ACTC1

actin, alpha, cardiac muscle 1
OMIM: 102540, Gene2Phenotype

12 panels

Panel Reviews Mode of inheritance Details
12 panels

Green ACTC1 in Arthrogryposis


Level 2: Neurology and neurodevelopmental disorders
Version 0.411

Component of the following Super Panels:

  • Neuromuscular Superpanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • MONDO:0019942 ACTC1 related distal arthrogrypsis

    Green ACTC1 in Congenital Heart Defect


    Level 2: Cardiovascular disorders
    Version 0.418

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Atrial septal defect 5, MIM# 612794
    Tags
    • founder

    Green ACTC1 in Dilated Cardiomyopathy


    Level 2: Cardiovascular disorders
    Version 1.33

    Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Cardiomyopathy_Adult_SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Cardiomyopathy, dilated, 1R, MIM# 613424
    Tags
    • for review

    Green ACTC1 in Hypertrophic cardiomyopathy_HCM


    Level 2: Cardiovascular disorders
    Version 0.178

    Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Cardiomyopathy_Adult_SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Cardiomyopathy, hypertrophic, 11 612098

    Green ACTC1 in Mendeliome


    Version 1.1902

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Atrial septal defect 5 MIM#612794
    • Cardiomyopathy, dilated, 1R MIM#613424
    • Cardiomyopathy, hypertrophic, 11 MIM#612098
    • ACTC1 related distal arthrogryposis MONDO:0019942

    Green ACTC1 in Additional findings_Adult


    Level 2: Screening
    Version 0.166

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Melbourne Genomics Health Alliance
    Phenotypes
    • Cardiomyopathy, dilated, 1R, MIM# 613424
    • Cardiomyopathy, hypertrophic, 11, MIM# 612098
    • Left ventricular noncompaction 4, MIM# 613424

    Green ACTC1 in Cardiomyopathy_Paediatric


    Level 2: Cardiovascular disorders
    Version 0.192

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • London South GLH
    • South West GLH
    • NHS GMS
    Phenotypes
    • Cardiomyopathy, dilated, 1R
    • Left ventricular noncompaction 4
    • Left Ventricular Noncompaction Cardiomyopathy
    • Hypertrophic Cardiomyopathy
    • Cardiomyopathy, familial hypertrophic, 11

    Red ACTC1 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • BabySeq Category C gene
    • BabySeq Category B gene
    Phenotypes
    • Left ventricular noncompaction
    • Cardiomyopathy, familial hypertrophic
    • Cardiomyopathy, dilated
    • Atrial septal defect

    Red ACTC1 in Incidentalome_PREGEN_DRAFT


    Version 0.43

    review Unknown
    Sources
    • Expert Review Red
    • NSW Health Pathology

    Green ACTC1 in Fetal anomalies


    Version 1.255

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Atrial septal defect 5, MIM# 612794
    • Cardiomyopathy, hypertrophic, 11 MIM# 612098

    Red ACTC1 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.114

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • BabySeq Category C gene
    • BabySeq Category B gene
    • Expert Review Red
    Phenotypes
    • Left ventricular noncompaction
    • Atrial septal defect
    • Cardiomyopathy, familial hypertrophic
    • Cardiomyopathy, dilated

    Green ACTC1 in Transplant Co-Morbidity Superpanel


    Level 2: Screening
    Version 0.18

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Cardiomyopathy, dilated, 1R, MIM# 613424
    • Cardiomyopathy, hypertrophic, 11, MIM# 612098
    • Left ventricular noncompaction 4, MIM# 613424