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XPNPEP1

Gene

X-prolyl aminopeptidase 1

HGNCHGNC:12822EnsemblENSG00000108039NCBI Gene7511
Locus: gene with protein productLocation: 10q25.1

Also known as

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

Also known asXPNPEP · XPNPEPL1 · XPNPEPL
View full nomenclature history (6)
Previous symbolsXPNPEP, XPNPEPL1, XPNPEPL
Previous namesX-prolyl aminopeptidase (aminopeptidase P)-like, X-prolyl aminopeptidase (aminopeptidase P) 1, soluble
Alias namesXaa-Pro aminopeptidase 1

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.

Bipolar Disorder
bipolar I disorder
Pre-Eclampsia
Alcohol drinking
Urolithiasis
Escherichia coli Infections
Leukemia, Myeloid, Acute

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.

AminopeptidasesM24 metallopeptidase family

Provenance

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