GABBR1

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

GABBR1

Gamma-aminobutyric acid B receptor, 1 (GABAB1), is a G-protein coupled receptor subunit encoded by the GABBR1 gene.

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GABBR1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesGABBR1, GABABR1, GABBR1-3, GB1, GPRC3A, dJ271M21.1.1, dJ271M21.1.2, gamma-aminobutyric acid type B receptor subunit 1
External IDsOMIM: 603540; MGI: 1860139; HomoloGene: 1132; GeneCards: GABBR1; OMA:GABBR1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001470
NM_021903
NM_021904
NM_021905
NM_001319053

NM_019439

RefSeq (protein)

NP_001305982
NP_001461
NP_068703
NP_068704

NP_062312

Location (UCSC)Chr 6: 29.56 – 29.63 MbChr 17: 37.36 – 37.39 Mb
PubMed search[3][4]
Wikidata
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Function

GABAB1 is a receptor for Gamma-aminobutyric acid. Upon binding, GABAB1 will produce a slow and prolonged inhibitory effect. GABAB1 is one part of a heterodimer, which is the GABAB receptor, consisting of it and the related GABAB2 protein. The GABA(B) receptor 1 gene is mapped to chromosome 6p21.3 within the HLA class I region close to the HLA-F gene. Susceptibility loci for multiple sclerosis, epilepsy, and schizophrenia have also been mapped in this region. Alternative splicing of this gene generates 4 transcript variants.[5]

Interactions

GABBR1 has been shown to interact with ATF4[6] and GABBR2.[7]

See also

References

Further reading

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