Serine hydroxymethyltransferase, mitochondrial

Preferred Label : Serine hydroxymethyltransferase, mitochondrial;

Symbol : SHMT2;

CISMeF acronym : SHMT2;

Type : Gene;

Alternative titles and symbols : Glycine auxotroph a, human complement for hamster; GLY A ;

Ensembl ID : ENSG00000182199;

Prefixed ID : *138450;

Details

Origin ID

138450;

UMLS CUI

C1420040;

Automatic exact mappings (from CISMeF team)
- serine hydroxymethyltransferase 2 [HGNC gene]
HGNC gene
- serine hydroxymethyltransferase 2 [HGNC gene]
NCIt concept(s)
- SHMT2 Gene [NCIt concept]
- SHMT2 wt Allele [NCIt concept]
- Serine Hydroxymethyltransferase 2, Mitochondrial [NCIt concept]
Phenotypes related
- Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- serine hydroxymethyltransferase 2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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