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MeSH keywords -> Related genes, diseases (OMIM)


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01 Ketoglutaric Acids [NCBI]


Gene


Gene Link Information
Gain
01
GLUDP5 [NCBI] 0.000398916
SLC25A11 [NCBI] 6.90995e-05
HIF1A [NCBI] 2.29007e-05
HIF1AN [NCBI] 1.92883e-05
PHYH [NCBI] 1.02386e-05
GLUD1 [NCBI] 8.00721e-06
L2HGDH [NCBI] 6.7018e-06
PLOD1 [NCBI] 6.22232e-06
VHL [NCBI] 4.84397e-06
ALKBH1 [NCBI] 4.01106e-06
DLST [NCBI] 3.98616e-06
MDH2 [NCBI] 3.93958e-06
IREB2 [NCBI] 3.89673e-06
DLD [NCBI] 3.73765e-06
PTH [NCBI] 3.72081e-06
SLC13A2 [NCBI] 3.49585e-06
FH [NCBI] 3.44047e-06
EGLN1 [NCBI] 3.35928e-06
FTO [NCBI] 3.34442e-06
OAT [NCBI] 3.11081e-06
PC [NCBI] 3.02371e-06
TAT [NCBI] 2.55319e-06
SLC25A21 [NCBI] 2.38989e-06
SLC22A10 [NCBI] 2.38989e-06
SUCNR1 [NCBI] 2.23138e-06
OXGR1 [NCBI] 2.09436e-06
JMJD1A [NCBI] 2.09436e-06
P4HTM [NCBI] 2.06084e-06
SLC13A3 [NCBI] 2.03105e-06
OGDH [NCBI] 2.00426e-06
TMLHE [NCBI] 1.97991e-06
JMJD1B [NCBI] 1.95759e-06
OXCT1 [NCBI] 1.93699e-06
LEPRE1 [NCBI] 1.91787e-06
ALKBH3 [NCBI] 1.91787e-06
JMJD2C [NCBI] 1.90002e-06
IDH2 [NCBI] 1.8833e-06
SLC25A19 [NCBI] 1.8833e-06
SLC25A3 [NCBI] 1.85269e-06
SLC22A9 [NCBI] 1.8386e-06
GLUD2 [NCBI] 1.82523e-06
SLC25A20 [NCBI] 1.80032e-06
GOT2 [NCBI] 1.75656e-06
HIF3A [NCBI] 1.75656e-06
SLC22A7 [NCBI] 1.74665e-06
SLC22A11 [NCBI] 1.71033e-06
PYCR1 [NCBI] 1.55891e-06
SHMT1 [NCBI] 1.55414e-06
LDHD [NCBI] 1.52716e-06
EPAS1 [NCBI] 1.43423e-06
SDHD [NCBI] 1.4139e-06
OXCT2 [NCBI] 1.39763e-06
VDAC1 [NCBI] 1.37015e-06
NFKBIA [NCBI] 1.21867e-06
SCP2 [NCBI] 1.10562e-06
NFKB1 [NCBI] 7.98346e-07
VEGFA [NCBI] 4.84628e-07
EPO [NCBI] 4.5929e-07
CCK [NCBI] 4.48177e-07
EGF [NCBI] 1.94001e-07




OMIM


OMIM Link Information
gain
01
deafness, congenital, and onychodystrophy, recessive form [NCBI] 0.00446791
thyroid hormonogenesis, genetic defect in, 3 [NCBI] 0.00182656
ehlers-danlos syndrome, type vib [NCBI] 0.0015281
beta-aminoisobutyric acid, urinary excretion of [NCBI] 0.00128562
maple syrup urine disease [NCBI] 0.00029812
refsum disease [NCBI] 0.000226869
hyperoxaluria, primary, type i [NCBI] 0.000211853
SLC25A11 [NCBI] 0.000161187
MCPHA [NCBI] 0.00015942
alaninuria with microcephaly, dwarfism, enamel hypoplasia, and diabetes mellitus [NCBI] 0.000147501
lactic acidosis, fatal infantile [NCBI] 0.000122354
l-2-hydroxyglutaric aciduria [NCBI] 0.000116971
ehlers-danlos syndrome, type vi [NCBI] 0.000104419
3-@methylcrotonyl-coa carboxylase 1 deficiency [NCBI] 0.000103083
GLUD1 [NCBI] 9.70477e-05
pyruvate decarboxylase deficiency [NCBI] 8.24612e-05
PHYH [NCBI] 6.88771e-05
FH [NCBI] 5.08258e-05
SLC22A10 [NCBI] 4.83165e-05
SLC25A21 [NCBI] 4.83165e-05
PC [NCBI] 4.21383e-05
GPR91 [NCBI] 4.08937e-05
GPR80 [NCBI] 4.08937e-05
AD [NCBI] 3.86801e-05
FTO [NCBI] 3.62734e-05
JMJD1A [NCBI] 3.62734e-05
SLC22A9 [NCBI] 3.4921e-05
SLC25A19 [NCBI] 3.4921e-05
L2HGDH [NCBI] 3.4921e-05
SLC25A3 [NCBI] 3.4921e-05
alpha-ketoglutarate dehydrogenase deficiency [NCBI] 3.38434e-05
SLC22A7 [NCBI] 3.38434e-05
GLUD2 [NCBI] 3.21803e-05
VDAC2 [NCBI] 3.21803e-05
PTH [NCBI] 3.05054e-05
VDAC1 [NCBI] 3.03785e-05
AGXT [NCBI] 2.79608e-05
SLC22A8 [NCBI] 2.70679e-05
SLC25A20 [NCBI] 2.50412e-05
ornithine aminotransferase deficiency [NCBI] 2.23176e-05
DAO [NCBI] 2.11191e-05
CCK [NCBI] 1.2874e-06
EGF [NCBI] 3.15334e-07
VEGF [NCBI] 1.83187e-07




Database Center for Life Science