phosphatidylethanolamine N-methyltransferase

Preferred Label : phosphatidylethanolamine N-methyltransferase;

Approved symbol HGNC : PEMT;

Alias symbols HGNC : PEMT2; PEMPT;

Chromosome HGNC : 17p11.2;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000133027;

Details

Origin ID

HGNC:8830;

UMLS CUI

C1418456;

Automatic exact mappings (from CISMeF team)
- Phosphatidylethanolamine N-Methyltransferase [NCIt concept]
- Phosphatidylethanolamine n-methyltransferase [OMIM gene]
- phosphatidylethanolamine N-Methyltransferase [MeSH concept]
- phosphatidylethanolamine n-methyltransferase [MeSH Descriptor]
NCIt concept
- PEMT Gene [NCIt concept]
OMIM gene
- Phosphatidylethanolamine n-methyltransferase [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PEMT Gene [NCIt concept]
- Phosphatidylethanolamine n-methyltransferase [OMIM gene]

Keyword's position in hierarchy(ies) :

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