Entity Details

Primary name ZMY10_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionO75800
EntryNameZMY10_HUMAN
FullNameZinc finger MYND domain-containing protein 10
TaxID9606
Evidenceevidence at protein level
Length440
SequenceStatuscomplete
DateCreated2002-11-08
DateModified2021-06-02

Ontological Relatives

GenesZMYND10

GO terms

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GOName
GO:0003341 cilium movement
GO:0005737 cytoplasm
GO:0016324 apical plasma membrane
GO:0034451 centriolar satellite
GO:0036158 outer dynein arm assembly
GO:0036159 inner dynein arm assembly
GO:0044183 protein folding chaperone
GO:0044458 motile cilium assembly
GO:0046872 metal ion binding
GO:0060090 molecular adaptor activity
GO:0061512 protein localization to cilium
GO:0120293 dynein axonemal particle
GO:1905505 positive regulation of motile cilium assembly

Subcellular Location

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Subcellular Location
Apical cell membrane
Cytoplasm
Dynein axonemal particle

Domains

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DomainNameCategoryType
IPR002893 Zinc finger, MYND-typeDomainDomain
IPR017333 Uncharacterised conserved protein UCP037948, zinc finger MYND-typeFamilyFamily

Diseases

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Disease IDSourceNameDescription
615444 OMIMCiliary dyskinesia, primary, 22 (CILD22)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.