IGF2

insulin like growth factor 2
OMIM: 147470
PanelMode of inheritanceDetails
3 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
Phenotypes
BECKWITH-WIEDEMANN SYNDROME 130650, CHROMOSOME 11P15.5-RELATED RUSSELL-SILVER SYNDROME 180860
R-numbers: R21
Signed-off version 1.92
MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
Phenotypes
CHROMOSOME 11P15.5-RELATED RUSSELL-SILVER SYNDROME, BECKWITH-WIEDEMANN SYNDROME
R-numbers: R147
Signed-off version 1.4
MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
Phenotypes
SRS, IUGR, Pre- and post-natal growth failure, ?Growth restriction, severe, with distinctive facies, 616489, Silver-Russell phenptype