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LOXL3

Official Full Name
lysyl oxidase like 3
Organism
Homo sapiens
GeneID
84695
Background
This gene encodes a lysyl oxidase, which likely functions as an amine oxidase and plays a role in the formation of crosslinks in collagens and elastin. Deletion of the related gene in mouse causes neonatal mortality with cleft palate, spine deformity, and defects in collagen organization. A mutation in this gene was found in a family with Stickler syndrome. [provided by RefSeq, Sep 2016]
Synonyms
LOXL; MYP28;

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