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Gene: ASB11 |
Gene summary for ASB11 |
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Gene information | Species | Human | Gene symbol | ASB11 | Gene ID | 140456 |
Gene name | ankyrin repeat and SOCS box containing 11 | |
Gene Alias | ASB11 | |
Cytomap | Xp22.2 | |
Gene Type | protein-coding | GO ID | GO:0006464 | UniProtAcc | Q7Z670 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
140456 | ASB11 | HCC1 | Human | Liver | HCC | 7.77e-09 | 4.14e-01 | 0.5336 |
140456 | ASB11 | HCC2 | Human | Liver | HCC | 1.30e-15 | 1.02e+00 | 0.5341 |
140456 | ASB11 | HCC5 | Human | Liver | HCC | 3.25e-10 | 7.16e-01 | 0.4932 |
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Tissue | Expression Dynamics | Abbreviation |
Liver | ![]() | HCC: Hepatocellular carcinoma |
NAFLD: Non-alcoholic fatty liver disease |
∗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:000989622 | Liver | HCC | positive regulation of catabolic process | 335/7958 | 492/18723 | 3.83e-31 | 1.87e-28 | 335 |
GO:004217622 | Liver | HCC | regulation of protein catabolic process | 267/7958 | 391/18723 | 2.45e-25 | 7.38e-23 | 267 |
GO:004573222 | Liver | HCC | positive regulation of protein catabolic process | 163/7958 | 231/18723 | 4.00e-18 | 4.69e-16 | 163 |
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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 |
ASB11 | SNV | Missense_Mutation | novel | c.224A>G | p.Gln75Arg | p.Q75R | Q8WXH4 | protein_coding | deleterious(0.04) | possibly_damaging(0.652) | TCGA-34-2604-01 | Lung | lung squamous cell carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
ASB11 | SNV | Missense_Mutation | novel | c.805G>T | p.Ala269Ser | p.A269S | Q8WXH4 | protein_coding | tolerated(0.24) | benign(0.003) | TCGA-58-8390-01 | Lung | lung squamous cell carcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
ASB11 | SNV | Missense_Mutation | c.452T>A | p.Leu151Gln | p.L151Q | Q8WXH4 | protein_coding | deleterious(0) | possibly_damaging(0.828) | TCGA-60-2698-01 | Lung | lung squamous cell carcinoma | Male | <65 | I/II | Chemotherapy | mithramycin | PD | |
ASB11 | SNV | Missense_Mutation | c.491C>A | p.Ala164Asp | p.A164D | Q8WXH4 | protein_coding | tolerated(0.1) | possibly_damaging(0.855) | TCGA-60-2720-01 | Lung | lung squamous cell carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | SD | |
ASB11 | SNV | Missense_Mutation | novel | c.724N>A | p.Glu242Lys | p.E242K | Q8WXH4 | protein_coding | deleterious(0.05) | probably_damaging(0.996) | TCGA-63-A5MG-01 | Lung | lung squamous cell carcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
ASB11 | deletion | Frame_Shift_Del | novel | c.851delN | p.Pro284HisfsTer65 | p.P284Hfs*65 | Q8WXH4 | protein_coding | TCGA-55-8299-01 | Lung | lung adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | PD | ||
ASB11 | SNV | Missense_Mutation | c.674G>A | p.Gly225Asp | p.G225D | Q8WXH4 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-BR-8372-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Chemotherapy | etoposide | CR | |
ASB11 | SNV | Missense_Mutation | c.128G>A | p.Gly43Glu | p.G43E | Q8WXH4 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-BR-8680-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Chemotherapy | oxaliplatin | CR | |
ASB11 | SNV | Missense_Mutation | c.309N>A | p.His103Gln | p.H103Q | Q8WXH4 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-CD-5813-01 | Stomach | stomach adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | PD | |
ASB11 | SNV | Missense_Mutation | c.422N>A | p.Ser141Asn | p.S141N | Q8WXH4 | protein_coding | tolerated(0.06) | benign(0.355) | TCGA-CG-5721-01 | Stomach | stomach adenocarcinoma | Male | <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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