Mitochondrial DNA Analysis (Whole Genome)
| TEST CODE | MG01900 |
| TEST NAME | Mitochondrial DNA Analysis (Whole Genome) |
| RELATED GENE | MT-ND5, MT-ND6, MT-ND2, MT-ND4, MT-ND1, MTND4L, TNRF, RNR1, TRNV, RNR2, TRNL1, TRNI, TRNQ, TRNM, TRNW, TRNN, TRNC, TRNY, COX1, TRNK, COX3, TRNG, MTND3, TRNR, TRNL2, TRNE, CYTB, TRNT, TRNP, ATP6 |
| SYNONYMOUS | MT-ND5, MT-ND6, MT-ND2, MT-ND4, MT-ND1, MTND4L, TNRF, RNR1, TRNV, RNR2, TRNL1, TRNI, TRNQ, TRNM, TRNW, TRNN, TRNC, TRNY, COX1, TRNK, COX3, TRNG, MTND3, TRNR, TRNL2, TRNE, CYTB, TRNT, TRNP, ATP6 |
| OMIM | |
| HEREDITY | |
| CLINICAL AREA | “These 30 genes are screened and associated with disease phenotypes such as Leigh Syndrome, Kearns-Sayre Syndrome, neuropathy, ataxia and retinitis pigmentosa, mitochondrial encephalopathy and MELAS. |
| METHOD | Next Generation Sequencing |
| SAMPLE TYPE | Blood with EDTA |
| QUANTITY | 3 mL |
| TAT | 40 DAYS |
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