PRDM12

Gene

PR/SET domain 12

HGNCHGNC:13997 EnsemblENSG00000130711 NCBI Gene59335

Locus: gene with protein productLocation: 9q34.12

Also known as

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

Also known asPFM9

View full nomenclature history (5)

Alias symbolsPFM9

Previous namesPR domain containing 12, PR domain 12

Alias namesPR-domain containing protein 12, PR-domain zinc finger protein 12

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.

Genetic Diseases, Inborn

Hereditary sensory and autonomic neuropathy

Neurodegenerative Diseases

Thrombophilia

Wolff-Parkinson's-White syndrome

Arrhythmogenic Right Ventricular Dysplasia

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.

Zinc fingers C2H2-typePR/SET domain familyPutative lysine methyltransferases

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.