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
Signed-off version 2.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Peutz-Jeghers syndrome, OMIM:175200, Peutz-Jeghers syndrome, MONDO:0008280
R-numbers: R236
Signed-off version 2.1
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
PJS, Peutz-Jeghers syndrome, PEUTZ-JEGHERS SYNDROME
R-numbers: R359
Signed-off version 3.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Peutz Jeghers syndrome, Peutz-Jeghers syndrome, 175200