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Gene: GNAL |
Gene summary for GNAL |
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Gene information | Species | Human | Gene symbol | GNAL | Gene ID | 2774 |
Gene name | G protein subunit alpha L | |
Gene Alias | DYT25 | |
Cytomap | 18p11.21 | |
Gene Type | protein-coding | GO ID | GO:0003008 | UniProtAcc | A8K1Y9 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
2774 | GNAL | HCC1_Meng | Human | Liver | HCC | 2.78e-08 | 5.66e-03 | 0.0246 |
2774 | GNAL | HCC1 | Human | Liver | HCC | 1.72e-15 | 2.38e+00 | 0.5336 |
2774 | GNAL | HCC2 | Human | Liver | HCC | 2.59e-18 | 2.53e+00 | 0.5341 |
2774 | GNAL | HCC5 | Human | Liver | HCC | 8.93e-03 | 5.12e-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 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0501222 | Liver | HCC | Parkinson disease | 198/4020 | 266/8465 | 9.40e-20 | 1.58e-17 | 8.76e-18 | 198 |
hsa05142 | Liver | HCC | Chagas disease | 61/4020 | 102/8465 | 8.04e-03 | 2.17e-02 | 1.21e-02 | 61 |
hsa0501232 | Liver | HCC | Parkinson disease | 198/4020 | 266/8465 | 9.40e-20 | 1.58e-17 | 8.76e-18 | 198 |
hsa051421 | Liver | HCC | Chagas disease | 61/4020 | 102/8465 | 8.04e-03 | 2.17e-02 | 1.21e-02 | 61 |
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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 |
GNAL | SNV | Missense_Mutation | c.1093G>A | p.Val365Ile | p.V365I | P38405 | protein_coding | tolerated(0.51) | benign(0.025) | TCGA-HF-7132-01 | Stomach | stomach adenocarcinoma | Male | Unknown | I/II | Chemotherapy | fluorouracil | SD | |
GNAL | SNV | Missense_Mutation | rs753374463 | c.284N>C | p.Val95Ala | p.V95A | P38405 | protein_coding | tolerated(0.75) | benign(0) | TCGA-VQ-A8P2-01 | Stomach | stomach adenocarcinoma | Male | >=65 | III/IV | Unspecific | Complete Response | |
GNAL | SNV | Missense_Mutation | c.430N>A | p.Val144Ile | p.V144I | P38405 | protein_coding | tolerated(0.5) | benign(0.02) | TCGA-DJ-A2Q0-01 | Thyroid | thyroid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
GNAL | SNV | Missense_Mutation | c.493N>A | p.Asp165Asn | p.D165N | P38405 | protein_coding | deleterious(0.01) | probably_damaging(0.925) | TCGA-DJ-A2Q3-01 | Thyroid | thyroid carcinoma | Female | <65 | III/IV | 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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