CHD3 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human CHD3 wild-type allele is located in the vicinity of 17p13.1 and is approximately 28 kb in length. This allele, which encodes chromodomain-helicase-DNA-binding protein 3, plays a role in mitosis, transcriptional repression and chromatin remodeling. Mutation of the gene is associated with Snijders Blok-Campeau syndrome.

**Synonyms:** - Chromodomain Helicase DNA Binding Protein 3 wt Allele - Mi-2a - Mi2-ALPHA - SNIBCPS - ZFH - Zinc-Finger Helicase (Snf2-Like) Gene