" /> MYO7A wt Allele - CISMeF





Preferred Label : MYO7A wt Allele;

NCIt synonyms : MYOVIIA; MYU7A; DFNA11; Myosin VIIA wt Allele; USH1B; NSRD2; DFNB2; Myosin VIIA (Usher Syndrome 1B (Autosomal Recessive, Severe)) Gene; Myosin, Unconventional Family VII, Member A Gene;

NCIt definition : Human MYO7A wild-type allele is located in the vicinity of 11q13.5 and is approximately 87 kb in length. This allele, which encodes unconventional myosin-VIIa protein, plays a role in intracellular transport affecting sight and hearing. Mutations in the gene are associated with autosomal dominant deafness 11, autosomal recessive deafness 2 and Usher syndrome type 1B.;

GenBank Accession Number : U39226;

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28/07/2025


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