Gene Gene information from NCBI Gene database.
Entrez ID 2835
Gene name G protein-coupled receptor 12
Gene symbol GPR12
Synonyms (NCBI Gene)
GPCR12GPCR21PPP1R84
Chromosome 13
Chromosome location 13q12.13
miRNA miRNA information provided by mirtarbase database.
129
miRTarBase ID miRNA Experiments Reference
MIRT1030031 hsa-miR-103a CLIP-seq
MIRT1030032 hsa-miR-107 CLIP-seq
MIRT1030033 hsa-miR-122 CLIP-seq
MIRT1030034 hsa-miR-1260 CLIP-seq
MIRT1030035 hsa-miR-1260b CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
15
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 8530049
GO:0005737 Component Cytoplasm IBA
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
600752 4466 ENSG00000132975
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P47775
Protein name G-protein coupled receptor 12
Protein function Promotes neurite outgrowth and blocks myelin inhibition in neurons (By similarity). Receptor with constitutive G(s) signaling activity that stimulates cyclic AMP production.
PDB 7Y3G
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 61 301 7 transmembrane receptor (rhodopsin family) Family
Sequence
Sequence length 334
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
6
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
ASTHMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CEREBRAL ATHEROSCLEROSIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
EOSINOPHILIC ESOPHAGITIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HEARING LOSS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Carcinogenesis Associate 33742771
★☆☆☆☆
Found in Text Mining only
Esophageal Neoplasms Inhibit 33742771
★☆☆☆☆
Found in Text Mining only
Hypopharyngeal Neoplasms Associate 33742771
★☆☆☆☆
Found in Text Mining only
Inflammation Associate 33742771
★☆☆☆☆
Found in Text Mining only
Neoplasms Inhibit 33742771
★☆☆☆☆
Found in Text Mining only
Squamous Cell Carcinoma of Head and Neck Associate 33742771
★☆☆☆☆
Found in Text Mining only