Nuclear receptor subfamily 2, group f, member 2

Preferred Label : Nuclear receptor subfamily 2, group f, member 2;

Symbol : NR2F2;

CISMeF acronym : NR2F2;

Type : Gene;

Alternative titles and symbols : Transcription factor coup 2; Chicken ovalbumin upstream promoter transcription factor 2; Apolipoprotein regulatory protein I; TFCOUP2; COUPTFII; ARP1;

Ensembl ID : ENSG00000185551;

Prefixed ID : *107773;

Details

Origin ID

107773;

UMLS CUI

C1417834;

Automatic exact mappings (from CISMeF team)
- ANGPTL1 wt Allele [NCIt concept]
- ARFRP1 wt Allele [NCIt concept]
- COUP Transcription Factor 2 [NCIt concept]
- NR2F2 Gene [NCIt concept]
- NR2F2 wt Allele [NCIt concept]
- PITX2 wt Allele [NCIt concept]
- coup transcription factor ii [MeSH Descriptor]
- nuclear receptor subfamily 2 group F member 2 [ORDO Gene]
- nuclear receptor subfamily 2 group F member 2 [HGNC gene]
- paired like homeodomain 2 [ORDO Gene]
HGNC gene
- nuclear receptor subfamily 2 group F member 2 [HGNC gene]
NCIt concept(s)
- COUP Transcription Factor 2 [NCIt concept]
- NR2F2 Gene [NCIt concept]
- NR2F2 wt Allele [NCIt concept]
ORDO concept(s)
- nuclear receptor subfamily 2 group F member 2 [ORDO Gene]
Phenotypes related
- 46,XX sex reversal 5 [OMIM Phenotype]
- Congenital heart defects, multiple types, 4 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- NR2F2 Gene [NCIt concept]
- nuclear receptor subfamily 2 group F member 2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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