Gene Gene information from NCBI Gene database.
Entrez ID 54329
Gene name G protein-coupled receptor 85
Gene symbol GPR85
Synonyms (NCBI Gene)
SREBSREB2
Chromosome 7
Chromosome location 7q31.1
Summary Members of the G protein-coupled receptor (GPCR) family, such as GPR85, have a similar structure characterized by 7 transmembrane domains. Activation of GPCRs by extracellular stimuli, such as neurotransmitters, hormones, or light, induces an intracellula
miRNA miRNA information provided by mirtarbase database.
83
miRTarBase ID miRNA Experiments Reference
MIRT438267 hsa-miR-29a-3p Luciferase reporter assay 24085298
MIRT438267 hsa-miR-29a-3p Luciferase reporter assay 24085298
MIRT530915 hsa-miR-548aa PAR-CLIP 22012620
MIRT530914 hsa-miR-548ap-3p PAR-CLIP 22012620
MIRT530913 hsa-miR-548t-3p PAR-CLIP 22012620
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13
GO ID Ontology Definition Evidence Reference
GO:0004930 Function G protein-coupled receptor activity IBA
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0004930 Function G protein-coupled receptor activity TAS 10833454
GO:0005515 Function Protein binding IPI 25780553
GO:0005783 Component Endoplasmic reticulum IDA 25780553
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605188 4536 ENSG00000164604
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P60893
Protein name Probable G-protein coupled receptor 85 (Super conserved receptor expressed in brain 2)
Protein function Orphan receptor.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 37 338 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Highly expressed in brain and testis. Lower levels in small intestine, placenta and spleen. In brain regions, detected in all regions tested, but somewhat lower levels in the corpus callosum, medulla and spinal cord. {ECO:0000269|PubMe
Sequence
Sequence length 370
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 Evidence Score
CHOLELITHIASIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Mental disorders Mental Disorders BEFREE 18413613
★☆☆☆☆
Found in Text Mining only
Schizophrenia Schizophrenia BEFREE 18413613, 22968816
★☆☆☆☆
Found in Text Mining only