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Gene: TMEM106C |
Gene summary for TMEM106C |
| Gene information | Species | Human | Gene symbol | TMEM106C | Gene ID | 79022 |
| Gene name | transmembrane protein 106C | |
| Gene Alias | TMEM106C | |
| Cytomap | 12q13.11 | |
| Gene Type | protein-coding | GO ID | GO:0008150 | UniProtAcc | Q9BVX2 |
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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 |
| Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
| 79022 | TMEM106C | P65T-E | Human | Esophagus | ESCC | 3.03e-24 | 7.63e-01 | 0.0978 |
| 79022 | TMEM106C | P74T-E | Human | Esophagus | ESCC | 2.61e-49 | 1.57e+00 | 0.1479 |
| 79022 | TMEM106C | P75T-E | Human | Esophagus | ESCC | 6.18e-50 | 1.26e+00 | 0.1125 |
| 79022 | TMEM106C | P76T-E | Human | Esophagus | ESCC | 3.47e-51 | 1.39e+00 | 0.1207 |
| 79022 | TMEM106C | P79T-E | Human | Esophagus | ESCC | 3.14e-48 | 1.15e+00 | 0.1154 |
| 79022 | TMEM106C | P80T-E | Human | Esophagus | ESCC | 2.70e-27 | 9.04e-01 | 0.155 |
| 79022 | TMEM106C | P82T-E | Human | Esophagus | ESCC | 1.11e-21 | 1.37e+00 | 0.1072 |
| 79022 | TMEM106C | P83T-E | Human | Esophagus | ESCC | 5.67e-48 | 1.60e+00 | 0.1738 |
| 79022 | TMEM106C | P84T-E | Human | Esophagus | ESCC | 9.14e-05 | 5.29e-01 | 0.0933 |
| 79022 | TMEM106C | P89T-E | Human | Esophagus | ESCC | 9.98e-17 | 1.64e+00 | 0.1752 |
| 79022 | TMEM106C | P91T-E | Human | Esophagus | ESCC | 9.42e-18 | 3.09e+00 | 0.1828 |
| 79022 | TMEM106C | P94T-E | Human | Esophagus | ESCC | 6.85e-04 | 1.08e+00 | 0.0879 |
| 79022 | TMEM106C | P107T-E | Human | Esophagus | ESCC | 9.40e-46 | 1.24e+00 | 0.171 |
| 79022 | TMEM106C | P126T-E | Human | Esophagus | ESCC | 5.43e-05 | 5.74e-01 | 0.1125 |
| 79022 | TMEM106C | P127T-E | Human | Esophagus | ESCC | 5.95e-14 | 2.83e-01 | 0.0826 |
| 79022 | TMEM106C | P128T-E | Human | Esophagus | ESCC | 2.10e-59 | 1.98e+00 | 0.1241 |
| 79022 | TMEM106C | P130T-E | Human | Esophagus | ESCC | 6.90e-105 | 2.45e+00 | 0.1676 |
| 79022 | TMEM106C | HCC1_Meng | Human | Liver | HCC | 1.81e-98 | 4.07e-01 | 0.0246 |
| 79022 | TMEM106C | HCC2_Meng | Human | Liver | HCC | 1.01e-36 | 7.12e-02 | 0.0107 |
| 79022 | TMEM106C | cirrhotic1 | Human | Liver | Cirrhotic | 7.86e-16 | 1.09e-01 | 0.0202 |
| Page: 1 2 3 4 5 6 7 |
| ∗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 |
| 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 |
| Page: 1 |
| 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 |
| TMEM106C | insertion | Nonsense_Mutation | novel | c.409_410insCAGGCTAAGCTCAACCTGGCAGTATGAACAAAGAAACCCACCCAT | p.Met137delinsThrGlyTerAlaGlnProGlySerMetAsnLysGluThrHisProLeu | p.M137delinsTG*AQPGSMNKETHPL | Q9BVX2 | protein_coding | TCGA-A8-A08S-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | anastrozole | SD | ||
| TMEM106C | insertion | Nonsense_Mutation | novel | c.335_336insAGAAAACTGATACCAGAAGTGGGGCATTGCTATAAAGATACC | p.Leu112_Val113insGluAsnTerTyrGlnLysTrpGlyIleAlaIleLysIlePro | p.L112_V113insEN*YQKWGIAIKIP | Q9BVX2 | protein_coding | TCGA-A8-A09C-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | ||
| TMEM106C | insertion | Nonsense_Mutation | novel | c.351_352insTGAGAG | p.Gly117_Ile118insTer | p.G117_I118ins* | Q9BVX2 | protein_coding | TCGA-A8-A0A6-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | epirubicin | CR | ||
| TMEM106C | insertion | Frame_Shift_Ins | novel | c.353_354insTCGACGACTCTGCCAAGCCCATGCAGTAAAGCCAGAA | p.Lys119ArgfsTer20 | p.K119Rfs*20 | Q9BVX2 | protein_coding | TCGA-A8-A0A6-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | epirubicin | CR | ||
| TMEM106C | insertion | Nonsense_Mutation | novel | c.380_381insTAGAAACAAGCGATTTCTGTCGTGATTCACTGGGGCC | p.Lys127AsnfsTer9 | p.K127Nfs*9 | Q9BVX2 | protein_coding | TCGA-AO-A0JF-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | doxorubicin | SD | ||
| TMEM106C | SNV | Missense_Mutation | c.127N>C | p.Phe43Leu | p.F43L | Q9BVX2 | protein_coding | tolerated(0.07) | probably_damaging(0.992) | TCGA-AA-3715-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
| TMEM106C | SNV | Missense_Mutation | novel | c.415A>C | p.Thr139Pro | p.T139P | Q9BVX2 | protein_coding | deleterious(0) | probably_damaging(0.99) | TCGA-AA-A01D-01 | Colorectum | colon adenocarcinoma | Female | <65 | III/IV | Chemotherapy | capecitabine | PD |
| TMEM106C | SNV | Missense_Mutation | c.617T>C | p.Val206Ala | p.V206A | Q9BVX2 | protein_coding | deleterious(0.01) | benign(0.089) | TCGA-CM-5348-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD | |
| TMEM106C | SNV | Missense_Mutation | novel | c.350G>A | p.Gly117Asp | p.G117D | Q9BVX2 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
| TMEM106C | SNV | Missense_Mutation | novel | c.242C>A | p.Pro81His | p.P81H | Q9BVX2 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <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 |
| Page: 1 |