Mn1 protooncogene, transcriptional regulator

Preferred Label : Mn1 protooncogene, transcriptional regulator;

Symbol : MN1;

CISMeF acronym : MN1;

Type : Gene;

Alternative titles and symbols : Mn1 gene; Meningioma chromosome region 1; MGCR1;

Included titles and symbols : Mn1/tel fusion gene;

Ensembl ID : ENSG00000169184;

Prefixed ID : *156100;

Details

Origin ID

156100;

UMLS CUI

C1417217;

Automatic exact mappings (from CISMeF team)
- ETV6/MN1 Fusion Gene [NCIt concept]
- MN1 Gene [NCIt concept]
- MN1 Gene Mutation [NCIt concept]
- MN1 proto-oncogene, transcriptional regulator [ORDO Gene]
- MN1 proto-oncogene, transcriptional regulator [HGNC gene]
- MN1 wt Allele [NCIt concept]
- MN1/ETV6 Fusion Gene [NCIt concept]
- Transcriptional Activator MN1 [NCIt concept]
- symbol withdrawn MGCR [HGNC gene]
HGNC gene
- MN1 proto-oncogene, transcriptional regulator [HGNC gene]
NCIt concept(s)
- MN1 Gene [NCIt concept]
- MN1 wt Allele [NCIt concept]
- Transcriptional Activator MN1 [NCIt concept]
ORDO concept(s)
- MN1 proto-oncogene, transcriptional regulator [ORDO Gene]
Phenotypes related
- Cebalid syndrome [OMIM Phenotype]
- Meningioma, familial, susceptibility to [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MN1 Gene [NCIt concept]
- MN1 proto-oncogene, transcriptional regulator [HGNC gene]

Keyword's position in hierarchy(ies) :

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