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ANPEP

Gene

alanyl aminopeptidase, membrane

HGNCHGNC:500EnsemblENSG00000166825NCBI Gene290
Locus: gene with protein productLocation: 15q26.1

Also known as

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

Also known asCD13 · PEPN · LAP1 · gp150 · p150 · AP-N · hAPN
View full nomenclature history (12)
Previous symbolsCD13, PEPN
Alias symbolsLAP1, gp150, p150, AP-N, hAPN
Previous namesalanyl (membrane) aminopeptidase
Alias namesaminopeptidase N, aminopeptidase M, microsomal aminopeptidase, membrane alanyl aminopeptidase

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.

Cholelithiasis
Gallstones
Leukemia, Myeloid, Acute
Neoplasms
Carcinoma, Non-Small-Cell Lung
Carcinoma, Hepatocellular
Myelodysplastic syndrome
Alzheimer's Disease

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.

AminopeptidasesCD moleculesM1 metallopeptidases

Provenance

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