![]() |
|||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Gene: TMCO3 |
Gene summary for TMCO3 |
![]() |
Gene information | Species | Human | Gene symbol | TMCO3 | Gene ID | 55002 |
Gene name | transmembrane and coiled-coil domains 3 | |
Gene Alias | C13orf11 | |
Cytomap | 13q34 | |
Gene Type | protein-coding | GO ID | GO:0006810 | UniProtAcc | A0A024RE09 |
Top |
Malignant transformation analysis |
![]() |
![]() |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
55002 | TMCO3 | LZE4T | Human | Esophagus | ESCC | 1.09e-03 | 1.26e-01 | 0.0811 |
55002 | TMCO3 | LZE7T | Human | Esophagus | ESCC | 2.41e-04 | 2.74e-01 | 0.0667 |
55002 | TMCO3 | LZE8T | Human | Esophagus | ESCC | 1.34e-04 | 1.40e-01 | 0.067 |
55002 | TMCO3 | LZE22T | Human | Esophagus | ESCC | 6.09e-04 | 5.05e-01 | 0.068 |
55002 | TMCO3 | LZE24T | Human | Esophagus | ESCC | 8.74e-17 | 4.31e-01 | 0.0596 |
55002 | TMCO3 | P1T-E | Human | Esophagus | ESCC | 8.75e-04 | 4.15e-01 | 0.0875 |
55002 | TMCO3 | P2T-E | Human | Esophagus | ESCC | 9.36e-20 | 3.19e-01 | 0.1177 |
55002 | TMCO3 | P4T-E | Human | Esophagus | ESCC | 9.13e-23 | 5.52e-01 | 0.1323 |
55002 | TMCO3 | P5T-E | Human | Esophagus | ESCC | 3.52e-02 | 3.08e-02 | 0.1327 |
55002 | TMCO3 | P8T-E | Human | Esophagus | ESCC | 2.64e-34 | 7.38e-01 | 0.0889 |
55002 | TMCO3 | P9T-E | Human | Esophagus | ESCC | 9.43e-09 | 2.94e-01 | 0.1131 |
55002 | TMCO3 | P10T-E | Human | Esophagus | ESCC | 1.97e-82 | 1.78e+00 | 0.116 |
55002 | TMCO3 | P11T-E | Human | Esophagus | ESCC | 9.33e-14 | 6.01e-01 | 0.1426 |
55002 | TMCO3 | P12T-E | Human | Esophagus | ESCC | 1.09e-41 | 8.78e-01 | 0.1122 |
55002 | TMCO3 | P15T-E | Human | Esophagus | ESCC | 3.26e-15 | 2.80e-01 | 0.1149 |
55002 | TMCO3 | P16T-E | Human | Esophagus | ESCC | 8.59e-16 | 2.18e-01 | 0.1153 |
55002 | TMCO3 | P17T-E | Human | Esophagus | ESCC | 1.22e-07 | 4.72e-01 | 0.1278 |
55002 | TMCO3 | P19T-E | Human | Esophagus | ESCC | 1.13e-07 | 6.65e-01 | 0.1662 |
55002 | TMCO3 | P20T-E | Human | Esophagus | ESCC | 1.52e-14 | 2.81e-01 | 0.1124 |
55002 | TMCO3 | P21T-E | Human | Esophagus | ESCC | 1.56e-25 | 4.68e-01 | 0.1617 |
Page: 1 2 3 4 5 6 |
![]() |
∗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. |
Top |
Malignant transformation related pathway analysis |
![]() |
![]() |
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 |
![]() |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:190260018 | Esophagus | ESCC | proton transmembrane transport | 88/8552 | 157/18723 | 5.62e-03 | 2.10e-02 | 88 |
GO:19026007 | Liver | HCC | proton transmembrane transport | 87/7958 | 157/18723 | 7.27e-04 | 4.42e-03 | 87 |
GO:1902600110 | Skin | cSCC | proton transmembrane transport | 57/4864 | 157/18723 | 2.66e-03 | 1.50e-02 | 57 |
GO:1902600111 | Thyroid | PTC | proton transmembrane transport | 72/5968 | 157/18723 | 1.64e-04 | 1.26e-03 | 72 |
GO:190260032 | Thyroid | ATC | proton transmembrane transport | 73/6293 | 157/18723 | 5.25e-04 | 3.06e-03 | 73 |
Page: 1 |
![]() |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
Page: 1 |
Top |
Cell-cell communication analysis |
![]() |
Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
Page: 1 |
Top |
Single-cell gene regulatory network inference analysis |
![]() |
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. |
Page: 1 |
Top |
Somatic mutation of malignant transformation related genes |
![]() |
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 |
TMCO3 | SNV | Missense_Mutation | c.1915N>T | p.Arg639Trp | p.R639W | Q6UWJ1 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AR-A0TW-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | doxorubicin | PD | |
TMCO3 | SNV | Missense_Mutation | c.1492G>C | p.Glu498Gln | p.E498Q | Q6UWJ1 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-C8-A12T-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
TMCO3 | SNV | Missense_Mutation | c.583G>C | p.Glu195Gln | p.E195Q | Q6UWJ1 | protein_coding | tolerated(0.09) | possibly_damaging(0.601) | TCGA-D8-A1J8-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | nolvadex | SD | |
TMCO3 | SNV | Missense_Mutation | rs755051458 | c.139N>T | p.Arg47Trp | p.R47W | Q6UWJ1 | protein_coding | deleterious(0.01) | benign(0.405) | TCGA-D8-A1XZ-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Hormone Therapy | tamoxiphen+anastrozolum | SD |
TMCO3 | SNV | Missense_Mutation | c.746A>T | p.Gln249Leu | p.Q249L | Q6UWJ1 | protein_coding | tolerated(0.19) | benign(0.039) | TCGA-E2-A1LB-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | SD | |
TMCO3 | SNV | Missense_Mutation | c.1390N>G | p.Leu464Val | p.L464V | Q6UWJ1 | protein_coding | tolerated(0.08) | possibly_damaging(0.46) | TCGA-EW-A1J5-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | SD | |
TMCO3 | insertion | Frame_Shift_Ins | novel | c.1183_1184insCTTCACAAAAGCTCAGCTCTGCCTCCTT | p.Val395AlafsTer21 | p.V395Afs*21 | Q6UWJ1 | protein_coding | TCGA-AO-A0J5-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Other, specify in notesBisphosphonate | zoledronic | PD | ||
TMCO3 | SNV | Missense_Mutation | rs761196028 | c.1888C>T | p.Arg630Trp | p.R630W | Q6UWJ1 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
TMCO3 | SNV | Missense_Mutation | novel | c.1730N>T | p.Thr577Met | p.T577M | Q6UWJ1 | protein_coding | deleterious(0.01) | possibly_damaging(0.863) | TCGA-EA-A3HU-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
TMCO3 | SNV | Missense_Mutation | rs550159257 | c.1906G>A | p.Val636Ile | p.V636I | Q6UWJ1 | protein_coding | tolerated(1) | benign(0) | TCGA-A6-6780-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
Page: 1 2 3 4 5 6 7 8 |
Top |
Related drugs of malignant transformation related genes |
![]() |
(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
Page: 1 |