STK11:Ensemblv90

serine/threonine kinase 11
OMIM: 602216, ClinGen, DECIPHER

9 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 9 panels
Green STK11 in Incidentalome Version 0.370	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Melbourne Genomics Health Alliance Victorian Clinical Genetics Services Phenotypes Peutz-Jeghers syndrome, MIM# 175200
Green STK11 in Cancer Predisposition_Paediatric Level 2: Cancer Version 0.132	0 reviews	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green STK11 in Additional findings_Adult Level 2: Screening Version 1.130	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Melbourne Genomics Health Alliance Phenotypes Peutz-Jeghers syndrome, MIM# 175200
Red STK11 in CGC_86 Version 0.3	0 reviews	Other	Sources CGC_86 Phenotypes Peutz-Jeghers syndrome
Red STK11 in NCGC Version 0.3	0 reviews	Other	Sources NCGC Phenotypes Peutz-Jeghers syndrome
Red STK11 in TCGA_PANCAN_2018 Version 0.3	0 reviews	Other	Sources TCGA_PANCAN_2018 Phenotypes Peutz-Jeghers syndrome
Green STK11 in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category A gene Expert Review Green Phenotypes Peutz-Jeghers syndrome
Amber STK11 in Incidentalome_PREGEN_DRAFT Version 0.43	1 review	Unknown	Sources Expert Review Amber NSW Health Pathology
Amber STK11 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.141	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber BabySeq Category A gene Phenotypes Peutz-Jeghers syndrome, MIM# 175200 Tags for review cancer treatable