SOS2

SOS Ras/Rho guanine nucleotide exchange factor 2
OMIM: 601247
PanelMode of inheritanceDetails
6 panels
R-numbers: R135
Signed-off version 1.4
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Noonan syndrome 9 616559, Noonan syndrome 9
R-numbers: R21
Signed-off version 1.92
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Fetal hydrops, Noonan syndrome 9, 616559
R-numbers: R147
Signed-off version 1.4
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Noonan syndrome 9
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 3.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Noonan syndrome 9
R-numbers: R236
Signed-off version 1.4
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
NS9, NOONAN SYNDROME 9, Noonan syndrome 9 616559
R-numbers: R136
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Noonan syndrome 9 616559