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DTNA, dystrobrevin alpha

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DTNA, dystrobrevin alpha

  • The protein encoded by this gene belongs to the dystrobrevin subfamily of the dystrophin family. This protein is a component of the dystrophin-associated protein complex (DPC), which consists of dystrophin and several integral and peripheral membrane proteins, including dystroglycans, sarcoglycans, syntrophins and alpha- and beta-dystrobrevin. The DPC localizes to the sarcolemma and its disruption is associated with various forms of muscular dystrophy. Mutations in this gene are associated with left ventricular noncompaction with congenital heart defects. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]

  • Gene Synonyms (D18S892E, DRP3, DTN, DTN-A, LVNC1, dystrobrevin alpha, dystrophin-related protein 3,)
  • NCBI Gene ID: 1837
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A0A024RC32
    UNIPROT ID#>>B7Z3X3
    UNIPROT ID#>>Q9Y4J8
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

dystrobrevin alpha interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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