SEPTIN9 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human SEPT9 wild-type allele is located in the vicinity of 17q25.3 and is approximately 219 kb in length. This allele, which encodes septin-9 protein, is involved in the regulation of microfilament formation. Mutation of the gene is associated with hereditary neuralgic amyotrophy. A chromosomal translocation t(11;17)(q23;q25) of this gene and the MLL gene is associated with acute myeloid leukemia.

**Synonyms:** - AF17q25 - FLJ75490 - KIAA0991 - MLL Septin-Like Fusion Gene - MSF - MSF1 - NAPB - Ov/Br Septin Gene - PNUTL4 - Peanut-Like 4 Gene - SEPT9 - SEPT9 wt Allele - SINT1 - SeptD1 - Septin 9 wt Allele