Runt-related transcription factor 2

Preferred Label : Runt-related transcription factor 2;

Symbol : RUNX2;

CISMeF acronym : RUNX2;

Type : Gene;

Alternative titles and symbols : Core-binding factor, runt domain, alpha subunit 1; Aml3 gene; CBFA1; AML3; PEBP2-ALPHA-A; OSF2;

Ensembl ID : ENSG00000124813;

Prefixed ID : *600211;

Détails

Origin ID

600211;

UMLS CUI

C1419771;

Automatic exact mappings (from CISMeF team)
- POSTN wt Allele [NCIt concept]
- Periostin [NCIt concept]
- Periostin Measurement [NCIt concept]
- RUNX family transcription factor 2 [ORDO Gene]
- RUNX family transcription factor 2 [HGNC gene]
- RUNX2 Gene [NCIt concept]
- RUNX2 wt Allele [NCIt concept]
- Runt-Related Transcription Factor 2 [NCIt concept]
HGNC gene
- RUNX family transcription factor 2 [HGNC gene]
NCIt concept(s)
- RUNX2 Gene [NCIt concept]
- RUNX2 wt Allele [NCIt concept]
- Runt-Related Transcription Factor 2 [NCIt concept]
ORDO concept(s)
- RUNX family transcription factor 2 [ORDO Gene]
Phenotypes related
- Cleidocranial dysplasia 1 [OMIM Phenotype]
- Metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- RUNX family transcription factor 2 [HGNC gene]
- RUNX2 Gene [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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