Short Description

List of genes tested using NGS technology for detection of variant and mutation in NGSMito Comprehensive are AARS2, AASS, ABAT, ABCB6, ABCB7, ABCD1, ABCD3, ACACA, ACAD8, ACAD9, ACADM, ACADS, ACADSB, ACADVL, ACAT1, ACO2, ACOX1, ACSF3, ACSL4, AFG3L2, AGK, AGXT, AIFM1, AK2, ALAS2, ALDH18A1, ALDH2, ALDH3A2, ALDH4A1, ALDH5A1, ALDH6A1, ALDH7A1, AMACR, AMT, APTX, ATIC, ATP5F1A, ATP5F1E, ATP7B, ATPAF2, ATXN2, AUH, BAX, BCKDHA, BCKDHB, BCKDK, BCL2, BCS1L, BOLA3, BRIP1, BTD, C12orf65, CA5A, CASP8, CAT, CAVIN1, CEL, CHCHD10, CISD2, CLPB, CLPP, COA5, COA6, COA8, COASY, COMT, COQ2, COQ4, COQ6, COQ8A, COQ8B, COQ9, COX10, COX14, COX15, COX20, COX4I2, COX6A1, COX6B1, COX7B, CPOX, CPS1, CPT1A, CPT1C, CPT2, CRBN, CYB5A, CYB5R3, CYC1, CYCS, CYP11A1, CYP11B1, CYP11B2, CYP24A1, CYP27A1, CYP27B1, D2HGDH, DARS2, DBT, DGUOK, DHCR24, DHODH, DHTKD1, DIABLO, DLAT, DLD, DMGDH, DMPK, DNA2, DNAJC19, DNAJC3, DNM1L, EARS2, ECHS1, ELAC2, EPHX2, ETFA, ETFB, ETFDH, ETHE1, FAH, FARS2, FASTKD2, FBXL4, FECH, FH, FKBP10, FOXRED1, FTH1, FXN, GARS1, GATM, GCDH, GCSH, GDAP1, GFER, GFM1, GFM2, GK, GLDC, GLRX5, GLUD1, GLYCTK, GPI, GPT2, GPX1, GRHPR, GSR, GTPBP3, HADH, HADHA, HADHB, HAMP, HARS2, HAX1, HCCS, HIBCH, HINT1, HK1, HLCS, HMBS, HMGCL, HMGCS2, HOGA1, HSD17B10, HSD17B4, HSD3B2, HSPA9, HSPD1, HTRA2, IARS2, IBA57, IDH2, IDH3B, ISCA2, ISCU, IVD, KARS1, KIF1B, KRT5, L2HGDH, LARS2, LIAS, LIPT1, LONP1, LRPPRC, LYRM7, MAOA, MARS2, MCCC1, MCCC2, MCEE, MFN2, MGME1, MICU1, MIP, MLH1, MLYCD, MMAA, MMAB, MMACHC, MMADHC, MMUT, MOCS1, MPC1, MPV17, MRPL3, MRPL44, MRPS16, MRPS22, MSRB3, MTFMT, MTO1, MTPAP, MTRR, MUTYH, NADK2, NAGS, NARS2, NBAS, NDUFA1, NDUFA10, NDUFA11, NDUFA12, NDUFA2, NDUFA9, NDUFAF1, NDUFAF2, NDUFAF3, NDUFAF4, NDUFAF5, NDUFAF6, NDUFB11, NDUFB3, NDUFB9, NDUFS1, NDUFS2, NDUFS3, NDUFS4, NDUFS6, NDUFS7, NDUFS8, NDUFV1, NDUFV2, NFU1, NNT, NTHL1, NUBPL, OAT, OGDH, OGG1, OPA1, OPA3, OTC, OXCT1, P4HB, PAM16, PANK2, PARK7, PC, PCCA, PCCB, PCK2, PDHA1, PDHB, PDHX, PDK3, PDP1, PDSS1, PDSS2, PDX1, PET100, PEX11B, PHYH, PINK1, PKLR, PNPLA8, PNPO, PNPT1, POLG, POLG2, PPOX, PRODH, PTRH2, PTS, PUS1, PYCR1, PYCR2, QDPR, RARS1, RARS2, RDH11, RMND1, RNASEH1, RNASEL, RPIA, RPL35A, RPS14, RRM2B, SARS2, SBDS, SCO1, SCO2, SDHA, SDHAF1, SDHAF2, SDHB, SDHC, SDHD, SECISBP2, SERAC1, SFXN4, SLC16A1, SLC19A3, SLC25A1, SLC25A12, SLC25A13, SLC25A15, SLC25A19, SLC25A20, SLC25A22, SLC25A3, SLC25A38, SLC25A4, SLC25A46, SLC9A6, SNAP29, SOD1, SOD2, SPG7, SPR, SPTLC2, STAR, SUCLA2, SUCLG1, SUGCT, SUOX, SURF1, TACO1, TARS2, TCIRG1, TFR2, TIMM8A, TK2, TMEM126A, TMEM70, TMLHE, TPI1, TPK1, TRMU, TRNT1, TSFM, TTC19, TUBB3, TUFM, TWNK, TYMP, UNG, UQCC2, UQCRB, UQCRC2, UQCRQ, VARS2, WDR81, WFS1, XPNPEP3, YARS2

PreTest Information

Clinical History of Patient who is going for NGSMito Comprehensive NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NGSMito Comprehensive

Detail Description

NGSMito Comprehensive NGS Genetic DNA Test

DNA Labs India offers the NGSMito Comprehensive NGS Genetic DNA Test for INR 20,000. This test helps in the diagnosis of various genetic disorders by analyzing the mitochondrial DNA (mtDNA) present in the cells.

Symptoms

Various symptoms that may indicate the need for NGSMito Comprehensive NGS Genetic DNA Test are:

• Developmental delays
• Muscle weakness
• Memory loss
• Vision loss
• Hearing loss
• Seizures
• Stroke-like episodes
• Heart problems
• Diabetes
• Liver disease

Diagnosis

NGSMito Comprehensive NGS Genetic DNA Test helps in the diagnosis of various genetic disorders such as:

• Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS)
• Leber hereditary optic neuropathy (LHON)
• Mitochondrial myopathy
• Mitochondrial neurogastrointestinal encephalopathy (MNGIE)

The test involves sequencing the entire mitochondrial genome, which helps in identifying any mutations or changes in the mtDNA. These mutations can affect the functioning of the mitochondria, leading to various genetic disorders.

Cost

The NGSMito Comprehensive NGS Genetic DNA Test costs INR 20,000 at DNA Labs India. The cost may vary depending on the location and other factors.

Conclusion

The NGSMito Comprehensive NGS Genetic DNA Test is a powerful tool in the diagnosis of various genetic disorders. It helps in identifying any mutations or changes in the mitochondrial genome, which can affect the functioning of the mitochondria. The test is available at DNA Labs India for INR 20,000.

Before getting tested ask for Raw Data, FASTQ, and VCF files along with clinical test report from DNA Testing Lab. DNA Labs India is the Only lab that is transparent and will share Raw Data, FASTQ, and VCF files along with the conclusive clinical report for NGSMito Comprehensive NGS Genetic DNA Test