CHD7 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human CHD7 wild-type allele is located in the vicinity of 8q12.2 and is approximately 188 kb in length. This allele, which encodes chromodomain-helicase-DNA-binding protein 7, may be involved in both transcriptional regulation and chromatin modification. Mutation of the gene is associated with CHARGE syndrome.

**Synonyms:** - Chromodomain Helicase DNA Binding Protein 7 wt Allele - FLJ20357 - FLJ20361 - IS3 - KIAA1416