×
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
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
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
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
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
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
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
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
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
Clinical application of whole-exome sequencing across clinical indications.
26633542
2016
×
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
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
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
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
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
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
The orphan nuclear receptor COUP-TFII is required for angiogenesis and heart development.
10215630
1999
×
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
Prevalence and architecture of de novo mutations in developmental disorders.
28135719
2017
×
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