Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Metabolism [NCBI]

Gene


 Gene Link Information
Gain		 01
UCP3 [NCBI] 6.17844e-06
GALP [NCBI] 6.11887e-06
GSTT1 [NCBI] 5.79972e-06
CNR1 [NCBI] 5.28552e-06
LEPR [NCBI] 4.60577e-06
NQO1 [NCBI] 4.14903e-06
CYP1A1 [NCBI] 3.93518e-06
LEP [NCBI] 3.88837e-06
INS [NCBI] 3.82008e-06
CHDH [NCBI] 3.70718e-06
EML3 [NCBI] 3.56577e-06
PRL [NCBI] 3.43233e-06
CIDEA [NCBI] 3.23526e-06
OR1D2 [NCBI] 3.10805e-06
ALMS1 [NCBI] 2.89845e-06
FGF19 [NCBI] 2.79838e-06
CNR2 [NCBI] 2.69805e-06
GSTT2 [NCBI] 2.65513e-06
LPL [NCBI] 2.65192e-06
SIRT2 [NCBI] 2.63904e-06
PEMT [NCBI] 2.6235e-06
BHMT [NCBI] 2.58683e-06
APOA2 [NCBI] 2.53369e-06
CDC7 [NCBI] 2.53369e-06
E2F2 [NCBI] 2.48052e-06
CCK [NCBI] 2.35954e-06
CUBN [NCBI] 2.30671e-06
IL1R1 [NCBI] 2.27023e-06
TP53 [NCBI] 2.25839e-06
ADH1C [NCBI] 2.24302e-06
TTPA [NCBI] 2.22364e-06
XPNPEP2 [NCBI] 2.19013e-06
E2F4 [NCBI] 2.17568e-06
DIO2 [NCBI] 2.13752e-06
UCP1 [NCBI] 2.12974e-06
COMP [NCBI] 2.08571e-06
EPHX1 [NCBI] 2.08108e-06
FAAH [NCBI] 2.01869e-06
TNFRSF1A [NCBI] 1.98952e-06
PPARGC1A [NCBI] 1.95335e-06
RETN [NCBI] 1.93462e-06
SIRT1 [NCBI] 1.92148e-06
CYP2E1 [NCBI] 1.87243e-06
LMNA [NCBI] 1.85255e-06
IGFBP3 [NCBI] 1.8484e-06
GHR [NCBI] 1.83618e-06
MATN1 [NCBI] 1.82298e-06
DDIT3 [NCBI] 1.8191e-06
DBH [NCBI] 1.81397e-06
CS [NCBI] 1.81016e-06
CCR3 [NCBI] 1.77493e-06
NR3C1 [NCBI] 1.75214e-06
ADIPOQ [NCBI] 1.64066e-06
CFLAR [NCBI] 1.58999e-06
TGFBR1 [NCBI] 1.49508e-06
PPARG [NCBI] 1.46845e-06
E2F1 [NCBI] 1.43022e-06
CYP2C19 [NCBI] 1.37182e-06
ARID4A [NCBI] 1.36341e-06
GSTM1 [NCBI] 1.34707e-06
GSTP1 [NCBI] 1.3207e-06
G6PD [NCBI] 1.31819e-06
IRS1 [NCBI] 1.30545e-06
TNF [NCBI] 1.24598e-06
NOS2 [NCBI] 1.07159e-06
HIF1A [NCBI] 1.02008e-06
VWF [NCBI] 8.94767e-07
BDNF [NCBI] 8.76146e-07
NPY [NCBI] 7.59349e-07



OMIM


 OMIM Link Information
gain		 01
thyroid hormonogenesis, genetic defect in, 3 [NCBI] 0.00116883
MCDU [NCBI] 0.00110387
cerebellar ataxia and hypogonadotropic hypogonadism [NCBI] 0.00105558
hypermetabolism due to defect in mitochondria [NCBI] 0.000141401
xanthinuria, type i [NCBI] 0.000124118
thyroid hormonogenesis, genetic defect in, 1 [NCBI] 0.00011906
enchondromatosis, multiple [NCBI] 0.00011503
hyperbilirubinemia, transient familial neonatal [NCBI] 0.000108812
mitochondrial myopathy [NCBI] 0.000106305
NSHPT [NCBI] 0.000106305
ADHR [NCBI] 0.000106305
IFD [NCBI] 0.000102076
dent disease 1 [NCBI] 9.56224e-05
CGL2 [NCBI] 8.8708e-05
megaloblastic anemia 1 [NCBI] 8.77578e-05
HHC1 [NCBI] 8.14526e-05
CLN3 [NCBI] 7.77681e-05
PDS [NCBI] 7.66783e-05
maple syrup urine disease [NCBI] 7.11659e-05
gaucher disease, type i [NCBI] 6.68671e-05
GALP [NCBI] 5.46499e-05
isoniazid inactivation [NCBI] 5.39454e-05
AIS [NCBI] 4.94388e-05
ATE1 [NCBI] 3.73207e-05
COQ7 [NCBI] 3.61237e-05
FGF19 [NCBI] 3.35317e-05
INS [NCBI] 3.20288e-05
PFKL [NCBI] 3.03575e-05
LDHC [NCBI] 2.99614e-05
TP73 [NCBI] 2.99614e-05
TXNIP [NCBI] 2.95903e-05
orotic aciduria i [NCBI] 2.9241e-05
adenylyl cyclase, soluble [NCBI] 2.6349e-05
PRSS1 [NCBI] 2.61447e-05
E2F1 [NCBI] 2.57562e-05
EPHX1 [NCBI] 2.48842e-05
IFNG [NCBI] 2.32039e-05
HS [NCBI] 2.2736e-05
RLBP1 [NCBI] 2.25154e-05
UCP3 [NCBI] 1.9596e-05
UCP1 [NCBI] 1.67159e-05
FAAH [NCBI] 1.45904e-05
COMP [NCBI] 1.45632e-05
GPI [NCBI] 1.24326e-05
LPL [NCBI] 1.22664e-05
PRL [NCBI] 1.14193e-05
CCK [NCBI] 8.32328e-06
TNFRSF11B [NCBI] 7.25334e-06
PPARA [NCBI] 6.29034e-06
G6PD [NCBI] 4.95623e-06
CRH [NCBI] 1.57177e-06
BDNF [NCBI] 1.53151e-06
TNF [NCBI] 5.77687e-07
NPY [NCBI] 4.33032e-07



Database Center for Life Science