Tel: 1-631-626-9181 (USA)   44-207-097-1828 (Europe)


Official Full Name
myosin VI
This gene encodes a protein involved intracellular vesicle and organelle transport, especially in the hair cell of the inner ear. Mutations in this gene have been found in patients with non-syndromic autosomal dominant and recessive hearing loss.
MYO6; myosin VI; deafness, autosomal recessive 37 , DFNA22, DFNB37; myosin-VI; KIAA0389; Deafness autosomal recessive 37; DFNA 22; DFNA22; DFNB 37; DFNB37; MYO 6; MYO6_HUMAN; Myosin 6; Myosin6; MyosinVI; Unconventional myosin-6; CMY6; unconventional myosin-VI

Interested in learning more?

Contact us today for a free consultation with the scientific team and discover how Creative Biogene can be a valuable resource and partner for your organization.

Request a quote today!