Entity Details

Primary name RSPH3
Entity type gene
Source Source Link

Details

PrimaryID83861
RefseqGeneNG_051819
SymbolRSPH3
Nameradial spoke head 3
Chromosome6
Location6q25.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-05-06
ModificationDate2021-06-22

Ontological Relatives

UniProt IDsRSPH3_HUMAN

GO terms

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GOName
GO:0005737 cytoplasm
GO:0005856 cytoskeleton
GO:0005929 cilium

Diseases

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Disease IDSourceNameDescription
616481 OMIMCiliary dyskinesia, primary, 32 (CILD32)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. The disease is caused by variants affecting the gene represented in this entry.

Interactions

8 interactions

InteractorPartnerSourcesPublicationsLink
RSPH3HSPB1BioGRID, IntAct25277244 details
RSPH3ROPN1LBioGRID, IntAct25416956 31515488 32296183 details
RSPH3RSPH14BioGRID, IntAct32296183 details
RSPH3FAM124BBioGRID, IntAct32296183 details
RSPH3MLH1BioGRID, IntAct32296183 details
RSPH3PRKAR1ABioGRID, IntAct32296183 details
RSPH3DPY30BioGRID, IntAct32296183 details
RSPH3APPBioGRID21832049 details