" /> CLRN1 wt Allele - CISMeF





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;

Details


Keyword's position in hierarchy(ies) : arborescence

You can consult :


Nous contacter.
09/09/2025


[Home] [Top]

© Rouen University Hospital. Any partial or total use of this material must mention the source.