Ribonucleotide reductase regulatory tp53 inducible subunit m2b

Preferred Label : Ribonucleotide reductase regulatory tp53 inducible subunit m2b;

Symbol : RRM2B;

CISMeF acronym : RRM2B;

Type : Gene;

Alternative titles and symbols : Ribonucleotide reductase small subunit 2-like, p53-inducible; P53-inducible and ribonucleotide reductase small subunit 2-like; P53R2; Ribonucleotide reductase, m2 b;

Ensembl ID : ENSG00000048392;

Prefixed ID : *604712;

Details

Origin ID

604712;

UMLS CUI

C1424883;

Automatic exact mappings (from CISMeF team)
- RRM2B Gene [NCIt concept]
- RRM2B gene [LOINC component]
- RRM2B wt Allele [NCIt concept]
- Ribonucleoside-Diphosphate Reductase Subunit M2 B [NCIt concept]
- ribonucleotide reductase regulatory TP53 inducible subunit M2B [ORDO Gene]
- ribonucleotide reductase regulatory TP53 inducible subunit M2B [HGNC gene]
HGNC gene
- ribonucleotide reductase regulatory TP53 inducible subunit M2B [HGNC gene]
NCIt concept(s)
- RRM2B Gene [NCIt concept]
- RRM2B wt Allele [NCIt concept]
- Ribonucleoside-Diphosphate Reductase Subunit M2 B [NCIt concept]
ORDO concept(s)
- ribonucleotide reductase regulatory TP53 inducible subunit M2B [ORDO Gene]
Phenotypes related
- Mitochondrial dna depletion syndrome 8a (encephalomyopathic type with renal tubulopathy) [OMIM Phenotype]
- Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 5 [OMIM Phenotype]
- Rod-cone dystrophy, sensorineural deafness, and fanconi-type renal dysfunction [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- RRM2B Gene [NCIt concept]
- RRM2B gene [LOINC component]
- ribonucleotide reductase regulatory TP53 inducible subunit M2B [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients