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PRDM15

Gene

PR/SET domain 15

HGNCHGNC:13999EnsemblENSG00000141956NCBI Gene63977
Locus: gene with protein productLocation: 21q22.3

Also known as

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

Also known asZNF298 · C21orf83
View full nomenclature history (5)
Previous symbolsZNF298, C21orf83
Previous nameschromosome 21 open reading frame 83, PR domain containing 15, PR domain 15

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.

Nephrotic Syndrome
Dementia
Parkinson's Disease
Child Development Disorders, Pervasive
Diabetes Mellitus, Type 2
Sleep Initiation and Maintenance Disorders
Mycoses
Cholangiocarcinoma
Lymphoma

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.