DNAH5
HGNC:2950 · SaudiVarKB evidence summary derived from retained literature mentions.
4Gene mentions
4Publications
0Linked variants
2Associated phenotypes
Associated phenotypes
Co-mentioned in DNAH5 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| primary ciliary dyskinesia | — | 3 | 3 |
| asthma | — | 1 | 1 |
Linked variants
Variants normalized to DNAH5| Variant | HGVS / rsID | Articles | Mentions |
|---|
No normalized variants are linked to this gene.
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|---|---|---|
| Not specified | — | 25 | 1 |
| Saudi Arabia | — | 2,023 | 1 |
| Not specified | — | 19 | 1 |
Supporting publications
4 records- 2025Genetic Analysis of Heterotaxy in a Consanguineous Cohort.Clinical geneticsPubMed ↗
- 2024Cystic Lung Changes, Bronchiectasis, and a Heterozygous-Primary Ciliary Dyskinesia-Associated Variant in the DNAH5 Gene: A Diagnostic Challenge.The American journal of case reportsPubMed ↗
- 2023Clinical and Genetic Characterization of Patients with Primary Ciliary Dyskinesia in Southwest Saudi Arabia: A Cross Sectional Study.Children (Basel, Switzerland)PubMed ↗
- 2022Vestibular and Balance Impairment Is Common in Children With Primary Ciliary Dyskinesia.Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and NeurotologyPubMed ↗