USH1G wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human USH1G wild-type allele is located in the vicinity of 17q25.1 and is approximately 7 kb in length. This allele, which encodes Usher syndrome type-1G protein, is involved in the development of both the retina and cochlear hair cells. Mutation of the gene is associated with Usher syndrome 1G.

**Synonyms:** - ANKS4A - FLJ33924 - SANS - Sans - Usher Syndrome 1G (Autosomal Recessive) wt Allele