CLRN1 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human CLRN1 wild-type allele is located in the vicinity of 3q25.1 and is approximately 47 kb in length. This allele, which encodes clarin-1 protein, plays a role in sight and hearing. Mutations in the gene are associated with Usher syndrome 3A and retinitis pigmentosa 61.

**Synonyms:** - Clarin 1 wt Allele - RP61 - USH3 - USH3A - Usher Syndrome 3A Gene