Entity Details

Primary name DNAAF3
Entity type gene
Source Source Link

Details

PrimaryID352909
RefseqGeneNG_032759
SymbolDNAAF3
Namedynein axonemal assembly factor 3
Chromosome19
Location19q13.42
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2003-04-22
ModificationDate2021-06-19

Ontological Relatives

UniProt IDsDAAF3_HUMAN

GO terms

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GOName
GO:0044458 motile cilium assembly
GO:0070286 axonemal dynein complex assembly
GO:0120293 dynein axonemal particle

Diseases

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Disease IDSourceNameDescription
606763 OMIMCiliary dyskinesia, primary, 2 (CILD2)A disorder characterized by abnormalities of motile cilia. Respiratory infections leading to chronic inflammation and bronchiectasis are recurrent, due to defects in the respiratory cilia; reduced fertility is often observed in male patients due to abnormalities of sperm tails. Half of the patients exhibit randomization of left-right body asymmetry and situs inversus, due to dysfunction of monocilia at the embryonic node. Primary ciliary dyskinesia associated with situs inversus is referred to as Kartagener syndrome. The disease is caused by variants affecting the gene represented in this entry.

Interactions

5 interactions

InteractorPartnerSourcesPublicationsLink
DNAAF3SP6BioGRID, IntAct26186194 28514442 details
DNAAF3RANBP2BioGRID, IntAct30021884 details
DNAAF3XPO1BioGRID26673895 details
DNAAF3TMEM259BioGRID32738194 details
DNAAF3SYVN1BioGRID32738194 details