DIS3L2 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human DIS3L2 wild-type allele is located in the vicinity of 2q37.1 and is approximately 383 kb in length. This allele, which encodes DIS3-like exonuclease 2 protein, plays a role in exosome-independent RNA degradation. Mutation of the gene is associated with Perlman syndrome.

**Synonyms:** - DIS3 Like 3'-5' Exoribonuclease 2 wt Allele - DIS3 Mitotic Control Homolog (S. cerevisiae)-Like 2 Gene - DIS3 Mitotic Control Homolog-Like 2 Gene - DIS3 Mitotic Control, S. cerevisiae, Homolog-Like 2 Gene - DIS3-Like 3-Prime-5-Prime Exoribonuclease 2 Gene - FAM6A - FLJ36974 - Family With Sequence Similarity 6, Member A Gene - MGC42174 - PRLMNS - hDIS3L2