Esophagus | ESCC | 1.51e-56 | 1.39e+00 | 0.0926 |
27075 | TSPAN13 | P61T-E | Human | Esophagus | ESCC | 2.78e-21 | 9.90e-01 | 0.099 |
27075 | TSPAN13 | P62T-E | Human | Esophagus | ESCC | 5.39e-68 | 1.51e+00 | 0.1302 |
27075 | TSPAN13 | P65T-E | Human | Esophagus | ESCC | 1.25e-44 | 1.22e+00 | 0.0978 |
27075 | TSPAN13 | P74T-E | Human | Esophagus | ESCC | 2.93e-48 | 1.96e+00 | 0.1479 |
27075 | TSPAN13 | P75T-E | Human | Esophagus | ESCC | 2.24e-91 | 2.23e+00 | 0.1125 |
27075 | TSPAN13 | P76T-E | Human | Esophagus | ESCC | 1.73e-56 | 1.37e+00 | 0.1207 |
27075 | TSPAN13 | P79T-E | Human | Esophagus | ESCC | 6.43e-49 | 1.08e+00 | 0.1154 |
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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:00109596 | Breast | Precancer | regulation of metal ion transport | 37/1080 | 406/18723 | 4.07e-03 | 3.22e-02 | 37 |
GO:001095913 | Breast | IDC | regulation of metal ion transport | 52/1434 | 406/18723 | 1.76e-04 | 2.97e-03 | 52 |
GO:0051924 | Breast | IDC | regulation of calcium ion transport | 32/1434 | 255/18723 | 3.94e-03 | 3.22e-02 | 32 |
GO:001095921 | Breast | DCIS | regulation of metal ion transport | 50/1390 | 406/18723 | 2.86e-04 | 4.22e-03 | 50 |
GO:0010959 | Colorectum | FAP | regulation of metal ion transport | 83/2622 | 406/18723 | 2.06e-04 | 2.96e-03 | 83 |
GO:1904062 | Colorectum | FAP | regulation of cation transmembrane transport | 69/2622 | 357/18723 | 3.06e-03 | 2.30e-02 | 69 |
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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 |
TSPAN13 | SNV | Missense_Mutation | c.270T>G | p.Phe90Leu | p.F90L | O95857 | protein_coding | tolerated(0.07) | benign(0.028) | TCGA-FU-A3HZ-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
TSPAN13 | SNV | Missense_Mutation | c.457N>T | p.Pro153Ser | p.P153S | O95857 | protein_coding | tolerated(0.26) | benign(0.175) | TCGA-AA-3833-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
TSPAN13 | SNV | Missense_Mutation | c.356G>A | p.Arg119Gln | p.R119Q | O95857 | protein_coding | tolerated(0.24) | benign(0.003) | TCGA-QL-A97D-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
TSPAN13 | SNV | Missense_Mutation | rs763710458 | c.283N>A | p.Ala95Thr | p.A95T | O95857 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-EI-6507-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
TSPAN13 | SNV | Missense_Mutation | novel | c.119T>G | p.Ile40Ser | p.I40S | O95857 | protein_coding | deleterious(0) | benign(0.398) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
TSPAN13 | SNV | Missense_Mutation | rs568219547 | c.244C>A | p.Leu82Met | p.L82M | O95857 | protein_coding | tolerated(0.05) | probably_damaging(0.999) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
TSPAN13 | SNV | Missense_Mutation | c.43N>A | p.Ala15Thr | p.A15T | O95857 | protein_coding | deleterious(0.05) | benign(0.066) | TCGA-AP-A0LE-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
TSPAN13 | SNV | Missense_Mutation | novel | c.112G>T | p.Gly38Trp | p.G38W | O95857 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-55-6979-01 | Lung | lung adenocarcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | PD |
TSPAN13 | SNV | Missense_Mutation | novel | c.200N>T | p.Ala67Val | p.A67V | O95857 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-KU-A66T-01 | Oral cavity | head & neck squamous cell carcinoma | Female | <65 | I/II | Unknown | Unknown | PD |
TSPAN13 | SNV | Missense_Mutation | novel | c.188N>A | p.Gly63Asp | p.G63D | O95857 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-UF-A7JF-01 | Oral cavity | head & neck squamous cell carcinoma | Male | >=65 | I/II | Chemotherapy | cisplatin | CR |
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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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