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Gene: GPR157 |
Gene summary for GPR157 |
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Gene information | Species | Human | Gene symbol | GPR157 | Gene ID | 80045 |
Gene name | G protein-coupled receptor 157 | |
Gene Alias | GPR157 | |
Cytomap | 1p36.22 | |
Gene Type | protein-coding | GO ID | GO:0006873 | UniProtAcc | Q5UAW9 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
80045 | GPR157 | P107T-E | Human | Esophagus | ESCC | 3.26e-20 | 4.44e-01 | 0.171 |
80045 | GPR157 | P126T-E | Human | Esophagus | ESCC | 1.74e-04 | 7.06e-01 | 0.1125 |
80045 | GPR157 | P127T-E | Human | Esophagus | ESCC | 6.56e-14 | 2.48e-01 | 0.0826 |
80045 | GPR157 | P128T-E | Human | Esophagus | ESCC | 1.41e-26 | 8.52e-01 | 0.1241 |
80045 | GPR157 | P130T-E | Human | Esophagus | ESCC | 4.70e-07 | 2.46e-01 | 0.1676 |
80045 | GPR157 | C30 | Human | Oral cavity | OSCC | 1.83e-14 | 6.07e-01 | 0.3055 |
80045 | GPR157 | C43 | Human | Oral cavity | OSCC | 2.25e-07 | 2.18e-01 | 0.1704 |
80045 | GPR157 | C46 | Human | Oral cavity | OSCC | 9.85e-05 | 8.55e-02 | 0.1673 |
80045 | GPR157 | C51 | Human | Oral cavity | OSCC | 6.23e-05 | 4.60e-01 | 0.2674 |
80045 | GPR157 | C57 | Human | Oral cavity | OSCC | 1.98e-08 | 2.49e-01 | 0.1679 |
80045 | GPR157 | LN22 | Human | Oral cavity | OSCC | 2.31e-09 | 1.06e+00 | 0.1733 |
80045 | GPR157 | LN46 | Human | Oral cavity | OSCC | 7.48e-04 | 2.20e-01 | 0.1666 |
80045 | GPR157 | SYSMH1 | Human | Oral cavity | OSCC | 1.12e-18 | 4.62e-01 | 0.1127 |
80045 | GPR157 | SYSMH3 | Human | Oral cavity | OSCC | 1.17e-15 | 4.54e-01 | 0.2442 |
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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:00420636 | Esophagus | ESCC | gliogenesis | 172/8552 | 301/18723 | 3.75e-05 | 3.04e-04 | 172 |
GO:00100016 | Esophagus | ESCC | glial cell differentiation | 129/8552 | 225/18723 | 2.73e-04 | 1.65e-03 | 129 |
GO:004851118 | Esophagus | ESCC | rhythmic process | 164/8552 | 298/18723 | 6.80e-04 | 3.57e-03 | 164 |
GO:000762319 | Esophagus | ESCC | circadian rhythm | 119/8552 | 210/18723 | 8.47e-04 | 4.36e-03 | 119 |
GO:004851116 | Oral cavity | OSCC | rhythmic process | 157/7305 | 298/18723 | 1.00e-06 | 1.36e-05 | 157 |
GO:00420635 | Oral cavity | OSCC | gliogenesis | 154/7305 | 301/18723 | 1.10e-05 | 1.14e-04 | 154 |
GO:000762316 | Oral cavity | OSCC | circadian rhythm | 110/7305 | 210/18723 | 5.40e-05 | 4.48e-04 | 110 |
GO:00100015 | Oral cavity | OSCC | glial cell differentiation | 110/7305 | 225/18723 | 1.56e-03 | 7.45e-03 | 110 |
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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 |
GPR157 | SNV | Missense_Mutation | c.593G>A | p.Arg198Lys | p.R198K | Q5UAW9 | protein_coding | tolerated(0.12) | benign(0.018) | TCGA-C8-A26Y-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
GPR157 | SNV | Missense_Mutation | c.974N>T | p.Ser325Phe | p.S325F | Q5UAW9 | protein_coding | tolerated_low_confidence(0.08) | benign(0) | TCGA-E9-A22E-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | cyclophosphane | SD | |
GPR157 | SNV | Missense_Mutation | rs555957933 | c.920C>T | p.Pro307Leu | p.P307L | Q5UAW9 | protein_coding | tolerated(0.17) | benign(0.001) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
GPR157 | SNV | Missense_Mutation | novel | c.670G>A | p.Asp224Asn | p.D224N | Q5UAW9 | protein_coding | tolerated(0.11) | benign(0.137) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
GPR157 | SNV | Missense_Mutation | c.1002N>A | p.Ser334Arg | p.S334R | Q5UAW9 | protein_coding | deleterious_low_confidence(0.01) | benign(0.157) | TCGA-A6-6654-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Chemotherapy | oxaliplatin | SD | |
GPR157 | SNV | Missense_Mutation | c.331G>A | p.Ala111Thr | p.A111T | Q5UAW9 | protein_coding | tolerated(0.44) | benign(0.007) | TCGA-A6-6781-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | oxaliplatin | SD | |
GPR157 | SNV | Missense_Mutation | rs374315465 | c.763N>A | p.Val255Met | p.V255M | Q5UAW9 | protein_coding | tolerated(0.14) | probably_damaging(0.963) | TCGA-AY-A69D-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
GPR157 | SNV | Missense_Mutation | c.770N>T | p.Thr257Met | p.T257M | Q5UAW9 | protein_coding | tolerated(0.19) | benign(0.036) | TCGA-CI-6622-01 | Colorectum | rectum adenocarcinoma | Male | >=65 | I/II | Chemotherapy | 5-fluorouracil | SD | |
GPR157 | SNV | Missense_Mutation | novel | c.1001N>T | p.Ser334Ile | p.S334I | Q5UAW9 | protein_coding | deleterious_low_confidence(0) | benign(0.205) | TCGA-A5-A0G1-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
GPR157 | SNV | Missense_Mutation | rs183530083 | c.860N>A | p.Arg287Gln | p.R287Q | Q5UAW9 | protein_coding | deleterious(0) | probably_damaging(0.994) | TCGA-A5-A2K5-01 | 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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