Back to discover

DNAAF5

Gene

dynein axonemal assembly factor 5

HGNCHGNC:26013EnsemblENSG00000164818NCBI Gene54919
Locus: gene with protein productLocation: 7p22.3

Also known as

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

Also known asHEATR2 · FLJ20397 · FLJ31671 · FLJ39381 · FLJ25564 · CILD18
View full nomenclature history (9)
Previous symbolsHEATR2
Alias symbolsFLJ20397, FLJ31671, FLJ39381, FLJ25564, CILD18
Previous namesHEAT repeat containing 2, dynein, axonemal, assembly factor 5, dynein (axonemal) assembly factor 5

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
Ovarian neoplasm
Heart Defects, Congenital
Schizophrenia
Carcinoma, Hepatocellular
Ciliopathy
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus

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.

TOG domain containingAxonemal 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.