Long QT Syndrome Panel (31 Genes)
| TEST CODE | MGT0320 |
| TEST NAME | Long QT Syndrome Panel (31 Genes) |
| RELATED GENE | AKAP9, ANK2, CACNA1C, CACNA2D1, CACNB2, CASQ2, CAV3, DES, DSC2, DSG2, DSP, GPD1L, JUP, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNQ1, LMNA, PKP2, RYR2, SCN1B, SCN3B, SCN4B, SCN5A, SNTA1, TMEM43, TRPM4 |
| SYNONYMOUS | AKAP9, ANK2, CACNA1C, CACNA2D1, CACNB2, CASQ2, CAV3, DES, DSC2, DSG2, DSP, GPD1L, JUP, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNQ1, LMNA, PKP2, RYR2, SCN1B, SCN3B, SCN4B, SCN5A, SNTA1, TMEM43, TRPM4 |
| OMIM | |
| HEREDITY | |
| CLINICAL AREA | Long QT syndrome (LQTS) is a genetically inherited arrhythmia disease caused by dysfunction of ion channels that affects the repolarization phase of the action potential of the heart muscle cell. Within the scope of the panel, 31 genes associated with the disease are examined. |
| METHOD | Next Generation Sequencing (NGS) |
| SAMPLE TYPE | Blood with EDTA |
| QUANTITY | 3 mL |
| TAT | 40 DAYS |
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