LOXL1

lysyl oxidase like 1

2 disorders 1 susceptibility 1 modifier 15q24.1 gene with protein product

HGNC:6665 Monarch NCBI Gene 4016 ENSG00000129038 UniProt Q08397 OMIM 153456

Aliases: LOXL, LOL.

Normal function · from ai-gene-review (Q08397, commit 79fe13b38970) · AI-generated, not KB evidence

ai-gene-review has this gene at status DRAFT; the description is shown only once the review is complete. Read the draft upstream.

In the knowledge base · computed from kb/ at build time

Disorders

Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.

Disorder	Relationship	Where the gene appears
Exfoliation Syndrome	susceptibility	mechanism: Dysregulated LOXL1 Expression and Elastic Microfibril Cross-Linking; LOXL1 Susceptibility Genotype
Pelvic Organ Prolapse	modifier

Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.