Entity Details

Primary name CCDC39
Entity type gene
Source Source Link

Details

PrimaryID339829
RefseqGeneNG_029581
SymbolCCDC39
Namecoiled-coil domain containing 39
Chromosome3
Location3q26.33
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2003-03-28
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsCCD39_HUMAN

GO terms

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GOName
GO:0001947 heart looping
GO:0003341 cilium movement
GO:0003356 regulation of cilium beat frequency
GO:0005576 extracellular region
GO:0005829 cytosol
GO:0005929 cilium
GO:0005930 axoneme
GO:0007420 brain development
GO:0030317 flagellated sperm motility
GO:0030324 lung development
GO:0035469 determination of pancreatic left/right asymmetry
GO:0036159 inner dynein arm assembly
GO:0044458 motile cilium assembly
GO:0051649 establishment of localization in cell
GO:0060285 cilium-dependent cell motility
GO:0060287 epithelial cilium movement involved in determination of left/right asymmetry
GO:0061512 protein localization to cilium
GO:0061966 establishment of left/right asymmetry
GO:0070286 axonemal dynein complex assembly
GO:0071907 determination of digestive tract left/right asymmetry
GO:0071910 determination of liver left/right asymmetry
GO:0090660 cerebrospinal fluid circulation

Diseases

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Disease IDSourceNameDescription
613807 OMIMCiliary dyskinesia, primary, 14 (CILD14)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. The disease is characterized by primary ciliary dyskinesia with inner dynein arm (IDA) defects and axonemal dizorganisation: defects in CCDC39 and CCDC40 constitute the major cause of this phenotype.

Interactions

4 interactions

InteractorPartnerSourcesPublicationsLink
CCDC39SEM1BioGRID24515614 details
CCDC39CUL3BioGRID, IntAct21145461 details
CCDC39HYOU1BioGRID, IntAct30021884 details
CCDC39RNF123BioGRID29676528 details