RNF168 protein, human

Preferred Label : RNF168 protein, human;

MeSH note : mutated in RIDDLE syndrome; GenBank BC033791;

MeSH synonym : ring finger protein 168, human;

Registry Number MeSH : EC 6.3.2.19; EC 2.3.2.27;

Is substance : O;

UNII : EC 2.3.2.27;

Details

Origin ID

C535210;

UMLS CUI

C2713934;

Automatic exact mappings (from CISMeF team)
- UBE3A wt Allele [NCIt concept]
- Ubiquitin-Conjugating Enzyme E2 C [NCIt concept]
- Ubiquitin-Conjugating Enzyme E2 D2 [NCIt concept]
- Ubiquitin-Protein Ligase E3A [NCIt concept]
MeSH indexing information
- zinc fingers [MeSH Descriptor]
MeSH term(s) associated for indexing
- ubiquitin-protein ligases [MeSH Descriptor]
Record concept(s)
- RNF168 protein, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Enzyme [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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