FTSJ1 protein, human

Preferred Label : FTSJ1 protein, human;

MeSH note : May play a role in the regulation of translation. Mutations cause X-linked mental retardation. RefSeq NM_012280;

MeSH synonym : FtsJ homolog 1 (E. coli) proteins, human;

Registry Number MeSH : EC 2.1.1.-;

Is substance : O;

Details

Origin ID

C490101;

UMLS CUI

C1506484;

Automatic exact mappings (from CISMeF team)
- Methyltransferase [NCIt concept]
MeSH term(s) associated for indexing
- methyltransferases [MeSH Descriptor]
- nuclear proteins [MeSH Descriptor]
Record concept(s)
- FTSJ1 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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