syntrophin, alpha 1

Symbol

SNTA1 (may also be known as: None)

Organism

Human

Description

Syntrophins are cytoplasmic peripheral membrane scaffold proteins that are components of the dystrophin-associated protein complex. This gene is a member of the syntrophin gene family and encodes the most common syntrophin isoform found in cardiac tissues. The N-terminal PDZ domain of this syntrophin protein interacts with the C-terminus of the pore-forming alpha subunit (SCN5A) of the cardiac sodium channel Nav1.5. This protein also associates cardiac sodium channels with the nitric oxide synthase-PMCA4b (plasma membrane Ca-ATPase subtype 4b) complex in cardiomyocytes. This gene is a susceptibility locus for Long-QT syndrome (LQT) - an inherited disorder associated with sudden cardiac death from arrhythmia - and sudden infant death syndrome (SIDS). This protein also associates with dystrophin and dystrophin-related proteins at the neuromuscular junction and alters intracellular calcium ion levels in muscle tissue. [provided by RefSeq, Jan 2013]

Orthologs

SymbolSpecies
stn-1 Caenorhabditis elegans
Syn1 Drosophila melanogaster
Snta1 Mus musculus
Snta1 Rattus norvegicus

Links to external resources

Changes associated with this gene

GO Terms

GO IDGO TermGO Category
GO:0006936 muscle contraction biological_process
GO:0007528 neuromuscular junction development biological_process
GO:0005622 intracellular cellular_component
GO:0005737 cytoplasm cellular_component
GO:0005856 cytoskeleton cellular_component
GO:0030054 cell junction cellular_component
GO:0042383 sarcolemma cellular_component
GO:0045211 postsynaptic membrane cellular_component
GO:0003779 actin binding molecular_function
GO:0005515 protein binding molecular_function
GO:0005516 calmodulin binding molecular_function
GO:0030165 PDZ domain binding molecular_function