UTRO Rabbit Polyclonal Antibody

This gene shares both structural and functional similarities with the dystrophin gene. It contains an actin-binding N-terminus, a triple coiled-coil repeat central region, and a C-terminus that consists of protein-protein interaction motifs which interact with dystroglycan protein components. The protein encoded by this gene is located at the neuromuscular synapse and myotendinous junctions, where it participates in post-synaptic membrane maintenance and acetylcholine receptor clustering. Mouse studies suggest that this gene may serve as a functional substitute for the dystrophin gene and therefore, may serve as a potential therapeutic alternative to muscular dystrophy which is caused by mutations in the dystrophin gene. Alternative splicing of the utrophin gene has been described; however, the full-length nature of these variants has not yet been determined. [provided by RefSeq, Jul 2008], function:May play a role in anchoring the cytoskeleton to the plasma membrane., online information:Utrophin entry, similarity:Contains 1 WW domain., similarity:Contains 1 ZZ-type zinc finger., similarity:Contains 2 CH (calponin-homology) domains., similarity:Contains 20 spectrin repeats., subcellular location:Neuromuscular junction., subunit:Interacts with the syntrophins SNTA1; SNTB1 and SNTB2. Interacts with SYNM., tissue specificity:Muscle.