Dilated Cardiomyopathy (DCM) and Conduction Defects - Expanded Panel

Overview

Test Name
Dilated Cardiomyopathy (DCM) and Conduction Defects - Expanded Panel
Test Code
CAE1008
Test Category
Gene Panels
Test Subcategory
Cardiology
Disease(s) Targeted
Dilated Cardiomyopathy (DCM) and Conduction Defects
Who Is The Test For?
Patients with a family history, clinical suspicion, or diagnosis of Dilated Cardiomyopathy (DCM) and Conduction Defects
Test Approach

Whole exome sequencing (WES) with in silico gene panel analysis

No. Of Genes
88
Panel Content
ABCC9, ACTC1, ACTN2, BAG3, CRYAB, CSRP3, DES, DMD, DSG2, DSP, EPG5, EYA4, FKTN, FLNC, GATAD1, HAMP, HFE, HJV, IDH2, JPH2, LAMA4, LDB3, LMNA, MT-ATP6, MT-ATP8, MT-CO1, MT-CO2, MT-CO3, MT-CYB, MT-ND1, MT-ND2, MT-ND3, MT-ND4, MT-ND4L, MT-ND5, MT-ND6, MT-RNR1, MT-RNR2, MT-TA, MT-TC, MT-TD, MT-TE, MT-TF, MT-TG, MT-TH, MT-TI, MT-TK, MT-TL1, MT-TL2, MT-TM, MT-TN, MT-TP, MT-TQ, MT-TR, MT-TS1, MT-TS2, MT-TT, MT-TV, MT-TW, MT-TY, MYBPC3, MYH6, MYH7, MYPN, NEXN, PLN, PPCS, PPP1R13L, PRDM16, PSEN1, PSEN2, RAF1, RBM20, SCN5A, SDHA, SGCD, SLC40A1, SPEG, TAFAZZIN, TCAP, TFR2, TNNC1, TNNI3, TNNI3K, TNNT2, TPM1, TTN, VCL
Mitochondrial Genome Included In The Analysis
Yes
Deliverables
Turnaround Time

~3-6 weeks*

Specimen Requirements

For detailed information about the sample requirements, please consult our clinical sample requirements page.

Alternative Panels Available
*Turnaround times are estimated from receipt of satisfactory specimen and test request form at the laboratory to release of clinical report. The turnaround time may vary depending on the nature of the specimen and the complexity of the investigation required. The above table is only a guideline and the complexity of a case and the requirement for further investigations may change this.

About Dilated Cardiomyopathy (DCM) and Conduction Defects

Cardiomyopathies are a heterogeneous group of pathologies of the heart which may affect its size, shape and/or thickness. Common cardiomyopathies include hypertrophic cardiomyopathy and dilated cardiomyopathy.

Conduction defects refer to abnormalities in the electrical conduction system of the heart, which is responsible for coordinating the heart's rhythm and ensuring that the heart muscles contract in a synchronized manner to effectively pump blood.

Cardiomyopathy is a clinically heterogenous disease, and one of the factors that differentiates clinical phenotypes is genotype.

Gene Panel Workflow

©2023 Genseq All Rights Reserved.

Terms & Conditions
Privacy Policy
Cookie Policy