B9D2 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human B9D2 wild-type allele is located in the vicinity of 19q13.2 and is approximately 10 kb in length. This allele, which encodes B9 domain-containing protein 2, is involved in ciliogenesis. Mutation of the gene is associated with Meckel syndrome 10.

**Synonyms:** - B9 Protein Domain 2 wt Allele - ICIS-1 - MGC4093 - MKS10 - MKSR2 - Stumpy, Mouse, Homolog of Gene