Entity Details

Primary name DNAAF1
Entity type gene
Source Source Link

Details

PrimaryID123872
RefseqGeneNG_021174
SymbolDNAAF1
Namedynein axonemal assembly factor 1
Chromosome16
Location16q24.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-11-29
ModificationDate2021-06-19

Ontological Relatives

UniProt IDsDAAF1_HUMAN

GO terms

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GOName
GO:0000922 spindle pole
GO:0001947 heart looping
GO:0003341 cilium movement
GO:0003356 regulation of cilium beat frequency
GO:0005576 extracellular region
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0005930 axoneme
GO:0016607 nuclear speck
GO:0030324 lung development
GO:0035469 determination of pancreatic left/right asymmetry
GO:0036158 outer dynein arm assembly
GO:0036159 inner dynein arm assembly
GO:0044458 motile cilium assembly
GO:0060271 cilium assembly
GO:0060287 epithelial cilium movement involved in determination of left/right asymmetry
GO:0060972 left/right pattern formation
GO:0070286 axonemal dynein complex assembly
GO:0070840 dynein complex binding
GO:0071907 determination of digestive tract left/right asymmetry
GO:0071910 determination of liver left/right asymmetry

Diseases

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Disease IDSourceNameDescription
613193 OMIMCiliary dyskinesia, primary, 13 (CILD13)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. At ultrastructural level, CILD13 is characterized by a marked reduction or absence of both dynein arms from the patients cilia. The disease is caused by variants affecting the gene represented in this entry.

Interactions

7 interactions