RecName: Full=E3 ubiquitin-protein ligase RNF216; AltName: Full=RING f - Protein

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Ring finger protein 216 loss-of-function induces white matter hyperintensities by inhibiting oligodendroglia proliferation. [Cell Biochem Funct. 2024]
Ring finger protein 216 loss-of-function induces white matter hyperintensities by inhibiting oligodendroglia proliferation.
Xu W, Chen K, Yuan Y, Guo M, Dong Q, Cui M. Cell Biochem Funct. 2024 Jun; 42(4):e4057.
Clinical and genetic spectrum of RNF216-related disorder: a new case and literature review. [J Med Genet. 2024]
Clinical and genetic spectrum of RNF216-related disorder: a new case and literature review.
Wu C, Zhang Z. J Med Genet. 2024 Apr 19; 61(5):430-434. Epub 2024 Apr 19.
Whole-Exome Sequencing Identified a Novel Mutation in RNF216 in a Family with Gordon Holmes Syndrome. [J Mol Neurosci. 2022]
Whole-Exome Sequencing Identified a Novel Mutation in RNF216 in a Family with Gordon Holmes Syndrome.
Chen KL, Wang H, Zhao GX, Wei L, Huang YY, Chen SD, Sun J, Dong Q, Cui M, Yu JT. J Mol Neurosci. 2022 Apr; 72(4):691-694. Epub 2022 Jan 28.

RefSeq genomic sequence
See the genomic reference sequence for the RNF216 gene (NG_029374.2).
RefSeq protein isoforms
See 18 reference sequence protein isoforms for the RNF216 gene.

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Q9NWF9 [Domain Mapping of Disease Mut...]
Q9NWF9
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
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Reactome [Reactome]
Reactome
reagents [ExactAntigen/Labome]
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RecName: Full=E3 ubiquitin-protein ligase RNF216; AltName: Full=RING finger prot...
RecName: Full=E3 ubiquitin-protein ligase RNF216; AltName: Full=RING finger protein 216; AltName: Full=RING-type E3 ubiquitin transferase RNF216; AltName: Full=Triad domain-containing protein 3; AltName: Full=Ubiquitin-conjugating enzyme 7-interacting protein 1; AltName: Full=Zinc finger protein inhibiting NF-kappa-B
gi|57015417|sp|Q9NWF9.3|RN216_HUMAN

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