Your search for "myo7a" returned 447 TaqMan® SNP Genotyping Assays
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. [provided by RefSeq, Jul 2008]
DFNA11, DFNB2, HDB, MYO7, MYO7A, MYOVIIA, MYU7A, NMF371, NSRD2, POLKA, SH-1, SH1, USH1B
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