AOPEP

Gene

aminopeptidase O (putative)

HGNCHGNC:1361 EnsemblENSG00000148120 NCBI Gene84909

Locus: gene with protein productLocation: 9q22.32

Also known as

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

Also known asC9orf3 · C90RF3 · FLJ14675 · APO · AP-O

View full nomenclature history (7)

Previous symbolsC9orf3

Alias symbolsC90RF3, FLJ14675, APO, AP-O

Previous nameschromosome 9 open reading frame 3

Alias namesaminopeptidase O

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.

Atrial Fibrillation

Polycystic Ovary 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.

M1 metallopeptidasesMicroRNA protein coding host genes

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-11-12.

Open TargetsGene–disease associations from the Open Targets Platform.