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MeSH keywords -> Related genes, diseases (OMIM)


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01 Pyruvate Dehydrogenase Complex [NCBI]

Gene


 Gene Link Information
Gain		 01
PDHX [NCBI] 9.75289e-05
PDHA1 [NCBI] 9.60185e-05
DLAT [NCBI] 3.6135e-05
PDHB [NCBI] 3.42746e-05
PDK2 [NCBI] 2.32425e-05
PDK3 [NCBI] 1.91437e-05
PDK1 [NCBI] 1.65517e-05
PC [NCBI] 1.62547e-05
PDK4 [NCBI] 1.48715e-05
DLD [NCBI] 1.47521e-05
PDHA2 [NCBI] 1.46786e-05
PPM2C [NCBI] 6.28006e-06
MDH2 [NCBI] 5.89167e-06
ACLY [NCBI] 3.85179e-06
CS [NCBI] 3.66109e-06
ABCC5 [NCBI] 3.13289e-06
ABCC4 [NCBI] 2.93458e-06
GAPDH [NCBI] 2.91877e-06
MSH3 [NCBI] 2.52342e-06
PDP2 [NCBI] 2.17852e-06
SREBF1 [NCBI] 2.05986e-06
PPM1K [NCBI] 1.94039e-06
OGDH [NCBI] 1.88382e-06
CRAT [NCBI] 1.7796e-06
CIDEA [NCBI] 1.7796e-06
NDUFS1 [NCBI] 1.76287e-06
BCKDHB [NCBI] 1.71819e-06
ATP5J [NCBI] 1.69208e-06
DLST [NCBI] 1.67992e-06
SOX13 [NCBI] 1.67992e-06
GOT2 [NCBI] 1.63616e-06
DBT [NCBI] 1.59858e-06
BCKDHA [NCBI] 1.58996e-06
HK2 [NCBI] 1.58996e-06
ABCC3 [NCBI] 1.55058e-06
GSTO1 [NCBI] 1.4386e-06
ANP32A [NCBI] 1.40688e-06
OXCT2 [NCBI] 1.27746e-06
SP100 [NCBI] 1.24532e-06
LPL [NCBI] 1.23889e-06
SLC19A2 [NCBI] 1.20043e-06
SET [NCBI] 1.17964e-06
PIGR [NCBI] 1.17247e-06
MYOM2 [NCBI] 1.16206e-06
SFRS2 [NCBI] 1.15368e-06
FOXO3 [NCBI] 1.09746e-06
CASP6 [NCBI] 1.08958e-06
VIP [NCBI] 1.06204e-06
C1QBP [NCBI] 1.03068e-06
CD93 [NCBI] 1.02053e-06
NR1I3 [NCBI] 9.61869e-07
CDK5 [NCBI] 8.51203e-07
PRKCD [NCBI] 7.98149e-07
GZMB [NCBI] 7.40599e-07
SLC2A1 [NCBI] 7.24823e-07
CYP2C19 [NCBI] 6.73372e-07
CASP9 [NCBI] 5.06971e-07
CHAT [NCBI] 4.67935e-07
HIF1A [NCBI] 4.64169e-07
TGFB1 [NCBI] 3.81235e-07
TP53 [NCBI] 3.70919e-07
GFAP [NCBI] 3.52522e-07
CASP3 [NCBI] 2.45882e-07
NGF [NCBI] 2.20921e-07
PRL [NCBI] 2.14954e-07
TNF [NCBI] 8.37389e-08



OMIM


 OMIM Link Information
gain		 01
pyruvate decarboxylase deficiency [NCBI] 0.00331945
wernicke-korsakoff syndrome [NCBI] 0.00230594
PDHA1 [NCBI] 0.0017703
pyruvate dehydrogenase e3-binding protein deficiency [NCBI] 0.00141306
maple syrup urine disease [NCBI] 0.000375909
LS [NCBI] 0.000349999
PDHX [NCBI] 0.000339698
DLD [NCBI] 0.000248269
DLAT [NCBI] 0.000239069
RA [NCBI] 0.000223289
PDHB [NCBI] 0.000211896
PC [NCBI] 0.000181427
TRMA [NCBI] 0.000166289
pyruvate carboxylase deficiency [NCBI] 0.000163847
adrenoleukodystrophy, autosomal neonatal form [NCBI] 0.000128233
pyruvate dehydrogenase e2 deficiency [NCBI] 0.000124053
carnitine acetyltransferase deficiency [NCBI] 0.000124053
leigh syndrome, x-linked [NCBI] 0.000112153
FRDA [NCBI] 9.56291e-05
pyruvate dehydrogenase phosphatase deficiency [NCBI] 9.41369e-05
mitochondrial complex iii deficiency [NCBI] 9.41369e-05
lactic acidosis, fatal infantile [NCBI] 8.71034e-05
PBC [NCBI] 8.71034e-05
PDHA2 [NCBI] 8.45957e-05
alpers diffuse degeneration of cerebral gray matter with hepatic cirrhosis [NCBI] 8.42719e-05
carnitine palmitoyltransferase ii deficiency, lethal neonatal [NCBI] 8.17592e-05
glucose transport defect, blood-brain barrier [NCBI] 6.67841e-05
glutaric acidemia i [NCBI] 6.24205e-05
mitochondrial complex i deficiency [NCBI] 5.05708e-05
MTATP6 [NCBI] 4.03945e-05
CROT [NCBI] 3.48495e-05
PPM1K [NCBI] 3.48495e-05
DLST [NCBI] 3.0232e-05
SLE [NCBI] 2.92293e-05
NDUFV1 [NCBI] 2.88809e-05
KSS [NCBI] 2.7251e-05
ABCC5 [NCBI] 2.61443e-05
ABCC4 [NCBI] 2.61443e-05
CRAT [NCBI] 2.54752e-05
BCKDHB [NCBI] 2.54752e-05
SLC19A2 [NCBI] 2.4881e-05
MJD [NCBI] 2.45642e-05
HK2 [NCBI] 2.43466e-05
GAPDH [NCBI] 2.09772e-05
DBT [NCBI] 2.07822e-05
PPARA [NCBI] 1.91263e-05
MTTK [NCBI] 1.80223e-05
ABCC2 [NCBI] 1.19398e-05
PIGR [NCBI] 1.16248e-05
TNF [NCBI] 9.59289e-06
VEGF [NCBI] 8.5368e-06
CDK5 [NCBI] 7.3239e-06
PRL [NCBI] 2.97735e-06
LPL [NCBI] 2.87267e-06
NGFB [NCBI] 2.77672e-06
VIP [NCBI] 8.90528e-07
GFAP [NCBI] 2.3913e-07
CHAT [NCBI] 8.99183e-08



Database Center for Life Science