SNTA1 Rabbit Polyclonal Antibody, 50ul Immuno Plates The encoded protein acts as

The encoded protein acts as an intermediary factor for the ligand-dependent activity of these nuclear receptors

Mutations in this gene cause nocturnal frontal lobe epilepsy type 1

Mutations in this gene cause atrial septal defect with atrioventricular conduction defect

and cleft lip/palate syndrome 3 (EEC3)| split-hand/foot malformation 4 (SHFM4)| ankyloblepharon-ectodermal defects-cleft lip/palate| ADULT syndrome (acro-dermato-ungual-lacrim

The phosphorylated form of this protein forms a complex with SMAD4

SNTA1 Rabbit Polyclonal Antibody, 50ul Immuno Plates The encoded protein acts asSyntrophins 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