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  3. MYLK2
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Sudden death in young people

Gene: MYLK2

No list
MYLK2 (myosin light chain kinase 2)
EnsemblGeneIds (GRCh38): ENSG00000101306
EnsemblGeneIds (GRCh37): ENSG00000101306
OMIM: 606566, Gene2Phenotype
MYLK2 is in 4 panels

1 review

Rebecca Foulger (Genomics England curator)

Comment on list classification: Changed rating from red to grey: MYLK2 is amber on the V1.8 Hypertrophic Cardiomyopathy panel.
Created: 6 Dec 2016, 4:36 p.m.
Created: 6 Dec 2016, 4:36 p.m.

Panel version: 0.26

Details

Mode of Inheritance
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
OMIM
606566
Clinvar variants
Variants in MYLK2
Penetrance
Complete
Panels with this gene

History Filter Activity

26 Feb 2021, Gel status: 0

Added Tag

Arina Puzriakova (Genomics England Curator)

Tag curated_removed tag was added to gene: MYLK2.

19 Dec 2016, Gel status: 0

panel promoted to version 1

Ellen Thomas (Genomics England Curator)

This panel contains genes which aren't arrhythmic or metabolic causes of sudden death with normal post mortem.

6 Dec 2016, Gel status: 0

Gene classified by Genomics England curator

Rebecca Foulger (Genomics England curator)

This gene has been removed from the panel.

6 Dec 2016, Gel status: 1

Added New Source

Rebecca Foulger (Genomics England curator)

MYLK2 was added to Sudden death in young peoplepanel. Source: UKGTN

6 Dec 2016, Gel status: 0

Added New Source

Rebecca Foulger (Genomics England curator)

MYLK2 was added to Sudden death in young peoplepanel. Sources: Other

6 Dec 2016, Gel status: 0

Created

Rebecca Foulger (Genomics England curator)

MYLK2 was created by rfoulger