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01 Mitochondrial Encephalomyopathies [NCBI]

Gene


 Gene Link Information
Gain		 01
TRNL1 [NCBI] 0.000767057
TRNR [NCBI] 0.000401057
TRNE [NCBI] 0.000317391
TYMP [NCBI] 9.31889e-05
SUCLA2 [NCBI] 5.55538e-05
POLG [NCBI] 4.94702e-05
SCO2 [NCBI] 3.43139e-05
FASTKD2 [NCBI] 1.67242e-05
MSTN [NCBI] 1.6175e-05
MB [NCBI] 1.56993e-05
TMEM70 [NCBI] 1.43438e-05
COX7B [NCBI] 1.34454e-05
NDUFA12 [NCBI] 1.34454e-05
GFM1 [NCBI] 1.34454e-05
MPV17L [NCBI] 1.2862e-05
COX3 [NCBI] 1.2862e-05
PDSS1 [NCBI] 1.2862e-05
COQ2 [NCBI] 1.24282e-05
C1D [NCBI] 1.20826e-05
NDUFA1 [NCBI] 1.17951e-05
NDUFB7 [NCBI] 1.17951e-05
VDAC2 [NCBI] 1.15491e-05
NDUFS2 [NCBI] 1.1334e-05
NDUFS7 [NCBI] 1.11429e-05
NDUFS4 [NCBI] 1.11429e-05
NDUFS8 [NCBI] 1.0971e-05
SCO1 [NCBI] 1.06716e-05
SDHA [NCBI] 1.05395e-05
COX1 [NCBI] 1.05395e-05
COX2 [NCBI] 9.99873e-06
TUFM [NCBI] 9.99873e-06
ND5 [NCBI] 9.74091e-06
CASP3 [NCBI] 9.64664e-06
VDAC1 [NCBI] 9.58835e-06
SLC25A4 [NCBI] 9.3188e-06
SDHC [NCBI] 8.98047e-06
C10orf2 [NCBI] 8.83348e-06
ND1 [NCBI] 8.65531e-06
FES [NCBI] 8.65531e-06
TFAM [NCBI] 8.38223e-06
FH [NCBI] 8.17857e-06
SDHB [NCBI] 7.43772e-06
SDHD [NCBI] 7.31777e-06
APAF1 [NCBI] 5.97623e-06
XIAP [NCBI] 4.91933e-06
PTGS1 [NCBI] 3.7045e-06
SOD1 [NCBI] 3.06497e-06
CAT [NCBI] 2.94905e-06
BCL2L1 [NCBI] 2.93978e-06
BAX [NCBI] 2.06498e-06



OMIM


 OMIM Link Information
gain		 01
MNGIE [NCBI] 0.00124021
KSS [NCBI] 0.00107182
coenzyme q10 deficiency [NCBI] 0.000564618
mitochondrial complex i deficiency [NCBI] 0.000399754
MTTL1 [NCBI] 0.000388696
MTTK [NCBI] 0.000329144
ECGF1 [NCBI] 0.000327928
MTATP6 [NCBI] 0.000253537
SUCLA2 [NCBI] 0.000160618
MERRF [NCBI] 0.000153596
mitochondrial dna depletion syndrome, myopathic form [NCBI] 0.000151004
POLG [NCBI] 0.000136233
COQ2 [NCBI] 0.000133062
MELAS [NCBI] 0.000128619
MTTW [NCBI] 0.000127176
COXPD4 [NCBI] 0.00012182
COXPD1 [NCBI] 9.93556e-05
MTCYB [NCBI] 9.60411e-05
MTND5 [NCBI] 9.50234e-05
neuropathy, ataxia, and retinitis pigmentosa [NCBI] 9.08822e-05
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency [NCBI] 8.12954e-05
MTRNR2 [NCBI] 8.01986e-05
MTND4 [NCBI] 7.53716e-05
mitochondrial myopathy with diabetes [NCBI] 7.30194e-05
wolfram syndrome, mitochondrial form [NCBI] 7.30194e-05
NDUFA1 [NCBI] 6.64209e-05
NDUFS7 [NCBI] 6.64209e-05
UPP1 [NCBI] 6.64209e-05
TUFM [NCBI] 6.64209e-05
PDSS1 [NCBI] 6.64209e-05
VDAC2 [NCBI] 6.64209e-05
NDUFS2 [NCBI] 6.64209e-05
leber optic atrophy [NCBI] 6.63553e-05
GFM1 [NCBI] 6.12225e-05
MTTA [NCBI] 6.12225e-05
MTTR [NCBI] 6.12225e-05
NDUFV2 [NCBI] 6.12225e-05
MB [NCBI] 5.95323e-05
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1 [NCBI] 5.84695e-05
MTND4L [NCBI] 5.78478e-05
MTND3 [NCBI] 5.53391e-05
MTTH [NCBI] 5.33406e-05
MTND2 [NCBI] 5.33406e-05
MTTE [NCBI] 5.02572e-05
mitochondrial complex iv deficiency [NCBI] 4.80514e-05
MTCO2 [NCBI] 4.44276e-05
MTCO1 [NCBI] 4.13098e-05
MTND6 [NCBI] 3.98249e-05
APTX [NCBI] 3.93759e-05
MTND1 [NCBI] 3.73963e-05
CSTB [NCBI] 3.70443e-05
LS [NCBI] 3.30252e-05
FRDA [NCBI] 2.94958e-05
RP [NCBI] 2.84109e-05
CAT [NCBI] 3.76661e-06



Database Center for Life Science