UNC119 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human UNC119 wild-type allele is located in the vicinity of 17q11.2 and is approximately 6 kb in length. This allele, which encodes protein unc-119 homolog A, is involved in the modulation of subcellular protein localization. Mutation of the gene is associated with cone-rod dystrophy.

**Synonyms:** - HRG4 - POC7 - POC7A - RG4 - Unc-119 Homolog (C. elegans) wt Allele