DNAJC5 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human DNAJC5 wild-type allele is located in the vicinity of 20q13.33 and is approximately 41 kb in length. This allele, which encodes DnaJ homolog subfamily C member 5 protein, plays a role in chaperone activity for proteins that are subjected to exocytosis. Mutation of the gene is associated with ceroid neuronal lipofuscinosis 4.

**Synonyms:** - CLN4 - CLN4B - CSP - CSP-Alpha Gene - Ceroid-Lipofuscinosis, Neuronal 4 (Kufs Disease) Gene - Cysteine String Protein Alpha Gene - DNAJC5A - DnaJ (Hsp40) Homolog, Subfamily C, Member 5 Gene - DnaJ Heat Shock Protein Family (Hsp40) Member C5 wt Allele - DnaJ/Hsp40 Homolog, Subfamily C, Member 5 Gene - DnaJ/Hsp40 Homolog, Subfamily C, Member 5, Alpha Gene - FLJ00118 - FLJ13070 - NCL