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Gene: TMEM135 |
Gene summary for TMEM135 |
Gene summary. |
Gene information | Species | Human | Gene symbol | TMEM135 | Gene ID | 65084 |
Gene name | transmembrane protein 135 | |
Gene Alias | PMP52 | |
Cytomap | 11q14.2 | |
Gene Type | protein-coding | GO ID | GO:0000266 | UniProtAcc | Q86UB9 |
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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 |
65084 | TMEM135 | HTA11_3410_2000001011 | Human | Colorectum | AD | 5.88e-15 | -5.60e-01 | 0.0155 |
65084 | TMEM135 | HTA11_3361_2000001011 | Human | Colorectum | AD | 7.04e-04 | -4.64e-01 | -0.1207 |
65084 | TMEM135 | HTA11_696_2000001011 | Human | Colorectum | AD | 3.21e-02 | -2.59e-01 | -0.1464 |
65084 | TMEM135 | HTA11_5212_2000001011 | Human | Colorectum | AD | 6.01e-03 | -6.26e-01 | -0.2061 |
65084 | TMEM135 | HTA11_866_3004761011 | Human | Colorectum | AD | 7.39e-12 | -5.51e-01 | 0.096 |
65084 | TMEM135 | HTA11_10711_2000001011 | Human | Colorectum | AD | 8.40e-04 | -4.62e-01 | 0.0338 |
65084 | TMEM135 | HTA11_7696_3000711011 | Human | Colorectum | AD | 1.17e-07 | -4.45e-01 | 0.0674 |
65084 | TMEM135 | HTA11_6818_2000001021 | Human | Colorectum | AD | 4.03e-02 | -3.44e-01 | 0.0588 |
65084 | TMEM135 | HTA11_99999970781_79442 | Human | Colorectum | MSS | 1.45e-07 | -3.38e-01 | 0.294 |
65084 | TMEM135 | HTA11_99999971662_82457 | Human | Colorectum | MSS | 1.76e-14 | -4.83e-01 | 0.3859 |
65084 | TMEM135 | HTA11_99999973899_84307 | Human | Colorectum | MSS | 2.31e-07 | -6.63e-01 | 0.2585 |
65084 | TMEM135 | HTA11_99999974143_84620 | Human | Colorectum | MSS | 1.20e-17 | -5.44e-01 | 0.3005 |
65084 | TMEM135 | F007 | Human | Colorectum | FAP | 1.93e-02 | -2.50e-01 | 0.1176 |
65084 | TMEM135 | A002-C-010 | Human | Colorectum | FAP | 5.59e-05 | -2.15e-01 | 0.242 |
65084 | TMEM135 | A001-C-207 | Human | Colorectum | FAP | 1.62e-08 | -4.10e-01 | 0.1278 |
65084 | TMEM135 | A015-C-203 | Human | Colorectum | FAP | 2.09e-34 | -5.67e-01 | -0.1294 |
65084 | TMEM135 | A015-C-204 | Human | Colorectum | FAP | 2.89e-09 | -3.74e-01 | -0.0228 |
65084 | TMEM135 | A014-C-040 | Human | Colorectum | FAP | 6.17e-09 | -6.78e-01 | -0.1184 |
65084 | TMEM135 | A002-C-201 | Human | Colorectum | FAP | 5.46e-20 | -5.06e-01 | 0.0324 |
65084 | TMEM135 | A002-C-203 | Human | Colorectum | FAP | 1.11e-05 | -2.10e-01 | 0.2786 |
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Transcriptomic changes along malignancy continuum. |
∗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). |
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Enriched GO biological processes. |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:0010821 | Colorectum | AD | regulation of mitochondrion organization | 57/3918 | 144/18723 | 2.43e-07 | 9.92e-06 | 57 |
GO:0031667 | Colorectum | AD | response to nutrient levels | 138/3918 | 474/18723 | 1.22e-05 | 2.68e-04 | 138 |
GO:0009409 | Colorectum | AD | response to cold | 22/3918 | 49/18723 | 1.40e-04 | 1.98e-03 | 22 |
GO:00108212 | Colorectum | MSS | regulation of mitochondrion organization | 53/3467 | 144/18723 | 1.67e-07 | 7.55e-06 | 53 |
GO:00316672 | Colorectum | MSS | response to nutrient levels | 125/3467 | 474/18723 | 1.24e-05 | 2.88e-04 | 125 |
GO:00094092 | Colorectum | MSS | response to cold | 19/3467 | 49/18723 | 7.20e-04 | 7.70e-03 | 19 |
GO:00316673 | Colorectum | FAP | response to nutrient levels | 95/2622 | 474/18723 | 1.59e-04 | 2.43e-03 | 95 |
GO:00108213 | Colorectum | FAP | regulation of mitochondrion organization | 35/2622 | 144/18723 | 6.44e-04 | 7.05e-03 | 35 |
GO:00094093 | Colorectum | FAP | response to cold | 14/2622 | 49/18723 | 5.95e-03 | 3.75e-02 | 14 |
GO:00316678 | Lung | IAC | response to nutrient levels | 76/2061 | 474/18723 | 4.87e-04 | 7.08e-03 | 76 |
GO:003166713 | Lung | AIS | response to nutrient levels | 64/1849 | 474/18723 | 6.13e-03 | 4.98e-02 | 64 |
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Enriched KEGG pathways. |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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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 |
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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. |
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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 |
TMEM135 | SNV | Missense_Mutation | c.809N>A | p.Cys270Tyr | p.C270Y | Q86UB9 | protein_coding | deleterious(0) | probably_damaging(0.979) | TCGA-D8-A1JA-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | adriamycin | PD | |
TMEM135 | SNV | Missense_Mutation | c.777C>G | p.Ile259Met | p.I259M | Q86UB9 | protein_coding | tolerated(0.13) | possibly_damaging(0.751) | TCGA-C5-A7UH-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Chemotherapy | cisplatin | SD | |
TMEM135 | SNV | Missense_Mutation | novel | c.288N>G | p.Phe96Leu | p.F96L | Q86UB9 | protein_coding | deleterious(0.01) | benign(0.168) | TCGA-DS-A7WH-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
TMEM135 | SNV | Missense_Mutation | c.692N>G | p.Asp231Gly | p.D231G | Q86UB9 | protein_coding | deleterious(0.04) | possibly_damaging(0.462) | TCGA-AA-3713-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | 5-fluorouracil | PR | |
TMEM135 | SNV | Missense_Mutation | c.47N>A | p.Gly16Asp | p.G16D | Q86UB9 | protein_coding | tolerated(0.08) | possibly_damaging(0.859) | TCGA-AD-5900-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
TMEM135 | SNV | Missense_Mutation | rs202089067 | c.955N>T | p.Arg319Cys | p.R319C | Q86UB9 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-AD-6899-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD |
TMEM135 | SNV | Missense_Mutation | c.1259N>G | p.Asn420Ser | p.N420S | Q86UB9 | protein_coding | tolerated(0.45) | probably_damaging(0.998) | TCGA-AY-6197-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
TMEM135 | SNV | Missense_Mutation | novel | c.284N>C | p.Lys95Thr | p.K95T | Q86UB9 | protein_coding | tolerated(0.1) | benign(0.177) | TCGA-CA-6717-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | CR |
TMEM135 | SNV | Missense_Mutation | novel | c.653N>T | p.Gly218Val | p.G218V | Q86UB9 | protein_coding | tolerated(0.59) | benign(0.049) | TCGA-CA-6717-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | CR |
TMEM135 | SNV | Missense_Mutation | novel | c.645A>C | p.Glu215Asp | p.E215D | Q86UB9 | protein_coding | tolerated(0.4) | benign(0) | TCGA-F5-6814-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
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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 |
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