SNTG2 syntrophin gamma 2 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 54221)
Symbol: SNTG2
Full name: syntrophin gamma 2
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: G2SYN; SYN5
Summary: This gene encodes a protein belonging to the syntrophin family. Syntrophins are cytoplasmic peripheral membrane proteins that bind to components of mechanosenstive sodium channels and the extreme carboxy-terminal domain of dystrophin and dystrophin-related proteins. The PDZ domain of this protein product interacts with a protein component of a mechanosensitive sodium channel that affects channel gating. Absence or reduction of this protein product has been associated with Duchenne muscular dystrophy. There is evidence of alternative splicing yet the full-length nature of these variants has not been described. [provided by RefSeq, Jul 2008]
Expression: Low expression observed in reference dataset
Orthologs: mouse
Gene size: 416765bp
Exon count: 26