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ZMYND8

Gene

zinc finger MYND-type containing 8

HGNCHGNC:9397EnsemblENSG00000101040NCBI Gene23613
Locus: gene with protein productLocation: 20q13.12

Also known as

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

Also known asPRKCBP1 · RACK7 · KIAA1125
View full nomenclature history (5)
Previous symbolsPRKCBP1
Alias symbolsRACK7, KIAA1125
Previous namesprotein kinase C binding protein 1
Alias namesRACK like clone 7

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.

Autoimmune disorder of central nervous system
Neurodevelopmental Disorders
Hypothyroidism
Major depressive disorder
Sleep Initiation and Maintenance Disorders
Coffee consumption
Neurodegenerative Diseases

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-typePHD finger proteinsPWWP domain containingBromodomain containing

Provenance

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