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Gene: THOC5 |
Gene summary for THOC5 |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | THOC5 | Gene ID | 8563 |
| Gene name | THO complex 5 | |
| Gene Alias | C22orf19 | |
| Cytomap | 22q12.2 | |
| Gene Type | protein-coding | GO ID | GO:0000075 | UniProtAcc | A0A024R1D6 |
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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 |
| 8563 | THOC5 | LZE4T | Human | Esophagus | ESCC | 2.73e-07 | 1.80e-01 | 0.0811 |
| 8563 | THOC5 | LZE7T | Human | Esophagus | ESCC | 1.59e-15 | 5.03e-01 | 0.0667 |
| 8563 | THOC5 | LZE8T | Human | Esophagus | ESCC | 3.30e-02 | 8.89e-02 | 0.067 |
| 8563 | THOC5 | LZE24T | Human | Esophagus | ESCC | 5.17e-10 | 2.53e-01 | 0.0596 |
| 8563 | THOC5 | LZE21T | Human | Esophagus | ESCC | 4.00e-03 | 1.74e-01 | 0.0655 |
| 8563 | THOC5 | P2T-E | Human | Esophagus | ESCC | 5.72e-14 | 2.33e-01 | 0.1177 |
| 8563 | THOC5 | P4T-E | Human | Esophagus | ESCC | 4.30e-15 | 3.37e-01 | 0.1323 |
| 8563 | THOC5 | P5T-E | Human | Esophagus | ESCC | 2.15e-05 | 9.44e-02 | 0.1327 |
| 8563 | THOC5 | P8T-E | Human | Esophagus | ESCC | 8.04e-11 | 1.72e-01 | 0.0889 |
| 8563 | THOC5 | P9T-E | Human | Esophagus | ESCC | 3.11e-12 | 2.58e-01 | 0.1131 |
| 8563 | THOC5 | P10T-E | Human | Esophagus | ESCC | 1.11e-26 | 4.17e-01 | 0.116 |
| 8563 | THOC5 | P11T-E | Human | Esophagus | ESCC | 4.72e-07 | 3.17e-01 | 0.1426 |
| 8563 | THOC5 | P12T-E | Human | Esophagus | ESCC | 2.08e-15 | 2.95e-01 | 0.1122 |
| 8563 | THOC5 | P15T-E | Human | Esophagus | ESCC | 1.90e-29 | 5.50e-01 | 0.1149 |
| 8563 | THOC5 | P16T-E | Human | Esophagus | ESCC | 5.84e-17 | 3.32e-01 | 0.1153 |
| 8563 | THOC5 | P17T-E | Human | Esophagus | ESCC | 1.58e-07 | 3.40e-01 | 0.1278 |
| 8563 | THOC5 | P19T-E | Human | Esophagus | ESCC | 1.88e-03 | 3.43e-01 | 0.1662 |
| 8563 | THOC5 | P20T-E | Human | Esophagus | ESCC | 1.04e-13 | 3.04e-01 | 0.1124 |
| 8563 | THOC5 | P21T-E | Human | Esophagus | ESCC | 1.32e-11 | 2.38e-01 | 0.1617 |
| 8563 | THOC5 | P22T-E | Human | Esophagus | ESCC | 1.67e-16 | 3.71e-01 | 0.1236 |
| Page: 1 2 3 4 5 |
| 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 |
| ∗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:0008380111 | Esophagus | ESCC | RNA splicing | 336/8552 | 434/18723 | 1.74e-42 | 3.67e-39 | 336 |
| GO:0006913110 | Esophagus | ESCC | nucleocytoplasmic transport | 230/8552 | 301/18723 | 6.04e-28 | 2.02e-25 | 230 |
| GO:0051169110 | Esophagus | ESCC | nuclear transport | 230/8552 | 301/18723 | 6.04e-28 | 2.02e-25 | 230 |
| GO:0006403110 | Esophagus | ESCC | RNA localization | 166/8552 | 201/18723 | 1.95e-27 | 6.18e-25 | 166 |
| GO:005123617 | Esophagus | ESCC | establishment of RNA localization | 134/8552 | 166/18723 | 1.23e-20 | 1.81e-18 | 134 |
| GO:0051168110 | Esophagus | ESCC | nuclear export | 126/8552 | 154/18723 | 1.88e-20 | 2.65e-18 | 126 |
| GO:005102815 | Esophagus | ESCC | mRNA transport | 110/8552 | 130/18723 | 2.76e-20 | 3.80e-18 | 110 |
| GO:005065717 | Esophagus | ESCC | nucleic acid transport | 131/8552 | 163/18723 | 6.94e-20 | 8.46e-18 | 131 |
| GO:005065817 | Esophagus | ESCC | RNA transport | 131/8552 | 163/18723 | 6.94e-20 | 8.46e-18 | 131 |
| GO:001593117 | Esophagus | ESCC | nucleobase-containing compound transport | 162/8552 | 222/18723 | 9.87e-17 | 7.93e-15 | 162 |
| GO:000635414 | Esophagus | ESCC | DNA-templated transcription, elongation | 76/8552 | 91/18723 | 8.35e-14 | 4.11e-12 | 76 |
| GO:007116612 | Esophagus | ESCC | ribonucleoprotein complex localization | 66/8552 | 77/18723 | 2.94e-13 | 1.38e-11 | 66 |
| GO:007142612 | Esophagus | ESCC | ribonucleoprotein complex export from nucleus | 65/8552 | 76/18723 | 5.56e-13 | 2.50e-11 | 65 |
| GO:000640512 | Esophagus | ESCC | RNA export from nucleus | 68/8552 | 84/18723 | 2.99e-11 | 1.01e-09 | 68 |
| GO:190198713 | Esophagus | ESCC | regulation of cell cycle phase transition | 242/8552 | 390/18723 | 3.86e-11 | 1.26e-09 | 242 |
| GO:00064064 | Esophagus | ESCC | mRNA export from nucleus | 51/8552 | 59/18723 | 7.98e-11 | 2.47e-09 | 51 |
| GO:00714274 | Esophagus | ESCC | mRNA-containing ribonucleoprotein complex export from nucleus | 51/8552 | 59/18723 | 7.98e-11 | 2.47e-09 | 51 |
| GO:0044403111 | Esophagus | ESCC | biological process involved in symbiotic interaction | 186/8552 | 290/18723 | 1.43e-10 | 4.16e-09 | 186 |
| GO:00457865 | Esophagus | ESCC | negative regulation of cell cycle | 236/8552 | 385/18723 | 3.62e-10 | 9.93e-09 | 236 |
| GO:00000754 | Esophagus | ESCC | cell cycle checkpoint | 117/8552 | 169/18723 | 4.47e-10 | 1.17e-08 | 117 |
| 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 |
| hsa0301321 | Esophagus | ESCC | Nucleocytoplasmic transport | 89/4205 | 108/8465 | 1.20e-12 | 2.37e-11 | 1.21e-11 | 89 |
| hsa0301331 | Esophagus | ESCC | Nucleocytoplasmic transport | 89/4205 | 108/8465 | 1.20e-12 | 2.37e-11 | 1.21e-11 | 89 |
| hsa03013 | Liver | HCC | Nucleocytoplasmic transport | 81/4020 | 108/8465 | 4.28e-09 | 6.83e-08 | 3.80e-08 | 81 |
| hsa030131 | Liver | HCC | Nucleocytoplasmic transport | 81/4020 | 108/8465 | 4.28e-09 | 6.83e-08 | 3.80e-08 | 81 |
| hsa030136 | Oral cavity | OSCC | Nucleocytoplasmic transport | 82/3704 | 108/8465 | 7.93e-12 | 1.33e-10 | 6.77e-11 | 82 |
| hsa0301311 | Oral cavity | OSCC | Nucleocytoplasmic transport | 82/3704 | 108/8465 | 7.93e-12 | 1.33e-10 | 6.77e-11 | 82 |
| hsa030132 | Oral cavity | LP | Nucleocytoplasmic transport | 53/2418 | 108/8465 | 4.68e-06 | 4.10e-05 | 2.64e-05 | 53 |
| hsa030133 | Oral cavity | LP | Nucleocytoplasmic transport | 53/2418 | 108/8465 | 4.68e-06 | 4.10e-05 | 2.64e-05 | 53 |
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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 |
| THOC5 | SNV | Missense_Mutation | c.25N>G | p.Arg9Gly | p.R9G | Q13769 | protein_coding | deleterious(0) | probably_damaging(0.924) | TCGA-BH-A0C0-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | SD | |
| THOC5 | SNV | Missense_Mutation | c.639G>C | p.Glu213Asp | p.E213D | Q13769 | protein_coding | tolerated(0.12) | benign(0.177) | TCGA-C8-A26Y-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
| THOC5 | insertion | Frame_Shift_Ins | novel | c.727_728insA | p.Val243AspfsTer17 | p.V243Dfs*17 | Q13769 | protein_coding | TCGA-A2-A0CP-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | SD | ||
| THOC5 | insertion | In_Frame_Ins | novel | c.725_726insTGTGGCTGCAGATGACGAGAGTGACTCAGATGCCGAGGA | p.Val243_Gln244insAlaAlaAspAspGluSerAspSerAspAlaGluGluVal | p.V243_Q244insAADDESDSDAEEV | Q13769 | protein_coding | TCGA-A2-A0CP-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | SD | ||
| THOC5 | insertion | Frame_Shift_Ins | novel | c.206_207insGG | p.Ile69MetfsTer5 | p.I69Mfs*5 | Q13769 | protein_coding | TCGA-AN-A03X-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | ||
| THOC5 | insertion | Frame_Shift_Ins | novel | c.205_206insCATTTGTAAATTTGATAAGAATCCCTTCTGAGTCTTTAATTCA | p.Ile69ThrfsTer48 | p.I69Tfs*48 | Q13769 | protein_coding | TCGA-AN-A03X-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | ||
| THOC5 | SNV | Missense_Mutation | novel | c.1003N>A | p.Asp335Asn | p.D335N | Q13769 | protein_coding | tolerated(0.08) | possibly_damaging(0.878) | TCGA-DS-A1OB-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | carboplatin | PD |
| THOC5 | SNV | Missense_Mutation | c.352G>A | p.Glu118Lys | p.E118K | Q13769 | protein_coding | tolerated(0.07) | probably_damaging(0.98) | TCGA-EA-A3HR-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | |
| THOC5 | SNV | Missense_Mutation | novel | c.1294N>A | p.Asp432Asn | p.D432N | Q13769 | protein_coding | tolerated(0.07) | possibly_damaging(0.617) | TCGA-A6-3807-01 | Colorectum | colon adenocarcinoma | Female | <65 | III/IV | Ancillary | leucovorin | SD |
| THOC5 | SNV | Missense_Mutation | c.1957N>T | p.Pro653Ser | p.P653S | Q13769 | protein_coding | tolerated(0.05) | benign(0.386) | TCGA-AA-3492-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| Page: 1 2 3 4 5 6 7 |
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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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