Ataxia Report

Ataxia Report

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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 Atassia Report is based on Whole Genome Sequencing Test. As such, it analyzes all Common and Rare Variants associated with Atassia instead of a limited set of genes, like old genetic target panels. 

Ataxia describes a lack of muscle control or coordination of voluntary movements.

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

 

Click here to see what your report will look like

 

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

 

List of genes:

MTFMT,MTPAP,MTTP,NDUFAF6,NDUFS2,NDUFS4,NDUFS7,NDUFS8,
NDUFV1,NOL3,NPHP1,NUBPL,OFD1,OPA1,OPHN1,PAX6,PDYN,PEX7,
PHYH,PNKD,PNKP,PNPLA6,POLG,PPP2R2B,PRKCG,PRRT2,RNF216,
RPGRIP1L,RUBCN,SACS,SERAC1,SETX,SIL1,SLC1A3,SLC2A1,SLC9A6,
SLC20A2,SLC25A46,SLC52A2,SNX14,SPG7,SPTBN2,STUB1,SYNE1,
SYT14,TCTN1,TCTN2,TCTN3,TDP1,TGM6,TMEM67,TMEM138,TMEM216,
TMEM231,TMEM237,TMEM240,TPP1,TRIM32,TTBK2,TTC8,TTC19,TTPA,
TUBB4A,UBA5,VAMP1,VLDLR,WDPCP,WDR81,WFS1,WWOX,ZFYVE26,
ABCB7,ABHD12,ACO2,ADCK3,AFG3L2,AHI1,ALDH5A1,ALS2,ANO10,
APTX,ARL6,ARL13B,ATCAY,ATL1,ATM,ATP1A3,ATP8A2,B9D1,BBS1,BBS2,
BBS4,BBS5,BBS7,BBS9,BBS10,BBS12,BSCL2,BEAN1,C5ORF42,C10ORF2,
C12orf65,C19orf12,CA8,CACNA1A,CACNB4,CAMTA1,CAPN1,CASK,CC2D2A,
CCDC88C,CEP290,CEP41,CLCN2,CLN5,CLPP,COASY,COQ2,COQ6,COQ8A,
COQ9,COX20,CP,CPLANE1,CSTB,CWF19L1,CYP2U1,CYP27A1,CYP7B1,
DNAJC19,DNMT1,EBF3,EEF2,EIF2B1,EIF2B2,EIF2B3,EIF2B4,EIF2B5,
ELOVL4,ELOVL5,FA2H,FBXL4,FDXR,FGF14,FLVCR1,FMR1,FXN,GALC,
GBA2,GFAP,GJC2,GOSR2,GRID2,GRM1,GSS,HARS2,HEPACAM,HIBCH,
INPP5E,ITM2B,ITPR1,KCNA1,KCNC3,KCND3,KCNJ10,KIF1A,KIF1C,KIF5A,
KIF7,LAMA1,LARS2,LMNB1,LRPPRC,MARS2,MKKS,MKS1,MKKS,MKS1,
MLC1,MME,MRE11,MRE11A,NDUFS1,NOTCH3,OPA3,PDSS1,PDSS2,
PEX10,PLP1,POLR3A,POLR3B,RRM2B,SLC16A2,SLC52A3,SPAST,SPG11,
SPR,TWNK,TYMP,WASHC5,WDR73,ZNF423