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Gene: OR51E1 |
Gene summary for OR51E1 |
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Gene information | Species | Human | Gene symbol | OR51E1 | Gene ID | 143503 |
Gene name | olfactory receptor family 51 subfamily E member 1 | |
Gene Alias | D-GPCR | |
Cytomap | 11p15.4 | |
Gene Type | protein-coding | GO ID | GO:0003008 | UniProtAcc | A0A126GVF8 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
143503 | OR51E1 | S014 | Human | Liver | HCC | 4.86e-10 | 6.48e-01 | 0.2254 |
143503 | OR51E1 | S016 | Human | Liver | HCC | 1.04e-22 | 1.35e+00 | 0.2243 |
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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 |
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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 |
OR51E1 | SNV | Missense_Mutation | rs200993659 | c.910C>T | p.Arg304Cys | p.R304C | Q8TCB6 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-A8-A07F-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | tamoxiphen | SD |
OR51E1 | SNV | Missense_Mutation | rs192878981 | c.401N>A | p.Arg134His | p.R134H | Q8TCB6 | protein_coding | tolerated(0.15) | benign(0.024) | TCGA-E9-A1N8-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | SD |
OR51E1 | SNV | Missense_Mutation | rs201979094 | c.805N>T | p.Arg269Trp | p.R269W | Q8TCB6 | protein_coding | tolerated(0.06) | possibly_damaging(0.54) | TCGA-E9-A1RC-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Hormone Therapy | tamoxiphen | SD |
OR51E1 | SNV | Missense_Mutation | rs575981363 | c.808N>T | p.Arg270Cys | p.R270C | Q8TCB6 | protein_coding | tolerated(0.14) | possibly_damaging(0.54) | TCGA-FU-A23L-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
OR51E1 | SNV | Missense_Mutation | rs779396777 | c.428N>A | p.Arg143His | p.R143H | Q8TCB6 | protein_coding | deleterious(0.03) | probably_damaging(0.979) | TCGA-5M-AAT6-01 | Colorectum | colon adenocarcinoma | Female | <65 | III/IV | Unknown | Unknown | PD |
OR51E1 | SNV | Missense_Mutation | rs575981363 | c.808N>T | p.Arg270Cys | p.R270C | Q8TCB6 | protein_coding | tolerated(0.14) | possibly_damaging(0.54) | TCGA-AA-3492-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
OR51E1 | SNV | Missense_Mutation | rs146565220 | c.826G>A | p.Val276Ile | p.V276I | Q8TCB6 | protein_coding | tolerated(1) | benign(0.012) | TCGA-AA-3866-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
OR51E1 | SNV | Missense_Mutation | c.722G>A | p.Gly241Asp | p.G241D | Q8TCB6 | protein_coding | deleterious(0.03) | possibly_damaging(0.682) | TCGA-DM-A1HB-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD | |
OR51E1 | SNV | Missense_Mutation | c.252N>T | p.Met84Ile | p.M84I | Q8TCB6 | protein_coding | tolerated(0.48) | probably_damaging(0.986) | TCGA-DM-A28F-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD | |
OR51E1 | SNV | Missense_Mutation | rs575981363 | c.808N>T | p.Arg270Cys | p.R270C | Q8TCB6 | protein_coding | tolerated(0.14) | possibly_damaging(0.54) | TCGA-G4-6299-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Ancillary | leucovorin | 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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