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GPR155

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

Integral membrane protein GPR155, also known as G protein-coupled receptor 155, is a protein that in humans is encoded by the GPR155 gene.[5][6] Mutations in this gene may be associated with autism.[7]

AliasesGPR155, DEP.7, DEPDC3, PGR22, G protein-coupled receptor 155
External IDsMGI: 1915776; GeneCards: GPR155
End174,487,094 bp[1]
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GPR155
Identifiers
AliasesGPR155, DEP.7, DEPDC3, PGR22, G protein-coupled receptor 155
External IDsMGI: 1915776; GeneCards: GPR155
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001033045
NM_001267050
NM_001267051
NM_152529

NM_001080707
NM_001190297
NM_001276443
NM_001276444

RefSeq (protein)

NP_001028217
NP_001253979
NP_001253980
NP_689742
NP_001253980.1

n/a

Location (UCSC)Chr 2: 174.43 – 174.49 MbChr 2: 73.17 – 73.22 Mb
PubMed search[3][4]
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