VMA21 protein, human

Preferred Label : VMA21 protein, human;

MeSH note : mutations in this protein are associated with X-linked myopathy with excessive autophagy; GenBank AL833596;

Registry Number MeSH : EC 3.6.1.-;

Is substance : O;

Details

Origin ID

C540401;

UMLS CUI

C2715590;

Automatic exact mappings (from CISMeF team)
- Fanconi Anemia Group J Protein [NCIt concept]
- Fanconi Anemia Group M Protein [NCIt concept]
- General Transcription and DNA Repair Factor IIH Helicase Subunit XPD [NCIt concept]
- RNA Helicase [NCIt concept]
- TFIIH Basal Transcription Factor Complex Helicase XPB Subunit [NCIt concept]
MeSH term(s) associated for indexing
- vacuolar Proton-Translocating ATPases [MeSH Descriptor]
Record concept(s)
- VMA21 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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