Gendoo

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01 Apoenzymes [NCBI]

Gene


 Gene Link Information
Gain		 01
GLUDP5 [NCBI] 0.000351113
COX17P [NCBI] 0.000216972
SOD1 [NCBI] 7.53818e-06
AGXT2L1 [NCBI] 6.66478e-06
GSTA1 [NCBI] 5.1597e-06
GAPDH [NCBI] 4.96509e-06
COX17 [NCBI] 3.90798e-06
MUT [NCBI] 3.81858e-06
GLUD1 [NCBI] 3.75404e-06
METAP2 [NCBI] 3.71875e-06
CCS [NCBI] 3.70749e-06
PTGS1 [NCBI] 3.26742e-06
GSTA5 [NCBI] 3.06698e-06
DCT [NCBI] 2.57962e-06
PAH [NCBI] 2.49855e-06
GNPNAT1 [NCBI] 2.30043e-06
PLEKHB1 [NCBI] 2.20177e-06
PTGS2 [NCBI] 2.09725e-06
MGAM [NCBI] 2.07331e-06
GSTP1 [NCBI] 2.03283e-06
METAP1 [NCBI] 2.00604e-06
IMPA1 [NCBI] 1.96907e-06
GNGT1 [NCBI] 1.95234e-06
USP5 [NCBI] 1.90764e-06
HGD [NCBI] 1.90764e-06
GLUD2 [NCBI] 1.89426e-06
GOT1 [NCBI] 1.85773e-06
ADH5 [NCBI] 1.80613e-06
GLUL [NCBI] 1.78799e-06
CRABP2 [NCBI] 1.78799e-06
GYS1 [NCBI] 1.77936e-06
PGK2 [NCBI] 1.77936e-06
TKT [NCBI] 1.73273e-06
CYP3A4 [NCBI] 1.73165e-06
TNK2 [NCBI] 1.71883e-06
GLO1 [NCBI] 1.71883e-06
LTA4H [NCBI] 1.71215e-06
AHCY [NCBI] 1.69926e-06
TDP1 [NCBI] 1.68696e-06
GCKR [NCBI] 1.67521e-06
ACAT1 [NCBI] 1.66952e-06
GNMT [NCBI] 1.63276e-06
ASPA [NCBI] 1.6279e-06
LTC4S [NCBI] 1.60484e-06
NP [NCBI] 1.56019e-06
PDE4A [NCBI] 1.53865e-06
APBA1 [NCBI] 1.50018e-06
KIF11 [NCBI] 1.45122e-06
PRKAR2A [NCBI] 1.44875e-06
OAT [NCBI] 1.43672e-06
PIM1 [NCBI] 1.3894e-06
ATP7B [NCBI] 1.38355e-06
ERCC4 [NCBI] 1.37595e-06
GCK [NCBI] 1.34924e-06
MTRR [NCBI] 1.28884e-06
TYMS [NCBI] 1.26189e-06
GNAS [NCBI] 1.17432e-06
CYP2E1 [NCBI] 1.16483e-06
TAT [NCBI] 1.15897e-06
GSK3B [NCBI] 1.15486e-06
DPP4 [NCBI] 1.1375e-06
APAF1 [NCBI] 1.10997e-06
PAM [NCBI] 1.08818e-06
ALDH2 [NCBI] 1.06282e-06
NOS1 [NCBI] 9.99188e-07
ZAP70 [NCBI] 9.97386e-07
TF [NCBI] 8.49915e-07
DHFR [NCBI] 7.55565e-07
TH [NCBI] 4.94968e-07
ACHE [NCBI] 4.69318e-07



OMIM


 OMIM Link Information
gain		 01
CTS1 [NCBI] 0.00429663
methylmalonic aciduria and homocystinuria, cbld type [NCBI] 0.00175075
methylmalonic aciduria due to methylmalonyl-coa mutase deficiency [NCBI] 0.000591989
methylmalonic aciduria, cbla type [NCBI] 0.000135247
thyroid hormonogenesis, genetic defect in, 2a [NCBI] 0.000117736
holocarboxylase synthetase deficiency [NCBI] 0.000112772
acyl-coa dehydrogenase, medium-chain, deficiency of [NCBI] 0.000107969
SOD1 [NCBI] 8.53262e-05
GAPDH [NCBI] 6.09941e-05
MTR [NCBI] 4.75497e-05
H6PD [NCBI] 4.71882e-05
COX17 [NCBI] 3.89868e-05
PLEKHB1 [NCBI] 3.89868e-05
MTRR [NCBI] 3.24037e-05
CCS [NCBI] 3.0339e-05
PCCB [NCBI] 2.74388e-05
LTC4S [NCBI] 2.63216e-05
MUT [NCBI] 2.5933e-05
GNMT [NCBI] 2.36765e-05
DCT [NCBI] 2.25738e-05
FPGS [NCBI] 1.85784e-05
AKR1B1 [NCBI] 1.32122e-05
ACE [NCBI] 1.08305e-05
TF [NCBI] 7.73055e-06
TYMS [NCBI] 6.73342e-06
DHFR [NCBI] 5.67653e-06
TH [NCBI] 1.57752e-06
ACHE [NCBI] 1.28346e-06



Database Center for Life Science