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ZMYND10

Gene

zinc finger MYND-type containing 10

HGNCHGNC:19412EnsemblENSG00000004838NCBI Gene51364
Locus: gene with protein productLocation: 3p21.31

Also known as

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

Also known asCILD22 · DNAAF7 · BLU
View full nomenclature history (6)
Alias symbolsCILD22, DNAAF7, BLU
Alias namesdynein axonemal assembly factor 7, Ciliary dyskinesia, primary, 22, tumor suppressor BLU

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.

Kartagener Syndrome
Genetic Diseases, Inborn
Nasopharyngeal Carcinoma
Neoplasms
Schizophrenia

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-typeAxonemal dynein assembly factors

Provenance

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