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Gene: COMMD7 |
Gene summary for COMMD7 |
Gene summary. |
Gene information | Species | Human | Gene symbol | COMMD7 | Gene ID | 149951 |
Gene name | COMM domain containing 7 | |
Gene Alias | C20orf92 | |
Cytomap | 20q11.21 | |
Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q86VX2 |
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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 |
Malignant transformation involving gene list. |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
149951 | COMMD7 | HTA11_2487_2000001011 | Human | Colorectum | SER | 1.32e-08 | 2.15e-01 | -0.1808 |
149951 | COMMD7 | HTA11_2951_2000001011 | Human | Colorectum | AD | 3.40e-03 | 2.80e-01 | 0.0216 |
149951 | COMMD7 | HTA11_1938_2000001011 | Human | Colorectum | AD | 1.67e-02 | 1.39e-01 | -0.0811 |
149951 | COMMD7 | HTA11_78_2000001011 | Human | Colorectum | AD | 6.68e-05 | 1.98e-01 | -0.1088 |
149951 | COMMD7 | HTA11_347_2000001011 | Human | Colorectum | AD | 2.93e-13 | 2.57e-01 | -0.1954 |
149951 | COMMD7 | HTA11_411_2000001011 | Human | Colorectum | SER | 2.78e-05 | 3.68e-01 | -0.2602 |
149951 | COMMD7 | HTA11_3361_2000001011 | Human | Colorectum | AD | 7.91e-05 | 2.02e-01 | -0.1207 |
149951 | COMMD7 | HTA11_83_2000001011 | Human | Colorectum | SER | 1.79e-04 | 2.04e-01 | -0.1526 |
149951 | COMMD7 | HTA11_696_2000001011 | Human | Colorectum | AD | 4.28e-10 | 2.09e-01 | -0.1464 |
149951 | COMMD7 | HTA11_866_2000001011 | Human | Colorectum | AD | 9.55e-09 | 1.85e-01 | -0.1001 |
149951 | COMMD7 | HTA11_1391_2000001011 | Human | Colorectum | AD | 7.00e-13 | 2.74e-01 | -0.059 |
149951 | COMMD7 | HTA11_2992_2000001011 | Human | Colorectum | SER | 1.72e-05 | 3.10e-01 | -0.1706 |
149951 | COMMD7 | HTA11_5212_2000001011 | Human | Colorectum | AD | 5.12e-05 | 2.37e-01 | -0.2061 |
149951 | COMMD7 | HTA11_5216_2000001011 | Human | Colorectum | SER | 2.79e-07 | 4.15e-01 | -0.1462 |
149951 | COMMD7 | HTA11_546_2000001011 | Human | Colorectum | AD | 2.65e-04 | 2.15e-01 | -0.0842 |
149951 | COMMD7 | HTA11_866_3004761011 | Human | Colorectum | AD | 3.29e-15 | 3.14e-01 | 0.096 |
149951 | COMMD7 | HTA11_4255_2000001011 | Human | Colorectum | SER | 3.40e-03 | 2.22e-01 | 0.0446 |
149951 | COMMD7 | HTA11_10623_2000001011 | Human | Colorectum | AD | 8.98e-03 | 1.87e-01 | -0.0177 |
149951 | COMMD7 | HTA11_6801_2000001011 | Human | Colorectum | SER | 9.67e-09 | 3.87e-01 | 0.0171 |
149951 | COMMD7 | HTA11_10711_2000001011 | Human | Colorectum | AD | 1.67e-03 | 1.54e-01 | 0.0338 |
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Transcriptomic changes along malignancy continuum. |
∗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 |
Figure of enriched GO biological processes. |
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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Enriched GO biological processes. |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:0051090 | Colorectum | MSS | regulation of DNA-binding transcription factor activity | 106/3467 | 440/18723 | 1.88e-03 | 1.65e-02 | 106 |
GO:00510908 | Esophagus | ESCC | regulation of DNA-binding transcription factor activity | 252/8552 | 440/18723 | 5.22e-07 | 6.97e-06 | 252 |
GO:003320914 | Esophagus | ESCC | tumor necrosis factor-mediated signaling pathway | 67/8552 | 99/18723 | 7.87e-06 | 7.72e-05 | 67 |
GO:003461220 | Esophagus | ESCC | response to tumor necrosis factor | 149/8552 | 253/18723 | 1.47e-05 | 1.33e-04 | 149 |
GO:007135620 | Esophagus | ESCC | cellular response to tumor necrosis factor | 132/8552 | 229/18723 | 1.69e-04 | 1.11e-03 | 132 |
GO:00434332 | Esophagus | ESCC | negative regulation of DNA-binding transcription factor activity | 103/8552 | 185/18723 | 3.86e-03 | 1.57e-02 | 103 |
GO:00320882 | Esophagus | ESCC | negative regulation of NF-kappaB transcription factor activity | 54/8552 | 93/18723 | 1.08e-02 | 3.67e-02 | 54 |
GO:003461218 | Oral cavity | OSCC | response to tumor necrosis factor | 143/7305 | 253/18723 | 1.09e-08 | 2.23e-07 | 143 |
GO:007135618 | Oral cavity | OSCC | cellular response to tumor necrosis factor | 128/7305 | 229/18723 | 1.49e-07 | 2.49e-06 | 128 |
GO:00510907 | Oral cavity | OSCC | regulation of DNA-binding transcription factor activity | 221/7305 | 440/18723 | 9.06e-07 | 1.23e-05 | 221 |
GO:00332099 | Oral cavity | OSCC | tumor necrosis factor-mediated signaling pathway | 61/7305 | 99/18723 | 4.31e-06 | 4.98e-05 | 61 |
GO:00192214 | Oral cavity | OSCC | cytokine-mediated signaling pathway | 222/7305 | 472/18723 | 2.02e-04 | 1.35e-03 | 222 |
GO:0032088 | Oral cavity | OSCC | negative regulation of NF-kappaB transcription factor activity | 47/7305 | 93/18723 | 1.55e-02 | 4.99e-02 | 47 |
GO:005109015 | Oral cavity | LP | regulation of DNA-binding transcription factor activity | 147/4623 | 440/18723 | 2.00e-05 | 3.35e-04 | 147 |
GO:003320913 | Oral cavity | LP | tumor necrosis factor-mediated signaling pathway | 38/4623 | 99/18723 | 1.72e-03 | 1.31e-02 | 38 |
GO:003461219 | Oral cavity | LP | response to tumor necrosis factor | 83/4623 | 253/18723 | 2.10e-03 | 1.54e-02 | 83 |
GO:007135619 | Oral cavity | LP | cellular response to tumor necrosis factor | 76/4623 | 229/18723 | 2.24e-03 | 1.62e-02 | 76 |
GO:0043433 | Oral cavity | LP | negative regulation of DNA-binding transcription factor activity | 61/4623 | 185/18723 | 6.68e-03 | 3.89e-02 | 61 |
GO:003461216 | Prostate | BPH | response to tumor necrosis factor | 68/3107 | 253/18723 | 2.22e-05 | 2.67e-04 | 68 |
GO:007135616 | Prostate | BPH | cellular response to tumor necrosis factor | 60/3107 | 229/18723 | 1.42e-04 | 1.26e-03 | 60 |
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Enriched KEGG pathways. |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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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 |
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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 |
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 |
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 |
COMMD7 | SNV | Missense_Mutation | novel | c.252G>T | p.Lys84Asn | p.K84N | Q86VX2 | protein_coding | deleterious(0) | possibly_damaging(0.823) | TCGA-EO-A3KX-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
COMMD7 | insertion | Nonsense_Mutation | novel | c.539_540insCAGCTAATTTTTTGTATTTT | p.Gln181SerfsTer2 | p.Q181Sfs*2 | Q86VX2 | protein_coding | TCGA-AP-A056-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | ||
COMMD7 | SNV | Missense_Mutation | novel | c.406G>T | p.Asp136Tyr | p.D136Y | Q86VX2 | protein_coding | deleterious(0) | probably_damaging(0.99) | TCGA-64-5781-01 | Lung | lung adenocarcinoma | Female | <65 | I/II | Chemotherapy | cisplatin | PD |
COMMD7 | SNV | Missense_Mutation | novel | c.394N>G | p.Asn132Asp | p.N132D | Q86VX2 | protein_coding | deleterious(0.01) | probably_damaging(0.986) | TCGA-22-1016-01 | Lung | lung squamous cell carcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
COMMD7 | SNV | Missense_Mutation | novel | c.280G>T | p.Ala94Ser | p.A94S | Q86VX2 | protein_coding | tolerated(0.49) | benign(0.023) | TCGA-NC-A5HN-01 | Lung | lung squamous cell carcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
COMMD7 | SNV | Missense_Mutation | novel | c.279G>T | p.Gln93His | p.Q93H | Q86VX2 | protein_coding | tolerated(0.1) | benign(0.183) | TCGA-NC-A5HN-01 | Lung | lung squamous cell carcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
COMMD7 | SNV | Missense_Mutation | novel | c.542N>T | p.Gln181Leu | p.Q181L | Q86VX2 | protein_coding | deleterious(0) | possibly_damaging(0.658) | TCGA-O2-A52S-01 | Lung | lung squamous cell carcinoma | Female | <65 | III/IV | Unknown | Unknown | PD |
COMMD7 | SNV | Missense_Mutation | c.541N>G | p.Gln181Glu | p.Q181E | Q86VX2 | protein_coding | deleterious(0.04) | benign(0.086) | TCGA-CV-5970-01 | Oral cavity | head & neck squamous cell carcinoma | Male | <65 | I/II | Unknown | Unknown | PD | |
COMMD7 | SNV | Missense_Mutation | rs781670155 | c.511G>A | p.Glu171Lys | p.E171K | Q86VX2 | protein_coding | deleterious(0.04) | possibly_damaging(0.81) | TCGA-CD-5800-01 | Stomach | stomach adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
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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 |
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