Gendoo

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01 Cytochrome Reductases [NCBI]

Gene


 Gene Link Information
Gain		 01
TRNAP1 [NCBI] 0.000227613
CYB5R3 [NCBI] 7.60948e-05
GFER [NCBI] 2.81389e-05
CYB5A [NCBI] 1.14049e-05
TMEM217 [NCBI] 2.39376e-06
CYB5R2 [NCBI] 2.39376e-06
CHCHD4 [NCBI] 2.33989e-06
CYB5R4 [NCBI] 2.25674e-06
CYB5R1 [NCBI] 2.25674e-06
AADAC [NCBI] 2.16662e-06
NDUFB6 [NCBI] 2.11995e-06
TST [NCBI] 1.89942e-06
TOMM20 [NCBI] 1.79254e-06
HEPH [NCBI] 1.76848e-06
ND1 [NCBI] 1.75722e-06
RPL14 [NCBI] 1.69372e-06
DHDH [NCBI] 1.63189e-06
MAS1 [NCBI] 1.58459e-06
NOX1 [NCBI] 1.52524e-06
CYP19A1 [NCBI] 1.2612e-06
CS [NCBI] 1.20701e-06
NQO1 [NCBI] 1.18549e-06
MB [NCBI] 1.10293e-06
CTSG [NCBI] 9.86359e-07
CYP2C9 [NCBI] 9.27545e-07
SOD1 [NCBI] 8.64458e-07
CYP3A4 [NCBI] 7.73627e-07



OMIM


 OMIM Link Information
gain		 01
succinic acidemia [NCBI] 0.003491
methemoglobinemia due to deficiency of methemoglobin reductase [NCBI] 0.00141
mitochondrial complex i deficiency [NCBI] 0.000224173
MTND1 [NCBI] 0.000141713
mitochondrial myopathy [NCBI] 0.000135247
coumarin resistance [NCBI] 0.000115454
blood group, p system [NCBI] 0.000111431
thyroid hormonogenesis, genetic defect in, 2a [NCBI] 0.000109097
GFER [NCBI] 8.90919e-05
CGD [NCBI] 8.17592e-05
MTND4 [NCBI] 7.34057e-05
KSS [NCBI] 6.9813e-05
methemoglobinemia due to deficiency of cytochrome b5 [NCBI] 6.64976e-05
leber optic atrophy [NCBI] 6.19716e-05
MTND4L [NCBI] 5.97521e-05
MTND3 [NCBI] 5.47223e-05
MTND2 [NCBI] 5.38666e-05
MTND6 [NCBI] 5.19869e-05
MTND5 [NCBI] 5.1319e-05
NQO3A2 [NCBI] 4.59563e-05
cytochrome b5 reductase 2 [NCBI] 4.59563e-05
NCB5OR [NCBI] 3.85338e-05
HEPH [NCBI] 2.59402e-05
CYP2A6 [NCBI] 2.10903e-05
CYP1A1 [NCBI] 2.08919e-05
MTCYB [NCBI] 2.03206e-05
CF [NCBI] 1.7489e-05
MB [NCBI] 7.45164e-06



Database Center for Life Science