Entity Details

Primary name ARMC2
Entity type gene
Source Source Link

Details

PrimaryID84071
RefseqGene
SymbolARMC2
Namearmadillo repeat containing 2
Chromosome6
Location6q21
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-05-27
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsARMC2_HUMAN

GO terms

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GOName
GO:0007288 sperm axoneme assembly
GO:0044782 cilium organization

Diseases

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Disease IDSourceNameDescription
618433 OMIMSpermatogenic failure 38 (SPGF38)An autosomal recessive infertility disorder characterized by asthenoteratozoospermia. Spermatozoa exhibit multiple morphologic abnormalities including short, absent, coiled, bent, or irregular-caliber flagella. The disease is caused by variants affecting the gene represented in this entry.

Interactions

4 interactions

InteractorPartnerSourcesPublicationsLink
ARMC2PYCARDBioGRID, HPIDb24407287 details
ARMC2NDUFA9BioGRID, IntAct30021884 details
ARMC2PTENBioGRID30631154 details
ARMC2HNRNPLBioGRID28611215 details