NR2F2 wt Allele

Preferred Label : NR2F2 wt Allele;

NCIt synonyms : Nuclear Receptor Subfamily 2, Group F, Member 2 wt Allele; SVP40; TFCOUP2; COUP-TFII; COUPTFB; ARP1; MGC117452;

NCIt definition : Human NR2F2 wild-type allele is located in the vicinity of 15q26 and is approximately 14 kb in length. This allele, which encodes COUP transcription factor 2 protein, plays a role in transcriptional activation. Deletion of the gene may be associated with congenital diaphragmatic hernia.;

GenBank Accession Number : M64497;

Details

Origin ID

C75868;

UMLS CUI

C2698420;

Currated CISMeF NLP mapping
- Arbitrary restriction polymorphism 1 [OMIM Phenotype]
OMIM relation
- Nuclear receptor subfamily 2, group f, member 2 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 15q26 [NCIt concept]
gene_is_element_in_pathway
- FOXA1 Transcription Factor Signaling Pathway [NCIt concept]
- Telomerase Regulation Pathway [NCIt concept]
gene_plays_role_in_process
- Cell Differentiation Process [NCIt concept]
- Cell Proliferation [NCIt concept]
- DNA Binding [NCIt concept]
- Homeostatic Process [NCIt concept]
- Ligand Binding [NCIt concept]
- Maturation [NCIt concept]
- Pattern Formation [NCIt concept]
- Receptor Signaling [NCIt concept]
- Signal Transduction [NCIt concept]
- Transcriptional Regulation [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients