Entity Details

Primary name ARMC2_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8NEN0
EntryNameARMC2_HUMAN
FullNameArmadillo repeat-containing protein 2
TaxID9606
Evidenceevidence at transcript level
Length867
SequenceStatuscomplete
DateCreated2007-04-17
DateModified2021-06-02

Ontological Relatives

GenesARMC2

GO terms

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

Subcellular Location

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Domains

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DomainNameCategoryType
IPR000225 ArmadilloRepeatRepeat
IPR011989 Armadillo-like helicalFamilyHomologous superfamily
IPR016024 Armadillo-type foldFamilyHomologous superfamily
IPR038905 Armadillo repeat-containing protein 2FamilyFamily

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

0 interactions

InteractorPartnerSourcesPublicationsLink