Entity Details

Primary name ODAD1
Entity type gene
Source Source Link

Details

PrimaryID93233
RefseqGeneNG_033251
SymbolODAD1
Nameouter dynein arm docking complex subunit 1
Chromosome19
Location19q13.33
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-07-12
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsODAD1_HUMAN

GO terms

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GOName
GO:0003341 cilium movement
GO:0005929 cilium
GO:0005930 axoneme
GO:0036157 outer dynein arm
GO:0036158 outer dynein arm assembly

Diseases

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Disease IDSourceNameDescription
615067 OMIMCiliary dyskinesia, primary, 20 (CILD20)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. Unlike other forms of CILD characterized by reduced fertility, patients with CILD20 do not appear to be infertile. The disease is caused by variants affecting the gene represented in this entry.

Interactions

8 interactions

InteractorPartnerSourcesPublicationsLink
ODAD1ODAD3BioGRID, IntAct25416956 details
ODAD1HGSBioGRID, IntAct25416956 26871637 32296183 details
ODAD1KLC1BioGRID, IntAct25416956 details
ODAD1C1orf216BioGRID, IntAct25416956 32296183 details
ODAD1LNX1BioGRID, IntAct25416956 details
ODAD1HAUS1BioGRID, IntAct25416956 details
ODAD1TXN2BioGRID, IntAct25416956 details
ODAD1TPM3BioGRID25416956 details