SNTB1
Protein-coding gene in the species Homo sapiens
From Wikipedia, the free encyclopedia
Beta-1-syntrophin is a protein that in humans is encoded by the SNTB1 gene.[4][5][6]
External IDsOMIM: 600026; MGI: 101781; HomoloGene: 9618; GeneCards: SNTB1; OMA:SNTB1 - orthologs
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| Aliases | SNTB1, 59-DAP, A1B, BSYN2, DAPA1B, SNT2, SNT2B1, TIP-43, syntrophin beta 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 600026; MGI: 101781; HomoloGene: 9618; GeneCards: SNTB1; OMA:SNTB1 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Function
Dystrophin is a large, rod-like cytoskeletal protein found at the inner surface of muscle fibers. Dystrophin is missing in Duchenne Muscular Dystrophy patients and is present in reduced amounts in Becker Muscular Dystrophy patients. The protein encoded by this gene is a peripheral membrane protein found associated with dystrophin and dystrophin-related proteins. This gene is a member of the syntrophin gene family, which contains at least two other structurally related genes.[6]
Interactions
SNTB1 has been shown to interact with Dystrophin.[7]
