MYO3A Polyclonal Antibody

catalytic activity:ATP + a protein = ADP + a phosphoprotein.,disease:Defects in MYO3A are the cause of non-syndromic sensorineural deafness autosomal recessive type 30 (DFNB30) [MIM:607101]. DFNB30 is a form of sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information.,function:Probable actin-based motor with a protein kinase activity. Probably plays a role in vision and hearing.,similarity:Contains 1 myosin head-like domain.,similarity:Contains 1 protein kinase domain.,similarity:Contains 3 IQ domains.,similarity:In the N-terminal section; belongs to the protein kinase superfamily. STE Ser/Thr protein kinase family.,tissue specificity:Strongest expression in retina, retinal pigment epithelial cells, cochlea and pancreas.,