LPAR2

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

LPAR2

Lysophosphatidic acid receptor 2 also known as LPA2 is a protein that in humans is encoded by the LPAR2 gene.[5][6][7] LPA2 is a G protein-coupled receptor that binds the lipid signaling molecule lysophosphatidic acid (LPA).[8]

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LPAR2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesLPAR2, EDG-4, EDG4, LPA-2, LPA2, lysophosphatidic acid receptor 2
External IDsOMIM: 605110; MGI: 1858422; HomoloGene: 3465; GeneCards: LPAR2; OMA:LPAR2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004720
NM_001395660

NM_020028

RefSeq (protein)

NP_004711

NP_064412

Location (UCSC)Chr 19: 19.62 – 19.63 MbChr 8: 70.28 – 70.28 Mb
PubMed search[3][4]
Wikidata
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Function

This gene encodes a member of family I of the G protein-coupled receptors, as well as the EDG family of proteins. This protein functions as a lysophosphatidic acid (LPA) receptor and contributes to Ca2+ mobilization, a critical cellular response to LPA in cells, through association with Gi and Gq proteins.[5]

Interactions

LPAR2 has been shown to interact with TRIP6.[9]

Evolution

Paralogues

Source:[10][11]

See also

References

Further reading

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