Gene: SNTG1

Alternate names for this Gene: G1SYN|SYN4

Gene Summary: 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 family member plays a role in mediating gamma-enolase trafficking to the plasma membrane and in enhancing its neurotrophic activity. Mutations in this gene are associated with idiopathic scoliosis. Alternatively spliced transcript variants have been found for this gene.

Gene is located in Chromosome: 8

Location in Chromosome : 8q11.21

Description of this Gene: syntrophin gamma 1

Type of Gene: protein-coding

Gene: LOC105375829

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