Back to discover

DNAH1

Gene

dynein axonemal heavy chain 1

HGNCHGNC:2940EnsemblENSG00000114841NCBI Gene25981
Locus: gene with protein productLocation: 3p21.1

Also known as

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

Also known asXLHSRF-1 · DNAHC1 · HDHC7 · HL-11 · HL11
View full nomenclature history (6)
Alias symbolsXLHSRF-1, DNAHC1, HDHC7, HL-11, HL11
Previous namesdynein, axonemal, heavy polypeptide 1

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
Non-syndromic male infertility due to sperm motility disorder
Neurodegenerative Diseases
Osteoarthritis

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.

Dyneins, axonemal inner arm I1/f complex subunits

Provenance

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