Entity Details

Primary name CC103_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8IW40
EntryNameCC103_HUMAN
FullNameCoiled-coil domain-containing protein 103
TaxID9606
Evidenceevidence at protein level
Length242
SequenceStatuscomplete
DateCreated2006-12-12
DateModified2021-06-02

Ontological Relatives

GenesCCDC103

GO terms

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GOName
GO:0001947 heart looping
GO:0003341 cilium movement
GO:0003351 epithelial cilium movement involved in extracellular fluid movement
GO:0005576 extracellular region
GO:0005737 cytoplasm
GO:0005930 axoneme
GO:0007368 determination of left/right symmetry
GO:0031514 motile cilium
GO:0036157 outer dynein arm
GO:0036158 outer dynein arm assembly
GO:0036159 inner dynein arm assembly
GO:0042803 protein homodimerization activity
GO:0060287 epithelial cilium movement involved in determination of left/right asymmetry
GO:0070286 axonemal dynein complex assembly
GO:0071907 determination of digestive tract left/right asymmetry

Subcellular Location

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Subcellular Location
Cell projection
Cytoplasm

Domains

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DomainNameCategoryType
IPR025986 RNA-polymerase II-associated protein 3-like, C-terminal domainDomainDomain
IPR031733 Dynein attachment factor, N-terminalDomainDomain
IPR042422 Coiled-coil domain-containing protein 103FamilyFamily

Diseases

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Disease IDSourceNameDescription
614679 OMIMCiliary dyskinesia, primary, 17 (CILD17)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.