TNNC1

troponin C1, slow skeletal and cardiac type
OMIM: 191040, Gene2Phenotype

8 panels

Panel Reviews Mode of inheritance Details
8 panels

Green TNNC1 in Dilated Cardiomyopathy


Level 2: Cardiovascular disorders
Version 1.48

Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Cardiomyopathy_Adult_SuperPanel
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Cardiomyopathy, dilated, 1Z, MIM# 611879
    • MONDO:0012745

    Green TNNC1 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 MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Cardiomyopathy, hypertrophic, 13 (MIM# 613243)

    Green TNNC1 in Mendeliome


    Version 1.3520

    1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Cardiomyopathy, dilated, 1Z, MIM# 611879
    • Cardiomyopathy, hypertrophic, 13 (MIM# 613243)

    Green TNNC1 in Additional findings_Adult


    Level 2: Screening
    Version 1.130

    0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Cardiomyopathy, dilated, 1Z, MIM# 611879

    Green TNNC1 in Cardiomyopathy_Paediatric


    Level 2: Cardiovascular disorders
    Version 0.207

    2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert Review Green
    • London South GLH
    • South West GLH
    • NHS GMS
    Phenotypes
    • Cardiomyopathy, familial hypertrophic, 13,
    • Cardiomyopathy, dilated, 1Z

    Amber TNNC1 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • BabySeq Category B gene
    Phenotypes
    • Cardiomyopathy, dilated

    Amber TNNC1 in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.140

    0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • BabySeq Category B gene
    • Expert Review Amber
    Phenotypes
    • Cardiomyopathy, dilated

    Green TNNC1 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
    • MONDO:0012745
    • Cardiomyopathy, dilated, 1Z, MIM# 611879