LOXL1 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human LOXL1 wild-type allele is located in the vicinity of 15q24.1 and is approximately 26 kb in length. This allele, which encodes lysyl oxidase homolog 1 protein, is involved in elastin fibril formation. Mutation of the gene is associated with exfoliation syndrome.

**Synonyms:** - LOL - LOXL - Lysyl Oxidase Like 1 wt Allele - Lysyl Oxidase-Like 1 Gene