Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 GeneticVariation disease BEFREE Novel de novo pathogenic variant in the NR2F2 gene in a boy with congenital heart defect and dysmorphic features. 29663647 2018
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 GeneticVariation disease CLINVAR Prevalence and architecture of de novo mutations in developmental disorders. 28135719 2017
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 CausalMutation disease CLINVAR Prevalence and architecture of de novo mutations in developmental disorders. 28135719 2017
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 GeneticVariation disease CLINVAR Clinical application of whole-exome sequencing across clinical indications. 26633542 2016
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 CausalMutation disease CLINVAR Clinical application of whole-exome sequencing across clinical indications. 26633542 2016
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 GeneticVariation disease CLINVAR Prevalence and penetrance of ZFPM2 mutations and deletions causing congenital diaphragmatic hernia. 24702427 2015
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 CausalMutation disease CLINVAR Prevalence and penetrance of ZFPM2 mutations and deletions causing congenital diaphragmatic hernia. 24702427 2015
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 GeneticVariation disease CLINVAR Rare variants in NR2F2 cause congenital heart defects in humans. 24702954 2014
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 CausalMutation disease CLINVAR Rare variants in NR2F2 cause congenital heart defects in humans. 24702954 2014
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 CausalMutation disease CLINVAR 5.78 Mb terminal deletion of chromosome 15q in a girl, evaluation of NR2F2 as candidate gene for congenital heart defects. 21172461 2011
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 GeneticVariation disease CLINVAR 5.78 Mb terminal deletion of chromosome 15q in a girl, evaluation of NR2F2 as candidate gene for congenital heart defects. 21172461 2011
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 CausalMutation disease CLINVAR Breakpoint mapping and array CGH in translocations: comparison of a phenotypically normal and an abnormal cohort. 18371933 2008
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 GeneticVariation disease CLINVAR Breakpoint mapping and array CGH in translocations: comparison of a phenotypically normal and an abnormal cohort. 18371933 2008
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 CausalMutation disease CLINVAR Identification of COUP-TFII orphan nuclear receptor as a retinoic acid-activated receptor. 18798693 2008
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 GeneticVariation disease CLINVAR Identification of COUP-TFII orphan nuclear receptor as a retinoic acid-activated receptor. 18798693 2008
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 CausalMutation disease CLINVAR Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization. 15750894 2005
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 GeneticVariation disease CLINVAR Mouse lacking COUP-TFII as an animal model of Bochdalek-type congenital diaphragmatic hernia. 16251273 2005
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 GeneticVariation disease CLINVAR Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization. 15750894 2005
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 CausalMutation disease CLINVAR Mouse lacking COUP-TFII as an animal model of Bochdalek-type congenital diaphragmatic hernia. 16251273 2005
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 GeneticVariation disease CLINVAR The orphan nuclear receptor COUP-TFII is required for angiogenesis and heart development. 10215630 1999
Entrez Id: 7026
Gene Symbol: NR2F2
NR2F2
0.110 CausalMutation disease CLINVAR The orphan nuclear receptor COUP-TFII is required for angiogenesis and heart development. 10215630 1999