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01 Cytochrome-c Oxidase Deficiency [NCBI]

Gene


 Gene Link Information
Gain		 01
COX7AP1 [NCBI] 0.000438875
COX7AP2 [NCBI] 0.000438875
TRNL1 [NCBI] 0.000226878
SCO2 [NCBI] 0.00020466
SURF1 [NCBI] 0.000115874
SCO1 [NCBI] 0.000101432
COX10 [NCBI] 6.5023e-05
COX15 [NCBI] 2.84531e-05
LRPPRC [NCBI] 2.4622e-05
COX1 [NCBI] 2.33558e-05
TFAM [NCBI] 1.89425e-05
COX19 [NCBI] 1.65908e-05
FASTKD2 [NCBI] 1.65908e-05
COX7A2L [NCBI] 1.65908e-05
COX6A2 [NCBI] 1.42104e-05
COX16 [NCBI] 1.42104e-05
COX6A1 [NCBI] 1.42104e-05
SURF4 [NCBI] 1.42104e-05
COX6B1 [NCBI] 1.42104e-05
COX7A1 [NCBI] 1.3312e-05
COX7A2 [NCBI] 1.3312e-05
FXN [NCBI] 1.30254e-05
PUS1 [NCBI] 1.22948e-05
COX17 [NCBI] 1.19492e-05
CYTB [NCBI] 1.00617e-05
COX2 [NCBI] 9.86543e-06
SPG7 [NCBI] 8.95279e-06
TYMP [NCBI] 7.72566e-06
OPA1 [NCBI] 7.0373e-06
ATP7A [NCBI] 6.18124e-06
CYP2D6 [NCBI] 5.87962e-06
SMN1 [NCBI] 5.27998e-06
UCP3 [NCBI] 5.03218e-06
HMOX1 [NCBI] 4.41874e-06
SOD1 [NCBI] 2.94067e-06
GFAP [NCBI] 1.9015e-06
CASP3 [NCBI] 1.39804e-06



OMIM


 OMIM Link Information
gain		 01
mitochondrial complex iv deficiency [NCBI] 0.00275817
LS [NCBI] 0.00231876
LSFC [NCBI] 0.000626614
SURF1 [NCBI] 0.000582628
KSS [NCBI] 0.000290896
SCO2 [NCBI] 0.000280964
MTCO1 [NCBI] 0.000238904
mitochondrial dna depletion syndrome, hepatocerebral form [NCBI] 0.000223663
LIMM [NCBI] 0.000201267
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency [NCBI] 0.000177697
COX15 [NCBI] 0.00013984
MTTW [NCBI] 0.000133953
MTCO3 [NCBI] 0.00012269
MTCO2 [NCBI] 0.000110347
COX7A3 [NCBI] 8.35435e-05
LRPPRC [NCBI] 8.35435e-05
MLASA [NCBI] 7.54786e-05
SCO1 [NCBI] 6.9765e-05
COX7A1 [NCBI] 6.9765e-05
mitochondrial myopathy with diabetes [NCBI] 6.72141e-05
wolfram syndrome, mitochondrial form [NCBI] 6.72141e-05
ETHE1 [NCBI] 6.45657e-05
MTTV [NCBI] 6.45657e-05
PGAM1 [NCBI] 6.11901e-05
PUS1 [NCBI] 6.11901e-05
MERRF [NCBI] 5.89884e-05
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive [NCBI] 5.89884e-05
PCK2 [NCBI] 5.86805e-05
COX10 [NCBI] 5.86805e-05
mitochondrial dna depletion syndrome, myopathic form [NCBI] 5.77528e-05
phosphoglycerate mutase, muscle, deficiency of [NCBI] 5.50187e-05
MNGIE [NCBI] 5.03074e-05
cutis laxa, x-linked [NCBI] 4.82273e-05
mitochondrial complex i deficiency [NCBI] 4.63923e-05
CYP2D6 [NCBI] 4.63915e-05
MTTS1 [NCBI] 4.51891e-05
WFS1 [NCBI] 3.84557e-05
MTTL1 [NCBI] 3.01559e-05
menkes disease [NCBI] 2.85571e-05
SOD2 [NCBI] 1.54706e-05
GFAP [NCBI] 2.02163e-06



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