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01 Mitochondria, Muscle [NCBI]

Gene


 Gene Link Information
Gain		 01
TRNI [NCBI] 0.000453044
UCP3 [NCBI] 0.000423639
TRNAL1 [NCBI] 0.000353973
TRNAL2 [NCBI] 0.000353973
CS [NCBI] 0.00018358
PPARGC1A [NCBI] 7.12908e-05
MS [NCBI] 3.15998e-05
TFAM [NCBI] 2.91757e-05
UCP2 [NCBI] 2.16439e-05
CASQ1 [NCBI] 1.90762e-05
POLG [NCBI] 1.88257e-05
ND5 [NCBI] 1.75364e-05
C10orf2 [NCBI] 1.62895e-05
SPG7 [NCBI] 1.60711e-05
SLC25A4 [NCBI] 1.52477e-05
MFN2 [NCBI] 1.40194e-05
CRAT [NCBI] 1.30247e-05
NDUFS1 [NCBI] 1.18052e-05
NOTCH3 [NCBI] 1.13193e-05
ND1 [NCBI] 1.09329e-05
TK2 [NCBI] 1.09329e-05
NDUFS4 [NCBI] 1.06077e-05
SLC2A4 [NCBI] 1.04715e-05
FXN [NCBI] 1.01677e-05
RRM2B [NCBI] 9.6681e-06
SLC16A1 [NCBI] 9.54702e-06
SLC16A4 [NCBI] 9.1733e-06
TYMP [NCBI] 8.38121e-06
SPAST [NCBI] 8.31697e-06
NRF1 [NCBI] 7.96998e-06
OPA1 [NCBI] 7.62979e-06
DCTN6 [NCBI] 7.21881e-06
MYOM2 [NCBI] 7.15606e-06
SOD2 [NCBI] 6.8938e-06
UCP1 [NCBI] 6.81856e-06
PDP2 [NCBI] 6.69505e-06
GOLPH3 [NCBI] 6.35498e-06
NT5M [NCBI] 6.35498e-06
NDUFA8 [NCBI] 6.10216e-06
ETFDH [NCBI] 6.10216e-06
SIRT1 [NCBI] 6.02869e-06
POLG2 [NCBI] 5.90072e-06
MB [NCBI] 5.80615e-06
PDSS1 [NCBI] 5.73323e-06
PUS1 [NCBI] 5.73323e-06
ASAH2C [NCBI] 5.73323e-06
NT5C [NCBI] 5.58988e-06
SOD1 [NCBI] 5.54759e-06
DMPK [NCBI] 5.51431e-06
NDUFB6 [NCBI] 5.46457e-06
HCCS [NCBI] 5.46457e-06
MRPS22 [NCBI] 5.46457e-06
COX4I2 [NCBI] 5.35327e-06
PARL [NCBI] 5.35327e-06
ECHS1 [NCBI] 5.35327e-06
KCNJ8 [NCBI] 5.32142e-06
COX2 [NCBI] 5.25315e-06
PPM2C [NCBI] 5.25315e-06
PDK2 [NCBI] 5.16218e-06
COX1 [NCBI] 5.16218e-06
NDUFS8 [NCBI] 5.16218e-06
DLST [NCBI] 5.07883e-06
SLC25A3 [NCBI] 5.00191e-06
KLHL1 [NCBI] 4.93051e-06
SLC27A4 [NCBI] 4.86389e-06
CKMT2 [NCBI] 4.86389e-06
SLC25A15 [NCBI] 4.86389e-06
SLC25A12 [NCBI] 4.86389e-06
NDUFV1 [NCBI] 4.86389e-06
ME2 [NCBI] 4.86389e-06
DLD [NCBI] 4.80145e-06
PCCB [NCBI] 4.80145e-06
SDHA [NCBI] 4.7427e-06
VDAC3 [NCBI] 4.7427e-06
PARK2 [NCBI] 4.60179e-06
ACADVL [NCBI] 4.58478e-06
LDB3 [NCBI] 4.58478e-06
MDH2 [NCBI] 4.53727e-06
ACADM [NCBI] 4.53727e-06
PDK4 [NCBI] 4.49192e-06
TAZ [NCBI] 4.44856e-06
MCTS1 [NCBI] 4.32879e-06
ASAH2 [NCBI] 4.32879e-06
CPT2 [NCBI] 4.22194e-06
TUFM [NCBI] 4.22194e-06
PPARGC1B [NCBI] 4.18875e-06
MYBBP1A [NCBI] 4.18875e-06
FIS1 [NCBI] 4.15662e-06
PDHA1 [NCBI] 4.06608e-06
MYOT [NCBI] 4.03765e-06
TOMM20 [NCBI] 4.03765e-06
HSD17B10 [NCBI] 3.90662e-06
RRM1 [NCBI] 3.88238e-06
TRIM63 [NCBI] 3.74827e-06
RRM2 [NCBI] 3.72759e-06
CYCS [NCBI] 3.57619e-06
DNM1L [NCBI] 3.4922e-06
CDH15 [NCBI] 3.41485e-06
PTGS1 [NCBI] 3.30818e-06
OXCT2 [NCBI] 3.27642e-06
PPARD [NCBI] 3.25095e-06
PINK1 [NCBI] 3.21395e-06
PRKAA2 [NCBI] 3.13274e-06
GSTA5 [NCBI] 3.09991e-06
CAMK2A [NCBI] 3.09991e-06
SLC19A2 [NCBI] 3.0578e-06
ATF3 [NCBI] 2.90566e-06
CD36 [NCBI] 2.85428e-06
STC1 [NCBI] 2.71489e-06
CACNA1A [NCBI] 2.69351e-06
DMD [NCBI] 2.61902e-06
ALDH2 [NCBI] 2.59332e-06
AKT2 [NCBI] 2.57449e-06
MUSK [NCBI] 2.5683e-06
DCK [NCBI] 2.43072e-06
ATXN1 [NCBI] 2.4254e-06
CYP27A1 [NCBI] 2.37886e-06
MSTN [NCBI] 2.37383e-06
GPX1 [NCBI] 2.3589e-06
AIFM1 [NCBI] 2.27404e-06
LPL [NCBI] 2.11377e-06
HIF1A [NCBI] 2.04438e-06
CAT [NCBI] 2.00843e-06
LEP [NCBI] 1.93226e-06
CNN1 [NCBI] 1.62053e-06
SRF [NCBI] 1.56811e-06
ITPR1 [NCBI] 1.53035e-06
MAPT [NCBI] 1.45074e-06
XIAP [NCBI] 1.4281e-06
MCL1 [NCBI] 1.32356e-06
GAPDH [NCBI] 1.16817e-06
PLN [NCBI] 9.00407e-07
IL1RN [NCBI] 7.66998e-07
NOS3 [NCBI] 5.24205e-07
TGFB1 [NCBI] 2.47042e-07
BAX [NCBI] 2.19726e-07
TNF [NCBI] 1.9993e-07
AKT1 [NCBI] 1.99008e-07
GFAP [NCBI] 9.01157e-08
EGFR [NCBI] 8.06893e-08
PTH [NCBI] 5.02049e-08
CASP3 [NCBI] 1.09685e-11



OMIM


 OMIM Link Information
gain		 01
KSS [NCBI] 0.0028049
myopathy with deficiency of succinate dehydrogenase and aconitase [NCBI] 0.00237807
cataract and cardiomyopathy [NCBI] 0.00106946
inclusion body myositis [NCBI] 0.00102443
AUTS4 [NCBI] 0.000987008
MELAS [NCBI] 0.000868893
mitochondrial dna depletion syndrome, hepatocerebral form [NCBI] 0.00083399
mitochondrial myopathy [NCBI] 0.000803374
mitochondrial myopathy with diabetes [NCBI] 0.000654426
mitochondrial complex i deficiency [NCBI] 0.00064618
mitochondrial dna depletion syndrome, myopathic form [NCBI] 0.00055945
RA [NCBI] 0.000546169
mitochondrial complex iii deficiency [NCBI] 0.000534935
coenzyme q10 deficiency [NCBI] 0.000534536
mitochondrial complex ii deficiency [NCBI] 0.000486223
UCP3 [NCBI] 0.000462311
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1 [NCBI] 0.000439335
MERRF [NCBI] 0.000439335
mitochondrial complex iv deficiency [NCBI] 0.000434056
MNGIE [NCBI] 0.000406604
MLASA [NCBI] 0.000386821
SLE [NCBI] 0.000350693
MTTL1 [NCBI] 0.000337867
mitochondrial myopathy with lactic acidosis [NCBI] 0.000321151
acyl-coa dehydrogenase, short-chain, deficiency of [NCBI] 0.00027694
LIMM [NCBI] 0.000267146
MTTK [NCBI] 0.000255328
carnitine palmitoyltransferase ii deficiency, late-onset [NCBI] 0.000244088
BTHS [NCBI] 0.000181579
trifunctional protein deficiency [NCBI] 0.000180154
OPMD [NCBI] 0.000175329
SLC25A4 [NCBI] 0.000171698
COXPD5 [NCBI] 0.000160495
mitochondrial phosphate carrier deficiency [NCBI] 0.000160495
neuropathy, ataxia, and retinitis pigmentosa [NCBI] 0.000160495
hypomagnesemia, hypertension, and hypercholesterolemia, mitochondrial [NCBI] 0.000160495
muscular dystrophy, congenital, megaconial type [NCBI] 0.000160495
myopathy due to malate-aspartate shuttle defect [NCBI] 0.000160495
mitochondrial myopathy with a defect in mitochondrial-protein transport [NCBI] 0.000160495
myopathy with abnormal lipid metabolism [NCBI] 0.000160495
myoglobinuria, recurrent [NCBI] 0.000160495
pearson marrow-pancreas syndrome [NCBI] 0.000159646
SDHC [NCBI] 0.000154679
LS [NCBI] 0.000141103
MTATP6 [NCBI] 0.000126299
MTTF [NCBI] 0.00012492
pleoconial myopathy with salt craving [NCBI] 0.000121316
hypermetabolism due to defect in mitochondria [NCBI] 0.000121316
ophthalmoplegic neuromuscular disorder with abnormal mitochondria [NCBI] 0.000121316
TK2 [NCBI] 0.00012045
MTCYB [NCBI] 0.000118951
MTTI [NCBI] 0.000113632
myopathy with giant abnormal mitochondria [NCBI] 0.000106589
fumarase deficiency [NCBI] 0.000106589
wolfram syndrome, mitochondrial form [NCBI] 9.70597e-05
DLD [NCBI] 9.5262e-05
MTCO1 [NCBI] 9.08275e-05
SANDO [NCBI] 8.9999e-05
pyruvate dehydrogenase e3-binding protein deficiency [NCBI] 8.9999e-05
MTTY [NCBI] 8.94436e-05
PPARGC1A [NCBI] 8.8018e-05
MTND4 [NCBI] 8.47691e-05
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 2 [NCBI] 8.43922e-05
cardiomyopathy, infantile histiocytoid [NCBI] 8.43922e-05
PUS1 [NCBI] 8.32338e-05
myopathy, centronuclear, autosomal dominant [NCBI] 7.97461e-05
NDUFS8 [NCBI] 7.89725e-05
lipomatosis, familial benign cervical [NCBI] 7.57828e-05
glycogen storage disease ii [NCBI] 7.27018e-05
bartter syndrome, antenatal, type 2 [NCBI] 7.23301e-05
TRMA [NCBI] 7.23301e-05
gracile syndrome [NCBI] 6.92736e-05
parkinson disease, mitochondrial [NCBI] 6.92736e-05
diabetes-deafness syndrome, maternally transmitted [NCBI] 6.92736e-05
AD [NCBI] 6.87611e-05
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive [NCBI] 6.65338e-05
aging [NCBI] 6.40526e-05
hyperornithinemia-hyperammonemia-homocitrullinuria syndrome [NCBI] 6.40526e-05
ACADM [NCBI] 6.39709e-05
SNDI [NCBI] 6.1787e-05
leber optic atrophy [NCBI] 5.96558e-05
CMH [NCBI] 5.96558e-05
ACADVL [NCBI] 5.80593e-05
UCP2 [NCBI] 5.79283e-05
UCMD [NCBI] 5.77762e-05
bethlem myopathy [NCBI] 5.77762e-05
MTND5 [NCBI] 5.64667e-05
AAA [NCBI] 5.5984e-05
MFN2 [NCBI] 5.37349e-05
ACADS [NCBI] 5.25443e-05
NT5M [NCBI] 5.15718e-05
POLG [NCBI] 5.04277e-05
MSS [NCBI] 4.85512e-05
MTND1 [NCBI] 4.73512e-05
MADD [NCBI] 4.49755e-05
OPA1 [NCBI] 4.49755e-05
MM [NCBI] 4.18654e-05
RSMD1 [NCBI] 4.18654e-05
PPM2C [NCBI] 4.15937e-05
PDSS1 [NCBI] 4.15937e-05
UQCRC2 [NCBI] 4.15937e-05
MTTG [NCBI] 4.15937e-05
MTTS2 [NCBI] 4.15937e-05
CD36 [NCBI] 4.03619e-05
XPA [NCBI] 3.9121e-05
NEM3 [NCBI] 3.9121e-05
pyruvate decarboxylase deficiency [NCBI] 3.82746e-05
PDCD8 [NCBI] 3.82311e-05
CKMT1B [NCBI] 3.7831e-05
MTTN [NCBI] 3.7831e-05
MTTL2 [NCBI] 3.7831e-05
RRM2B [NCBI] 3.7831e-05
NDUFB6 [NCBI] 3.7831e-05
ASAH2 [NCBI] 3.7831e-05
MRPS22 [NCBI] 3.7831e-05
NDUFA8 [NCBI] 3.7831e-05
BMD [NCBI] 3.66713e-05
ATP5C1 [NCBI] 3.53895e-05
NDUFV1 [NCBI] 3.53895e-05
NDUFS7 [NCBI] 3.53895e-05
MTTW [NCBI] 3.53895e-05
CDSP [NCBI] 3.37751e-05
SLC25A3 [NCBI] 3.35754e-05
CASQ1 [NCBI] 3.35754e-05
SLC25A15 [NCBI] 3.35754e-05
PDHX [NCBI] 3.35754e-05
SLC25A19 [NCBI] 3.35754e-05
SLC25A12 [NCBI] 3.21308e-05
NDUFS1 [NCBI] 3.21308e-05
CRAT [NCBI] 3.21308e-05
CMT1B [NCBI] 3.18315e-05
C10ORF2 [NCBI] 3.09305e-05
CAMK4 [NCBI] 3.09305e-05
SLC19A2 [NCBI] 3.09305e-05
SLC16A7 [NCBI] 3.09305e-05
PCK2 [NCBI] 3.09305e-05
maple syrup urine disease [NCBI] 3.00519e-05
UCP1 [NCBI] 2.99133e-05
SDHA [NCBI] 2.99037e-05
PGAM1 [NCBI] 2.99037e-05
DGUOK [NCBI] 2.99037e-05
MTTE [NCBI] 2.99037e-05
NT5C [NCBI] 2.99037e-05
NDUFS4 [NCBI] 2.99037e-05
BCS1L [NCBI] 2.99037e-05
NPS [NCBI] 2.94911e-05
PPARA [NCBI] 2.94123e-05
TNF [NCBI] 2.83999e-05
ECGF1 [NCBI] 2.82105e-05
VDAC1 [NCBI] 2.74947e-05
ATP5O [NCBI] 2.62494e-05
phosphoglycerate mutase, muscle, deficiency of [NCBI] 2.62494e-05
TAZ [NCBI] 2.47163e-05
HADHA [NCBI] 2.47163e-05
MTM1 [NCBI] 2.46103e-05
MG [NCBI] 2.45959e-05
SLC22A5 [NCBI] 2.34584e-05
PPARD [NCBI] 2.34584e-05
SLC25A20 [NCBI] 2.30848e-05
PPID [NCBI] 2.30848e-05
SPG4 [NCBI] 2.30848e-05
MTND6 [NCBI] 2.27301e-05
MB [NCBI] 2.26008e-05
COL6A1 [NCBI] 2.01588e-05
FRDA [NCBI] 2.00551e-05
TPI1 [NCBI] 1.94779e-05
ATF3 [NCBI] 1.53896e-05
VEGF [NCBI] 1.42581e-05
PPARG [NCBI] 1.30477e-05
SOD2 [NCBI] 1.27006e-05
ZS [NCBI] 1.13646e-05
DMD [NCBI] 9.7226e-06
SLC2A4 [NCBI] 8.97212e-06
dystrophia myotonica 1 [NCBI] 6.56446e-06
PTH [NCBI] 6.35571e-06
GFAP [NCBI] 4.88129e-06
SRF [NCBI] 3.2167e-06
EGFR [NCBI] 3.09872e-06
LPL [NCBI] 1.47007e-06
GAPDH [NCBI] 1.30532e-06
CAT [NCBI] 1.2111e-06
PTK2 [NCBI] 2.18606e-08



Database Center for Life Science