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01 MELAS Syndrome [NCBI]

Gene


 Gene Link Information
Gain		 01
TRNL1 [NCBI] 0.0019939
TRNV [NCBI] 0.000288064
TRNA [NCBI] 0.000288064
TRNK [NCBI] 0.00021682
TRNS1 [NCBI] 0.000202104
MS [NCBI] 7.35891e-05
ND1 [NCBI] 3.60449e-05
ND5 [NCBI] 2.47269e-05
POLG [NCBI] 1.92347e-05
GFM2 [NCBI] 1.56978e-05
TOMM20 [NCBI] 1.47993e-05
TOMM34 [NCBI] 1.3782e-05
LARS2 [NCBI] 1.31488e-05
NDUFV3 [NCBI] 1.31488e-05
ASNS [NCBI] 1.15482e-05
COX2 [NCBI] 1.13518e-05
TUFM [NCBI] 1.13518e-05
PRCC [NCBI] 1.04937e-05
FES [NCBI] 1.00071e-05
ATF4 [NCBI] 9.88455e-06
HSPD1 [NCBI] 9.03246e-06
TFE3 [NCBI] 8.93916e-06
CS [NCBI] 8.13837e-06
NOTCH3 [NCBI] 7.19265e-06
DDIT3 [NCBI] 6.90813e-06
ALDH2 [NCBI] 6.50518e-06
IGF1 [NCBI] 5.8626e-06
STAT1 [NCBI] 5.31428e-06
PTGS1 [NCBI] 5.0169e-06
CASP3 [NCBI] 2.6877e-06
PTGS2 [NCBI] 2.30422e-06



OMIM


 OMIM Link Information
gain		 01
MTTL1 [NCBI] 0.00195421
MELAS [NCBI] 0.00107505
MTND5 [NCBI] 0.000500416
KSS [NCBI] 0.000398277
MERRF [NCBI] 0.000286926
MTTK [NCBI] 0.000138251
leber optic atrophy [NCBI] 8.80295e-05
MTND1 [NCBI] 8.69882e-05
vasculopathy, retinal, with cerebral leukodystrophy [NCBI] 8.63791e-05
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive [NCBI] 7.57931e-05
MNGIE [NCBI] 6.70381e-05
MTATP8 [NCBI] 6.53848e-05
FHM1 [NCBI] 6.08897e-05
MTTQ [NCBI] 6.01867e-05
MTTS2 [NCBI] 6.01867e-05
MTTH [NCBI] 5.23058e-05
MTTF [NCBI] 5.06447e-05
NPS [NCBI] 4.84579e-05
TREX1 [NCBI] 4.68774e-05
LS [NCBI] 4.36936e-05
MTTS1 [NCBI] 4.08287e-05
MTCYB [NCBI] 3.97595e-05
MTND6 [NCBI] 3.87956e-05
MTND4 [NCBI] 2.96616e-05
CJD [NCBI] 7.94684e-06



Database Center for Life Science