LOXL1 Chromosome 15

Lysyl oxidase like 1
3 variants 3 Health Risk

Upload your DNA to see your personal genotypes for variants in LOXL1.

What This Gene Does
This gene encodes a member of the lysyl oxidase family of proteins. The prototypic member of the family is essential to the biogenesis of connective tissue, encoding an extracellular copper-dependent amine oxidase that catalyzes the first step in the formation of crosslinks in collagen and elastin. The encoded preproprotein is proteolytically processed to generate the mature enzyme. A highly conserved amino acid sequence at the C-terminus end appears to be sufficient for amine oxidase activity, suggesting that each family member may retain this function. The N-terminus is poorly conserved and may impart additional roles in developmental regulation, senescence, tumor suppression, cell growth control, and chemotaxis to each member of the family. Mutations in this gene are associated with exfoliation syndrome. [provided by RefSeq, Jan 2016]
Associated Conditions (3)
Exfoliation syndrome
susceptibility to
LOXL1-related disorder
Key Variants
All Variants (3)
RSID Category Clinical Significance Conditions
RS3825942 Health Risk Benign; risk factor Exfoliation syndrome, susceptibility to, LOXL1-related disorder
RS1048661 Health Risk risk factor Exfoliation syndrome, susceptibility to, Exfoliation syndrome
RS2165241 Health Risk risk factor Exfoliation syndrome, susceptibility to, Exfoliation syndrome
Sign Up to Analyze Your DNA Log In