MYLK2

myosin light chain kinase 2
OMIM: 606566, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Red MYLK2 in Hypertrophic cardiomyopathy_HCM


Level 2: Cardiovascular disorders
Version 1.10

Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Cardiomyopathy_Adult_SuperPanel
  • 2 reviews Other
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Cardiomyopathy, hypertrophic, 1, digenic, 192600

    Red MYLK2 in Mendeliome


    Version 1.3512

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

    Red MYLK2 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    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 1.140

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