Gene: LOXL1

Alternate names for this Gene: LOL|LOXL

Gene Summary: 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.

Gene is located in Chromosome: 15

Location in Chromosome : 15q24.1

Description of this Gene: lysyl oxidase like 1

Type of Gene: protein-coding

Gene: LOXL1-AS1

Alternate names for this Gene: -

Gene Summary:

Gene is located in Chromosome: 15

Location in Chromosome : 15q24.1

Description of this Gene: LOXL1 antisense RNA 1

Type of Gene: ncRNA

rs3825942 in LOXL1;LOXL1-AS1 gene and Exfoliation Syndrome PMID 17690259 2007 Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma.