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Gene: DDX10 |
Gene summary for DDX10 |
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Gene information | Species | Human | Gene symbol | DDX10 | Gene ID | 1662 |
Gene name | DEAD-box helicase 10 | |
Gene Alias | Dbp4 | |
Cytomap | 11q22.3 | |
Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q13206 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
1662 | DDX10 | HTA11_696_2000001011 | Human | Colorectum | AD | 1.13e-02 | -2.86e-01 | -0.1464 |
1662 | DDX10 | HTA11_866_2000001011 | Human | Colorectum | AD | 1.02e-10 | -3.63e-01 | -0.1001 |
1662 | DDX10 | HTA11_546_2000001011 | Human | Colorectum | AD | 3.37e-02 | -4.10e-01 | -0.0842 |
1662 | DDX10 | HTA11_866_3004761011 | Human | Colorectum | AD | 1.14e-05 | -4.40e-01 | 0.096 |
1662 | DDX10 | HTA11_10711_2000001011 | Human | Colorectum | AD | 1.22e-02 | -4.39e-01 | 0.0338 |
1662 | DDX10 | HTA11_7696_3000711011 | Human | Colorectum | AD | 9.94e-06 | -3.52e-01 | 0.0674 |
1662 | DDX10 | HTA11_99999974143_84620 | Human | Colorectum | MSS | 8.21e-13 | -4.56e-01 | 0.3005 |
1662 | DDX10 | A001-C-207 | Human | Colorectum | FAP | 7.39e-03 | -2.30e-01 | 0.1278 |
1662 | DDX10 | A015-C-203 | Human | Colorectum | FAP | 4.36e-29 | -4.30e-01 | -0.1294 |
1662 | DDX10 | A015-C-204 | Human | Colorectum | FAP | 2.72e-04 | -2.38e-01 | -0.0228 |
1662 | DDX10 | A014-C-040 | Human | Colorectum | FAP | 7.64e-05 | -5.04e-01 | -0.1184 |
1662 | DDX10 | A002-C-201 | Human | Colorectum | FAP | 1.03e-12 | -3.67e-01 | 0.0324 |
1662 | DDX10 | A001-C-119 | Human | Colorectum | FAP | 5.79e-07 | -3.83e-01 | -0.1557 |
1662 | DDX10 | A001-C-108 | Human | Colorectum | FAP | 1.11e-18 | -3.24e-01 | -0.0272 |
1662 | DDX10 | A002-C-205 | Human | Colorectum | FAP | 7.12e-17 | -2.31e-01 | -0.1236 |
1662 | DDX10 | A001-C-104 | Human | Colorectum | FAP | 1.18e-03 | -2.28e-01 | 0.0184 |
1662 | DDX10 | A015-C-005 | Human | Colorectum | FAP | 2.86e-04 | -2.86e-01 | -0.0336 |
1662 | DDX10 | A015-C-006 | Human | Colorectum | FAP | 4.78e-11 | -1.67e-01 | -0.0994 |
1662 | DDX10 | A015-C-106 | Human | Colorectum | FAP | 2.73e-12 | -2.09e-01 | -0.0511 |
1662 | DDX10 | A002-C-114 | Human | Colorectum | FAP | 2.85e-15 | -3.65e-01 | -0.1561 |
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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:0022613 | Colorectum | AD | ribonucleoprotein complex biogenesis | 151/3918 | 463/18723 | 1.96e-09 | 1.39e-07 | 151 |
GO:0042254 | Colorectum | AD | ribosome biogenesis | 84/3918 | 299/18723 | 1.82e-03 | 1.50e-02 | 84 |
GO:00226132 | Colorectum | MSS | ribonucleoprotein complex biogenesis | 144/3467 | 463/18723 | 2.76e-11 | 3.67e-09 | 144 |
GO:00422542 | Colorectum | MSS | ribosome biogenesis | 79/3467 | 299/18723 | 4.32e-04 | 5.23e-03 | 79 |
GO:0006364 | Colorectum | MSS | rRNA processing | 58/3467 | 225/18723 | 4.17e-03 | 3.03e-02 | 58 |
GO:0016072 | Colorectum | MSS | rRNA metabolic process | 60/3467 | 236/18723 | 5.01e-03 | 3.46e-02 | 60 |
GO:00226134 | Colorectum | FAP | ribonucleoprotein complex biogenesis | 91/2622 | 463/18723 | 4.28e-04 | 5.12e-03 | 91 |
GO:00226135 | Colorectum | CRC | ribonucleoprotein complex biogenesis | 76/2078 | 463/18723 | 3.04e-04 | 4.78e-03 | 76 |
GO:0022613111 | Esophagus | ESCC | ribonucleoprotein complex biogenesis | 365/8552 | 463/18723 | 1.74e-49 | 1.11e-45 | 365 |
GO:0042254111 | Esophagus | ESCC | ribosome biogenesis | 252/8552 | 299/18723 | 3.27e-44 | 1.04e-40 | 252 |
GO:003447015 | Esophagus | ESCC | ncRNA processing | 300/8552 | 395/18723 | 3.09e-35 | 3.26e-32 | 300 |
GO:0016072110 | Esophagus | ESCC | rRNA metabolic process | 197/8552 | 236/18723 | 1.31e-33 | 1.18e-30 | 197 |
GO:0006364110 | Esophagus | ESCC | rRNA processing | 189/8552 | 225/18723 | 4.88e-33 | 3.87e-30 | 189 |
GO:003466012 | Esophagus | ESCC | ncRNA metabolic process | 346/8552 | 485/18723 | 4.35e-31 | 2.51e-28 | 346 |
GO:00226137 | Liver | NAFLD | ribonucleoprotein complex biogenesis | 76/1882 | 463/18723 | 1.19e-05 | 3.67e-04 | 76 |
GO:00422547 | Liver | NAFLD | ribosome biogenesis | 52/1882 | 299/18723 | 6.03e-05 | 1.32e-03 | 52 |
GO:00344704 | Liver | NAFLD | ncRNA processing | 57/1882 | 395/18723 | 3.34e-03 | 2.93e-02 | 57 |
GO:00063644 | Liver | NAFLD | rRNA processing | 35/1882 | 225/18723 | 6.04e-03 | 4.54e-02 | 35 |
GO:002261322 | Liver | HCC | ribonucleoprotein complex biogenesis | 355/7958 | 463/18723 | 7.76e-52 | 4.92e-48 | 355 |
GO:004225422 | Liver | HCC | ribosome biogenesis | 246/7958 | 299/18723 | 4.99e-46 | 1.58e-42 | 246 |
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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 |
DDX10 | SNV | Missense_Mutation | c.2209A>G | p.Lys737Glu | p.K737E | Q13206 | protein_coding | deleterious(0) | probably_damaging(0.994) | TCGA-37-4135-01 | Lung | lung squamous cell carcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
DDX10 | SNV | Missense_Mutation | novel | c.331N>C | p.Gly111Arg | p.G111R | Q13206 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-43-2581-01 | Lung | lung squamous cell carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | SD |
DDX10 | SNV | Missense_Mutation | novel | c.2541N>T | p.Arg847Ser | p.R847S | Q13206 | protein_coding | deleterious(0.04) | benign(0) | TCGA-56-8082-01 | Lung | lung squamous cell carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
DDX10 | SNV | Missense_Mutation | novel | c.1078N>A | p.Glu360Lys | p.E360K | Q13206 | protein_coding | tolerated(0.13) | benign(0.141) | TCGA-58-A46M-01 | Lung | lung squamous cell carcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
DDX10 | SNV | Missense_Mutation | novel | c.1265C>T | p.Ser422Leu | p.S422L | Q13206 | protein_coding | deleterious(0) | probably_damaging(0.969) | TCGA-90-A4EE-01 | Lung | lung squamous cell carcinoma | Male | <65 | I/II | Chemotherapy | cisplatin | CR |
DDX10 | SNV | Missense_Mutation | rs145766863 | c.269G>A | p.Arg90His | p.R90H | Q13206 | protein_coding | tolerated(0.55) | benign(0.005) | TCGA-CR-7382-01 | Oral cavity | head & neck squamous cell carcinoma | Male | <65 | I/II | Unspecific | PD | |
DDX10 | SNV | Missense_Mutation | rs777793234 | c.1043N>A | p.Arg348Gln | p.R348Q | Q13206 | protein_coding | tolerated(0.1) | benign(0.309) | TCGA-F7-A624-01 | Oral cavity | head & neck squamous cell carcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
DDX10 | SNV | Missense_Mutation | rs368051511 | c.1526N>A | p.Arg509His | p.R509H | Q13206 | protein_coding | deleterious(0.01) | probably_damaging(0.965) | TCGA-F7-A624-01 | Oral cavity | head & neck squamous cell carcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
DDX10 | SNV | Missense_Mutation | c.409N>G | p.Thr137Ala | p.T137A | Q13206 | protein_coding | deleterious(0.01) | benign(0.151) | TCGA-BR-6452-01 | Stomach | stomach adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
DDX10 | SNV | Missense_Mutation | novel | c.1211G>A | p.Gly404Asp | p.G404D | Q13206 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-BR-8362-01 | Stomach | stomach adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | etoposide | PD |
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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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