Hu, Mu, RtApplications:
ICC/IF, IHC, IHC-PHost:
Hu, Mu, Rt, Bv, Ca, GP, PmApplications:
Host: Mouse Monoclonal
Applications: WB, ELISA, PA, AP
Applications: RNAi, RNAi SP
Myosin VIIa is a member of the myosin superfamily of actin-based motor proteins. Defects in the myosin VIIa gene are responsible for hearing impairment in shaker-1 (sh1) mice and causes Usher syndrome IB in humans. Usher syndrome associates congenital deafness, vestibular dysfunction, and retinitis pigmentosa and is the most common form of combined deafness and blindness. Structural features of myosin VIIa protein include an ATP binding N-terminal motor domain, a central region which possess five light-chain binding (IQ) motifs, and a C-terminal domain with three myosin tail homology (MyTH4) and talin-like homology regions.
|Product By Gene ID
- deafness, autosomal recessive 2
- deafness, autosomal dominant 11
- myosin VIIA
Research Areas for Myosin VIIa
Find related products by research area and learn more about each of the different research areas below.Cytoskeleton Markers
Bioinformatics Tool for Myosin VIIa
Discover related pathways, diseases and genes to Myosin VIIa. Need help? Read the Bioinformatics Tool Guide
for instructions on using this tool.