Nibrin - CISMeF

Preferred Label : Nibrin;

Symbol : NBN;

CISMeF acronym : NBN;

Type : Gene;

Alternative titles and symbols : P95 protein of the mre11/rad50 complex; NBS1;

Ensembl ID : ENSG00000104320;

Prefixed ID : *602667;

Details

Origin ID

602667;

UMLS CUI

C1334862;

Automatic exact mappings (from CISMeF team)
- ARTN wt Allele [NCIt concept]
- NBN Gene [NCIt concept]
- NBN gene [LOINC component]
- NBN wt Allele [NCIt concept]
- NLRP2 wt Allele [NCIt concept]
- artemin [HGNC gene]
- nibrin [ORDO Gene]
- nibrin [HGNC gene]
HGNC gene
- nibrin [HGNC gene]
NCIt concept(s)
- NBN Gene [NCIt concept]
- NBN wt Allele [NCIt concept]
- Nibrin [NCIt concept]
ORDO concept(s)
- nibrin [ORDO Gene]
Phenotypes related
- Aplastic anemia [OMIM Phenotype]
- Leukemia, acute lymphoblastic [OMIM Phenotype]
- Nijmegen breakage syndrome [OMIM Phenotype]
See also inter- (CISMeF)
- Nibrin [NCIt concept]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- NBN Gene [NCIt concept]
- NBN gene [LOINC component]
- nibrin [HGNC gene]

Keyword's position in hierarchy(ies) :

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