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Gene: TMEM54 |
Gene summary for TMEM54 |
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Gene information | Species | Human | Gene symbol | TMEM54 | Gene ID | 113452 |
Gene name | transmembrane protein 54 | |
Gene Alias | BCLP | |
Cytomap | 1p35.1 | |
Gene Type | protein-coding | GO ID | GO:0008150 | UniProtAcc | Q969K7 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
113452 | TMEM54 | GSM4909281 | Human | Breast | IDC | 2.94e-17 | 6.39e-01 | 0.21 |
113452 | TMEM54 | GSM4909282 | Human | Breast | IDC | 2.35e-24 | 7.17e-01 | -0.0288 |
113452 | TMEM54 | GSM4909286 | Human | Breast | IDC | 2.17e-22 | 6.80e-01 | 0.1081 |
113452 | TMEM54 | GSM4909291 | Human | Breast | IDC | 1.02e-02 | 3.36e-01 | 0.1753 |
113452 | TMEM54 | GSM4909296 | Human | Breast | IDC | 4.10e-05 | -1.26e-01 | 0.1524 |
113452 | TMEM54 | GSM4909297 | Human | Breast | IDC | 1.52e-09 | 2.62e-01 | 0.1517 |
113452 | TMEM54 | GSM4909311 | Human | Breast | IDC | 2.00e-17 | -3.71e-02 | 0.1534 |
113452 | TMEM54 | GSM4909312 | Human | Breast | IDC | 1.18e-04 | 1.53e-01 | 0.1552 |
113452 | TMEM54 | GSM4909319 | Human | Breast | IDC | 6.20e-21 | -1.07e-01 | 0.1563 |
113452 | TMEM54 | GSM4909321 | Human | Breast | IDC | 6.01e-07 | 8.32e-02 | 0.1559 |
113452 | TMEM54 | P1 | Human | Breast | IDC | 7.91e-07 | -1.60e-01 | 0.1527 |
113452 | TMEM54 | DCIS2 | Human | Breast | DCIS | 2.31e-63 | 2.86e-01 | 0.0085 |
113452 | TMEM54 | CA_HPV_1 | Human | Cervix | CC | 1.93e-03 | -1.32e-01 | 0.0264 |
113452 | TMEM54 | CA_HPV_3 | Human | Cervix | CC | 2.39e-03 | 1.86e-01 | 0.0414 |
113452 | TMEM54 | HSIL_HPV_2 | Human | Cervix | HSIL_HPV | 2.27e-09 | 3.78e-01 | 0.0208 |
113452 | TMEM54 | Tumor | Human | Cervix | CC | 6.28e-51 | 8.74e-01 | 0.1241 |
113452 | TMEM54 | sample3 | Human | Cervix | CC | 8.06e-59 | 8.75e-01 | 0.1387 |
113452 | TMEM54 | T3 | Human | Cervix | CC | 3.50e-52 | 8.22e-01 | 0.1389 |
113452 | TMEM54 | HTA11_2487_2000001011 | Human | Colorectum | SER | 4.35e-20 | 1.08e+00 | -0.1808 |
113452 | TMEM54 | HTA11_1938_2000001011 | Human | Colorectum | AD | 7.99e-03 | 2.84e-01 | -0.0811 |
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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 |
TMEM54 | SNV | Missense_Mutation | rs751814809 | c.208N>A | p.Val70Met | p.V70M | Q969K7 | protein_coding | deleterious(0.05) | benign(0.054) | TCGA-AN-A0AK-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
TMEM54 | SNV | Missense_Mutation | rs746007733 | c.625N>T | p.Arg209Cys | p.R209C | Q969K7 | protein_coding | deleterious(0.01) | benign(0) | TCGA-AA-3506-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
TMEM54 | SNV | Missense_Mutation | novel | c.575N>A | p.Gly192Glu | p.G192E | Q969K7 | protein_coding | deleterious(0.02) | probably_damaging(0.971) | TCGA-A5-A0G1-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
TMEM54 | SNV | Missense_Mutation | rs779851836 | c.155N>T | p.Ala52Val | p.A52V | Q969K7 | protein_coding | tolerated(0.06) | probably_damaging(0.919) | TCGA-AX-A06F-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatin | SD |
TMEM54 | SNV | Missense_Mutation | novel | c.293G>T | p.Ser98Ile | p.S98I | Q969K7 | protein_coding | deleterious(0) | possibly_damaging(0.745) | TCGA-AX-A2HD-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
TMEM54 | SNV | Missense_Mutation | c.449N>T | p.Thr150Ile | p.T150I | Q969K7 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-BS-A0TJ-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
TMEM54 | SNV | Missense_Mutation | rs775486263 | c.247N>T | p.Arg83Cys | p.R83C | Q969K7 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-EO-A22U-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
TMEM54 | SNV | Missense_Mutation | rs779851836 | c.155N>T | p.Ala52Val | p.A52V | Q969K7 | protein_coding | tolerated(0.06) | probably_damaging(0.919) | TCGA-EO-A22U-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
TMEM54 | SNV | Missense_Mutation | c.127C>G | p.Leu43Val | p.L43V | Q969K7 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-55-A57B-01 | Lung | lung adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
TMEM54 | SNV | Missense_Mutation | novel | c.626N>T | p.Arg209Leu | p.R209L | Q969K7 | protein_coding | tolerated(0.07) | benign(0.029) | TCGA-D6-8569-01 | Oral cavity | head & neck squamous cell carcinoma | Male | <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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