Galanin receptor 2

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GALR2
Identifiers
AliasesGALR2, GAL2-R, GALNR2, GALR-2, Galanin receptor 2
External IDsOMIM: 603691 MGI: 1337018 HomoloGene: 2863 GeneCards: GALR2
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_003857

NM_010254

RefSeq (protein)

NP_003848

NP_034384

Location (UCSC)Chr 17: 76.07 – 76.08 MbChr 11: 116.17 – 116.17 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Galanin receptor 2, (GAL2) is a G-protein coupled receptor encoded by the GALR2 gene.[5]

Function

Galanin is an important neuromodulator present in the brain, gastrointestinal system, and hypothalamopituitary axis. It is a 30-amino acid non-C-terminally amidated peptide that potently stimulates growth hormone secretion, inhibits cardiac vagal slowing of heart rate, abolishes sinus arrhythmia, and inhibits postprandial gastrointestinal motility. The actions of galanin are mediated through interaction with specific membrane receptors that are members of the 7-transmembrane family of G protein-coupled receptors. GALR2 interacts with the N-terminal residues of the galanin peptide. The primary signaling mechanism for GALR2 is through the phospholipase C/protein kinase C pathway (via Gq), in contrast to GALR1, which communicates its intracellular signal by inhibition of adenylyl cyclase through Gi. However, it has been demonstrated that GALR2 couples efficiently to both the Gq and Gi proteins to simultaneously activate 2 independent signal transduction pathways.[5]

See also

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000182687Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000020793Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b "Entrez Gene: GALR2 galanin receptor 2".

Further reading

External links

  • "Galanin Receptors: GAL2". IUPHAR Database of Receptors and Ion Channels. International Union of Basic and Clinical Pharmacology.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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