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DNAAF2

Gene

dynein axonemal assembly factor 2

HGNCHGNC:20188EnsemblENSG00000165506NCBI Gene55172
Locus: gene with protein productLocation: 14q21.3

Also known as

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

Also known asC14orf104 · FLJ10563 · KTU · pf13 · CILD10
View full nomenclature history (9)
Previous symbolsC14orf104
Alias symbolsFLJ10563, KTU, pf13, CILD10
Previous nameschromosome 14 open reading frame 104, dynein, axonemal, assembly factor 2, dynein (axonemal) assembly factor 2
Alias nameskintoun

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
Neurodegenerative Diseases
Bronchiectasis
Corneal Neovascularization
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus
Autosomal recessive primary microcephaly
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.