APOE

apolipoprotein E
OMIM: 107741
PanelMode of inheritanceDetails
3 panels
R-numbers: R134
Signed-off version 1.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Hyperlipoproteinemia, type III 617347
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R98
Signed-off version 2.3
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Familial dysbetalipoproteinaemia (Inherited mixed hyperlipidaemias), Hyperlipoproteinemia, type III 617347, Sea-blue histiocyte disease 269600, Lipoprotein glomerulopathy 611771
R-numbers: R324
Signed-off version 1.3
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Sea-blue histiocyte disease 269600, Hyperlipoproteinemia, type III 617347, Lipoprotein glomerulopathy 611771, Alzheimer disease-2 104310