# Dynein axonemal heavy chain 5

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21114318](https://www.wikidata.org/wiki/Q21114318)  
**Source**: https://4ort.xyz/entity/dynein-axonemal-heavy-chain-5-q21114318


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q8TE73)
3. Q20641742
4. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73)
5. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73)
6. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73)
7. [Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73)
8. [Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate gene](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73)
9. [High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxy](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73)
10. [DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73)
11. [Combined exome and whole-genome sequencing identifies mutations in ARMC4 as a cause of primary ciliary dyskinesia with defects in the outer dynein arm.](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73)
12. [Axonemal localization of the dynein component DNAH5 is not altered in secondary ciliary dyskinesia](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73)
13. [DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73)
14. [Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73)
15. [ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73)
16. [Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory Complex](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73)
17. [DNAH11 Localization in the Proximal Region of Respiratory Cilia Defines Distinct Outer Dynein Arm Complexes](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73)
18. [DNAH11 Localization in the Proximal Region of Respiratory Cilia Defines Distinct Outer Dynein Arm Complexes](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73)
19. [Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73)
20. [DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73)
21. [Axonemal localization of the dynein component DNAH5 is not altered in secondary ciliary dyskinesia](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73)
22. [Combined exome and whole-genome sequencing identifies mutations in ARMC4 as a cause of primary ciliary dyskinesia with defects in the outer dynein arm.](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73)
23. [ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73)
24. [Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory Complex](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73)
25. [Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate gene](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73)
26. [Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73)
27. [High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxy](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73)
28. [DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73)
29. [Mutations in dynein genes in patients affected by isolated non-syndromic asthenozoospermia](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73)
30. [Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73)
31. [Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesia](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73)
32. [Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73)
33. [Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesia](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73)
34. Ensembl Release 99