CALM2

calmodulin 2
OMIM: 114182, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green CALM2 in Catecholaminergic Polymorphic Ventricular Tachycardia


Level 2: Cardiovascular disorders
Version 0.35

Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Arrhythmia_SuperPanel
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Long QT syndrome 15 616249
    • sudden unexplained death
    • idopathic VF

    Green CALM2 in Long QT Syndrome


    Level 2: Cardiovascular disorders
    Version 0.61

    Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Arrhythmia_SuperPanel
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Long QT syndrome 15, MIM# 616249

    Green CALM2 in Mendeliome


    Version 1.3512

    1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Long QT syndrome 15 MIM#616249
    • CPVT

    Green CALM2 in Additional findings_Adult


    Level 2: Screening
    Version 1.130

    1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Catecholaminergic polymorphic ventricular tachycardia MONDO:0017990
    • Long QT syndrome 15 616249

    Amber CALM2 in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.140

    1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • ClinGen
    Phenotypes
    • Catecholaminergic polymorphic ventricular tachycardia MONDO:0017990
    Tags
    • cardiac
    • treatable

    Green CALM2 in Transplant Co-Morbidity


    Level 2: Screening
    Version 0.20

    0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Long QT syndrome 15 616249
    • idopathic VF
    • sudden unexplained death