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MeSH keywords -> Related genes, diseases (OMIM)


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01 Ketone Bodies [NCBI]

Gene


 Gene Link Information
Gain		 01
OXCT2 [NCBI] 7.6224e-05
SLC2A1 [NCBI] 8.24463e-06
OXCT1 [NCBI] 6.90637e-06
ACAT1 [NCBI] 5.85022e-06
LPL [NCBI] 5.14809e-06
TNF [NCBI] 4.77087e-06
AACS [NCBI] 4.69502e-06
SLC16A7 [NCBI] 4.03407e-06
INS [NCBI] 2.28543e-06
HMGCS2 [NCBI] 2.02691e-06
ACADL [NCBI] 2.00459e-06
SLC22A16 [NCBI] 1.9303e-06
ACSL6 [NCBI] 1.8856e-06
HMGCL [NCBI] 1.84732e-06
ACAT2 [NCBI] 1.83569e-06
EBI3 [NCBI] 1.79364e-06
SLC5A8 [NCBI] 1.76595e-06
ZBTB17 [NCBI] 1.5918e-06
GABRA1 [NCBI] 1.54962e-06
HGF [NCBI] 1.50343e-06
EGF [NCBI] 1.48483e-06
TXNIP [NCBI] 1.46936e-06
THRSP [NCBI] 1.43934e-06
FOXA2 [NCBI] 1.31082e-06
IL12A [NCBI] 1.30452e-06
SLC22A5 [NCBI] 1.27509e-06
PPARGC1A [NCBI] 1.189e-06
TAT [NCBI] 1.13704e-06
SLC6A2 [NCBI] 1.12254e-06
MECP2 [NCBI] 1.01415e-06
SREBF1 [NCBI] 1.01105e-06
GIP [NCBI] 9.88891e-07
MYC [NCBI] 9.10686e-07
AHR [NCBI] 8.20439e-07
SNCA [NCBI] 8.10964e-07
CALCA [NCBI] 8.09537e-07
IRS1 [NCBI] 8.07646e-07
G6PD [NCBI] 7.87933e-07
CETP [NCBI] 7.60054e-07
IL6 [NCBI] 6.93297e-07
HIF1A [NCBI] 6.22993e-07
APOE [NCBI] 5.04916e-07
PCNA [NCBI] 4.8572e-07
CDKN1A [NCBI] 4.25989e-07
NPY [NCBI] 4.20001e-07
CASP3 [NCBI] 3.9161e-07



OMIM


 OMIM Link Information
gain		 01
methionine malabsorption syndrome [NCBI] 0.00264194
succinyl-coa:3-oxoacid coa transferase deficiency [NCBI] 0.000565525
carnitine palmitoyltransferase ii deficiency, late-onset [NCBI] 0.000481577
acyl-coa dehydrogenase, short-chain, deficiency of [NCBI] 0.000221788
3-@hydroxy-3-methylglutaryl-coa synthase 2, mitochondrial, deficiency of [NCBI] 0.000139612
carnitine palmitoyltransferase ii deficiency, infantile [NCBI] 0.000126126
glycogen storage disease 0, liver [NCBI] 0.000117736
acyl-coa dehydrogenase, long-chain, deficiency of [NCBI] 0.000117736
hyperlipidemia, combined, 1 [NCBI] 0.000114476
creatine phosphokinase, elevated serum [NCBI] 0.000114476
alpers diffuse degeneration of cerebral gray matter with hepatic cirrhosis [NCBI] 0.000111627
methylmalonic aciduria, cbla type [NCBI] 0.000109097
glucose transport defect, blood-brain barrier [NCBI] 9.39667e-05
pyruvate carboxylase deficiency [NCBI] 9.27739e-05
propionic acidemia [NCBI] 8.76075e-05
methylmalonic aciduria due to methylmalonyl-coa mutase deficiency [NCBI] 8.26583e-05
FCHL [NCBI] 8.19303e-05
MADD [NCBI] 7.92347e-05
OXCT1 [NCBI] 7.34396e-05
3-@hydroxy-3-methylglutaryl-coa lyase deficiency [NCBI] 5.65863e-05
LPL [NCBI] 4.62049e-05
MODY [NCBI] 4.03429e-05
alpha-ketoglutarate dehydrogenase deficiency [NCBI] 3.24077e-05
GYS2 [NCBI] 3.24077e-05
ACAT2 [NCBI] 3.15119e-05
HMGCS2 [NCBI] 3.07451e-05
CPT1A [NCBI] 2.72178e-05
ACAT1 [NCBI] 2.72178e-05
FOXA2 [NCBI] 2.68614e-05
TXNIP [NCBI] 2.5635e-05
TNF [NCBI] 2.53296e-05
CPT2 [NCBI] 2.44167e-05
SLC16A1 [NCBI] 2.1119e-05
ACADM [NCBI] 1.37952e-05
ABP1 [NCBI] 1.24305e-05
INS [NCBI] 1.00928e-05
HGF [NCBI] 8.4721e-06
GIP [NCBI] 8.23522e-06
ADCYAP1 [NCBI] 6.71097e-06
AHR [NCBI] 5.52008e-06
AVP [NCBI] 4.7131e-06
G6PD [NCBI] 4.12795e-06
EGF [NCBI] 1.90443e-06
APOE [NCBI] 1.6647e-06
PCNA [NCBI] 6.05605e-07
NPY [NCBI] 1.26573e-07



Database Center for Life Science