QuickView for SNTG2;jsessionid=35AAE21D68A6D86C30868AEC78D23342;jsessionid=5D6EC365B14478EE6A4A0C5099D98855;jsessionid=E51604A0BA76FFE98BC148B6794A540F;jsessionid=26629A1B8EFB3762BE7949E6919EB0DF;jsessionid=8A9FA66A47683114E8A19E9877D7BC98 (gene)

Gene Symbol:

SNTG2 Homo sapiens

Full name:

syntrophin gamma 2

Synonyms:

G2SYN, SYN5, gamma-2-syntrophin, syntrophin-5

Genomic Location:

Chr 2: 936555-1253924

Description:

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 mech...

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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.

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Orthologs:

Mus musculus ,  Rattus norvegicus ,  Macaca mulatta ,  Gallus gallus ,  Danio rerio ,  Canis lupus familiaris ,  Bos taurus ,  Pan troglodytes

External Links:

Entrez Gene

Cytogenetic Map:

2p25.3

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