NIN wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human NIN wild-type allele is located in the vicinity of 14q22.1 and is approximately 111 kb in length. This allele, which encodes ninein protein, plays a role in the modulation of centrosome structure. A chromosomal translocation t(5;14)(q33;q24) of this gene and the PDGFRB is associated with chronic myeloproliferative disorder with eosinophilia.

**Synonyms:** - KIAA1565 - Ninein (GSK3B Interacting Protein) Gene - Ninein Centrosomal Protein Gene - Ninein wt Allele - SCKL7