Gene Gene information from NCBI Gene database.
Entrez ID 9293
Gene name G protein-coupled receptor 52
Gene symbol GPR52
Synonyms (NCBI Gene)
-
Chromosome 1
Chromosome location 1q25.1
Summary Members of the G protein-coupled receptor (GPR) family play important roles in signal transduction from the external environment to the inside of the cell.[supplied by OMIM, Jul 2002]
miRNA miRNA information provided by mirtarbase database.
4
miRTarBase ID miRNA Experiments Reference
MIRT1031506 hsa-miR-548aa CLIP-seq
MIRT1031507 hsa-miR-640 CLIP-seq
MIRT2005981 hsa-miR-4659a-3p CLIP-seq
MIRT2005982 hsa-miR-4659b-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
19
GO ID Ontology Definition Evidence Reference
GO:0004930 Function G protein-coupled receptor activity IDA 24587241
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0004930 Function G protein-coupled receptor activity TAS 9931487
GO:0005515 Function Protein binding IPI 32814053
GO:0005886 Component Plasma membrane IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604106 4508 ENSG00000203737
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9Y2T5
Protein name G-protein coupled receptor 52
Protein function Gs-coupled receptor activated by antipsychotics reserpine leading to an increase in intracellular cAMP and its internalization (PubMed:24587241). May play a role in locomotor activity through modulation of dopamine, NMDA and ADORA2A-induced loco
PDB 6LI0 , 6LI1 , 6LI2 , 6LI3 , 8HMP
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 57 317 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Expressed in brain, especially in striatum. {ECO:0000269|PubMed:24587241}.
Sequence
Sequence length 361
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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
NONORGANIC PSYCHOSIS Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PSYCHIATRIC DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PSYCHOTIC DISORDERS Disgenet
★★☆☆☆
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
Congenital anomaly of brain Brain malformation BEFREE 26680650
★☆☆☆☆
Found in Text Mining only
Huntington Disease Huntington Disease BEFREE 25738228, 29608652
★☆☆☆☆
Found in Text Mining only
Intellectual Disability Mental retardation BEFREE 26680650
★☆☆☆☆
Found in Text Mining only
Mental disorders Mental Disorders BEFREE 24587241, 28433511
★☆☆☆☆
Found in Text Mining only
Nonorganic psychosis Nonorganic Psychosis PSYGENET_DG 24587241
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Psychotic Disorders Psychosis PSYGENET_DG 24587241
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Psychotic Disorders Psychosis BEFREE 29478803
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Schizophrenia Schizophrenia BEFREE 28583861, 28851764
★☆☆☆☆
Found in Text Mining only