Myosin VIIa Products

Myosin VIIa Antibody
Myosin VIIa Antibody
Species: Hu, Mu, Rt
Applications: WB
Host: Rabbit Polyclonal
Myosin VIIa Antibody (1D3)
Myosin VIIa Antibody (1D3)
Species: Hu
Applications: ELISA, S-ELISA
Host: Mouse Monoclonal
Recombinant Human Myosin VIIa ...
Recombinant Human Myosin VIIa GST ...
Species: Hu
Applications: WB, ELISA, PA, PAGE, AP


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.


Uniprot Human
Product By Gene ID 4647
Alternate Names
  • deafness, autosomal dominant 11
  • deafness, autosomal recessive 2
  • DFNA11
  • DFNB2
  • myosin VIIA
  • myosin-VIIa
  • MYU7A
  • USH1Bsevere))

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.
Vizit™, under license from BioVista Inc.