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Gene: GPR146 |
Gene summary for GPR146 |
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Gene information | Species | Human | Gene symbol | GPR146 | Gene ID | 115330 |
Gene name | G protein-coupled receptor 146 | |
Gene Alias | PGR8 | |
Cytomap | 7p22.3 | |
Gene Type | protein-coding | GO ID | GO:0007154 | UniProtAcc | A4D2Q3 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
115330 | GPR146 | S014 | Human | Liver | HCC | 1.49e-13 | 5.36e-01 | 0.2254 |
115330 | GPR146 | S015 | Human | Liver | HCC | 4.31e-17 | 6.75e-01 | 0.2375 |
115330 | GPR146 | S016 | Human | Liver | HCC | 5.90e-17 | 5.31e-01 | 0.2243 |
115330 | GPR146 | S029 | Human | Liver | HCC | 3.71e-03 | 2.17e-01 | 0.2581 |
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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 |
Cervix | N_HPV | ![]() |
Endometrium | AEH | ![]() |
Endometrium | EEC | ![]() |
Prostate | BPH | ![]() |
Prostate | Tumor | ![]() |
∗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 |
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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 |
GPR146 | deletion | Frame_Shift_Del | novel | c.532delN | p.Cys178AlafsTer74 | p.C178Afs*74 | Q96CH1 | protein_coding | TCGA-D8-A27V-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD | ||
GPR146 | SNV | Missense_Mutation | c.632N>T | p.Ser211Phe | p.S211F | Q96CH1 | protein_coding | tolerated(0.14) | benign(0.311) | TCGA-EK-A2PM-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Unknown | Unknown | SD | |
GPR146 | SNV | Missense_Mutation | c.346G>A | p.Ala116Thr | p.A116T | Q96CH1 | protein_coding | tolerated(1) | benign(0.005) | TCGA-AA-3492-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
GPR146 | SNV | Missense_Mutation | rs761700064 | c.653N>T | p.Thr218Met | p.T218M | Q96CH1 | protein_coding | deleterious(0.01) | benign(0.224) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
GPR146 | SNV | Missense_Mutation | rs754291447 | c.361N>A | p.Ala121Thr | p.A121T | Q96CH1 | protein_coding | tolerated(0.66) | benign(0.012) | TCGA-CK-5916-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
GPR146 | SNV | Missense_Mutation | rs145638311 | c.401N>T | p.Pro134Leu | p.P134L | Q96CH1 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-D5-6929-01 | Colorectum | colon adenocarcinoma | Female | <65 | III/IV | Chemotherapy | oxaliplatinum+ | SD |
GPR146 | SNV | Missense_Mutation | rs750356197 | c.25N>A | p.Gly9Ser | p.G9S | Q96CH1 | protein_coding | tolerated(0.2) | benign(0.005) | TCGA-A5-A0VP-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
GPR146 | SNV | Missense_Mutation | c.521G>C | p.Arg174Pro | p.R174P | Q96CH1 | protein_coding | deleterious(0.01) | possibly_damaging(0.613) | TCGA-AJ-A23O-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
GPR146 | SNV | Missense_Mutation | novel | c.55N>C | p.Cys19Arg | p.C19R | Q96CH1 | protein_coding | deleterious(0.03) | probably_damaging(0.996) | TCGA-AJ-A3BG-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Chemotherapy | carboplatin | PD |
GPR146 | SNV | Missense_Mutation | c.994C>A | p.Leu332Met | p.L332M | Q96CH1 | protein_coding | tolerated_low_confidence(0.74) | benign(0.003) | TCGA-AP-A051-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | 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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