Entity Details

Primary name CCDC65
Entity type gene
Source Source Link

Details

PrimaryID85478
RefseqGeneNG_033837
SymbolCCDC65
Namecoiled-coil domain containing 65
Chromosome12
Location12q13.12
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-06-19
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsDRC2_HUMAN

GO terms

Show/Hide Table
GOName
GO:0003352 regulation of cilium movement
GO:0005858 axonemal dynein complex
GO:0005930 axoneme
GO:0031514 motile cilium
GO:0036064 ciliary basal body
GO:0060271 cilium assembly
GO:0060285 cilium-dependent cell motility
GO:0070286 axonemal dynein complex assembly

Diseases

Show/Hide Table
Disease IDSourceNameDescription
615504 OMIMCiliary dyskinesia, primary, 27 (CILD27)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. Patients may 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. Cilia ultrastructure show normal outer dynein arms, radial spokes and central pairs, but a reduction in inner dynein arms and nexin links. In 5%-15% of cilia, microtubules are disorganized. Nasal epithelial cilia reveal a stiff, dyskinetic cilia waveform.

Interactions

8 interactions

InteractorPartnerSourcesPublicationsLink
CCDC65NEURL4BioGRID, IntAct28514442 details
CCDC65HERC1BioGRID, IntAct28514442 details
CCDC65PCM1BioGRID, IntAct28514442 details
CCDC65HERC2BioGRID, IntAct28514442 details
CCDC65MYCBP2BioGRID, IntAct28514442 details
CCDC65MRPL12BioGRID, IntAct30021884 details
CCDC65NCLBioGRID, IntAct30021884 details
CCDC65SLTMBioGRID, IntAct30021884 details