# Dynein axonemal intermediate chain 1

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21110042](https://www.wikidata.org/wiki/Q21110042)  
**Source**: https://4ort.xyz/entity/dynein-axonemal-intermediate-chain-1-q21110042


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q9UI46)
3. Q20641742
4. [Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia.](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9UI46)
5. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9UI46)
6. [Molecular defects in the motor adaptor BICD2 cause proximal spinal muscular atrophy with autosomal-dominant inheritance](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9UI46)
7. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9UI46)
8. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9UI46&geneProductId=UniProtKB:Q9UI46)
9. [Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome)](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9UI46&geneProductId=UniProtKB:Q9UI46)
10. [Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutation](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9UI46&geneProductId=UniProtKB:Q9UI46)
11. [Mutations in GAS8, a Gene Encoding a Nexin-Dynein Regulatory Complex Subunit, Cause Primary Ciliary Dyskinesia with Axonemal Disorganization.](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9UI46)
12. [Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome)](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9UI46)
13. [Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutation](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9UI46)
14. [Mutations in dynein genes in patients affected by isolated non-syndromic asthenozoospermia](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9UI46)
15. [High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxy](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9UI46)
16. [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:Q9UI46)
17. [DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9UI46&geneProductId=UniProtKB:Q9UI46)
18. [Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9UI46&geneProductId=UniProtKB:Q9UI46)
19. [DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9UI46)
20. [Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9UI46)
21. Ensembl Release 99