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Protein-coding gene in the species Homo sapiens

GPRC5A

GPRC5A
All data from the card 17
Aliases
GPRC5A, GPCR5A, RAI3, RAIG1, PEIG-1, TIG1, G protein-coupled receptor class C group 5 member A
External IDs
OMIM: 604138; MGI: 1891250; GeneCards: GPRC5A
Chr.
Chromosome 12 (human)
Band
12p13.1
End
12,917,937 bp
Chr.
Chromosome 6 (mouse)
Band
6|6 G1
End
135,061,707 bp
BioGPS
n/a
Databases
NCBI: entry; OMA: entry
Species
Human
Entrez
9052
Ensembl
ENSG00000013588
UniProt
Q8NFJ5
RefSeq (mRNA)
NM_003979
RefSeq (protein)
NP_003970
Location (UCSC)
Chr 12: 12.89 – 12.92 Mb

Retinoic acid-induced protein 3 is a protein that in humans is encoded by the GPRC5A gene. This gene and its encoded mRNA was first identified as a phorbol ester-induced gene, and named Phorbol Ester Induced Gen 1 (PEIG-1); two years later it was rediscovered as a retinoic acid-inducible gene, and named Retinoic Acid-Inducible Gene 1 (RAIG1). Its encoded protein was later named Retinoic acid-induced protein 3.

Function

This gene encodes a member of the type 3 G protein-coupled receptor family, characterized by the signature 7-transmembrane domain motif. The encoded protein may be involved in interaction between retinoic acid and G protein signalling pathways. Retinoic acid plays an important role in development, cellular growth, and differentiation. This gene may play a role in embryonic development and epithelial cell differentiation. Tryptamine and other indole related chemicals produced by gut microflora bind and activate the receptor.

Post transcriptional regulation

GPRC5A is one of only a handful of genes known in the literature that are post-transcriptionally controlled by miRNAs through their 5'UTR.

Clinical significance

GPRC5A is dysregulated in many human cancers and in other diseases.

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Text from Wikipedia, CC BY-SA 4.0 · Source article