Entity Details

Primary name DAAF6_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9NQM4
EntryNameDAAF6_HUMAN
FullNameDynein axonemal assembly factor 6
TaxID9606
Evidenceevidence at protein level
Length214
SequenceStatuscomplete
DateCreated2005-07-19
DateModified2021-06-02

Ontological Relatives

GenesDNAAF6

GO terms

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GOName
GO:0003341 cilium movement
GO:0005737 cytoplasm
GO:0005802 trans-Golgi network
GO:0030317 flagellated sperm motility
GO:0036158 outer dynein arm assembly
GO:0036159 inner dynein arm assembly
GO:0045505 dynein intermediate chain binding
GO:0051087 chaperone binding
GO:0070286 axonemal dynein complex assembly

Subcellular Location

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Subcellular Location
Cytoplasm
Golgi apparatus

Domains

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DomainNameCategoryType
IPR026697 Dynein axonemal assembly factor 6FamilyFamily
IPR041442 PIH1D1/2/3, CS-like domainDomainDomain

Diseases

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Disease IDSourceNameDescription
300991 OMIMCiliary dyskinesia, primary, 36, X-linked (CILD36)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. CILD36 inheritance is X-linked recessive. About half of CILD36 patients have laterality defects due to ciliary dysfunction at the embryonic node. The disease is caused by variants affecting the gene represented in this entry.