Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Electron Transport Complex III [NCBI]

Gene


 Gene Link Information
Gain		 01
RP11-278E11.2 [NCBI] 0.000564273
UQCRBP2 [NCBI] 0.000264782
UQCRBP1 [NCBI] 0.000264782
BCS1L [NCBI] 2.55762e-05
UQCRC1 [NCBI] 2.35704e-05
UQCRH [NCBI] 1.84126e-05
UQCRFS1 [NCBI] 1.61097e-05
UQCRB [NCBI] 1.284e-05
CYTB [NCBI] 1.02639e-05
UQCRC2 [NCBI] 9.94911e-06
OXA1L [NCBI] 7.6961e-06
UQCRQ [NCBI] 7.52895e-06
UCRC [NCBI] 7.08346e-06
CS [NCBI] 4.12186e-06
CYC1 [NCBI] 4.05109e-06
HTT [NCBI] 3.44766e-06
UQCRFSL1 [NCBI] 2.9331e-06
HIF1A [NCBI] 2.69624e-06
UQCR [NCBI] 2.42219e-06
RTN4IP1 [NCBI] 2.16502e-06
LETM1 [NCBI] 2.01221e-06
PATZ1 [NCBI] 1.95017e-06
NDUFS2 [NCBI] 1.88498e-06
NDUFS3 [NCBI] 1.8709e-06
NDUFS7 [NCBI] 1.85752e-06
NDUFS8 [NCBI] 1.84478e-06
SOD1 [NCBI] 1.84122e-06
TK2 [NCBI] 1.83262e-06
TAZ [NCBI] 1.76017e-06
ACO2 [NCBI] 1.76017e-06
H2AFY [NCBI] 1.75125e-06
TXNRD2 [NCBI] 1.75125e-06
VDAC2 [NCBI] 1.75125e-06
CRMP1 [NCBI] 1.75125e-06
TUFM [NCBI] 1.68896e-06
PDHX [NCBI] 1.63848e-06
MT2A [NCBI] 1.56813e-06
RTN4 [NCBI] 1.5469e-06
CYCS [NCBI] 1.52724e-06
TXNRD1 [NCBI] 1.4757e-06
CACNA1C [NCBI] 1.46952e-06
BAX [NCBI] 1.41614e-06
HEBP1 [NCBI] 1.35273e-06
POLG [NCBI] 1.34882e-06
AIFM1 [NCBI] 1.20305e-06
PPARGC1A [NCBI] 1.17436e-06
CASP3 [NCBI] 1.10391e-06
FXN [NCBI] 1.08684e-06
NID1 [NCBI] 1.07482e-06
DMPK [NCBI] 1.06599e-06
NQO1 [NCBI] 1.05615e-06
MARCKS [NCBI] 9.92393e-07
UCP3 [NCBI] 9.35777e-07
HMOX1 [NCBI] 8.68312e-07
DHFR [NCBI] 7.19692e-07
TNFSF10 [NCBI] 6.56884e-07
CASP9 [NCBI] 6.52925e-07
BCL2L1 [NCBI] 6.38839e-07
CAT [NCBI] 6.00816e-07
GFAP [NCBI] 4.92503e-07
TNF [NCBI] 1.89701e-07



OMIM


 OMIM Link Information
gain		 01
myopathy with deficiency of succinate dehydrogenase and aconitase [NCBI] 0.00415751
FSHMD1A [NCBI] 0.00088762
MTCYB [NCBI] 0.000688342
mitochondrial complex iii deficiency [NCBI] 0.000465476
gracile syndrome [NCBI] 0.000421068
coenzyme q10 deficiency [NCBI] 0.000234883
BCS1L [NCBI] 0.000203665
mitochondrial myopathy with a defect in mitochondrial-protein transport [NCBI] 0.000185453
diarrhea, chronic, with villous atrophy [NCBI] 0.000185453
BJS [NCBI] 0.000141951
LIMM [NCBI] 0.000141951
septooptic dysplasia [NCBI] 0.000107087
parkinson disease, mitochondrial [NCBI] 0.000105192
MERRF [NCBI] 0.000105192
mitochondrial dna depletion syndrome, myopathic form [NCBI] 0.000103444
EAOH [NCBI] 0.000101821
UQCRFS1 [NCBI] 9.2457e-05
CYCS [NCBI] 9.1183e-05
UQCRB [NCBI] 8.22324e-05
mitochondrial complex iv deficiency [NCBI] 8.15493e-05
mitochondrial complex i deficiency [NCBI] 7.97199e-05
NDUFS4 [NCBI] 6.69346e-05
LS [NCBI] 6.21042e-05
ZS [NCBI] 5.89275e-05
UQCR [NCBI] 4.61727e-05
RTN4IP1 [NCBI] 4.61727e-05
UQCRC1 [NCBI] 4.61727e-05
RTT [NCBI] 4.20214e-05
UQCRC2 [NCBI] 3.87501e-05
NDUFS2 [NCBI] 3.41305e-05
MTTE [NCBI] 3.00387e-05
VDAC2 [NCBI] 3.00387e-05
TK2 [NCBI] 2.93686e-05
APTX [NCBI] 2.37124e-05
MTTK [NCBI] 2.18888e-05
ACADS [NCBI] 2.04172e-05
PDCD8 [NCBI] 1.0938e-05
HD [NCBI] 8.33433e-06
SOD2 [NCBI] 6.92159e-06
DHFR [NCBI] 3.24208e-06
CF [NCBI] 1.9983e-06
TNF [NCBI] 1.76051e-06
CAT [NCBI] 1.65216e-06
GFAP [NCBI] 4.57724e-07



Database Center for Life Science