Multiple Tumours
Gene: STK11EnsemblGeneIds (GRCh38): ENSG00000118046
EnsemblGeneIds (GRCh37): ENSG00000118046
OMIM: 602216, Gene2Phenotype
STK11 is in 14 panels
1 review
Ellen McDonagh (Genomics England Curator)
Information from TruSight panel: Pathogenic Mutations are Inactivating.Created: 5 Feb 2016, 11:47 a.m.
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- TruSight Cancer Panel (Illumina)
- Phenotypes
-
- Peutz-Jeghers SyndromeColorectal cancer, hamartoma, adenoma
- Gastric cancer, hamartoma, adenoma
- Breast cancer
- Ovarian cancer (epithelial, sex cord-stromal tumor)
- Testicular cancer (sex cord-stromal tumor)
- Pancreatic cancer
- Cervical cancer (adenoma malignum)
- Familial breast cancer
- Familial colon cancer
- OMIM
- 602216
- Clinvar variants
- Variants in STK11
- Penetrance
- Complete
- Panels with this gene
-
- Childhood solid tumours cancer susceptibility
- Childhood solid tumours
- Colorectal cancer pertinent cancer susceptibility
- Adult solid tumours for rare disease
- Familial breast cancer
- Palmoplantar keratodermas
- GI tract tumours
- Multiple monogenic benign skin tumours
- Pigmentary skin disorders
- Adult solid tumours cancer susceptibility
- Peutz Jeghers Syndrome
- Inherited pancreatic cancer
- Inherited ovarian cancer (without breast cancer)
- Inherited polyposis and early onset colorectal cancer - germline testing
History Filter Activity
Set Mode of Inheritance, Added New Source
Ellen McDonagh (Genomics England Curator)STK11 was added to Multiple Tumourspanel. Source: Expert Review Green Model of inheritance for gene STK11 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Created
Ellen McDonagh (Genomics England Curator)STK11 was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)STK11 was added to Multiple Tumourspanel. Sources: TruSight Cancer Panel (Illumina)