Gene Dossiers

Show alternative names & symbols

Gene dossier Disorders Genes
Cantu Syndrome

Bristol RGC - 2013

  • Cantu Syndrome
    • Hypertrichotic Osteochondrodysplasia
  • ATP-binding cassette, sub-family C, member 9
    • ATP-binding cassette, sub-family C (CFTR/MRP), member 9
    • sulfonylurea receptor 2
Cardiac 67 Gene Panel (consisting of 10 tests)

Manchester RGC - 2014

  • Aortic Aneurysm, Familial Thoracic 4
    • Aortic Aneurysm/Aortic Dissection and Patent Ductus Arteriosus
  • Aortic Aneurysm, Familial Thoracic 6
    • Familial Thoracic Aortic Aneurysm With Livedo Reticularis And Iris Flocculi
  • Ehlers-Danlos Syndrome, Hypermobility Type
    • Benign Hypermobility Syndrome
    • Ehlers-Danlos Syndrome, Type III
  • Ehlers-Danlos Syndrome, Type IV, Autosomal Dominant
    • Eds IV
    • Ehlers-Danlos Syndrome, Arterial Type
    • Ehlers-Danlos Syndrome, Ecchymotic Type
    • Ehlers-Danlos Syndrome, Sack-Barabas Type
    • Ehlers-Danlos Syndrome, Vascular Type
  • Loeys-Dietz Syndrome 1
    • Aortic Aneurysm, Familial Thoracic 5
    • Furlong Syndrome
    • Loeys-Dietz Aortic Aneurysm Syndrome
    • Loeys-Dietz Syndrome, type 1
  • Loeys-Dietz Syndrome 2
    • Loeys-Dietz Syndrome, Type 2
  • Loeys-Dietz Syndrome 3
    • Aneurysms-Osteoarthritis Syndrome
    • Loeys-Dietz Syndrome With Osteoarthritis
    • Loeys-Dietz Syndrome, Type 1C, Formerly
    • Loeys-Dietz Syndrome, Type 3
  • Loeys-Dietz Syndrome 4
    • Aneurysm, Aortic and Cerebral, with Arterial Tortuosity and Skeletal Manifestations
    • Loeys-Dietz Syndrome, Type 4
  • Moyamoya Disease 5
  • Multisystemic Smooth Muscle Dysfunction Syndrome
    • Mydriasis, Congenital, With Patent Ductus Arteriosus, Thoracic Aortic Aneurysm, And Vasculopathy
  • actin, alpha 2, smooth muscle, aorta
    • actin, alpha, smooth muscle, aortic
    • actin, vascular smooth muscle
  • collagen, type III, alpha 1 chain
    • collagen, type III, alpha 1 ehlers-danlos syndrome type IV, autosomal dominant
  • fibrillin 1
    • fibrillin
    • fibrillin 1 (marfan syndrome)
  • myosin heavy chain 11
    • myosin, heavy chain 11, smooth muscle
    • myosin, smooth muscle, heavy chain 11
    • smooth muscle myosin heavy chain
  • potassium calcium-activated channel subfamily N member 1
    • potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 1
    • potassium intermediate/small conductance calcium-activated channel, subfamily N, member 1
  • SMAD family member 3
    • MAD, mothers against decapentaplegic homolog 3 (Drosophila)
    • mothers against decapentaplegic, drosophila, homolog of, 3
    • SMA- and MAD-related protein 3
    • SMAD, mothers against DPP homolog 3 (Drosophila)
  • transforming growth factor, beta 2
    • transforming growth factor, beta-2
  • transforming growth factor, beta receptor 1
    • activin a receptor type II-like kinase, 53kda
  • transforming growth factor, beta receptor 2
    • colorectal cancer, hereditary nonpolyposis type 6
    • transforming growth factor, beta receptor II (70-80kd)
Cardiac 67 Gene Panel (consisting of 10 tests)

Manchester RGC - 2014

  • Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
    • Arrhythmogenic Right Ventricular Cardiomyopathy 10
  • Arrhythmogenic Right Ventricular Dysplasia, Familial, 11
    • Arrhythmogenic Right Ventricular Cardiomyopathy 11
    • Arrhythmogenic Right Ventricular Dysplasia, Familial, 11, And Mild Palmoplantar Keratoderma With Or Without Woolly Hair, Included
  • Arrhythmogenic Right Ventricular Dysplasia, Familial, 12
    • Arrhythmogenic Right Ventricular Cardiomyopathy 12
  • Arrhythmogenic Right Ventricular Dysplasia, Familial, 5
    • Arrhythmogenic Right Ventricular Cardiomyopathy 5
  • Arrhythmogenic Right Ventricular Dysplasia, Familial, 8
    • Arrhythmogenic Right Ventricular Cardiomyopathy 8
  • Arrhythmogenic Right Ventricular Dysplasia, Familial, 9
    • Arrhythmogenic Right Ventricular Cardiomyopathy 9
  • Cardiomyopathy, Dilated, 1BB
  • desmocollin 2
    • desmocollin 3, formerly
    • desmosomal glycoprotein II/III
  • desmoglein 2
  • desmoplakin
    • desmoplakin I
    • desmoplakin II
  • junction plakoglobin
    • catenin (cadherin-associated protein), gamma 80kDa
    • catenin, gamma
    • desmoplakin III
    • plakoglobin
  • plakophilin 2
  • transmembrane protein 43
    • arrhythmogenic right ventricular dysplasia 5
Cardiac 67 Gene Panel (consisting of 10 tests)

Manchester RGC - 2014

  • Atrial Fibrillation, Familial, 10
  • Atrial Fibrillation, Familial, 13
  • Brugada Syndrome 1
    • Brugada Syndrome
    • Right Bundle Branch Block, St Segment Elevation, And Sudden Death Syndrome
    • Sudden Unexplained Nocturnal Death Syndrome
  • Brugada Syndrome 2
  • Brugada Syndrome 5
  • Brugada Syndrome 6
  • Brugada Syndrome 7
  • Brugada Syndrome 8
  • Cardiomyopathy, Dilated, 1E
    • Cardiomyopathy, Dilated, With Conduction Defect 2
    • Cardiomyopathy, Dilated, With Conduction Disorder And Arrhythmia
  • Long QT Syndrome 3
    • Long QT Syndrome 2/3, Included
    • Long QT Syndrome 3, Acquired, Susceptibility To, Included
    • Long QT Syndrome 3/6, Included
  • Ventricular Fibrillation, Paroxysmal Familial, 1
    • Ventricular Fibrillation During Myocardial Infarction, Susceptibility To
  • glycerol-3-phosphate dehydrogenase 1 like
    • glycerol-3-phosphate dehydrogenase 1-like
  • hyperpolarization activated cyclic nucleotide gated potassium channel 4
    • hyperpolarization activated cyclic nucleotide-gated potassium channel 4
  • potassium voltage-gated channel subfamily E regulatory subunit 3
    • potassium channel, voltage gated subfamily E regulatory beta subunit 3
    • potassium voltage-gated channel, Isk-related family, member 3
  • sodium voltage-gated channel alpha subunit 5
    • sodium channel, voltage-gated, type v, alpha (long qt syndrome 3)
    • sodium channel, voltage-gated, type V, alpha subunit
  • sodium voltage-gated channel beta subunit 1
    • sodium channel, voltage-gated, type I, beta
    • sodium channel, voltage-gated, type I, beta polypeptide
    • sodium channel, voltage-gated, type I, beta subunit
  • sodium voltage-gated channel beta subunit 3
    • sodium channel, voltage gated, type III beta subunit
    • sodium channel, voltage-gated, type III, beta
    • sodium channel, voltage-gated, type III, beta subunit
Cardiac 67 Gene Panel (consisting of 10 tests)

Manchester RGC - 2014

  • Arrhythmogenic Right Ventricular Dysplasia, Familial, 2
    • Arrhythmogenic Right Ventricular Cardiomyopathy 2
  • Atrial Fibrillation, Familial, 9
  • Short QT Syndrome 3
  • Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/or Dilated Cardiomyopathy
    • Ventricular Tachycardia, Stress-Induced Polymorphic
  • Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
    • Ventricular Tachycardia, Stress-Induced Polymorphic
  • Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
  • Ventricular Tachycardia, Catecholaminergic Polymorphic, 5, With Or Without Muscle Weakness
  • calmodulin 1
    • calmodulin 1 (phosphorylase kinase, delta)
  • calsequestrin 2
    • calsequestrin 2 (cardiac muscle)
  • potassium voltage-gated channel subfamily J member 2
    • potassium inwardly-rectifying channel, subfamily J, member 2
  • ryanodine receptor 2
    • arrhythmogenic right ventricular dysplasia 2
    • ryanodine receptor 2 (cardiac)
    • ryanodine receptor, cardiac
  • triadin
Cardiac 67 Gene Panel (consisting of 10 tests)

Manchester RGC - 2014

  • Atrial Fibrillation, Familial, 12
  • Atrial Septal Defect 3
  • Cardiomyopathy, Dilated, 1A
    • Cardiomyopathy, Congestive
    • Cardiomyopathy, Dilated, With Conduction Defect 1
    • Cardiomyopathy, Familial Idiopathic
    • Cardiomyopathy, Idiopathic Dilated
  • Cardiomyopathy, Dilated, 1AA, With Or Without Left Ventricular Noncompaction;
    • Cardiomyopathy, Familial Hypertrophic, 23, With Or Without Ventricular Noncompaction, Included;
  • Cardiomyopathy, Dilated, 1CC
  • Cardiomyopathy, Dilated, 1D
    • Left Ventricular Noncompaction 6, Included
  • Cardiomyopathy, Dilated, 1DD
  • Cardiomyopathy, Dilated, 1EE
  • Cardiomyopathy, Dilated, 1FF
  • Cardiomyopathy, Dilated, 1G
  • Cardiomyopathy, Dilated, 1I
  • Cardiomyopathy, Dilated, 1J
    • Cardiomyopathy, Dilated, With Sensorineural Hearing Loss, Autosomal Dominant
  • Cardiomyopathy, Dilated, 1L
  • Cardiomyopathy, Dilated, 1M
  • Cardiomyopathy, Dilated, 1O
    • Cardiomyopathy, Dilated, With Ventricular Tachycardia
  • Cardiomyopathy, Dilated, 1P
  • Cardiomyopathy, Dilated, 1R
  • Cardiomyopathy, Dilated, 1S
    • Left Ventricular Noncompaction 5
  • Cardiomyopathy, Dilated, 1T
  • Cardiomyopathy, Dilated, 1W
  • Cardiomyopathy, Dilated, 1Y
    • Left Ventricular Noncompaction 9
  • Cardiomyopathy, Dilated, 1Z
  • Cardiomyopathy, Dilated, 2A
    • Cardiomyopathy, Congestive, Autosomal Recessive
    • Cardiomyopathy, Dilated, Autosomal Recessive
  • Cardiomyopathy, Familial Hypertrophic, 1
    • Asymmetric Septal Hypertrophy
    • Cardiomyopathy, hypertrophic, 1, digenic
    • Cardiomyopathy, Sporadic Hypertrophic, 1, Included
    • Hypertrophic Subaortic Stenosis, Idiopathic
    • Ventricular Hypertrophy, Hereditary
  • Cardiomyopathy, Familial Hypertrophic, 11
  • Cardiomyopathy, Familial Hypertrophic, 12
  • Cardiomyopathy, Familial Hypertrophic, 13
  • Cardiomyopathy, Familial Hypertrophic, 14
  • Cardiomyopathy, Familial Hypertrophic, 15
  • Cardiomyopathy, Familial Hypertrophic, 18
  • Cardiomyopathy, Familial Hypertrophic, 2
  • Cardiomyopathy, Familial Hypertrophic, 20
  • Cardiomyopathy, Familial Hypertrophic, 25
    • Cardiomyopathy, Dilated, 1N
  • Cardiomyopathy, Familial Hypertrophic, 3
  • Cardiomyopathy, Familial Hypertrophic, 4
  • Cardiomyopathy, Familial Hypertrophic, 7
  • Cardiomyopathy, Familial Hypertrophic, 9
  • Cardiomyopathy, Familial Restrictive, 1
  • Cardiomyopathy, Familial Restrictive, 3
  • Left Ventricular Noncompaction 10
    • Cardiomyopathy, Dilated, 1MM
  • actin, alpha, cardiac muscle 1
    • actin, alpha
    • actin, alpha, cardiac muscle
    • smooth muscle actin
  • actinin, alpha 2
  • ATP-binding cassette, sub-family C, member 9
    • ATP-binding cassette, sub-family C (CFTR/MRP), member 9
    • sulfonylurea receptor 2
  • cysteine and glycine rich protein 3
    • CLP LIM domain protein, muscle
    • cysteine-rich protein 3
    • lim domain protein, cardiac
  • desmin
  • EYA transcriptional coactivator and phosphatase 4
    • eyes absent (Drosophila) homolog 4
    • eyes absent homolog 4 (Drosophila)
  • lamin A/C
    • lamin A
    • lamin C
    • prelamin A
  • myosin binding protein C, cardiac
    • cardiac myosin-binding protein C
    • myosin-binding protein C, cardiac
  • myosin heavy chain 6
    • myosin, heavy chain 6, cardiac muscle, alpha
    • myosin, heavy polypeptide 6, cardiac muscle, alpha (cardiomyopathy, hypertrophic 1)
  • myosin heavy chain 7
    • myopathy, distal 1
    • myosin, cardiac, heavy chain, beta
    • myosin, heavy chain 7, cardiac muscle, beta
    • myosin, heavy polypeptide 7, cardiac muscle, beta
  • nexilin F-actin binding protein
    • nexilin (F actin binding protein)
  • phospholamban
  • RNA binding motif protein 20
  • sarcoglycan delta
    • sarcoglycan, delta (35kD dystrophin-associated glycoprotein)
    • sarcoglycan, delta (35kDa dystrophin-associated glycoprotein)
  • thymopoietin
  • titin
    • cardiomyopathy, dilated 1G (autosomal dominant
    • connectin
  • titin-cap
    • limb girdle muscular dystrophy 2G (autosomal recessive)
    • titin-cap (telethonin)
  • tropomyosin 1
    • cardiomyopathy, hypertrophic 3
    • chromosome 15 open reading frame 13
    • tropomyosin 1 (alpha)
    • tropomyosin, skeletal muscle alpha
  • troponin C1, slow skeletal and cardiac type
    • "troponin C type 1 (slow)"
    • TNNC, "troponin C type 1 (slow)"
    • troponin C, slow
  • troponin I3, cardiac type
    • cardiomyopathy, dilated 2A (autosomal recessive)
    • troponin I type 3
    • troponin I type 3 (cardiac)
    • troponin I type 3 cardiac
    • troponin I, cardiac
  • troponin T2, cardiac type
    • cardiomyopathy, dilated 1D (autosomal dominant)
    • troponin T type 2 (cardiac)
    • troponin t2, cardiac
  • vinculin
Cardiac 67 Gene Panel (consisting of 10 tests)

Manchester RGC - 2014

  • Cardiomyopathy, Dilated, 1CC
  • Cardiomyopathy, Dilated, 1D
    • Left Ventricular Noncompaction 6, Included
  • Cardiomyopathy, Dilated, 1EE
  • Cardiomyopathy, Dilated, 1FF
  • Cardiomyopathy, Dilated, 1G
  • Cardiomyopathy, Dilated, 1M
  • Cardiomyopathy, Dilated, 1P
  • Cardiomyopathy, Dilated, 1R
  • Cardiomyopathy, Dilated, 1S
    • Left Ventricular Noncompaction 5
  • Cardiomyopathy, Dilated, 1W
  • Cardiomyopathy, Dilated, 1Y
    • Left Ventricular Noncompaction 9
  • Cardiomyopathy, Dilated, 1Z
  • Cardiomyopathy, Dilated, 2A
    • Cardiomyopathy, Congestive, Autosomal Recessive
    • Cardiomyopathy, Dilated, Autosomal Recessive
  • Cardiomyopathy, Familial Hypertrophic, 1
    • Asymmetric Septal Hypertrophy
    • Cardiomyopathy, hypertrophic, 1, digenic
    • Cardiomyopathy, Sporadic Hypertrophic, 1, Included
    • Hypertrophic Subaortic Stenosis, Idiopathic
    • Ventricular Hypertrophy, Hereditary
  • Cardiomyopathy, Familial Hypertrophic, 10
    • Cardiomyopathy, Hypertrophic, Mid-Left Ventricular Chamber Type, 2
  • Cardiomyopathy, Familial Hypertrophic, 11
  • Cardiomyopathy, Familial Hypertrophic, 12
  • Cardiomyopathy, Familial Hypertrophic, 13
  • Cardiomyopathy, Familial Hypertrophic, 14
  • Cardiomyopathy, Familial Hypertrophic, 18
  • Cardiomyopathy, Familial Hypertrophic, 2
  • Cardiomyopathy, Familial Hypertrophic, 20
  • Cardiomyopathy, Familial Hypertrophic, 25
    • Cardiomyopathy, Dilated, 1N
  • Cardiomyopathy, Familial Hypertrophic, 3
  • Cardiomyopathy, Familial Hypertrophic, 4
  • Cardiomyopathy, Familial Hypertrophic, 6
  • Cardiomyopathy, Familial Hypertrophic, 7
  • Cardiomyopathy, Familial Hypertrophic, 8
    • Cardiomyopathy, Hypertrophic, Mid-Left Ventricular Chamber Type, 1
  • Cardiomyopathy, Familial Hypertrophic, 9
  • Cardiomyopathy, Familial Restrictive, 1
  • Cardiomyopathy, Familial Restrictive, 3
  • Danon Disease
    • Antopol Disease
    • Glycogen Storage Disease IIb
    • Lysosomal Glycogen Storage Disease Without Acid Maltase Deficiency, Formerly
    • Pseudoglycogenosis II
    • Vacuolar Cardiomyopathy And Myopathy, X-Linked
  • Emery-Dreifuss Muscular Dystrophy 6, X-Linked, Included
  • Fabry Disease
    • Alpha-Galactosidase A Deficiency
    • Alpha-Galactosidase A, Included
    • Anderson-Fabry Disease
    • Angiokeratoma, Diffuse
    • Ceramide Trihexosidase Deficiency
    • Fabry Disease, Cardiac Variant
    • Galactosidase, Alpha, Included
    • GLA Deficiency
    • Hereditary Dystopic Lipidosis
  • Left Ventricular Noncompaction 10
    • Cardiomyopathy, Dilated, 1MM
  • Mitochondrial DNA Depletion Syndrome 12B (Cardiomyopathic Type) Autosomal Recessive
  • actin, alpha, cardiac muscle 1
    • actin, alpha
    • actin, alpha, cardiac muscle
    • smooth muscle actin
  • cysteine and glycine rich protein 3
    • CLP LIM domain protein, muscle
    • cysteine-rich protein 3
    • lim domain protein, cardiac
  • four and a half LIM domains 1
    • KYOT, mouse, homolog of
  • galactosidase, alpha
    • alpha-galactosidase a deficiency
  • lysosomal associated membrane protein 2
    • lysosomal membrane glycoprotein, 110-kd
    • lysosome-associated membrane protein b
  • myosin binding protein C, cardiac
    • cardiac myosin-binding protein C
    • myosin-binding protein C, cardiac
  • myosin heavy chain 6
    • myosin, heavy chain 6, cardiac muscle, alpha
    • myosin, heavy polypeptide 6, cardiac muscle, alpha (cardiomyopathy, hypertrophic 1)
  • myosin heavy chain 7
    • myopathy, distal 1
    • myosin, cardiac, heavy chain, beta
    • myosin, heavy chain 7, cardiac muscle, beta
    • myosin, heavy polypeptide 7, cardiac muscle, beta
  • myosin light chain 2
    • myosin, light chain 2, regulatory, cardiac, slow
    • myosin, light chain, regulatory ventricular
    • myosin, light polypeptide 2, regulatory, cardiac, slow
    • regulatory light chain of myosin
    • RLC of myosin
  • myosin light chain 3
    • ELC of myosin
    • essential light chain of myosin
    • myosin, light chain 1, slow, b
    • myosin, light chain 1, ventricular
    • myosin, light chain 3, alkali, ventricular, skeletal, slow
    • myosin, light polypeptide 3, alkali; ventricular, skeletal, slow
  • myosin light chain kinase 2
    • myosin light chain kinase 2, skeletal muscle
  • nexilin F-actin binding protein
    • nexilin (F actin binding protein)
  • phospholamban
  • protein kinase AMP-activated non-catalytic subunit gamma 2
    • AMP-activated protein kinase, noncatalytic, gamma-2
    • AMPK-gamma-2
    • protein kinase AMP-activated, gamma 2 non-catalytic subunit
  • solute carrier family 25 member 4
    • adenine nucleotide translocator 1
    • ADP/ATP carrier 1
    • ADP/ATP translocator of skeletal muscle
    • solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator) member 4
  • titin
    • cardiomyopathy, dilated 1G (autosomal dominant
    • connectin
  • titin-cap
    • limb girdle muscular dystrophy 2G (autosomal recessive)
    • titin-cap (telethonin)
  • tropomyosin 1
    • cardiomyopathy, hypertrophic 3
    • chromosome 15 open reading frame 13
    • tropomyosin 1 (alpha)
    • tropomyosin, skeletal muscle alpha
  • troponin C1, slow skeletal and cardiac type
    • "troponin C type 1 (slow)"
    • TNNC, "troponin C type 1 (slow)"
    • troponin C, slow
  • troponin I3, cardiac type
    • cardiomyopathy, dilated 2A (autosomal recessive)
    • troponin I type 3
    • troponin I type 3 (cardiac)
    • troponin I type 3 cardiac
    • troponin I, cardiac
  • troponin T2, cardiac type
    • cardiomyopathy, dilated 1D (autosomal dominant)
    • troponin T type 2 (cardiac)
    • troponin t2, cardiac
  • vinculin
Cardiac 67 Gene Panel (consisting of 10 tests)

Manchester RGC - 2014

  • Atrial Fibrillation, Familial, 10
  • Atrial Fibrillation, Familial, 3
  • Atrial Fibrillation, Familial, 4
  • Atrial Fibrillation, Familial, 9
  • Brugada Syndrome 1
    • Brugada Syndrome
    • Right Bundle Branch Block, St Segment Elevation, And Sudden Death Syndrome
    • Sudden Unexplained Nocturnal Death Syndrome
  • Brugada Syndrome 3
  • Cardiac Arrhythmia, Ankyrin-B-Related
    • Ankyrin-B Syndrome
  • Cardiomyopathy, Dilated, 1E
    • Cardiomyopathy, Dilated, With Conduction Defect 2
    • Cardiomyopathy, Dilated, With Conduction Disorder And Arrhythmia
  • Long QT Syndrome 1
    • Jervell And Lange-Nielsen Syndrome (lqt1)
    • Long QT Syndrome 1, Acquired, Susceptibility To, Included
    • Long QT Syndrome 1/2, Included
    • Romano-Ward Syndrome
    • Ventricular Fibrillation With Prolonged Qt Interval
    • Ward-Romano Syndrome
  • Long QT Syndrome 10
  • Long QT Syndrome 11
  • Long QT Syndrome 12
  • Long QT Syndrome 13
  • Long QT Syndrome 2
    • Acquired Long QT Syndrome, Susceptibility To, Included
    • Ether-A-Go-Go-Related Gene, Human
    • Human Ether-A-Go-Go-Related Gene
    • Long QT Syndrome 2, Included
  • Long QT Syndrome 3
    • Long QT Syndrome 2/3, Included
    • Long QT Syndrome 3, Acquired, Susceptibility To, Included
    • Long QT Syndrome 3/6, Included
  • Long QT Syndrome 5
    • Long QT Syndrome 5, Included
    • Minimal Potassium Ion Channel
  • Long QT Syndrome 6
    • Long QT Syndrome 6, Included
    • Minimum Potassium Ion Channel-Related Peptide 1
    • Mink-Related Peptide 1
  • Short QT Syndrome 1
  • Short QT Syndrome 2
  • Short QT Syndrome 3
  • Ventricular Fibrillation, Paroxysmal Familial, 1
    • Ventricular Fibrillation During Myocardial Infarction, Susceptibility To
  • A kinase anchor protein 9
    • A kinase (PRKA) anchor protein 9
  • ankyrin 2
    • ankyrin 2, neuronal
    • long (electrocardiographic) QT syndrome 4
  • calcium voltage-gated channel subunit alpha 1C
    • calcium channel, voltage-dependent, L type, alpha 1C subunit
  • potassium voltage-gated channel subfamily E regulatory subunit 1
    • long qt syndrome 5, included
    • minimal potassium ion channel
    • potassium channel, voltage gated subfamily E regulatory beta subunit 1
    • potassium channel, voltage-gated, Isk-related subfamily, member 1
    • potassium voltage-gated channel, Isk-related family, member 1
  • potassium voltage-gated channel subfamily E regulatory subunit 2
    • minimum potassium ion channel-related peptide 1
    • mink-related peptide 1
    • potassium channel, voltage gated subfamily E regulatory beta subunit 2
    • potassium channel, voltage-gated, isk-related subfamily, member 2
    • potassium voltage-gated channel, Isk-related family, member 2
  • potassium voltage-gated channel subfamily H member 2
    • acquired long QT syndrome, susceptibility to, included
    • ether-a-go-go-related gene, human
    • human ether-a-go-go-related gene
    • long QT syndrome 2, included
    • potassium channel, voltage gated subfamily H, member 2
    • potassium channel, voltage-gated, subfamily H, member 2
    • potassium voltage-gated channel, subfamily H (eag-related), member 2
  • potassium voltage-gated channel subfamily J member 2
    • potassium inwardly-rectifying channel, subfamily J, member 2
  • potassium voltage-gated channel subfamily J member 5
    • potassium channel, inwardly rectifying subfamily J, member 5
    • potassium inwardly-rectifying channel, subfamily J, member 5
  • potassium voltage-gated channel subfamily Q member 1
    • potassium channel, voltage gated KQT-like subfamily Q, member 1
    • potassium channel, voltage-gated, KQT-like subfamily, member 1
    • potassium channel, voltage-gated, shaker-related subfamily, member 9
    • potassium voltage-gated channel, KQT-like subfamily, member 1
  • sodium voltage-gated channel alpha subunit 5
    • sodium channel, voltage-gated, type v, alpha (long qt syndrome 3)
    • sodium channel, voltage-gated, type V, alpha subunit
  • sodium voltage-gated channel beta subunit 4
    • sodium channel, voltage gated, type IV beta subunit
    • sodium channel, voltage-gated, type IV, beta
    • sodium channel, voltage-gated, type IV, beta subunit
  • syntrophin, alpha 1
    • syntrophin, alpha 1 (dystrophin-associated protein A1, 59kD, acidic component)
Cardiac 67 Gene Panel (consisting of 10 tests)

Manchester RGC - 2014

  • Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
    • Arrhythmogenic Right Ventricular Cardiomyopathy 10
  • Arrhythmogenic Right Ventricular Dysplasia, Familial, 11
    • Arrhythmogenic Right Ventricular Cardiomyopathy 11
    • Arrhythmogenic Right Ventricular Dysplasia, Familial, 11, And Mild Palmoplantar Keratoderma With Or Without Woolly Hair, Included
  • Arrhythmogenic Right Ventricular Dysplasia, Familial, 12
    • Arrhythmogenic Right Ventricular Cardiomyopathy 12
  • Arrhythmogenic Right Ventricular Dysplasia, Familial, 13
    • Arrhythmogenic Right Ventricular Cardiomyopathy 13
  • Arrhythmogenic Right Ventricular Dysplasia, Familial, 5
    • Arrhythmogenic Right Ventricular Cardiomyopathy 5
  • Arrhythmogenic Right Ventricular Dysplasia, Familial, 8
    • Arrhythmogenic Right Ventricular Cardiomyopathy 8
  • Arrhythmogenic Right Ventricular Dysplasia, Familial, 9
    • Arrhythmogenic Right Ventricular Cardiomyopathy 9
  • Atrial Fibrillation, Familial, 12
  • Atrial Septal Defect 3
  • Cardiomyopathy, Dilated, 1A
    • Cardiomyopathy, Congestive
    • Cardiomyopathy, Dilated, With Conduction Defect 1
    • Cardiomyopathy, Familial Idiopathic
    • Cardiomyopathy, Idiopathic Dilated
  • Cardiomyopathy, Dilated, 1AA, With Or Without Left Ventricular Noncompaction;
    • Cardiomyopathy, Familial Hypertrophic, 23, With Or Without Ventricular Noncompaction, Included;
  • Cardiomyopathy, Dilated, 1BB
  • Cardiomyopathy, Dilated, 1C, With Or Without Left Ventricular Noncompaction
    • Cardiomyopathy, Dilated, 1c, With Or Without Left Ventricular Noncompaction; CMD1C
    • Cardiomyopathy, Familial Hypertrophic, 24, Included; CMH24, Included
  • Cardiomyopathy, Dilated, 1CC
  • Cardiomyopathy, Dilated, 1D
    • Left Ventricular Noncompaction 6, Included
  • Cardiomyopathy, Dilated, 1DD
  • Cardiomyopathy, Dilated, 1EE
  • Cardiomyopathy, Dilated, 1FF
  • Cardiomyopathy, Dilated, 1G
  • Cardiomyopathy, Dilated, 1I
  • Cardiomyopathy, Dilated, 1J
    • Cardiomyopathy, Dilated, With Sensorineural Hearing Loss, Autosomal Dominant
  • Cardiomyopathy, Dilated, 1KK
    • Cardiomyopathy, Familial Hypertrophic, 22
    • Cardiomyopathy, Familial Restrictive, 4
  • Cardiomyopathy, Dilated, 1L
  • Cardiomyopathy, Dilated, 1M
  • Cardiomyopathy, Dilated, 1NN
  • Cardiomyopathy, Dilated, 1O
    • Cardiomyopathy, Dilated, With Ventricular Tachycardia
  • Cardiomyopathy, Dilated, 1P
  • Cardiomyopathy, Dilated, 1R
  • Cardiomyopathy, Dilated, 1S
    • Left Ventricular Noncompaction 5
  • Cardiomyopathy, Dilated, 1T
  • Cardiomyopathy, Dilated, 1W
  • Cardiomyopathy, Dilated, 1Y
    • Left Ventricular Noncompaction 9
  • Cardiomyopathy, Dilated, 1Z
  • Cardiomyopathy, Dilated, 2A
    • Cardiomyopathy, Congestive, Autosomal Recessive
    • Cardiomyopathy, Dilated, Autosomal Recessive
  • Cardiomyopathy, Dilated, 2B
  • Cardiomyopathy, Dilated, With Hypergonadotropic Hypogonadism
    • Cardiogenital Syndrome
    • Cardiomyopathy With Primary Testicular Failure
    • Cardiomyopathy, Congestive, With Hypergonadotropic Hypogonadism
    • Cardiomyopathy, Dilated, With Premature Ovarian Failure
    • Genital Anomaly With Cardiomyopathy
    • Malouf Syndrome
    • Najjar Syndrome
  • Cardiomyopathy, Dilated, With Woolly Hair, Keratoderma, And Tooth Agenesis
    • Dilated Cardiomyopathy With Woolly Hair, Keratoderma, And Tooth Agenesis
  • Cardiomyopathy, Familial Hypertrophic, 1
    • Asymmetric Septal Hypertrophy
    • Cardiomyopathy, hypertrophic, 1, digenic
    • Cardiomyopathy, Sporadic Hypertrophic, 1, Included
    • Hypertrophic Subaortic Stenosis, Idiopathic
    • Ventricular Hypertrophy, Hereditary
  • Cardiomyopathy, Familial Hypertrophic, 10
    • Cardiomyopathy, Hypertrophic, Mid-Left Ventricular Chamber Type, 2
  • Cardiomyopathy, Familial Hypertrophic, 11
  • Cardiomyopathy, Familial Hypertrophic, 12
  • Cardiomyopathy, Familial Hypertrophic, 13
  • Cardiomyopathy, Familial Hypertrophic, 14
  • Cardiomyopathy, Familial Hypertrophic, 15
  • Cardiomyopathy, Familial Hypertrophic, 16
  • Cardiomyopathy, Familial Hypertrophic, 18
  • Cardiomyopathy, Familial Hypertrophic, 2
  • Cardiomyopathy, Familial Hypertrophic, 20
  • Cardiomyopathy, Familial Hypertrophic, 25
    • Cardiomyopathy, Dilated, 1N
  • Cardiomyopathy, Familial Hypertrophic, 3
  • Cardiomyopathy, Familial Hypertrophic, 4
  • Cardiomyopathy, Familial Hypertrophic, 6
  • Cardiomyopathy, Familial Hypertrophic, 7
  • Cardiomyopathy, Familial Hypertrophic, 8
    • Cardiomyopathy, Hypertrophic, Mid-Left Ventricular Chamber Type, 1
  • Cardiomyopathy, Familial Hypertrophic, 9
  • Cardiomyopathy, Familial Restrictive, 1
  • Cardiomyopathy, Familial Restrictive, 3
  • Danon Disease
    • Antopol Disease
    • Glycogen Storage Disease IIb
    • Lysosomal Glycogen Storage Disease Without Acid Maltase Deficiency, Formerly
    • Pseudoglycogenosis II
    • Vacuolar Cardiomyopathy And Myopathy, X-Linked
  • Emery-Dreifuss Muscular Dystrophy 6, X-Linked, Included
  • Fabry Disease
    • Alpha-Galactosidase A Deficiency
    • Alpha-Galactosidase A, Included
    • Anderson-Fabry Disease
    • Angiokeratoma, Diffuse
    • Ceramide Trihexosidase Deficiency
    • Fabry Disease, Cardiac Variant
    • Galactosidase, Alpha, Included
    • GLA Deficiency
    • Hereditary Dystopic Lipidosis
  • Left Ventricular Noncompaction 10
    • Cardiomyopathy, Dilated, 1MM
  • Mitochondrial DNA Depletion Syndrome 12B (Cardiomyopathic Type) Autosomal Recessive
  • Naxos Disease
    • Cardiomyopathy, Arrhythmogenic Right Ventricular, With Skin, Hair, And Nail Abnormalities
    • Keratosis Palmoplantaris With Arrhythmogenic Cardiomyopathy
    • Mal De Naxos
    • Palmoplantar Keratoderma With Arrhythmogenic Right Ventricular Cardiomyopathy And Woolly Hair
    • Woolly Hair, Palmoplantar Keratoderma, And Cardiac Abnormalities
  • actin, alpha, cardiac muscle 1
    • actin, alpha
    • actin, alpha, cardiac muscle
    • smooth muscle actin
  • actinin, alpha 2
  • ATP-binding cassette, sub-family C, member 9
    • ATP-binding cassette, sub-family C (CFTR/MRP), member 9
    • sulfonylurea receptor 2
  • cysteine and glycine rich protein 3
    • CLP LIM domain protein, muscle
    • cysteine-rich protein 3
    • lim domain protein, cardiac
  • desmin
  • desmocollin 2
    • desmocollin 3, formerly
    • desmosomal glycoprotein II/III
  • desmoglein 2
  • desmoplakin
    • desmoplakin I
    • desmoplakin II
  • EYA transcriptional coactivator and phosphatase 4
    • eyes absent (Drosophila) homolog 4
    • eyes absent homolog 4 (Drosophila)
  • four and a half LIM domains 1
    • KYOT, mouse, homolog of
  • galactosidase, alpha
    • alpha-galactosidase a deficiency
  • junction plakoglobin
    • catenin (cadherin-associated protein), gamma 80kDa
    • catenin, gamma
    • desmoplakin III
    • plakoglobin
  • lamin A/C
    • lamin A
    • lamin C
    • prelamin A
  • lysosomal associated membrane protein 2
    • lysosomal membrane glycoprotein, 110-kd
    • lysosome-associated membrane protein b
  • myosin binding protein C, cardiac
    • cardiac myosin-binding protein C
    • myosin-binding protein C, cardiac
  • myosin heavy chain 6
    • myosin, heavy chain 6, cardiac muscle, alpha
    • myosin, heavy polypeptide 6, cardiac muscle, alpha (cardiomyopathy, hypertrophic 1)
  • myosin heavy chain 7
    • myopathy, distal 1
    • myosin, cardiac, heavy chain, beta
    • myosin, heavy chain 7, cardiac muscle, beta
    • myosin, heavy polypeptide 7, cardiac muscle, beta
  • myosin light chain 2
    • myosin, light chain 2, regulatory, cardiac, slow
    • myosin, light chain, regulatory ventricular
    • myosin, light polypeptide 2, regulatory, cardiac, slow
    • regulatory light chain of myosin
    • RLC of myosin
  • myosin light chain 3
    • ELC of myosin
    • essential light chain of myosin
    • myosin, light chain 1, slow, b
    • myosin, light chain 1, ventricular
    • myosin, light chain 3, alkali, ventricular, skeletal, slow
    • myosin, light polypeptide 3, alkali; ventricular, skeletal, slow
  • myosin light chain kinase 2
    • myosin light chain kinase 2, skeletal muscle
  • nexilin F-actin binding protein
    • nexilin (F actin binding protein)
  • phospholamban
  • plakophilin 2
  • protein kinase AMP-activated non-catalytic subunit gamma 2
    • AMP-activated protein kinase, noncatalytic, gamma-2
    • AMPK-gamma-2
    • protein kinase AMP-activated, gamma 2 non-catalytic subunit
  • RNA binding motif protein 20
  • sarcoglycan delta
    • sarcoglycan, delta (35kD dystrophin-associated glycoprotein)
    • sarcoglycan, delta (35kDa dystrophin-associated glycoprotein)
  • solute carrier family 25 member 4
    • adenine nucleotide translocator 1
    • ADP/ATP carrier 1
    • ADP/ATP translocator of skeletal muscle
    • solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator) member 4
  • thymopoietin
  • titin
    • cardiomyopathy, dilated 1G (autosomal dominant
    • connectin
  • titin-cap
    • limb girdle muscular dystrophy 2G (autosomal recessive)
    • titin-cap (telethonin)
  • transmembrane protein 43
    • arrhythmogenic right ventricular dysplasia 5
  • tropomyosin 1
    • cardiomyopathy, hypertrophic 3
    • chromosome 15 open reading frame 13
    • tropomyosin 1 (alpha)
    • tropomyosin, skeletal muscle alpha
  • troponin C1, slow skeletal and cardiac type
    • "troponin C type 1 (slow)"
    • TNNC, "troponin C type 1 (slow)"
    • troponin C, slow
  • troponin I3, cardiac type
    • cardiomyopathy, dilated 2A (autosomal recessive)
    • troponin I type 3
    • troponin I type 3 (cardiac)
    • troponin I type 3 cardiac
    • troponin I, cardiac
  • troponin T2, cardiac type
    • cardiomyopathy, dilated 1D (autosomal dominant)
    • troponin T type 2 (cardiac)
    • troponin t2, cardiac
  • vinculin
Cardiac 67 Gene Panel (consisting of 10 tests)

Manchester RGC - 2014

  • Arrhythmogenic Right Ventricular Dysplasia, Familial, 2
    • Arrhythmogenic Right Ventricular Cardiomyopathy 2
  • Atrial Fibrillation, Familial, 10
  • Atrial Fibrillation, Familial, 13
  • Atrial Fibrillation, Familial, 3
  • Atrial Fibrillation, Familial, 4
  • Atrial Fibrillation, Familial, 9
  • Brugada Syndrome 1
    • Brugada Syndrome
    • Right Bundle Branch Block, St Segment Elevation, And Sudden Death Syndrome
    • Sudden Unexplained Nocturnal Death Syndrome
  • Brugada Syndrome 2
  • Brugada Syndrome 3
  • Brugada Syndrome 5
  • Brugada Syndrome 6
  • Brugada Syndrome 7
  • Brugada Syndrome 8
  • Cardiac Arrhythmia, Ankyrin-B-Related
    • Ankyrin-B Syndrome
  • Cardiomyopathy, Dilated, 1E
    • Cardiomyopathy, Dilated, With Conduction Defect 2
    • Cardiomyopathy, Dilated, With Conduction Disorder And Arrhythmia
  • Long QT Syndrome 1
    • Jervell And Lange-Nielsen Syndrome (lqt1)
    • Long QT Syndrome 1, Acquired, Susceptibility To, Included
    • Long QT Syndrome 1/2, Included
    • Romano-Ward Syndrome
    • Ventricular Fibrillation With Prolonged Qt Interval
    • Ward-Romano Syndrome
  • Long QT Syndrome 10
  • Long QT Syndrome 11
  • Long QT Syndrome 12
  • Long QT Syndrome 13
  • Long QT Syndrome 2
    • Acquired Long QT Syndrome, Susceptibility To, Included
    • Ether-A-Go-Go-Related Gene, Human
    • Human Ether-A-Go-Go-Related Gene
    • Long QT Syndrome 2, Included
  • Long QT Syndrome 3
    • Long QT Syndrome 2/3, Included
    • Long QT Syndrome 3, Acquired, Susceptibility To, Included
    • Long QT Syndrome 3/6, Included
  • Long QT Syndrome 5
    • Long QT Syndrome 5, Included
    • Minimal Potassium Ion Channel
  • Long QT Syndrome 6
    • Long QT Syndrome 6, Included
    • Minimum Potassium Ion Channel-Related Peptide 1
    • Mink-Related Peptide 1
  • Short QT Syndrome 1
  • Short QT Syndrome 2
  • Short QT Syndrome 3
  • Ventricular Fibrillation, Paroxysmal Familial, 1
    • Ventricular Fibrillation During Myocardial Infarction, Susceptibility To
  • Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/or Dilated Cardiomyopathy
    • Ventricular Tachycardia, Stress-Induced Polymorphic
  • Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
    • Ventricular Tachycardia, Stress-Induced Polymorphic
  • Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
  • Ventricular Tachycardia, Catecholaminergic Polymorphic, 5, With Or Without Muscle Weakness
  • A kinase anchor protein 9
    • A kinase (PRKA) anchor protein 9
  • ankyrin 2
    • ankyrin 2, neuronal
    • long (electrocardiographic) QT syndrome 4
  • calcium voltage-gated channel subunit alpha 1C
    • calcium channel, voltage-dependent, L type, alpha 1C subunit
  • calmodulin 1
    • calmodulin 1 (phosphorylase kinase, delta)
  • calsequestrin 2
    • calsequestrin 2 (cardiac muscle)
  • glycerol-3-phosphate dehydrogenase 1 like
    • glycerol-3-phosphate dehydrogenase 1-like
  • hyperpolarization activated cyclic nucleotide gated potassium channel 4
    • hyperpolarization activated cyclic nucleotide-gated potassium channel 4
  • potassium voltage-gated channel subfamily E regulatory subunit 1
    • long qt syndrome 5, included
    • minimal potassium ion channel
    • potassium channel, voltage gated subfamily E regulatory beta subunit 1
    • potassium channel, voltage-gated, Isk-related subfamily, member 1
    • potassium voltage-gated channel, Isk-related family, member 1
  • potassium voltage-gated channel subfamily E regulatory subunit 2
    • minimum potassium ion channel-related peptide 1
    • mink-related peptide 1
    • potassium channel, voltage gated subfamily E regulatory beta subunit 2
    • potassium channel, voltage-gated, isk-related subfamily, member 2
    • potassium voltage-gated channel, Isk-related family, member 2
  • potassium voltage-gated channel subfamily E regulatory subunit 3
    • potassium channel, voltage gated subfamily E regulatory beta subunit 3
    • potassium voltage-gated channel, Isk-related family, member 3
  • potassium voltage-gated channel subfamily H member 2
    • acquired long QT syndrome, susceptibility to, included
    • ether-a-go-go-related gene, human
    • human ether-a-go-go-related gene
    • long QT syndrome 2, included
    • potassium channel, voltage gated subfamily H, member 2
    • potassium channel, voltage-gated, subfamily H, member 2
    • potassium voltage-gated channel, subfamily H (eag-related), member 2
  • potassium voltage-gated channel subfamily J member 2
    • potassium inwardly-rectifying channel, subfamily J, member 2
  • potassium voltage-gated channel subfamily J member 5
    • potassium channel, inwardly rectifying subfamily J, member 5
    • potassium inwardly-rectifying channel, subfamily J, member 5
  • potassium voltage-gated channel subfamily Q member 1
    • potassium channel, voltage gated KQT-like subfamily Q, member 1
    • potassium channel, voltage-gated, KQT-like subfamily, member 1
    • potassium channel, voltage-gated, shaker-related subfamily, member 9
    • potassium voltage-gated channel, KQT-like subfamily, member 1
  • ryanodine receptor 2
    • arrhythmogenic right ventricular dysplasia 2
    • ryanodine receptor 2 (cardiac)
    • ryanodine receptor, cardiac
  • sodium voltage-gated channel alpha subunit 5
    • sodium channel, voltage-gated, type v, alpha (long qt syndrome 3)
    • sodium channel, voltage-gated, type V, alpha subunit
  • sodium voltage-gated channel beta subunit 1
    • sodium channel, voltage-gated, type I, beta
    • sodium channel, voltage-gated, type I, beta polypeptide
    • sodium channel, voltage-gated, type I, beta subunit
  • sodium voltage-gated channel beta subunit 3
    • sodium channel, voltage gated, type III beta subunit
    • sodium channel, voltage-gated, type III, beta
    • sodium channel, voltage-gated, type III, beta subunit
  • sodium voltage-gated channel beta subunit 4
    • sodium channel, voltage gated, type IV beta subunit
    • sodium channel, voltage-gated, type IV, beta
    • sodium channel, voltage-gated, type IV, beta subunit
  • syntrophin, alpha 1
    • syntrophin, alpha 1 (dystrophin-associated protein A1, 59kD, acidic component)
  • triadin

Filters

Search filters