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Gene: CHD3 |
Gene summary for CHD3 |
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Gene information | Species | Human | Gene symbol | CHD3 | Gene ID | 1107 |
Gene name | chromodomain helicase DNA binding protein 3 | |
Gene Alias | Mi-2a | |
Cytomap | 17p13.1 | |
Gene Type | protein-coding | GO ID | GO:0000122 | UniProtAcc | B3KWV4 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
1107 | CHD3 | HTA11_3410_2000001011 | Human | Colorectum | AD | 2.26e-03 | 5.43e-02 | 0.0155 |
1107 | CHD3 | HTA11_1938_2000001011 | Human | Colorectum | AD | 1.75e-02 | 1.90e-01 | -0.0811 |
1107 | CHD3 | HTA11_347_2000001011 | Human | Colorectum | AD | 1.15e-02 | 1.59e-01 | -0.1954 |
1107 | CHD3 | HTA11_696_2000001011 | Human | Colorectum | AD | 3.35e-04 | 2.40e-01 | -0.1464 |
1107 | CHD3 | HTA11_1391_2000001011 | Human | Colorectum | AD | 1.07e-03 | 2.92e-01 | -0.059 |
1107 | CHD3 | HTA11_10711_2000001011 | Human | Colorectum | AD | 9.05e-03 | 3.80e-01 | 0.0338 |
1107 | CHD3 | HTA11_7696_3000711011 | Human | Colorectum | AD | 4.61e-03 | 2.76e-01 | 0.0674 |
1107 | CHD3 | A015-C-203 | Human | Colorectum | FAP | 2.48e-03 | 1.90e-01 | -0.1294 |
1107 | CHD3 | A001-C-119 | Human | Colorectum | FAP | 2.58e-05 | 5.94e-01 | -0.1557 |
1107 | CHD3 | A001-C-108 | Human | Colorectum | FAP | 1.23e-03 | 3.31e-01 | -0.0272 |
1107 | CHD3 | A002-C-021 | Human | Colorectum | FAP | 3.23e-02 | 3.38e-01 | 0.1171 |
1107 | CHD3 | A002-C-205 | Human | Colorectum | FAP | 6.14e-05 | 4.37e-01 | -0.1236 |
1107 | CHD3 | A001-C-104 | Human | Colorectum | FAP | 2.69e-05 | 4.05e-01 | 0.0184 |
1107 | CHD3 | A015-C-106 | Human | Colorectum | FAP | 1.15e-02 | 2.94e-01 | -0.0511 |
1107 | CHD3 | A015-C-104 | Human | Colorectum | FAP | 1.32e-10 | 3.70e-01 | -0.1899 |
1107 | CHD3 | A002-C-116 | Human | Colorectum | FAP | 7.12e-04 | 4.55e-02 | -0.0452 |
1107 | CHD3 | A014-C-008 | Human | Colorectum | FAP | 2.27e-07 | 6.29e-01 | -0.191 |
1107 | CHD3 | LZE4T | Human | Esophagus | ESCC | 1.28e-09 | 3.59e-01 | 0.0811 |
1107 | CHD3 | LZE5T | Human | Esophagus | ESCC | 2.79e-04 | 3.67e-01 | 0.0514 |
1107 | CHD3 | LZE7T | Human | Esophagus | ESCC | 1.06e-11 | 4.55e-01 | 0.0667 |
Page: 1 2 3 4 5 6 7 8 |
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∗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 |
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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 |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:00323928 | Thyroid | PTC | DNA geometric change | 41/5968 | 90/18723 | 4.47e-03 | 2.11e-02 | 41 |
GO:00080534 | Thyroid | PTC | mitochondrial fusion | 15/5968 | 27/18723 | 9.19e-03 | 3.79e-02 | 15 |
GO:000705122 | Thyroid | ATC | spindle organization | 109/6293 | 184/18723 | 7.99e-13 | 3.46e-11 | 109 |
GO:0007006111 | Thyroid | ATC | mitochondrial membrane organization | 69/6293 | 116/18723 | 9.55e-09 | 2.00e-07 | 69 |
GO:0006325110 | Thyroid | ATC | chromatin organization | 189/6293 | 409/18723 | 6.40e-08 | 1.13e-06 | 189 |
GO:004828413 | Thyroid | ATC | organelle fusion | 71/6293 | 141/18723 | 2.83e-05 | 2.38e-04 | 71 |
GO:003102311 | Thyroid | ATC | microtubule organizing center organization | 71/6293 | 143/18723 | 5.11e-05 | 3.99e-04 | 71 |
GO:000709811 | Thyroid | ATC | centrosome cycle | 65/6293 | 130/18723 | 7.95e-05 | 5.97e-04 | 65 |
GO:000700714 | Thyroid | ATC | inner mitochondrial membrane organization | 24/6293 | 38/18723 | 1.83e-04 | 1.24e-03 | 24 |
GO:000633813 | Thyroid | ATC | chromatin remodeling | 109/6293 | 255/18723 | 1.38e-03 | 7.15e-03 | 109 |
GO:003239216 | Thyroid | ATC | DNA geometric change | 42/6293 | 90/18723 | 6.81e-03 | 2.70e-02 | 42 |
Page: 1 2 3 4 5 6 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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Cell-cell communication analysis |
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Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
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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 |
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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 |
CHD3 | SNV | Missense_Mutation | c.2045N>A | p.Arg682His | p.R682H | Q12873 | protein_coding | deleterious(0) | possibly_damaging(0.791) | TCGA-A2-A0YM-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
CHD3 | SNV | Missense_Mutation | rs374465330 | c.5986N>A | p.Ala1996Thr | p.A1996T | Q12873 | protein_coding | tolerated_low_confidence(0.09) | benign(0) | TCGA-A8-A06R-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | 5-fluorouracil | CR |
CHD3 | SNV | Missense_Mutation | c.1012G>C | p.Asp338His | p.D338H | Q12873 | protein_coding | deleterious_low_confidence(0.01) | benign(0.443) | TCGA-A8-A0AB-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | 5-fluorouracil | CR | |
CHD3 | SNV | Missense_Mutation | c.2299N>A | p.Asp767Asn | p.D767N | Q12873 | protein_coding | tolerated(0.06) | benign(0.111) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
CHD3 | SNV | Missense_Mutation | c.2461N>A | p.Glu821Lys | p.E821K | Q12873 | protein_coding | deleterious(0) | probably_damaging(0.995) | TCGA-AC-A3W6-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
CHD3 | SNV | Missense_Mutation | novel | c.1929N>T | p.Lys643Asn | p.K643N | Q12873 | protein_coding | deleterious(0) | probably_damaging(0.991) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
CHD3 | SNV | Missense_Mutation | novel | c.90N>C | p.Glu30Asp | p.E30D | Q12873 | protein_coding | deleterious_low_confidence(0) | possibly_damaging(0.483) | TCGA-AO-A128-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | SD |
CHD3 | SNV | Missense_Mutation | rs765531902 | c.809N>T | p.Ala270Val | p.A270V | Q12873 | protein_coding | deleterious_low_confidence(0.03) | probably_damaging(0.986) | TCGA-AR-A1AI-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | PD |
CHD3 | SNV | Missense_Mutation | novel | c.3739G>A | p.Ala1247Thr | p.A1247T | Q12873 | protein_coding | deleterious(0.02) | probably_damaging(0.99) | TCGA-B6-A0RE-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
CHD3 | SNV | Missense_Mutation | rs551155540 | c.1396N>C | p.Asp466His | p.D466H | Q12873 | protein_coding | deleterious(0) | possibly_damaging(0.905) | TCGA-BH-A1FC-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 |
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Related drugs of malignant transformation related genes |
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(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
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