APC

APC, WNT signaling pathway regulator
OMIM: 611731
PanelMode of inheritanceDetails
3 panels
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Familial Adenomatous Polyposis
R-numbers: R211, R209
Signed-off version 1.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Desmoid disease, hereditary 135290, Brain tumor-polyposis syndrome 2 175100, Gardner syndrome 175100, Adenomatous polyposis coli 175100
R-numbers: R359
Signed-off version 2.5
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Familial Adenomatous Polyposis, 175100