Genomics England
GMS Panels
Panels
Genes and Entities

NR2F2

nuclear receptor subfamily 2 group F member 2
OMIM: 107773
PanelMode of inheritanceDetails
4 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.15
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CONGENITAL HEART DEFECTS and XX sex reversal
Green
in Differences in sex development
R-numbers: R146
Signed-off version 4.5
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
46,XX sex reversal 5, OMIM:618901, 46,XX sex reversal 5, MONDO:0030049
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.195
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4
Green
in Intellectual disability
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 7.51
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Congenital heart defects, multiple types, 4, 615779