phenylalanyl-tRNA synthetase 2, mitochondrial

Preferred Label : phenylalanyl-tRNA synthetase 2, mitochondrial;

Approved symbol HGNC : FARS2;

Name synonyms HGNC : phenylalanine tRNA ligase 2; mitochondrial;

Alias symbols HGNC : mtPheRS; dJ236A3.1;

Chromosome HGNC : 6p25.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000145982;

Details

Origin ID

HGNC:21062;

UMLS CUI

C1539476;

Automatic exact mappings (from CISMeF team)
- Mitochondrial inheritance [HPO term]
- Mitochondrion [NCIt concept]
- Muscular Dystrophy Secondary to Mitochondrial Disorder [NCIt concept]
- NADH:ubiquinone oxidoreductase core subunit S3 [ORDO Gene]
- Phenylalanyl-trna synthetase 2, mitochondrial [OMIM gene]
- phenylalanyl-tRNA synthetase 2, mitochondrial [ORDO Gene]
OMIM gene
- Phenylalanyl-trna synthetase 2, mitochondrial [OMIM gene]
Orphanet gene
- phenylalanyl-tRNA synthetase 2, mitochondrial [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FARS2 gene [LOINC component]
- Phenylalanyl-trna synthetase 2, mitochondrial [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients