Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Ketoglutarate Dehydrogenase Complex [NCBI]

Gene


 Gene Link Information
Gain		 01
DLSTP [NCBI] 0.000264782
OGDH [NCBI] 2.09694e-05
DLST [NCBI] 7.37047e-06
MDH2 [NCBI] 7.29897e-06
DLD [NCBI] 6.9905e-06
PDHX [NCBI] 4.27988e-06
CS [NCBI] 3.15039e-06
PPM1K [NCBI] 2.40177e-06
TPK1 [NCBI] 2.24093e-06
NDUFS1 [NCBI] 2.2242e-06
CHAT [NCBI] 2.20555e-06
SLC19A3 [NCBI] 2.12957e-06
GOT2 [NCBI] 2.09743e-06
SIAH2 [NCBI] 2.05981e-06
DBT [NCBI] 2.05981e-06
ACO1 [NCBI] 2.03472e-06
MAOB [NCBI] 1.74353e-06
ATP1A2 [NCBI] 1.73559e-06
PC [NCBI] 1.66494e-06
SLC19A2 [NCBI] 1.66096e-06
HNF1B [NCBI] 1.29837e-06
HNF1A [NCBI] 1.26642e-06
BMP4 [NCBI] 1.2537e-06
HIF1A [NCBI] 9.10311e-07
LPL [NCBI] 8.88081e-07
EGF [NCBI] 4.9207e-07



OMIM


 OMIM Link Information
gain		 01
deafness, congenital, and onychodystrophy, recessive form [NCBI] 0.00224712
wernicke-korsakoff syndrome [NCBI] 0.00178344
alpha-ketoglutarate dehydrogenase deficiency [NCBI] 0.000319628
maple syrup urine disease [NCBI] 0.000189277
FRDA [NCBI] 0.000176925
carnitine acetyltransferase deficiency [NCBI] 0.000164704
DLD [NCBI] 0.000149082
TRMA [NCBI] 0.000107087
AD [NCBI] 9.90848e-05
mitochondrial complex i deficiency [NCBI] 9.04625e-05
pyruvate decarboxylase deficiency [NCBI] 8.76997e-05
PPM1K [NCBI] 4.48588e-05
DLST [NCBI] 4.02379e-05
BCKDHB [NCBI] 3.54727e-05
DBT [NCBI] 3.07594e-05
PDHA1 [NCBI] 2.66157e-05
CHAT [NCBI] 1.97828e-05
LPL [NCBI] 6.10352e-06
SLE [NCBI] 3.30486e-06
EGF [NCBI] 4.05266e-07



Database Center for Life Science