Preferred Label : CLRN1 wt Allele;
NCIt synonyms : Clarin 1 wt Allele; USH3A; RP61; Usher Syndrome 3A Gene; USH3;
NCIt 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.;
GenBank Accession Number : AF388366;
Origin ID : C215706;
OMIM relation
- gene_found_in_organism
- gene_plays_role_in_process
