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Gene: COQ9 |
Gene summary for COQ9 |
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Gene information | Species | Human | Gene symbol | COQ9 | Gene ID | 57017 |
Gene name | coenzyme Q9 | |
Gene Alias | C16orf49 | |
Cytomap | 16q21 | |
Gene Type | protein-coding | GO ID | GO:0006091 | UniProtAcc | A0A024R6U3 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
57017 | COQ9 | P44T-E | Human | Esophagus | ESCC | 1.54e-13 | 3.14e-01 | 0.1096 |
57017 | COQ9 | P47T-E | Human | Esophagus | ESCC | 5.01e-18 | 3.16e-01 | 0.1067 |
57017 | COQ9 | P48T-E | Human | Esophagus | ESCC | 4.74e-29 | 5.47e-01 | 0.0959 |
57017 | COQ9 | P49T-E | Human | Esophagus | ESCC | 1.93e-16 | 1.05e+00 | 0.1768 |
57017 | COQ9 | P52T-E | Human | Esophagus | ESCC | 1.24e-52 | 1.01e+00 | 0.1555 |
57017 | COQ9 | P54T-E | Human | Esophagus | ESCC | 4.08e-40 | 8.07e-01 | 0.0975 |
57017 | COQ9 | P56T-E | Human | Esophagus | ESCC | 8.29e-08 | 8.60e-01 | 0.1613 |
57017 | COQ9 | P57T-E | Human | Esophagus | ESCC | 2.10e-20 | 4.54e-01 | 0.0926 |
57017 | COQ9 | P61T-E | Human | Esophagus | ESCC | 3.27e-23 | 4.42e-01 | 0.099 |
57017 | COQ9 | P62T-E | Human | Esophagus | ESCC | 2.88e-84 | 1.26e+00 | 0.1302 |
57017 | COQ9 | P65T-E | Human | Esophagus | ESCC | 8.39e-22 | 4.30e-01 | 0.0978 |
57017 | COQ9 | P74T-E | Human | Esophagus | ESCC | 2.87e-50 | 1.13e+00 | 0.1479 |
57017 | COQ9 | P75T-E | Human | Esophagus | ESCC | 4.55e-58 | 9.95e-01 | 0.1125 |
57017 | COQ9 | P76T-E | Human | Esophagus | ESCC | 4.69e-39 | 7.90e-01 | 0.1207 |
57017 | COQ9 | P79T-E | Human | Esophagus | ESCC | 4.51e-29 | 6.25e-01 | 0.1154 |
57017 | COQ9 | P80T-E | Human | Esophagus | ESCC | 8.98e-39 | 8.87e-01 | 0.155 |
57017 | COQ9 | P82T-E | Human | Esophagus | ESCC | 4.34e-18 | 8.31e-01 | 0.1072 |
57017 | COQ9 | P83T-E | Human | Esophagus | ESCC | 3.39e-59 | 1.48e+00 | 0.1738 |
57017 | COQ9 | P84T-E | Human | Esophagus | ESCC | 7.75e-10 | 4.83e-01 | 0.0933 |
57017 | COQ9 | P89T-E | Human | Esophagus | ESCC | 2.02e-21 | 9.86e-01 | 0.1752 |
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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:000611920 | Esophagus | HGIN | oxidative phosphorylation | 69/2587 | 141/18723 | 1.37e-23 | 2.05e-20 | 69 |
GO:000906020 | Esophagus | HGIN | aerobic respiration | 81/2587 | 189/18723 | 1.07e-22 | 9.26e-20 | 81 |
GO:004603427 | Esophagus | HGIN | ATP metabolic process | 101/2587 | 277/18723 | 1.53e-21 | 1.02e-18 | 101 |
GO:000609120 | Esophagus | HGIN | generation of precursor metabolites and energy | 145/2587 | 490/18723 | 3.41e-20 | 2.04e-17 | 145 |
GO:004533320 | Esophagus | HGIN | cellular respiration | 86/2587 | 230/18723 | 2.41e-19 | 1.20e-16 | 86 |
GO:001598020 | Esophagus | HGIN | energy derivation by oxidation of organic compounds | 105/2587 | 318/18723 | 1.16e-18 | 4.99e-16 | 105 |
GO:004277320 | Esophagus | HGIN | ATP synthesis coupled electron transport | 49/2587 | 95/18723 | 2.21e-18 | 7.36e-16 | 49 |
GO:004277520 | Esophagus | HGIN | mitochondrial ATP synthesis coupled electron transport | 49/2587 | 95/18723 | 2.21e-18 | 7.36e-16 | 49 |
GO:002290420 | Esophagus | HGIN | respiratory electron transport chain | 51/2587 | 114/18723 | 9.63e-16 | 2.41e-13 | 51 |
GO:001964620 | Esophagus | HGIN | aerobic electron transport chain | 43/2587 | 87/18723 | 1.98e-15 | 4.41e-13 | 43 |
GO:002290020 | Esophagus | HGIN | electron transport chain | 66/2587 | 175/18723 | 2.21e-15 | 4.73e-13 | 66 |
GO:000612020 | Esophagus | HGIN | mitochondrial electron transport, NADH to ubiquinone | 28/2587 | 51/18723 | 5.72e-12 | 7.30e-10 | 28 |
GO:19016614 | Esophagus | HGIN | quinone metabolic process | 13/2587 | 40/18723 | 2.04e-03 | 2.13e-02 | 13 |
GO:0006091110 | Esophagus | ESCC | generation of precursor metabolites and energy | 331/8552 | 490/18723 | 3.86e-23 | 8.45e-21 | 331 |
GO:0045333110 | Esophagus | ESCC | cellular respiration | 173/8552 | 230/18723 | 4.53e-20 | 5.99e-18 | 173 |
GO:0009060110 | Esophagus | ESCC | aerobic respiration | 145/8552 | 189/18723 | 2.16e-18 | 2.21e-16 | 145 |
GO:0015980110 | Esophagus | ESCC | energy derivation by oxidation of organic compounds | 220/8552 | 318/18723 | 1.20e-17 | 1.09e-15 | 220 |
GO:0022900110 | Esophagus | ESCC | electron transport chain | 133/8552 | 175/18723 | 2.18e-16 | 1.67e-14 | 133 |
GO:0046034111 | Esophagus | ESCC | ATP metabolic process | 189/8552 | 277/18723 | 1.99e-14 | 1.04e-12 | 189 |
GO:0006119111 | Esophagus | ESCC | oxidative phosphorylation | 106/8552 | 141/18723 | 8.19e-13 | 3.63e-11 | 106 |
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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 |
COQ9 | SNV | Missense_Mutation | c.76N>A | p.Ala26Thr | p.A26T | O75208 | protein_coding | tolerated_low_confidence(0.61) | benign(0) | TCGA-AA-3492-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
COQ9 | SNV | Missense_Mutation | c.743N>T | p.Ala248Val | p.A248V | O75208 | protein_coding | tolerated(0.07) | benign(0.068) | TCGA-AA-3663-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
COQ9 | SNV | Missense_Mutation | c.342N>A | p.His114Gln | p.H114Q | O75208 | protein_coding | deleterious(0.02) | probably_damaging(0.949) | TCGA-AA-3976-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | folinic | CR | |
COQ9 | SNV | Missense_Mutation | rs201097286 | c.467G>A | p.Arg156Gln | p.R156Q | O75208 | protein_coding | tolerated(0.49) | benign(0.003) | TCGA-AD-A5EJ-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
COQ9 | SNV | Missense_Mutation | rs763626877 | c.259G>A | p.Gly87Ser | p.G87S | O75208 | protein_coding | tolerated(0.05) | probably_damaging(0.999) | TCGA-AZ-6598-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
COQ9 | SNV | Missense_Mutation | c.275A>G | p.Asp92Gly | p.D92G | O75208 | protein_coding | tolerated(0.25) | benign(0) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
COQ9 | SNV | Missense_Mutation | c.227N>T | p.Ser76Phe | p.S76F | O75208 | protein_coding | tolerated(0.57) | benign(0.001) | TCGA-AG-A002-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
COQ9 | insertion | Frame_Shift_Ins | novel | c.481_482insA | p.Leu161HisfsTer38 | p.L161Hfs*38 | O75208 | protein_coding | TCGA-AG-A00Y-01 | Colorectum | rectum adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | ||
COQ9 | SNV | Missense_Mutation | novel | c.697N>T | p.Asp233Tyr | p.D233Y | O75208 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-A5-A0G1-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
COQ9 | SNV | Missense_Mutation | novel | c.98N>C | p.Val33Ala | p.V33A | O75208 | protein_coding | tolerated_low_confidence(0.69) | benign(0) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
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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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