STK11

serine/threonine kinase 11
OMIM: 602216
PanelMode of inheritanceDetails
4 panels
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Peutz Jeghers syndrome
R-numbers: R211, R209
Signed-off version 1.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Peutz-Jeghers syndrome 175200
R-numbers: R236
Signed-off version 1.4
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
PJS, Peutz-Jeghers syndrome, PEUTZ-JEGHERS SYNDROME
R-numbers: R359
Signed-off version 2.5
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Peutz Jeghers syndrome, Peutz-Jeghers syndrome, 175200