Identity
HGNC
LOCATION
15q26.2
LOCUSID
ALIAS
ARP-1,ARP1,CHTD4,COUPTF2,COUPTFB,COUPTFII,NF-E3,SRXX5,SVP40,TFCOUP2
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 7026
MIM: 107773
HGNC: 7976
Ensembl: ENSG00000185551
Variants:
dbSNP: 7026
ClinVar: 7026
TCGA: ENSG00000185551
COSMIC: NR2F2
RNA/Proteins
Expression (GTEx)
Pathways
| Pathway | Source | External ID |
|---|---|---|
| Developmental Biology | REACTOME | R-HSA-1266738 |
| Transcriptional regulation of white adipocyte differentiation | REACTOME | R-HSA-381340 |
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37015919 | 2023 | An epigenetic switch controls an alternative NR2F2 isoform that unleashes a metastatic program in melanoma. | 4 |
| 37039367 | 2023 | Inflammation and DKK1-induced AKT activation contribute to endothelial dysfunction following NR2F2 loss. | 6 |
| 37500725 | 2023 | Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays. | 4 |
| 37015919 | 2023 | An epigenetic switch controls an alternative NR2F2 isoform that unleashes a metastatic program in melanoma. | 4 |
| 37039367 | 2023 | Inflammation and DKK1-induced AKT activation contribute to endothelial dysfunction following NR2F2 loss. | 6 |
| 37500725 | 2023 | Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays. | 4 |
| 34315577 | 2022 | Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variants. | 5 |
| 34910830 | 2022 | Abnormal hsa_circ_0003948 expression affects chronic periodontitis development by regulating miR-144-3p/NR2F2/PTEN signaling. | 7 |
| 35666805 | 2022 | The nuclear receptors SF1 and COUP-TFII cooperate on the Insl3 promoter in Leydig cells. | 6 |
| 34315577 | 2022 | Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variants. | 5 |
| 34910830 | 2022 | Abnormal hsa_circ_0003948 expression affects chronic periodontitis development by regulating miR-144-3p/NR2F2/PTEN signaling. | 7 |
| 35666805 | 2022 | The nuclear receptors SF1 and COUP-TFII cooperate on the Insl3 promoter in Leydig cells. | 6 |
| 32107331 | 2021 | The Coup-TFII orphan nuclear receptor is an activator of the γ-globin gene. | 5 |
| 33200800 | 2021 | miR-194-5p serves a suppressive role in human keloid fibroblasts via targeting NR2F2. | 6 |
| 33664454 | 2021 | YAP1 overexpression contributes to the development of enzalutamide resistance by induction of cancer stemness and lipid metabolism in prostate cancer. | 27 |
Citation
Dessen P
NR2F2 (nuclear receptor subfamily 2 group F member 2)
Atlas Genet Cytogenet Oncol Haematol. 2007-04-01
Online version: http://atlasgeneticsoncology.org/gene/47203/nr2f2
