MYLK2

myosin light chain kinase 2
OMIM: 606566, Gene2Phenotype

4 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
No list MYLK2 in Sudden death in young people Level 3: Cardiac arrhythmia Level 2: Cardiovascular disorders Version 1.15	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Removed UKGTN Other Phenotypes Cardiomyopathy, hypertrophic, 1, digenic, 192600 sudden death in young subjects Molecular autopsy Familial Hypertrophic Cardiomyopathy HCM Tags curated_removed
Amber MYLK2 in Hypertrophic cardiomyopathy Level 3: Cardiomyopathy Level 2: Cardiovascular disorders Version 4.7 Latest signed off version: v4.0 (22 Mar 2023) Component of the following Super Panels: Sudden unexplained death or survivors of a cardiac event	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources South West GLH London South GLH North West GLH Expert list Illumina TruGenome Clinical Sequencing Services Radboud University Medical Center, Nijmegen Phenotypes Cardiomyopathy, hypertrophic, 1, digenic (192600) Cardiomyopathy, hypertrophic, midventricular, digenic,
Red MYLK2 in Thoracic aortic aneurysm or dissection (GMS) Version 3.11 Latest signed off version: v3.0 (22 Mar 2023)	review	Not set	Sources Expert Review Red London South GLH London South GLH
Red MYLK2 in Thoracic aortic aneurysm or dissection Level 3: Connective tissue disorders and aortopathies Level 2: Cardiovascular disorders Version 1.127	review	Not set	Sources London South GLH