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Gene Gene information from NCBI Gene database.
Entrez ID 27197
Gene name G protein-coupled receptor 82
Gene symbol GPR82
Synonyms (NCBI Gene)
-
Chromosome X
Chromosome location Xp11.4
Summary The protein encoded by this gene is an orphan G protein-coupled receptor of unknown function. The encoded protein is a member of a family of proteins that contain seven transmembrane domains and transduce extracellular signals through heterotrimeric G pro
miRNA miRNA information provided by mirtarbase database.
393 Show/Hide all (393)
miRTarBase ID miRNA Experiments Reference
MIRT017157 hsa-miR-335-5p Microarray 18185580
MIRT629811 hsa-miR-5197-5p HITS-CLIP 23824327
MIRT629810 hsa-miR-130a-3p HITS-CLIP 23824327
MIRT629809 hsa-miR-130b-3p HITS-CLIP 23824327
MIRT629808 hsa-miR-301a-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
11 Show/Hide all (11)
GO ID Ontology Definition Evidence Reference
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0005886 Component Plasma membrane IEA
GO:0006641 Process Triglyceride metabolic process IEA
GO:0007165 Process Signal transduction IEA
GO:0007186 Process G protein-coupled receptor signaling pathway IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
300748 4533 ENSG00000171657
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96P67
Protein name Probable G-protein coupled receptor 82
Protein function Orphan receptor.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 32 → 309 7 transmembrane receptor (rhodopsin family) Family
Sequence
Sequence length 336
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Reference Evidence Score
Prostate cancer Uncertain significance ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations