Back to discover

LRAT

Gene

lecithin retinol acyltransferase

HGNCHGNC:6685EnsemblENSG00000121207NCBI Gene9227
Locus: gene with protein productLocation: 4q32.1

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asLCA14
View full nomenclature history (3)
Alias symbolsLCA14
Previous nameslecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase)
Alias namesphosphatidylcholine--retinol O-acyltransferase

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Leber Congenital Amaurosis
Retinitis Pigmentosa
Neurodegenerative Diseases

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

LRAT domain containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.