LACC1

Gene

laccase domain multifunctional purine nucleosidase 1

HGNCHGNC:26789 EnsemblENSG00000179630 NCBI Gene144811

Locus: gene with protein productLocation: 13q14.11

Also known as

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

Also known asC13orf31 · FLJ38725 · FAMIN

View full nomenclature history (8)

Previous symbolsC13orf31

Alias symbolsFLJ38725, FAMIN

Previous nameslaccase (multicopper oxidoreductase) domain containing 1, laccase domain containing 1, chromosome 13 open reading frame 31

Alias namesfatty acid metabolism–immunity nexus, isocyanic acid synthase

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.

Cholangitis, Sclerosing

Spondylitis, Ankylosing

Behcet's Syndrome

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.

Carbon-nitrogen lyases

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2026-06-18.

Open TargetsGene–disease associations from the Open Targets Platform.