TMEM70 protein, human

Preferred Label : TMEM70 protein, human;

MeSH note : mutations result in ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy; GenBank BC002748;

Is substance : O;

Details

Origin ID

C533106;

UMLS CUI

C2605689;

MeSH term(s) associated for indexing
- membrane proteins [MeSH Descriptor]
- mitochondrial proteins [MeSH Descriptor]
Record concept(s)
- TMEM70 protein, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Biologically Active Substance [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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