A synthesized peptide derived from human MYO5A, corresponding to a region within C-terminal amino acids.
A synthesized peptide derived from human MYO5C, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human MYO6, corresponding to a region within N-terminal amino acids.
A synthesized peptide derived from human MYO7A, corresponding to a region within the internal amino acids.
This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants.
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