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ZMYND12

Gene

zinc finger MYND-type containing 12

HGNCHGNC:21192EnsemblENSG00000066185NCBI Gene84217
Locus: gene with protein productLocation: 1p34.2

Also known as

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

Also known asDKFZp434N2435
View full nomenclature history (1)
Alias symbolsDKFZp434N2435

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.

Neurodegenerative Diseases
Placental abruption
Coronary Artery Disease
Headache Disorders
Autosomal dominant macrothrombocytopenia

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 MYND-type

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.
Open TargetsGene–disease associations from the Open Targets Platform.