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01 Mitochondrial Myopathies [NCBI]


Gene


Gene Link Information
Gain
01
TRNL1 [NCBI] 0.000598298
NDUFB3P4 [NCBI] 0.000357173
TRNF [NCBI] 0.000357173
NDUFB3P3 [NCBI] 0.000357173
NDUFB3P2 [NCBI] 0.000357173
NDUFB3P1 [NCBI] 0.000357173
NDUFB3P5 [NCBI] 0.000357173
TRNV [NCBI] 0.000296439
TRNK [NCBI] 0.00022518
TRNS1 [NCBI] 0.000210456
RNR1 [NCBI] 0.000161195
TK2 [NCBI] 0.000110807
PUS1 [NCBI] 6.04204e-05
MS [NCBI] 5.07658e-05
POLG [NCBI] 4.64552e-05
TAZ [NCBI] 3.25358e-05
NDUFV1 [NCBI] 2.30249e-05
RPP14 [NCBI] 2.17363e-05
FXN [NCBI] 2.03091e-05
SLC25A4 [NCBI] 1.99393e-05
TIMM8A [NCBI] 1.99393e-05
TFAM [NCBI] 1.80379e-05
COX8A [NCBI] 1.61415e-05
PPM1B [NCBI] 1.37611e-05
SARS2 [NCBI] 1.37611e-05
IARS [NCBI] 1.37611e-05
PPA2 [NCBI] 1.37611e-05
COX7A1 [NCBI] 1.28627e-05
VARS2 [NCBI] 1.28627e-05
NDUFB3 [NCBI] 1.28627e-05
KCNIP1 [NCBI] 1.22794e-05
ISCU [NCBI] 1.22794e-05
MRPS22 [NCBI] 1.22794e-05
MPV17L [NCBI] 1.22794e-05
ETFDH [NCBI] 1.18456e-05
UCP3 [NCBI] 1.15521e-05
HADHB [NCBI] 1.15e-05
WARS [NCBI] 1.15e-05
IFI30 [NCBI] 1.12126e-05
DGUOK [NCBI] 1.09666e-05
CASQ1 [NCBI] 1.05605e-05
MYL3 [NCBI] 1.05605e-05
SUCLA2 [NCBI] 1.05605e-05
SCO1 [NCBI] 1.00893e-05
SLC16A4 [NCBI] 9.83463e-06
MYL2 [NCBI] 9.83463e-06
CYTB [NCBI] 9.61295e-06
ACADVL [NCBI] 9.51203e-06
HADHA [NCBI] 9.24069e-06
SETX [NCBI] 9.15903e-06
VDAC1 [NCBI] 9.00655e-06
NRF1 [NCBI] 8.93512e-06
ACTC1 [NCBI] 8.86655e-06
RRM2B [NCBI] 8.61688e-06
C10orf2 [NCBI] 8.25221e-06
TPM1 [NCBI] 7.76577e-06
TNNI3 [NCBI] 7.44527e-06
MYBPC3 [NCBI] 7.4163e-06
TYMP [NCBI] 7.27845e-06
GLA [NCBI] 7.25217e-06
HSPD1 [NCBI] 7.10251e-06
TNNT2 [NCBI] 6.92151e-06
ATP2A2 [NCBI] 6.64495e-06
OPA1 [NCBI] 6.59114e-06
MYH7 [NCBI] 6.31491e-06
SLC7A9 [NCBI] 6.256e-06
PREPL [NCBI] 6.256e-06
GCK [NCBI] 6.24159e-06
CS [NCBI] 6.21313e-06
PPARGC1A [NCBI] 5.9889e-06
DCK [NCBI] 5.9889e-06
NOTCH3 [NCBI] 5.27596e-06
GFAP [NCBI] 5.13996e-06
DAG1 [NCBI] 5.0019e-06
CASP3 [NCBI] 4.06081e-06
SOD1 [NCBI] 2.52796e-06
LPL [NCBI] 2.29715e-06




OMIM


OMIM Link Information
gain
01
myopathy with deficiency of succinate dehydrogenase and aconitase [NCBI] 0.00187142
cataract and cardiomyopathy [NCBI] 0.00182258
KSS [NCBI] 0.000510847
MTTL1 [NCBI] 0.000454447
MLASA [NCBI] 0.000429778
BTHS [NCBI] 0.000423375
mitochondrial dna depletion syndrome, myopathic form [NCBI] 0.000334661
SLC25A4 [NCBI] 0.00032333
PUS1 [NCBI] 0.000300398
MTATP6 [NCBI] 0.000283483
mitochondrial complex iv deficiency [NCBI] 0.00026711
MTCYB [NCBI] 0.000264104
mitochondrial dna depletion syndrome, hepatocerebral form [NCBI] 0.000227338
mitochondrial complex ii deficiency [NCBI] 0.000166818
mitochondrial myopathy with diabetes [NCBI] 0.000161791
carnitine palmitoyltransferase ii deficiency, lethal neonatal [NCBI] 0.000161791
MTS [NCBI] 0.000137087
diabetes-deafness syndrome, maternally transmitted [NCBI] 0.000135003
MTTN [NCBI] 0.000130961
MTTA [NCBI] 0.000130961
MELAS [NCBI] 0.000119364
COXPD5 [NCBI] 0.000117198
proximal myopathy with focal depletion of mitochondria [NCBI] 0.000117198
MTTG [NCBI] 0.000116502
TK2 [NCBI] 0.000111994
MTCO3 [NCBI] 0.000105249
MTTE [NCBI] 0.000105249
C10ORF2 [NCBI] 0.000100236
adrenoleukodystrophy, autosomal neonatal form [NCBI] 9.71836e-05
atpaf2 deficiency [NCBI] 9.47367e-05
MTCO2 [NCBI] 9.29243e-05
MTCO1 [NCBI] 8.64711e-05
hypotonia-cystinuria syndrome [NCBI] 8.62662e-05
neuropathy, ataxia, and retinitis pigmentosa [NCBI] 8.62662e-05
MTND1 [NCBI] 7.84511e-05
MTTK [NCBI] 7.5098e-05
NDUFB3 [NCBI] 7.49043e-05
MTIF2 [NCBI] 7.49043e-05
PPA2 [NCBI] 7.49043e-05
SFRS7 [NCBI] 7.49043e-05
POLG [NCBI] 7.17117e-05
SANDO [NCBI] 7.07301e-05
OPMD [NCBI] 6.76658e-05
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 2 [NCBI] 6.6398e-05
minicore myopathy with external ophthalmoplegia [NCBI] 6.46048e-05
acyl-coa dehydrogenase, short-chain, deficiency of [NCBI] 6.46048e-05
trifunctional protein deficiency [NCBI] 6.15286e-05
PPM1B [NCBI] 6.11289e-05
MDH1 [NCBI] 6.11289e-05
MTTP [NCBI] 6.11289e-05
ATP6V0E1 [NCBI] 6.11289e-05
NRF1 [NCBI] 6.11289e-05
COX7A1 [NCBI] 6.11289e-05
MERRF [NCBI] 6.01878e-05
USH1C [NCBI] 6.01878e-05
stuve-wiedemann syndrome [NCBI] 5.78041e-05
leber optic atrophy [NCBI] 5.75644e-05
coenzyme q10 deficiency [NCBI] 5.67342e-05
VDAC1 [NCBI] 5.59327e-05
MTTQ [NCBI] 5.59327e-05
PPA1 [NCBI] 5.59327e-05
PREPL [NCBI] 5.59327e-05
MRPS22 [NCBI] 5.59327e-05
pearson marrow-pancreas syndrome [NCBI] 5.57321e-05
MTTL2 [NCBI] 5.25601e-05
TFAM [NCBI] 5.25601e-05
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency [NCBI] 5.07731e-05
carnitine palmitoyltransferase ii deficiency, late-onset [NCBI] 5.00797e-05
PCK2 [NCBI] 5.00537e-05
WARS [NCBI] 5.00537e-05
MTTW [NCBI] 5.00537e-05
SDHA [NCBI] 4.80573e-05
mitochondrial complex i deficiency [NCBI] 4.7578e-05
MLYCD [NCBI] 4.63981e-05
CDSP [NCBI] 4.44484e-05
DGUOK [NCBI] 4.37378e-05
MTTI [NCBI] 4.26363e-05
RMRP [NCBI] 4.26363e-05
cystinuria [NCBI] 4.22515e-05
TIMM8A [NCBI] 4.16458e-05
SLC7A9 [NCBI] 3.99221e-05
CPT2 [NCBI] 3.99221e-05
HADHA [NCBI] 3.84565e-05
SLC25A20 [NCBI] 3.71822e-05
SLC16A1 [NCBI] 3.66024e-05
TAZ [NCBI] 3.66024e-05
SLC3A1 [NCBI] 3.37029e-05
ACADS [NCBI] 3.37029e-05
NPS [NCBI] 3.32611e-05
LS [NCBI] 2.86719e-05
ABCC8 [NCBI] 2.43395e-05
SOD2 [NCBI] 7.99229e-06
RP [NCBI] 3.20865e-06
GFAP [NCBI] 2.47394e-06
LPL [NCBI] 8.48007e-07
MG [NCBI] 1.35158e-07




Database Center for Life Science