Mitochondrial Diseases Report

Mitochondrial Diseases Report

Regular price $49.00
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Please note that these reports are recommended only for Whole Genome Test with 30X and up coverage

(Not compatible with WGL Longreads sequencing test)

 

The Mitochondrial Diseases test is based on the Whole Genome Sequencing Test. As such, it analyses all Common and Rare Variants associated with Mitochondrial Diseases instead of a limited set of genes.

Mitochondrial diseases are chronic (long-term), genetic, often inherited disorders that occur when mitochondria fail to produce enough energy for the body to function properly.

 

Along with environmental factors, Genetics plays a key role in the regulation of Mitochondrial Diseases.

 

Click here to see what your report will look like

 

  • 132 genes analyzed
  • 100% genomic regions covered
  • Intragenic and intergenic regions analyzed
  • All variants reported

 

 

List of genes:

HMGCS2,NDUFS4,NDUFAF2,NDUFAF1,NDUFA1,NDUFA2,NDUFA11,NDUFAF4,NDUFAF5,NDUFAF6,NDUFAF3,FOXRED1,NDUFS8,NUBPL,NDUFA10,NDUFA12,NDUFB9,NDUFB3,NDUFA9,MTFMT,NDUFA13,TMEM126B,NDUFS7,NDUFB11,TIMMDC1,NDUFB8,NDUFA6,NDUFV1,NDUFS1,NDUFS2,NDUFV2,NDUFS3,NDUFS6,SDHA,SDHAF1,SDHD,BCS1L,TTC19,UQCRB,UQCRQ,UQCRC2,CYC1,UQCC2,LYRM7,UQCC3,ATP5F1A,ATP5F1D,ATP5MD,ATP5F1E,ATPAF2,COA8,COX10,COX14,COX15,COX20,COX6B1,COX8A,DGUOK,DLAT,DLD,FASTKD2,FBXL4,LRPPRC,MGME1,MPV17,MT-ATP6,MT-CO1,MT-ND1,MT-ND4,MT-ND5,MT-ND6,MT-RNR1,MT-TA,MT-TC,MT-TD,MT-TF,MT-TH,MT-TK,MT-TL1,MT-TL2,MT TM,MT-TN,MT-TQ,MT-TR,MT-TS1,MT-TS2,MT-TT,MT-TV,MT-TW,MT-TY,PC,PDHA1,PDHB,PDHX,PET100,RRM2B,SCN4A,SCO1,SUCLA2,SUCLG1,SURF1,TACO1,TMEM70,TWNK,POLG,TYMP,SLC25A4,OPA1,TFAM,POLG2,MRM2,TK2,MT-CO3,MT-ND2,MT-ND3,MT-TI,FDX2,PUS1,YARS2,PNPLA8,SLC25A3,MPC1,ECHS1,HADHA,HADHB, MT-ATP8, MT-CO2, MT-CYB, ND4L, MT-RNR2, MT-TE,MT-TP