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DNAAF3

Gene

dynein axonemal assembly factor 3

HGNCHGNC:30492EnsemblENSG00000167646NCBI Gene352909
Locus: gene with protein productLocation: 19q13.42

Also known as

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

Also known asC19orf51 · CILD2 · FLJ40069 · FLJ36139 · pf22 · PCD
View full nomenclature history (10)
Previous symbolsC19orf51, CILD2
Alias symbolsFLJ40069, FLJ36139, pf22, PCD
Previous nameschromosome 19 open reading frame 51, ciliary dyskinesia, primary 2, dynein, axonemal, assembly factor 3, dynein (axonemal) assembly factor 3

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
Rare familial disorder with hypertrophic cardiomyopathy
Heterotaxia

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.

Axonemal dynein assembly factors

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2024-03-20.
Open TargetsGene–disease associations from the Open Targets Platform.