MYLK2

myosin light chain kinase 2
OMIM: 606566, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Red MYLK2 in Hypertrophic cardiomyopathy


Level 2: Cardiovascular disorders
Version 2.0

3 reviews Other
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Cardiomyopathy, hypertrophic, 1, digenic, 192600
Tags
  • disputed

Red MYLK2 in Mendeliome


Version 2.0

4 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Cardiomyopathy, hypertrophic, 1, digenic, 192600
Tags
  • disputed

Red MYLK2 in Additional findings_Paediatric


Level 2: Screening
Version 1.0

0 reviews Unknown
Sources
  • Expert Review Red
  • BabySeq Category C gene
Phenotypes
  • Cardiomyopathy, hypertrophic

Red MYLK2 in Genomic newborn screening: BabyScreen+


Level 2: Screening
Version 2.0

0 reviews Unknown
Sources
  • BabySeq Category C gene
  • Expert Review Red
Phenotypes
  • Cardiomyopathy, hypertrophic