Aliases for SNTG1 Gene
External Ids for SNTG1 Gene
Previous GeneCards Identifiers for SNTG1 Gene
The protein encoded by this gene is a member of the syntrophin family. Syntrophins are cytoplasmic peripheral membrane proteins that typically contain 2 pleckstrin homology (PH) domains, a PDZ domain that bisects the first PH domain, and a C-terminal domain that mediates dystrophin binding. This gene is specifically expressed in the brain. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2013]
GeneCards Summary for SNTG1 Gene
SNTG1 (Syntrophin, Gamma 1) is a Protein Coding gene. Diseases associated with SNTG1 include idiopathic scoliosis. GO annotations related to this gene include actin binding and protein C-terminus binding. An important paralog of this gene is SNTB1.
UniProtKB/Swiss-Prot for SNTG1 Gene
Adapter protein that binds to and probably organizes the subcellular localization of a variety of proteins. May link various receptors to the actin cytoskeleton and the dystrophin glycoprotein complex (By similarity). May participate in regulating the subcellular location of diacylglycerol kinase-zeta to ensure that diacylglycerol is rapidly inactivated following receptor activation.