Entity Details

Primary name ZMYND10
Entity type gene
Source Source Link

Details

PrimaryID51364
RefseqGeneNG_023270
SymbolZMYND10
Namezinc finger MYND-type containing 10
Chromosome3
Location3p21.31
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-05-11
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsZMY10_HUMAN

GO terms

Show/Hide Table
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

Diseases

Show/Hide Table
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.