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Gene: TMCC1 |
Gene summary for TMCC1 |
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Gene information | Species | Human | Gene symbol | TMCC1 | Gene ID | 23023 |
Gene name | transmembrane and coiled-coil domain family 1 | |
Gene Alias | TMCC1 | |
Cytomap | 3q22.1 | |
Gene Type | protein-coding | GO ID | GO:0006810 | UniProtAcc | O94876 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
23023 | TMCC1 | CCI_1 | Human | Cervix | CC | 1.80e-12 | 1.42e+00 | 0.528 |
23023 | TMCC1 | CCI_2 | Human | Cervix | CC | 1.31e-13 | 1.36e+00 | 0.5249 |
23023 | TMCC1 | CCI_3 | Human | Cervix | CC | 1.11e-38 | 2.01e+00 | 0.516 |
23023 | TMCC1 | HTA11_3410_2000001011 | Human | Colorectum | AD | 3.61e-11 | -5.30e-01 | 0.0155 |
23023 | TMCC1 | HTA11_866_3004761011 | Human | Colorectum | AD | 7.41e-03 | -3.40e-01 | 0.096 |
23023 | TMCC1 | A002-C-010 | Human | Colorectum | FAP | 9.47e-03 | -2.17e-02 | 0.242 |
23023 | TMCC1 | A001-C-207 | Human | Colorectum | FAP | 3.59e-03 | -1.46e-01 | 0.1278 |
23023 | TMCC1 | A015-C-203 | Human | Colorectum | FAP | 1.44e-31 | -5.14e-01 | -0.1294 |
23023 | TMCC1 | A015-C-204 | Human | Colorectum | FAP | 1.01e-03 | -2.64e-01 | -0.0228 |
23023 | TMCC1 | A014-C-040 | Human | Colorectum | FAP | 5.32e-07 | -5.08e-01 | -0.1184 |
23023 | TMCC1 | A002-C-201 | Human | Colorectum | FAP | 1.60e-12 | -2.50e-01 | 0.0324 |
23023 | TMCC1 | A002-C-203 | Human | Colorectum | FAP | 4.04e-02 | -7.23e-02 | 0.2786 |
23023 | TMCC1 | A001-C-119 | Human | Colorectum | FAP | 1.18e-04 | -1.41e-01 | -0.1557 |
23023 | TMCC1 | A001-C-108 | Human | Colorectum | FAP | 1.43e-14 | -2.60e-01 | -0.0272 |
23023 | TMCC1 | A002-C-205 | Human | Colorectum | FAP | 1.55e-20 | -3.31e-01 | -0.1236 |
23023 | TMCC1 | A001-C-104 | Human | Colorectum | FAP | 2.11e-03 | -1.49e-01 | 0.0184 |
23023 | TMCC1 | A015-C-005 | Human | Colorectum | FAP | 3.04e-03 | -2.22e-01 | -0.0336 |
23023 | TMCC1 | A015-C-006 | Human | Colorectum | FAP | 8.40e-17 | -4.28e-01 | -0.0994 |
23023 | TMCC1 | A015-C-106 | Human | Colorectum | FAP | 5.96e-15 | -3.00e-01 | -0.0511 |
23023 | TMCC1 | A002-C-114 | Human | Colorectum | FAP | 1.15e-18 | -3.60e-01 | -0.1561 |
Page: 1 2 3 4 5 6 7 8 9 10 |
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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:001605012 | Prostate | Tumor | vesicle organization | 87/3246 | 300/18723 | 3.44e-07 | 7.71e-06 | 87 |
GO:001619713 | Prostate | Tumor | endosomal transport | 62/3246 | 230/18723 | 1.65e-04 | 1.47e-03 | 62 |
GO:000703212 | Prostate | Tumor | endosome organization | 26/3246 | 82/18723 | 1.07e-03 | 6.87e-03 | 26 |
GO:000702912 | Prostate | Tumor | endoplasmic reticulum organization | 27/3246 | 87/18723 | 1.24e-03 | 7.83e-03 | 27 |
GO:001605017 | Thyroid | PTC | vesicle organization | 163/5968 | 300/18723 | 4.74e-16 | 3.69e-14 | 163 |
GO:001619718 | Thyroid | PTC | endosomal transport | 128/5968 | 230/18723 | 6.26e-14 | 3.52e-12 | 128 |
GO:000702915 | Thyroid | PTC | endoplasmic reticulum organization | 51/5968 | 87/18723 | 2.37e-07 | 4.15e-06 | 51 |
GO:000703210 | Thyroid | PTC | endosome organization | 48/5968 | 82/18723 | 5.65e-07 | 9.04e-06 | 48 |
GO:00482855 | Thyroid | PTC | organelle fission | 188/5968 | 488/18723 | 9.64e-04 | 5.77e-03 | 188 |
GO:001605023 | Thyroid | ATC | vesicle organization | 166/6293 | 300/18723 | 6.14e-15 | 3.92e-13 | 166 |
GO:001619719 | Thyroid | ATC | endosomal transport | 128/6293 | 230/18723 | 4.44e-12 | 1.75e-10 | 128 |
GO:004828512 | Thyroid | ATC | organelle fission | 229/6293 | 488/18723 | 4.79e-10 | 1.29e-08 | 229 |
GO:000702921 | Thyroid | ATC | endoplasmic reticulum organization | 51/6293 | 87/18723 | 1.47e-06 | 1.81e-05 | 51 |
GO:000703216 | Thyroid | ATC | endosome organization | 48/6293 | 82/18723 | 3.13e-06 | 3.56e-05 | 48 |
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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 |
TMCC1 | SNV | Missense_Mutation | novel | c.1217N>A | p.Gly406Glu | p.G406E | O94876 | protein_coding | deleterious(0.01) | probably_damaging(1) | TCGA-A7-A2KD-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | cytoxan | SD |
TMCC1 | SNV | Missense_Mutation | novel | c.1900N>A | p.Leu634Ile | p.L634I | O94876 | protein_coding | tolerated(0.08) | benign(0.188) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
TMCC1 | SNV | Missense_Mutation | c.1173N>G | p.Asp391Glu | p.D391E | O94876 | protein_coding | tolerated(0.1) | probably_damaging(0.992) | TCGA-BH-A0AW-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | SD | |
TMCC1 | SNV | Missense_Mutation | novel | c.1835N>G | p.Val612Gly | p.V612G | O94876 | protein_coding | deleterious(0.01) | probably_damaging(0.95) | TCGA-BH-A0BO-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
TMCC1 | SNV | Missense_Mutation | c.1094N>C | p.Val365Ala | p.V365A | O94876 | protein_coding | deleterious(0) | probably_damaging(0.989) | TCGA-D8-A1XK-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicine+cyclophosphamide | SD | |
TMCC1 | SNV | Missense_Mutation | c.1045N>C | p.Gly349Arg | p.G349R | O94876 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-EW-A1PD-01 | Breast | breast invasive carcinoma | Male | <65 | I/II | Chemotherapy | docetaxel | SD | |
TMCC1 | deletion | Frame_Shift_Del | novel | c.354delN | p.Thr119GlnfsTer27 | p.T119Qfs*27 | O94876 | protein_coding | TCGA-D8-A27V-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD | ||
TMCC1 | SNV | Missense_Mutation | rs148011506 | c.1321N>A | p.Ala441Thr | p.A441T | O94876 | protein_coding | tolerated(0.24) | benign(0.006) | TCGA-VS-A8EH-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Chemotherapy | cisplatin | CR |
TMCC1 | deletion | Frame_Shift_Del | novel | c.1840delN | p.Leu614SerfsTer2 | p.L614Sfs*2 | O94876 | protein_coding | TCGA-C5-A1BK-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | ||
TMCC1 | SNV | Missense_Mutation | novel | c.146N>A | p.Gly49Asp | p.G49D | O94876 | protein_coding | deleterious_low_confidence(0) | probably_damaging(0.998) | TCGA-A6-2672-01 | Colorectum | colon adenocarcinoma | Female | >=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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