APC

APC, WNT signaling pathway regulator
OMIM: 611731
PanelMode of inheritanceDetails
4 panels
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Familial Adenomatous Polyposis
Signed-off version 1.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Adult Glioma
R-numbers: R211
Signed-off version 2.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Desmoid disease, hereditary, OMIM:135290, Brain tumor-polyposis syndrome 2, OMIM:175100, Gardner syndrome, OMIM:175100, Adenomatous polyposis coli, OMIM:175100, Gastric adenocarcinoma and proximal polyposis of the stomach, OMIM:619182
R-numbers: R359
Signed-off version 3.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Familial Adenomatous Polyposis, 175100