Incidentalome_PREGEN_DRAFT
Gene: STK11EnsemblGeneIds (GRCh38): ENSG00000118046
EnsemblGeneIds (GRCh37): ENSG00000118046
OMIM: 602216, Gene2Phenotype
STK11 is in 9 panels
1 review
Tony Roscioli (New South Wales Health Pathology)
Comment on list classification: may present in younger adulthood - needs discussionCreated: 20 Jan 2021, 5:26 a.m. | Last Modified: 20 Jan 2021, 5:26 a.m.
Panel Version: 0.33
may present in young adulthood - requires additional discussionCreated: 20 Jan 2021, 5:25 a.m. | Last Modified: 20 Jan 2021, 5:25 a.m.
Panel Version: 0.32
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Amber
- NSW Health Pathology
- OMIM
- 602216
- Clinvar variants
- Variants in STK11
- Penetrance
- None
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Tony Roscioli (New South Wales Health Pathology)Gene: stk11 has been classified as Amber List (Moderate Evidence).
Created, Added New Source, Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: STK11 was added gene: STK11 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology Mode of inheritance for gene: STK11 was set to Unknown