rgs8

Entrez Gene Summary for RGS8 Gene

 
  • This gene is a member of the regulator of G protein signaling (RGS) family and encodes a protein with a single RGS domain. Regulator of G protein signaling (RGS) proteins are regulatory and structural components of G protein-coupled receptor complexes. They accelerate transit through the cycle of GTP binding and hydrolysis to GDP, thereby terminating signal transduction, but paradoxically, also accelerate receptor-stimulated activation. [provided by RefSeq, Jul 2008]

GeneCards Summary for RGS8 Gene

RGS8 (Regulator Of G Protein Signaling 8) is a Protein Coding gene. Diseases associated with RGS8 include Spinocerebellar Ataxia 1. Among its related pathways are G-AlphaQ Signaling and Signaling by GPCR. Gene Ontology (GO) annotations related to this gene include GTPase activator activity. An important paralog of this gene is RGS16.

UniProtKB/Swiss-Prot Summary for RGS8 Gene

  • Regulates G protein-coupled receptor signaling cascades, including signaling via muscarinic acetylcholine receptor CHRM2 and dopamine receptor DRD2 (By similarity). Inhibits signal transduction by increasing the GTPase activity of G protein alpha subunits, thereby driving them into their inactive GDP-bound form (PubMed:18434541). Modulates the activity of potassium channels that are activated in response to DRD2 and CHRM2 signaling (By similarity). 
    • RGS8_HUMAN,P57771

Gene Wiki entry for RGS8 Gene

 
 

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