MYOM1

myomesin 1
OMIM: 603508, ClinGen, DECIPHER

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Amber MYOM1 in Dilated Cardiomyopathy


Level 2: Cardiovascular disorders
Version 1.61

Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Cardiomyopathy_Adult_SuperPanel
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Victorian Clinical Genetics Services
    • Victorian Clinical Genetics Services
    Phenotypes
    • Dilated cardiomyopathy, MONDO:0005021, MYOM1-related
    Tags
    • disputed

    Red MYOM1 in Hypertrophic cardiomyopathy


    Level 2: Cardiovascular disorders
    Version 1.25

    Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Cardiomyopathy_Adult_SuperPanel
  • 3 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Hypertrophic cardiomyopathy, MONDO:0005045
    Tags
    • disputed

    Amber MYOM1 in Mendeliome


    Version 1.4566

    3 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Victorian Clinical Genetics Services
    Phenotypes
    • Dilated cardiomyopathy, MONDO:0005021, MYOM1-related
    • Hypertrophic cardiomyopathy, MONDO:0005045
    Tags
    • disputed

    Red MYOM1 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.280

    0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • BabySeq Category C gene
    Phenotypes
    • Cardiomyopathy, hypertrophic

    Red MYOM1 in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.147

    0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • BabySeq Category C gene
    • Expert Review Red
    Phenotypes
    • Cardiomyopathy, hypertrophic