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Gene: COPS6 |
Gene summary for COPS6 |
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Gene information | Species | Human | Gene symbol | COPS6 | Gene ID | 10980 |
Gene name | COP9 signalosome subunit 6 | |
Gene Alias | CSN6 | |
Cytomap | 7q22.1 | |
Gene Type | protein-coding | GO ID | GO:0000338 | UniProtAcc | Q7L5N1 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
10980 | COPS6 | P49T-E | Human | Esophagus | ESCC | 1.06e-25 | 2.47e+00 | 0.1768 |
10980 | COPS6 | P52T-E | Human | Esophagus | ESCC | 4.70e-59 | 1.51e+00 | 0.1555 |
10980 | COPS6 | P54T-E | Human | Esophagus | ESCC | 8.14e-43 | 1.04e+00 | 0.0975 |
10980 | COPS6 | P56T-E | Human | Esophagus | ESCC | 1.05e-11 | 1.90e+00 | 0.1613 |
10980 | COPS6 | P57T-E | Human | Esophagus | ESCC | 3.18e-33 | 8.13e-01 | 0.0926 |
10980 | COPS6 | P61T-E | Human | Esophagus | ESCC | 8.89e-20 | 6.79e-01 | 0.099 |
10980 | COPS6 | P62T-E | Human | Esophagus | ESCC | 1.02e-72 | 1.34e+00 | 0.1302 |
10980 | COPS6 | P65T-E | Human | Esophagus | ESCC | 8.13e-46 | 1.16e+00 | 0.0978 |
10980 | COPS6 | P74T-E | Human | Esophagus | ESCC | 1.92e-50 | 1.94e+00 | 0.1479 |
10980 | COPS6 | P75T-E | Human | Esophagus | ESCC | 7.27e-57 | 1.33e+00 | 0.1125 |
10980 | COPS6 | P76T-E | Human | Esophagus | ESCC | 1.52e-81 | 1.75e+00 | 0.1207 |
10980 | COPS6 | P79T-E | Human | Esophagus | ESCC | 1.15e-53 | 1.03e+00 | 0.1154 |
10980 | COPS6 | P80T-E | Human | Esophagus | ESCC | 3.31e-70 | 2.69e+00 | 0.155 |
10980 | COPS6 | P82T-E | Human | Esophagus | ESCC | 6.52e-27 | 1.31e+00 | 0.1072 |
10980 | COPS6 | P83T-E | Human | Esophagus | ESCC | 4.33e-66 | 2.32e+00 | 0.1738 |
10980 | COPS6 | P84T-E | Human | Esophagus | ESCC | 1.98e-15 | 9.48e-01 | 0.0933 |
10980 | COPS6 | P89T-E | Human | Esophagus | ESCC | 1.20e-36 | 2.82e+00 | 0.1752 |
10980 | COPS6 | P91T-E | Human | Esophagus | ESCC | 6.01e-25 | 2.59e+00 | 0.1828 |
10980 | COPS6 | P104T-E | Human | Esophagus | ESCC | 1.46e-02 | 8.74e-01 | 0.0931 |
10980 | COPS6 | P107T-E | Human | Esophagus | ESCC | 2.87e-81 | 2.48e+00 | 0.171 |
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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). |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:00003383 | Esophagus | HGIN | protein deneddylation | 6/2587 | 10/18723 | 8.81e-04 | 1.13e-02 | 6 |
GO:00706463 | Esophagus | HGIN | protein modification by small protein removal | 34/2587 | 157/18723 | 4.68e-03 | 4.02e-02 | 34 |
GO:007064612 | Esophagus | ESCC | protein modification by small protein removal | 95/8552 | 157/18723 | 1.25e-04 | 8.56e-04 | 95 |
GO:000033812 | Esophagus | ESCC | protein deneddylation | 10/8552 | 10/18723 | 3.94e-04 | 2.26e-03 | 10 |
GO:0000338 | Liver | Cirrhotic | protein deneddylation | 7/4634 | 10/18723 | 3.29e-03 | 1.83e-02 | 7 |
GO:00706461 | Liver | HCC | protein modification by small protein removal | 91/7958 | 157/18723 | 6.50e-05 | 5.92e-04 | 91 |
GO:00003381 | Liver | HCC | protein deneddylation | 9/7958 | 10/18723 | 2.79e-03 | 1.31e-02 | 9 |
GO:00003382 | Oral cavity | OSCC | protein deneddylation | 10/7305 | 10/18723 | 8.14e-05 | 6.26e-04 | 10 |
GO:00706462 | Oral cavity | OSCC | protein modification by small protein removal | 77/7305 | 157/18723 | 6.55e-03 | 2.43e-02 | 77 |
GO:000033811 | Oral cavity | LP | protein deneddylation | 9/4623 | 10/18723 | 2.64e-05 | 4.21e-04 | 9 |
GO:00003384 | Skin | cSCC | protein deneddylation | 10/4864 | 10/18723 | 1.39e-06 | 2.40e-05 | 10 |
GO:00706464 | Skin | cSCC | protein modification by small protein removal | 55/4864 | 157/18723 | 7.29e-03 | 3.46e-02 | 55 |
GO:00706465 | Thyroid | PTC | protein modification by small protein removal | 71/5968 | 157/18723 | 3.03e-04 | 2.12e-03 | 71 |
GO:007064613 | Thyroid | ATC | protein modification by small protein removal | 71/6293 | 157/18723 | 1.59e-03 | 7.99e-03 | 71 |
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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 |
COPS6 | SNV | Missense_Mutation | c.793N>T | p.His265Tyr | p.H265Y | Q7L5N1 | protein_coding | tolerated(0.16) | possibly_damaging(0.836) | TCGA-D8-A27G-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
COPS6 | insertion | Nonsense_Mutation | novel | c.170_171insTGGTCTCTTCCTTGTTCTATAATTGGGAAGATAAGCTTGTAATCAA | p.Met58GlyfsTer7 | p.M58Gfs*7 | Q7L5N1 | protein_coding | TCGA-A2-A04Y-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | SD | ||
COPS6 | insertion | Nonsense_Mutation | novel | c.547_548insAAGAAAGCAAAGGATGAGAGGAGACAGGATAGAAGGGAGTAGTTA | p.Phe183delinsTer | p.F183delins* | Q7L5N1 | protein_coding | TCGA-BH-A0E2-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | doxorubicin | SD | ||
COPS6 | SNV | Missense_Mutation | c.439G>A | p.Glu147Lys | p.E147K | Q7L5N1 | protein_coding | deleterious(0) | probably_damaging(0.99) | TCGA-AA-3655-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
COPS6 | SNV | Missense_Mutation | novel | c.664N>T | p.Ile222Leu | p.I222L | Q7L5N1 | protein_coding | tolerated(0.77) | benign(0.003) | TCGA-AA-3697-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
COPS6 | SNV | Missense_Mutation | c.472A>C | p.Thr158Pro | p.T158P | Q7L5N1 | protein_coding | tolerated(0.24) | benign(0.001) | TCGA-AA-3977-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
COPS6 | SNV | Missense_Mutation | c.313N>C | p.Tyr105His | p.Y105H | Q7L5N1 | protein_coding | deleterious(0) | probably_damaging(0.982) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR | |
COPS6 | SNV | Missense_Mutation | c.179N>T | p.Ser60Phe | p.S60F | Q7L5N1 | protein_coding | deleterious(0) | possibly_damaging(0.638) | TCGA-AZ-6599-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
COPS6 | SNV | Missense_Mutation | c.592N>T | p.Ile198Phe | p.I198F | Q7L5N1 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
COPS6 | SNV | Missense_Mutation | c.722N>T | p.Tyr241Phe | p.Y241F | Q7L5N1 | protein_coding | deleterious(0.04) | possibly_damaging(0.888) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | 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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