MYO6 Back

myosin VI

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NCBI Description of MYO6

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.

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Figure notes

• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


MYO6 is highly significantly mutated in
MYO6 is significantly mutated in
MYO6 is near significance in

Click on a tumor type to see its full list of significant genes.

Data details

Mutation list for MYO6