Automated description from the Alliance of Genome Resources
Exhibits actin filament binding activity; microfilament motor activity; and protein serine/threonine kinase activity. Involved in several processes, including cellular protein modification process; inner ear morphogenesis; and positive regulation of filopodium assembly. Localizes to the filopodium tip; photoreceptor inner segment; and stereocilium tip. Used to study autosomal recessive nonsyndromic deafness 30. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 30. Orthologous to human MYO3A (myosin IIIA).