Childhood solid tumours
Gene: STK11
As discussed at the Genomics Cancer Panel Workshop, 16th July 2019: the group agreed that there is enough evidence to rate this gene greenCreated: 2 Aug 2019, 11:03 a.m. | Last Modified: 2 Aug 2019, 11:03 a.m.
Panel Version: 1.27
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Peutz Jeghers syndrome
Source NHS GMS was added to STK11. Mode of inheritance for gene STK11 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Added phenotypes Peutz Jeghers syndrome for gene: STK11 Publications for gene STK11 were changed from to 23788249
Source Expert list was added to STK11. Source Expert Review Green was added to STK11. Mode of inheritance for gene STK11 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Added phenotypes Peutz-Jeghers syndrome, 175200 for gene: STK11 Rating Changed from Red List (low evidence) to Green List (high evidence)
gene: STK11 was added gene: STK11 was added to Tumour predisposition - childhood onset. Sources: Expert List Mode of inheritance for gene: STK11 was set to