Entity Details

Primary name ODAD3_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionA5D8V7
EntryNameODAD3_HUMAN
FullNameOuter dynein arm-docking complex subunit 3
TaxID9606
Evidenceevidence at protein level
Length595
SequenceStatuscomplete
DateCreated2008-02-26
DateModified2021-06-02

Ontological Relatives

GenesODAD3

GO terms

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GOName
GO:0003341 cilium movement
GO:0005814 centriole
GO:0005929 cilium
GO:0005930 axoneme
GO:0007368 determination of left/right symmetry
GO:0036064 ciliary basal body
GO:0036158 outer dynein arm assembly
GO:1902017 regulation of cilium assembly

Subcellular Location

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Subcellular Location
Cell projection
Cytoplasm

Domains

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DomainNameCategoryType
IPR033192 Outer dynein arm-docking complex subunit 3FamilyFamily

Diseases

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Disease IDSourceNameDescription
616037 OMIMCiliary dyskinesia, primary, 30 (CILD30)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.