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Gene: THOC2 |
Gene summary for THOC2 |
| Gene information | Species | Human | Gene symbol | THOC2 | Gene ID | 57187 |
| Gene name | THO complex 2 | |
| Gene Alias | CXorf3 | |
| Cytomap | Xq25 | |
| Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q8NI27 |
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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 |
| 57187 | THOC2 | CA_HPV_3 | Human | Cervix | CC | 4.66e-02 | 9.80e-02 | 0.0414 |
| 57187 | THOC2 | CCI_2 | Human | Cervix | CC | 1.82e-07 | 9.50e-01 | 0.5249 |
| 57187 | THOC2 | Tumor | Human | Cervix | CC | 2.34e-04 | 2.57e-01 | 0.1241 |
| 57187 | THOC2 | sample3 | Human | Cervix | CC | 8.51e-15 | 4.00e-01 | 0.1387 |
| 57187 | THOC2 | T3 | Human | Cervix | CC | 1.36e-12 | 3.79e-01 | 0.1389 |
| 57187 | THOC2 | HTA11_3410_2000001011 | Human | Colorectum | AD | 1.16e-21 | -6.83e-01 | 0.0155 |
| 57187 | THOC2 | HTA11_2487_2000001011 | Human | Colorectum | SER | 4.27e-04 | -4.77e-01 | -0.1808 |
| 57187 | THOC2 | HTA11_3361_2000001011 | Human | Colorectum | AD | 4.47e-06 | -6.03e-01 | -0.1207 |
| 57187 | THOC2 | HTA11_696_2000001011 | Human | Colorectum | AD | 4.75e-06 | -3.95e-01 | -0.1464 |
| 57187 | THOC2 | HTA11_866_2000001011 | Human | Colorectum | AD | 1.31e-10 | -4.36e-01 | -0.1001 |
| 57187 | THOC2 | HTA11_1391_2000001011 | Human | Colorectum | AD | 1.12e-03 | -3.33e-01 | -0.059 |
| 57187 | THOC2 | HTA11_866_3004761011 | Human | Colorectum | AD | 4.64e-11 | -5.45e-01 | 0.096 |
| 57187 | THOC2 | HTA11_10711_2000001011 | Human | Colorectum | AD | 1.20e-05 | -5.32e-01 | 0.0338 |
| 57187 | THOC2 | HTA11_7696_3000711011 | Human | Colorectum | AD | 1.07e-13 | -4.59e-01 | 0.0674 |
| 57187 | THOC2 | HTA11_6818_2000001021 | Human | Colorectum | AD | 8.57e-04 | -5.51e-01 | 0.0588 |
| 57187 | THOC2 | HTA11_99999965104_69814 | Human | Colorectum | MSS | 1.13e-03 | 5.78e-01 | 0.281 |
| 57187 | THOC2 | HTA11_99999974143_84620 | Human | Colorectum | MSS | 3.86e-05 | -3.74e-01 | 0.3005 |
| 57187 | THOC2 | A015-C-203 | Human | Colorectum | FAP | 1.01e-32 | 2.25e-01 | -0.1294 |
| 57187 | THOC2 | A015-C-204 | Human | Colorectum | FAP | 1.39e-04 | 1.22e-01 | -0.0228 |
| 57187 | THOC2 | A014-C-040 | Human | Colorectum | FAP | 1.19e-04 | 2.59e-01 | -0.1184 |
| Page: 1 2 3 4 5 6 7 8 9 10 11 |
| ∗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 |
| GO:005170110 | Cervix | CC | biological process involved in interaction with host | 57/2311 | 203/18723 | 1.18e-09 | 1.41e-07 | 57 |
| GO:004440310 | Cervix | CC | biological process involved in symbiotic interaction | 71/2311 | 290/18723 | 7.94e-09 | 6.98e-07 | 71 |
| GO:00069139 | Cervix | CC | nucleocytoplasmic transport | 71/2311 | 301/18723 | 4.04e-08 | 2.54e-06 | 71 |
| GO:00511699 | Cervix | CC | nuclear transport | 71/2311 | 301/18723 | 4.04e-08 | 2.54e-06 | 71 |
| GO:00109757 | Cervix | CC | regulation of neuron projection development | 88/2311 | 445/18723 | 4.26e-06 | 1.09e-04 | 88 |
| GO:00511689 | Cervix | CC | nuclear export | 38/2311 | 154/18723 | 1.86e-05 | 3.46e-04 | 38 |
| GO:00512368 | Cervix | CC | establishment of RNA localization | 39/2311 | 166/18723 | 4.76e-05 | 7.25e-04 | 39 |
| GO:00506578 | Cervix | CC | nucleic acid transport | 38/2311 | 163/18723 | 7.06e-05 | 9.85e-04 | 38 |
| GO:00506588 | Cervix | CC | RNA transport | 38/2311 | 163/18723 | 7.06e-05 | 9.85e-04 | 38 |
| GO:000640310 | Cervix | CC | RNA localization | 43/2311 | 201/18723 | 2.00e-04 | 2.29e-03 | 43 |
| GO:00510284 | Cervix | CC | mRNA transport | 31/2311 | 130/18723 | 2.05e-04 | 2.33e-03 | 31 |
| GO:00313456 | Cervix | CC | negative regulation of cell projection organization | 39/2311 | 186/18723 | 5.86e-04 | 5.57e-03 | 39 |
| GO:000838010 | Cervix | CC | RNA splicing | 76/2311 | 434/18723 | 9.79e-04 | 8.19e-03 | 76 |
| GO:00159318 | Cervix | CC | nucleobase-containing compound transport | 43/2311 | 222/18723 | 1.72e-03 | 1.30e-02 | 43 |
| GO:00714262 | Cervix | CC | ribonucleoprotein complex export from nucleus | 18/2311 | 76/18723 | 4.45e-03 | 2.71e-02 | 18 |
| GO:00109775 | Cervix | CC | negative regulation of neuron projection development | 28/2311 | 137/18723 | 4.74e-03 | 2.83e-02 | 28 |
| GO:00711662 | Cervix | CC | ribonucleoprotein complex localization | 18/2311 | 77/18723 | 5.15e-03 | 3.03e-02 | 18 |
| GO:00064054 | Cervix | CC | RNA export from nucleus | 19/2311 | 84/18723 | 6.02e-03 | 3.43e-02 | 19 |
| GO:0008380 | Colorectum | AD | RNA splicing | 169/3918 | 434/18723 | 3.59e-18 | 2.04e-15 | 169 |
| GO:0006913 | Colorectum | AD | nucleocytoplasmic transport | 102/3918 | 301/18723 | 1.00e-07 | 4.85e-06 | 102 |
| Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| hsa03040 | Colorectum | AD | Spliceosome | 73/2092 | 217/8465 | 1.73e-03 | 9.68e-03 | 6.18e-03 | 73 |
| hsa030401 | Colorectum | AD | Spliceosome | 73/2092 | 217/8465 | 1.73e-03 | 9.68e-03 | 6.18e-03 | 73 |
| hsa030402 | Colorectum | MSS | Spliceosome | 66/1875 | 217/8465 | 2.58e-03 | 1.27e-02 | 7.81e-03 | 66 |
| hsa030403 | Colorectum | MSS | Spliceosome | 66/1875 | 217/8465 | 2.58e-03 | 1.27e-02 | 7.81e-03 | 66 |
| hsa0301321 | Esophagus | ESCC | Nucleocytoplasmic transport | 89/4205 | 108/8465 | 1.20e-12 | 2.37e-11 | 1.21e-11 | 89 |
| hsa0304027 | Esophagus | ESCC | Spliceosome | 128/4205 | 217/8465 | 3.31e-03 | 8.79e-03 | 4.50e-03 | 128 |
| hsa0301331 | Esophagus | ESCC | Nucleocytoplasmic transport | 89/4205 | 108/8465 | 1.20e-12 | 2.37e-11 | 1.21e-11 | 89 |
| hsa0304037 | Esophagus | ESCC | Spliceosome | 128/4205 | 217/8465 | 3.31e-03 | 8.79e-03 | 4.50e-03 | 128 |
| hsa030407 | Liver | Cirrhotic | Spliceosome | 102/2530 | 217/8465 | 5.69e-08 | 9.47e-07 | 5.84e-07 | 102 |
| hsa0304012 | Liver | Cirrhotic | Spliceosome | 102/2530 | 217/8465 | 5.69e-08 | 9.47e-07 | 5.84e-07 | 102 |
| hsa03013 | Liver | HCC | Nucleocytoplasmic transport | 81/4020 | 108/8465 | 4.28e-09 | 6.83e-08 | 3.80e-08 | 81 |
| hsa0304022 | Liver | HCC | Spliceosome | 122/4020 | 217/8465 | 5.55e-03 | 1.60e-02 | 8.91e-03 | 122 |
| hsa030131 | Liver | HCC | Nucleocytoplasmic transport | 81/4020 | 108/8465 | 4.28e-09 | 6.83e-08 | 3.80e-08 | 81 |
| hsa0304032 | Liver | HCC | Spliceosome | 122/4020 | 217/8465 | 5.55e-03 | 1.60e-02 | 8.91e-03 | 122 |
| hsa030136 | Oral cavity | OSCC | Nucleocytoplasmic transport | 82/3704 | 108/8465 | 7.93e-12 | 1.33e-10 | 6.77e-11 | 82 |
| hsa0304016 | Oral cavity | OSCC | Spliceosome | 123/3704 | 217/8465 | 7.21e-05 | 2.74e-04 | 1.40e-04 | 123 |
| hsa0301311 | Oral cavity | OSCC | Nucleocytoplasmic transport | 82/3704 | 108/8465 | 7.93e-12 | 1.33e-10 | 6.77e-11 | 82 |
| hsa0304017 | Oral cavity | OSCC | Spliceosome | 123/3704 | 217/8465 | 7.21e-05 | 2.74e-04 | 1.40e-04 | 123 |
| 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 |
| ∗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 |
| THOC2 | SNV | Missense_Mutation | c.3679N>T | p.Thr1227Ser | p.T1227S | Q8NI27 | protein_coding | tolerated(0.66) | benign(0) | TCGA-AX-A063-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
| THOC2 | SNV | Missense_Mutation | novel | c.42N>T | p.Lys14Asn | p.K14N | Q8NI27 | protein_coding | deleterious(0) | probably_damaging(0.982) | TCGA-AX-A06F-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatin | SD |
| THOC2 | SNV | Missense_Mutation | c.2407N>A | p.Leu803Ile | p.L803I | Q8NI27 | protein_coding | deleterious(0.01) | possibly_damaging(0.824) | TCGA-AX-A0J0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
| THOC2 | SNV | Missense_Mutation | c.2271N>C | p.Glu757Asp | p.E757D | Q8NI27 | protein_coding | deleterious(0.01) | benign(0.225) | TCGA-AX-A0J0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
| THOC2 | SNV | Missense_Mutation | c.698N>G | p.Glu233Gly | p.E233G | Q8NI27 | protein_coding | tolerated(0.06) | benign(0.024) | TCGA-AX-A0J0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
| THOC2 | SNV | Missense_Mutation | rs757886087 | c.1291N>A | p.Val431Met | p.V431M | Q8NI27 | protein_coding | deleterious(0.01) | possibly_damaging(0.879) | TCGA-AX-A0J1-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| THOC2 | SNV | Missense_Mutation | novel | c.3522N>C | p.Lys1174Asn | p.K1174N | Q8NI27 | protein_coding | deleterious(0) | probably_damaging(0.995) | TCGA-AX-A1CE-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unspecific | Paclitaxel | SD |
| THOC2 | SNV | Missense_Mutation | novel | c.1286N>T | p.Arg429Ile | p.R429I | Q8NI27 | protein_coding | tolerated(0.08) | benign(0.045) | TCGA-AX-A1CE-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unspecific | Paclitaxel | SD |
| THOC2 | SNV | Missense_Mutation | novel | c.260N>C | p.Val87Ala | p.V87A | Q8NI27 | protein_coding | deleterious(0.02) | benign(0.023) | TCGA-AX-A1CE-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unspecific | Paclitaxel | SD |
| THOC2 | SNV | Missense_Mutation | novel | c.4640N>A | p.Ser1547Tyr | p.S1547Y | Q8NI27 | protein_coding | tolerated_low_confidence(0.37) | benign(0.06) | TCGA-AX-A2HC-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | paclitaxel | PD |
| Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 |
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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 |