Entity Details

Primary name RN213_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ63HN8
EntryNameRN213_HUMAN
FullNameE3 ubiquitin-protein ligase RNF213
TaxID9606
Evidenceevidence at protein level
Length5207
SequenceStatuscomplete
DateCreated2007-02-20
DateModified2021-06-02

Ontological Relatives

GenesRNF213

GO terms

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GOName
GO:0000209 protein polyubiquitination
GO:0001525 angiogenesis
GO:0002040 sprouting angiogenesis
GO:0004842 ubiquitin-protein transferase activity
GO:0005730 nucleolus
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0006511 ubiquitin-dependent protein catabolic process
GO:0016020 membrane
GO:0016567 protein ubiquitination
GO:0016887 ATP hydrolysis activity
GO:0033668 negative regulation by symbiont of host apoptotic process
GO:0046872 metal ion binding
GO:0051260 protein homooligomerization
GO:0051865 protein autoubiquitination
GO:2000051 negative regulation of non-canonical Wnt signaling pathway

Subcellular Location

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Subcellular Location
Cytoplasm

Domains

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DomainNameCategoryType
IPR001841 Zinc finger, RING-typeDomainDomain
IPR003593 AAA+ ATPase domainDomainDomain
IPR013083 Zinc finger, RING/FYVE/PHD-typeFamilyHomologous superfamily
IPR018957 Zinc finger, C3HC4 RING-typeDomainDomain
IPR027417 P-loop containing nucleoside triphosphate hydrolaseFamilyHomologous superfamily
IPR031248 E3 ubiquitin-protein ligase RNF213FamilyFamily

Diseases

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Disease IDSourceNameDescription
607151 OMIMMoyamoya disease 2 (MYMY2)A progressive cerebral angiopathy characterized by bilateral intracranial carotid artery stenosis and telangiectatic vessels in the region of the basal ganglia. The abnormal vessels resemble a 'puff of smoke' (moyamoya) on cerebral angiogram. Affected individuals can develop transient ischemic attacks and/or cerebral infarction, and rupture of the collateral vessels can cause intracranial hemorrhage. Hemiplegia of sudden onset and epileptic seizures constitute the prevailing presentation in childhood, while subarachnoid bleeding occurs more frequently in adults. Disease susceptibility is associated with variants affecting the gene represented in this entry.