Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Ketones [NCBI]

Gene


 Gene Link Information
Gain		 01
CTSL1 [NCBI] 1.64943e-05
PTGR1 [NCBI] 8.65571e-06
CASP3 [NCBI] 8.13276e-06
DHDH [NCBI] 5.25618e-06
PREPL [NCBI] 5.23569e-06
OXCT2 [NCBI] 5.03727e-06
AADACL1 [NCBI] 4.56597e-06
LRAT [NCBI] 3.842e-06
SLC2A1 [NCBI] 3.35867e-06
CTSG [NCBI] 3.30763e-06
GAPDH [NCBI] 3.2284e-06
VDR [NCBI] 2.78121e-06
PPARA [NCBI] 2.70602e-06
CYP3A4 [NCBI] 2.66565e-06
FAAH [NCBI] 2.65859e-06
CDKN1B [NCBI] 2.2242e-06
GFAP [NCBI] 2.18821e-06
FGF21 [NCBI] 1.91981e-06
OXCT1 [NCBI] 1.91981e-06
PRCP [NCBI] 1.88284e-06
CST3 [NCBI] 1.84464e-06
COMT [NCBI] 1.83957e-06
PDZD2 [NCBI] 1.8355e-06
BACE1 [NCBI] 1.81316e-06
PTGS1 [NCBI] 1.78803e-06
DLAT [NCBI] 1.70178e-06
BMP2 [NCBI] 1.69014e-06
CYP2J2 [NCBI] 1.60686e-06
ACAT1 [NCBI] 1.58334e-06
IMPDH1 [NCBI] 1.58334e-06
INSIG2 [NCBI] 1.57777e-06
INSIG1 [NCBI] 1.55659e-06
PLCB2 [NCBI] 1.50158e-06
AKR1C3 [NCBI] 1.45252e-06
LPL [NCBI] 1.43974e-06
PC [NCBI] 1.30733e-06
CTSB [NCBI] 1.29752e-06
RBL1 [NCBI] 1.18592e-06
MSRA [NCBI] 1.16995e-06
AIFM1 [NCBI] 1.15378e-06
LCAT [NCBI] 1.1428e-06
ACHE [NCBI] 1.12809e-06
PGGT1B [NCBI] 1.10479e-06
NFE2L2 [NCBI] 1.08766e-06
CDKN1A [NCBI] 1.08097e-06
CASP7 [NCBI] 1.02226e-06
PTGS2 [NCBI] 1.02054e-06
JAK3 [NCBI] 9.95095e-07
HLA-DQA1 [NCBI] 9.81912e-07
PDE5A [NCBI] 9.68803e-07
GIP [NCBI] 9.25358e-07
UCP3 [NCBI] 8.86893e-07
FAS [NCBI] 8.66575e-07
UMOD [NCBI] 8.63958e-07
PPARG [NCBI] 8.38462e-07
HMOX1 [NCBI] 8.19606e-07
IL2 [NCBI] 8.168e-07
HLA-DQB1 [NCBI] 7.99991e-07
AHR [NCBI] 7.57503e-07
CYP2C9 [NCBI] 7.50939e-07
SNCA [NCBI] 7.48075e-07
GSTP1 [NCBI] 7.46891e-07
PLN [NCBI] 7.38982e-07
IL10 [NCBI] 7.21502e-07
SOD1 [NCBI] 6.88654e-07
DHFR [NCBI] 6.71589e-07
EGF [NCBI] 6.71066e-07
TNFSF10 [NCBI] 6.09161e-07
HRAS [NCBI] 6.0807e-07
CASP9 [NCBI] 6.0523e-07
TRH [NCBI] 5.16654e-07
FASLG [NCBI] 4.62938e-07
NPY [NCBI] 3.61836e-07
EGFR [NCBI] 3.37996e-07
TNF [NCBI] 1.52559e-07



OMIM


 OMIM Link Information
gain		 01
glycogen storage disease 0, liver [NCBI] 0.000271966
glucose transport defect, blood-brain barrier [NCBI] 0.000221788
smell ketone compounds, ability to [NCBI] 0.000183113
mitochondrial myopathy with lactic acidosis [NCBI] 0.000151529
3-@hydroxy-3-methylglutaryl-coa synthase 2, mitochondrial, deficiency of [NCBI] 0.000139612
anemia, microcytic [NCBI] 0.000131876
carnitine palmitoyltransferase i deficiency [NCBI] 0.000106822
alpha-methylacetoacetic aciduria [NCBI] 9.79782e-05
propionic acidemia [NCBI] 8.76075e-05
carnitine palmitoyltransferase ii deficiency, late-onset [NCBI] 8.58334e-05
methylmalonic aciduria due to methylmalonyl-coa mutase deficiency [NCBI] 8.26583e-05
glycogen storage disease vii [NCBI] 7.8e-05
pyruvate decarboxylase deficiency [NCBI] 7.46609e-05
pyruvate kinase deficiency of red cells [NCBI] 7.22174e-05
maple syrup urine disease [NCBI] 6.48212e-05
LRAT [NCBI] 6.09261e-05
AIS [NCBI] 4.60248e-05
MODY [NCBI] 4.03429e-05
RA [NCBI] 3.68595e-05
GAPDH [NCBI] 3.39864e-05
FAAH [NCBI] 3.26385e-05
GYS2 [NCBI] 3.24077e-05
DLAT [NCBI] 3.15119e-05
SLC16A7 [NCBI] 3.15119e-05
HMGCS2 [NCBI] 3.07451e-05
ACAT1 [NCBI] 2.72178e-05
VDR [NCBI] 2.69837e-05
CBR1 [NCBI] 2.6213e-05
panencephalitis, subacute sclerosing [NCBI] 2.3737e-05
ADH5 [NCBI] 2.24398e-05
PDHA1 [NCBI] 2.12372e-05
COMT [NCBI] 1.96618e-05
PD [NCBI] 1.91825e-05
tyrosinemia, type i [NCBI] 1.91044e-05
PARP1 [NCBI] 1.81591e-05
PC [NCBI] 1.58797e-05
GFAP [NCBI] 1.41675e-05
AGER [NCBI] 1.39988e-05
PNPLA6 [NCBI] 1.37667e-05
SERPINA6 [NCBI] 1.12403e-05
LPL [NCBI] 9.467e-06
GIP [NCBI] 8.23522e-06
AHR [NCBI] 5.52008e-06
PPARA [NCBI] 5.23506e-06
ACHE [NCBI] 4.2982e-06
TNFSF6 [NCBI] 3.79974e-06
DHFR [NCBI] 3.7767e-06
TNF [NCBI] 1.11393e-06
VEGF [NCBI] 8.63842e-07
EGFR [NCBI] 2.41457e-07
NPY [NCBI] 1.26573e-07
EGF [NCBI] 6.49656e-08



Database Center for Life Science