Entity Details

Primary name ODAD4_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ96NG3
EntryNameODAD4_HUMAN
FullNameOuter dynein arm-docking complex subunit 4
TaxID9606
Evidenceevidence at protein level
Length672
SequenceStatuscomplete
DateCreated2007-04-17
DateModified2021-06-02

Ontological Relatives

GenesODAD4

GO terms

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GOName
GO:0003341 cilium movement
GO:0005576 extracellular region
GO:0005737 cytoplasm
GO:0005930 axoneme
GO:0007420 brain development
GO:0007507 heart development
GO:0030324 lung development
GO:0036158 outer dynein arm assembly
GO:0060287 epithelial cilium movement involved in determination of left/right asymmetry
GO:0090660 cerebrospinal fluid circulation
GO:0097729 9+2 motile cilium
GO:0120197 mucociliary clearance
GO:0120228 outer dynein arm docking complex
GO:0120229 protein localization to motile cilium

Subcellular Location

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Subcellular Location
Cytoplasm

Domains

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DomainNameCategoryType
IPR011990 Tetratricopeptide-like helical domain superfamilyFamilyHomologous superfamily
IPR019734 Tetratricopeptide repeatRepeatRepeat
IPR040111 Outer dynein arm-docking complex subunit 4FamilyFamily
IPR041617 MalT-like TPR regionDomainDomain

Diseases

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Disease IDSourceNameDescription
617092 OMIMCiliary dyskinesia, primary, 35 (CILD35)A form of primary ciliary dyskinesia, 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. Some patients exhibit randomization of left-right body asymmetry and situs inversus. Primary ciliary dyskinesia associated with situs inversus is referred to as Kartagener syndrome. CILD35 inheritance is autosomal recessive. The disease is caused by variants affecting the gene represented in this entry.