GPR12

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

GPR12

Probable G-protein coupled receptor 12 is a protein that in humans is encoded by the GPR12 gene.[5][6][7]

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GPR12
Identifiers
AliasesGPR12, GPCR12, GPCR21, PPP1R84, G protein-coupled receptor 12
External IDsOMIM: 600752; MGI: 101909; HomoloGene: 3868; GeneCards: GPR12; OMA:GPR12 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005288

RefSeq (protein)

NP_005279

Location (UCSC)Chr 13: 26.76 – 26.76 MbChr 5: 146.52 – 146.52 Mb
PubMed search[3][4]
Wikidata
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The gene product of GPR12 is an orphan receptor, meaning that its endogenous ligand is currently unknown. Gene disruption of GPR12 in mice results in dyslipidemia and obesity.[8]

Ligands

Inverse agonists

Evolution

Paralogues

Source:[10]

References

Further reading

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