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Gene: TMEM30A |
Gene summary for TMEM30A |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | TMEM30A | Gene ID | 55754 |
| Gene name | transmembrane protein 30A | |
| Gene Alias | C6orf67 | |
| Cytomap | 6q14.1 | |
| Gene Type | protein-coding | GO ID | GO:0006810 | UniProtAcc | Q9NV96 |
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Malignant transformation analysis |
| Identification of the aberrant gene expression in precancerous and cancerous lesions by comparing the gene expression of stem-like cells in diseased tissues with normal stem cells |
| Malignant transformation involving gene list. |
| Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
| 55754 | TMEM30A | LZE2T | Human | Esophagus | ESCC | 2.01e-03 | 3.80e-01 | 0.082 |
| 55754 | TMEM30A | LZE4T | Human | Esophagus | ESCC | 1.11e-13 | 3.95e-01 | 0.0811 |
| 55754 | TMEM30A | LZE7T | Human | Esophagus | ESCC | 1.20e-03 | 5.85e-01 | 0.0667 |
| 55754 | TMEM30A | LZE8T | Human | Esophagus | ESCC | 3.37e-08 | 3.47e-02 | 0.067 |
| 55754 | TMEM30A | LZE20T | Human | Esophagus | ESCC | 2.02e-05 | 1.27e-01 | 0.0662 |
| 55754 | TMEM30A | LZE24T | Human | Esophagus | ESCC | 1.31e-15 | 6.09e-01 | 0.0596 |
| 55754 | TMEM30A | LZE21T | Human | Esophagus | ESCC | 9.15e-04 | 7.20e-02 | 0.0655 |
| 55754 | TMEM30A | LZE6T | Human | Esophagus | ESCC | 2.45e-03 | 1.92e-01 | 0.0845 |
| 55754 | TMEM30A | P1T-E | Human | Esophagus | ESCC | 5.06e-07 | 2.98e-01 | 0.0875 |
| 55754 | TMEM30A | P2T-E | Human | Esophagus | ESCC | 1.92e-33 | 6.57e-01 | 0.1177 |
| 55754 | TMEM30A | P4T-E | Human | Esophagus | ESCC | 4.09e-20 | 6.67e-01 | 0.1323 |
| 55754 | TMEM30A | P5T-E | Human | Esophagus | ESCC | 2.83e-16 | 3.70e-01 | 0.1327 |
| 55754 | TMEM30A | P8T-E | Human | Esophagus | ESCC | 3.52e-40 | 9.84e-01 | 0.0889 |
| 55754 | TMEM30A | P9T-E | Human | Esophagus | ESCC | 1.06e-07 | 2.12e-01 | 0.1131 |
| 55754 | TMEM30A | P10T-E | Human | Esophagus | ESCC | 3.91e-35 | 7.01e-01 | 0.116 |
| 55754 | TMEM30A | P11T-E | Human | Esophagus | ESCC | 1.60e-16 | 9.80e-01 | 0.1426 |
| 55754 | TMEM30A | P12T-E | Human | Esophagus | ESCC | 1.69e-33 | 7.10e-01 | 0.1122 |
| 55754 | TMEM30A | P15T-E | Human | Esophagus | ESCC | 3.74e-31 | 9.14e-01 | 0.1149 |
| 55754 | TMEM30A | P16T-E | Human | Esophagus | ESCC | 2.63e-34 | 7.43e-01 | 0.1153 |
| 55754 | TMEM30A | P17T-E | Human | Esophagus | ESCC | 8.79e-08 | 5.30e-01 | 0.1278 |
| Page: 1 2 3 4 5 6 7 8 |
| Transcriptomic changes along malignancy continuum. |
| Tissue | Expression Dynamics | Abbreviation |
| Esophagus |  | ESCC: Esophageal squamous cell carcinoma |
| HGIN: High-grade intraepithelial neoplasias | ||
| LGIN: Low-grade intraepithelial neoplasias | ||
| Liver |  | HCC: Hepatocellular carcinoma |
| NAFLD: Non-alcoholic fatty liver disease | ||
| Oral Cavity |  | EOLP: Erosive Oral lichen planus |
| LP: leukoplakia | ||
| NEOLP: Non-erosive oral lichen planus | ||
| OSCC: Oral squamous cell carcinoma | ||
| Prostate |  | BPH: Benign Prostatic Hyperplasia |
| Skin |  | AK: Actinic keratosis |
| cSCC: Cutaneous squamous cell carcinoma | ||
| SCCIS:squamous cell carcinoma in situ | ||
| Thyroid |  | ATC: Anaplastic thyroid cancer |
| HT: Hashimoto's thyroiditis | ||
| PTC: Papillary thyroid cancer |
| ∗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 |
| Find out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer |
| Figure of enriched GO biological processes. |
| 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 |
| Enriched GO biological processes. |
| GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
| GO:003238618 | Esophagus | ESCC | regulation of intracellular transport | 243/8552 | 337/18723 | 3.20e-23 | 7.25e-21 | 243 |
| GO:0033157110 | Esophagus | ESCC | regulation of intracellular protein transport | 169/8552 | 229/18723 | 3.31e-18 | 3.23e-16 | 169 |
| GO:0032388110 | Esophagus | ESCC | positive regulation of intracellular transport | 152/8552 | 202/18723 | 7.89e-18 | 7.36e-16 | 152 |
| GO:1904951111 | Esophagus | ESCC | positive regulation of establishment of protein localization | 216/8552 | 319/18723 | 1.01e-15 | 6.86e-14 | 216 |
| GO:009031617 | Esophagus | ESCC | positive regulation of intracellular protein transport | 122/8552 | 160/18723 | 2.45e-15 | 1.49e-13 | 122 |
| GO:0051222111 | Esophagus | ESCC | positive regulation of protein transport | 204/8552 | 303/18723 | 1.56e-14 | 8.38e-13 | 204 |
| GO:003252714 | Esophagus | ESCC | protein exit from endoplasmic reticulum | 37/8552 | 48/18723 | 8.99e-06 | 8.65e-05 | 37 |
| GO:003134616 | Esophagus | ESCC | positive regulation of cell projection organization | 201/8552 | 353/18723 | 1.19e-05 | 1.11e-04 | 201 |
| GO:001097516 | Esophagus | ESCC | regulation of neuron projection development | 240/8552 | 445/18723 | 2.48e-04 | 1.53e-03 | 240 |
| GO:00360106 | Esophagus | ESCC | protein localization to endosome | 18/8552 | 24/18723 | 3.43e-03 | 1.41e-02 | 18 |
| GO:00109764 | Esophagus | ESCC | positive regulation of neuron projection development | 91/8552 | 163/18723 | 5.72e-03 | 2.13e-02 | 91 |
| GO:00708615 | Esophagus | ESCC | regulation of protein exit from endoplasmic reticulum | 19/8552 | 27/18723 | 8.35e-03 | 2.95e-02 | 19 |
| GO:003238611 | Liver | Cirrhotic | regulation of intracellular transport | 147/4634 | 337/18723 | 1.84e-14 | 1.72e-12 | 147 |
| GO:003315711 | Liver | Cirrhotic | regulation of intracellular protein transport | 108/4634 | 229/18723 | 1.23e-13 | 1.04e-11 | 108 |
| GO:190495112 | Liver | Cirrhotic | positive regulation of establishment of protein localization | 135/4634 | 319/18723 | 3.20e-12 | 2.28e-10 | 135 |
| GO:005122212 | Liver | Cirrhotic | positive regulation of protein transport | 126/4634 | 303/18723 | 6.85e-11 | 3.77e-09 | 126 |
| GO:003238811 | Liver | Cirrhotic | positive regulation of intracellular transport | 92/4634 | 202/18723 | 8.60e-11 | 4.66e-09 | 92 |
| GO:009031611 | Liver | Cirrhotic | positive regulation of intracellular protein transport | 77/4634 | 160/18723 | 1.17e-10 | 6.21e-09 | 77 |
| GO:00325271 | Liver | Cirrhotic | protein exit from endoplasmic reticulum | 29/4634 | 48/18723 | 1.63e-07 | 4.30e-06 | 29 |
| GO:00708611 | Liver | Cirrhotic | regulation of protein exit from endoplasmic reticulum | 17/4634 | 27/18723 | 2.89e-05 | 3.65e-04 | 17 |
| Page: 1 2 3 4 5 6 7 8 |
| Enriched KEGG pathways. |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| Page: 1 |
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Cell-cell communication analysis |
| Identification of potential cell-cell interactions between two cell types and their ligand-receptor pairs for different disease states |
| Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
| Page: 1 |
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Single-cell gene regulatory network inference analysis |
| Find out the significant the regulons (TFs) and the target genes of each regulon across cell types for different disease states |
| 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 |
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Somatic mutation of malignant transformation related genes |
| Annotation of somatic variants for genes involved in malignant transformation |
| 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 |
| TMEM30A | SNV | Missense_Mutation | novel | c.549A>C | p.Leu183Phe | p.L183F | Q9NV96 | protein_coding | tolerated(0.75) | benign(0.405) | TCGA-A7-A56D-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | arimidex | SD |
| TMEM30A | SNV | Missense_Mutation | rs766839161 | c.808C>T | p.Arg270Cys | p.R270C | Q9NV96 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| TMEM30A | SNV | Missense_Mutation | novel | c.149T>G | p.Val50Gly | p.V50G | Q9NV96 | protein_coding | deleterious(0) | possibly_damaging(0.885) | TCGA-LL-A8F5-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cyclophosphamide | SD |
| TMEM30A | deletion | Frame_Shift_Del | novel | c.216delN | p.Asn73ThrfsTer27 | p.N73Tfs*27 | Q9NV96 | protein_coding | TCGA-EW-A2FV-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | docetaxel | SD | ||
| TMEM30A | SNV | Missense_Mutation | novel | c.14N>G | p.Tyr5Cys | p.Y5C | Q9NV96 | protein_coding | tolerated_low_confidence(0.1) | benign(0.005) | TCGA-MA-AA41-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
| TMEM30A | SNV | Missense_Mutation | c.851C>T | p.Pro284Leu | p.P284L | Q9NV96 | protein_coding | tolerated(0.14) | benign(0.371) | TCGA-A6-2681-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
| TMEM30A | SNV | Missense_Mutation | c.200N>A | p.Gly67Asp | p.G67D | Q9NV96 | protein_coding | deleterious(0.04) | possibly_damaging(0.829) | TCGA-AA-3672-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
| TMEM30A | SNV | Missense_Mutation | rs766839161 | c.808C>T | p.Arg270Cys | p.R270C | Q9NV96 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AA-3977-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
| TMEM30A | SNV | Missense_Mutation | rs778890689 | c.920N>A | p.Arg307Gln | p.R307Q | Q9NV96 | protein_coding | tolerated(0.06) | benign(0.393) | TCGA-AA-3984-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| TMEM30A | SNV | Missense_Mutation | c.769T>G | p.Phe257Val | p.F257V | Q9NV96 | protein_coding | deleterious(0) | possibly_damaging(0.79) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
| Page: 1 2 3 4 |
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Related drugs of malignant transformation related genes |
| Identification of chemicals and drugs interact with genes involved in malignant transfromation |
| (DGIdb 4.0) |
| Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
| Page: 1 |
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