XomeDxSlice Tool

Now Available - NEW XomeDxSlice Xpanded – Custom slice testing with trio analysis for lists >150 genes.



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You may also use this search to review average exome sequencing coverage by entering the gene symbol below.


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Ventricular extrasystoles

Select all: Gene symbolChrAvg % covered at 10xLocus TypeNoteOMIMPrevious symbol(s)Phenotype(s)Slice(s)
DSG218q12.199.99%gene with protein product125671Autosomal dominant inheritance; Dilated cardiomyopathy; Heterogeneous; Palpitations; Right ventricular cardiomyopathy; Sudden cardiac death; Ventricular extrasystoles; Ventricular tachycardiaPalmoplantar keratoderma plus congenital ichthyosis
DSP6p24.3100%gene with protein product125647Abnormality of the cardiovascular system; Abnormality of the hair; Abnormality of the nail; Acantholysis; Alopecia; Alopecia universalis; Anonychia; Aplasia cutis congenita; Autosomal dominant inheritance; Autosomal recessive inheritance; Bronchiectasis; Clubbing of fingers; Congenital bullous ichthyosiform erythroderma; Congestive heart failure; Cough; Dilated cardiomyopathy; Exertional dyspnea; Failure to thrive; Fragile skin; Gastroesophageal reflux; Gingival recession; Ground-glass opacification on pulmonary HRCT; Heterogeneous; Honeycomb lung; Mitten deformity; Nail dysplasia; Nail dystrophy; Natal tooth; Neonatal death; Oral mucosal blisters; Palmoplantar keratoderma; Palmoplantar keratosis with erythema and scale; Parakeratosis; Patchy palmoplantar keratoderma; Phimosis; Pulmonary fibrosis; Rales; Reduced number of teeth; Reticular pattern on pulmonary HRCT; Right ventricular cardiomyopathy; Sandal gap; Skin erosion; Sparse and thin eyebrow; Sparse eyelashes; Sudden cardiac death; Tapered distal phalanges of finger; Ventricular extrasystoles; Ventricular fibrillation; Ventricular tachycardia; Widely spaced toes; Woolly hairEctodermal Dysplasia ; Palmoplantar keratoderma plus congenital ichthyosis
NAA10Xq2899.97%gene with protein product300013ARD1, ARD1AAbnormal palmar dermatoglyphics; Abnormality of dental morphology; Abnormality of the dentition; Abnormality of the nares; Abnormality of the pinna; Aganglionic megacolon; Agenesis of maxillary lateral incisor; Aggressive behavior; Anal atresia; Anophthalmia; Atrial septal defect; Bicuspid aortic valve; Blindness; Broad hallux; Camptodactyly; Camptodactyly of finger; Cerebral atrophy; Chorioretinal coloboma; Ciliary body coloboma; Cleft upper lip; Clinodactyly; Clinodactyly of the 5th finger; Coarse facial features; Complete duplication of thumb phalanx; Congenital onset; Cryptorchidism; Deep philtrum; Delayed cranial suture closure; Dental crowding; Depressed nasal bridge; Down-sloping shoulders; Downslanted palpebral fissures; Epicanthus; Everted upper lip vermilion; External ear malformation; Facial wrinkling; Finger syndactyly; Generalized hypotonia; Glaucoma; Global developmental delay; Growth delay; Hearing impairment; High palate; High, narrow palate; Hydronephrosis; Hydroureter; Hypertonia; Hypospadias; Inguinal hernia; Intellectual disability; Iris coloboma; Joint contracture of the hand; Kyphoscoliosis; Long eyelashes; Low-set ears; Low-set, posteriorly rotated ears; Lumbar hyperlordosis; Macrotia; Microcephaly; Microcornea; Microphthalmia; Microretrognathia; Minimal subcutaneous fat; Motor delay; Narrow chest; Optic nerve coloboma; Oral cleft; Overfolded helix; Pectus excavatum; Postnatal growth retardation; Prominent forehead; Proptosis; Ptosis; Pulmonary artery stenosis; Pyloric stenosis; Radial deviation of finger; Rectal prolapse; Recurrent infections; Recurrent otitis media; Redundant skin; Renal hypoplasia; Renal hypoplasia/aplasia; Seizures; Self-mutilation; Short clavicles; Short columella; Short stature; Sparse and thin eyebrow; Spastic diplegia; Stereotypy; Supraventricular tachycardia; Syndactyly; Thick upper lip vermilion; Thin upper lip vermilion; Torsade de pointes; Underdeveloped nasal alae; Variable expressivity; Ventricular extrasystoles; Ventricular septal defect; Ventricular tachycardia; Webbed neck; Wide nasal bridge; X-linked dominant inheritance; X-linked inheritance; X-linked recessive inheritance
SCN5A3p22.2100%gene with protein product600163CMD1EArrhythmia; Atrial fibrillation; Atrial flutter; Atrial standstill; Atrioventricular block; Autosomal dominant inheritance; Autosomal recessive inheritance; Cardiac arrest; Complete heart block with broad QRS complexes; Congenital onset; Dilated cardiomyopathy; Dyspnea; Heterogeneous; Left anterior fascicular block; Left bundle branch block; Left posterior fascicular block; Palpitations; Paroxysmal atrial fibrillation; Premature atrial contractions; Prolonged QT interval; Reduced systolic function; Right bundle branch block; Sick sinus syndrome; Sinus bradycardia; Stroke; Sudden cardiac death; Sudden death; Supraventricular tachycardia; Syncope; Torsade de pointes; Ventricular escape rhythm; Ventricular extrasystoles; Ventricular fibrillationHeterotaxy
SLC25A203p21.31100%gene with protein product613698CACTAbnormality of skeletal muscles; Atrioventricular block; Autosomal recessive inheritance; Bradycardia; Cardiomyopathy; Cardiorespiratory arrest; Coma; Decreased plasma carnitine; Dicarboxylic aciduria; Elevated creatine kinase after exercise; Elevated hepatic transaminases; Elevated plasma acylcarnitine levels; Elevated serum creatine phosphokinase; Encephalopathy; Fasting hypoglycemia; Generalized hypotonia; Global developmental delay; Hepatomegaly; Hyperammonemia; Hypoglycemia; Hypoketotic hypoglycemia; Hypotension; Irritability; Lethargy; Muscle weakness; Respiratory insufficiency; Rhabdomyolysis; Seizures; Ventricular extrasystoles; Ventricular hypertrophy; Ventricular tachycardiaRhabdomyolysis
TMEM433p25.1100%gene with protein product612048ARVD5Adult onset; Atrial fibrillation; Autosomal dominant inheritance; Bradycardia; Chest pain; Congestive heart failure; Muscular dystrophy; Neck muscle weakness; Palpitations; Prolonged QRS complex; Proximal amyotrophy; Proximal muscle weakness; Right ventricular cardiomyopathy; Slow progression; Sudden cardiac death; Ventricular extrasystoles; Ventricular tachycardia

The gene coverage data provided by GeneDx represent an estimate based on previous results, but the specific sequencing coverage data for the genes selected may vary from individual to individual, and cannot be predicted exactly. Changes to an approved gene list can only be made by contacting GeneDx directly at 888-729-1206 and asking to speak with a member of our Whole Exome Sequencing Laboratory.


Customize below OR enter Suggested Slice ID on printed requisition form
(e.g. 706 XomeDxSlice - Slice ID: CS-Albinism).

Suggested Slice IDSuggested Gene List Name
CS-AAAplastic Anemia
CS-AutoImmuneAutoimmune Disorders
CS-BBSBardet-Biedl Syndrome
CS-BMFBone Marrow Failure Syndromes
CS-CVIDCommon Variable Immune Deficiency
CS-CKUTCongenital Kidney and Urinary Tract (CKUT) Anomalies
CS-DSDDisorders of Sex Development
CS-EDEctodermal Dysplasia
CS-FAFanconi Anemia
CS-AnemiaHemolytic Anemia
CS-IBDInflammatory Bowel Disease
CS-MaleInfMale Infertility
CS-WWSMuscular dystropy-dystroglycanopathy (Walker-Warburg)
CS-NephroticNephrotic Syndrome
CS-PPKCIPalmoplantar keratoderma plus congenital ichthyosis
CS-Primary ImmunodefPrimary Immunodeficiency
CS-SRTDShort-Rib Thoracic Dysplasia
CS-WSWaardenburg Syndrome