Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Succinates [NCBI]

Gene


 Gene Link Information
Gain		 01
GER [NCBI] 0.000136461
SLC13A2 [NCBI] 1.82712e-05
OXCT2 [NCBI] 1.21797e-05
ADAM17 [NCBI] 5.74127e-06
ALDH5A1 [NCBI] 3.56201e-06
PC [NCBI] 3.2968e-06
CAT [NCBI] 2.9827e-06
SLC13A5 [NCBI] 2.19665e-06
SLC13A3 [NCBI] 2.16687e-06
CPZ [NCBI] 2.11572e-06
CTSL1 [NCBI] 2.07435e-06
CPA2 [NCBI] 2.03583e-06
IDH2 [NCBI] 2.0191e-06
ME2 [NCBI] 1.96102e-06
ME1 [NCBI] 1.94827e-06
PPP1R14A [NCBI] 1.8067e-06
ANTXR2 [NCBI] 1.7537e-06
SLC25A11 [NCBI] 1.69949e-06
RAD52 [NCBI] 1.59191e-06
STUB1 [NCBI] 1.56097e-06
CPB2 [NCBI] 1.54953e-06
PCNA [NCBI] 1.50231e-06
CPE [NCBI] 1.48963e-06
PANK2 [NCBI] 1.43158e-06
APOC3 [NCBI] 1.3609e-06
SMAD1 [NCBI] 1.34355e-06
CYP27A1 [NCBI] 1.2775e-06
HDLBP [NCBI] 1.25994e-06
MMP3 [NCBI] 1.25712e-06
HTR2A [NCBI] 1.25433e-06
TAT [NCBI] 1.22546e-06
KCNJ8 [NCBI] 1.22053e-06
RPA1 [NCBI] 1.14955e-06
MDM2 [NCBI] 1.13266e-06
PREPL [NCBI] 1.08764e-06
ALB [NCBI] 1.00282e-06
SMAD4 [NCBI] 9.93006e-07
FOLR1 [NCBI] 9.57945e-07
GAPDH [NCBI] 9.33802e-07
BACE1 [NCBI] 8.73295e-07
TG [NCBI] 8.28054e-07
JAK2 [NCBI] 8.01489e-07
SLC6A4 [NCBI] 7.90507e-07
MBP [NCBI] 6.70982e-07
TGFB1 [NCBI] 6.21455e-07
TP53 [NCBI] 6.10434e-07
VWF [NCBI] 6.0552e-07
CCK [NCBI] 5.76107e-07
NPY [NCBI] 5.02534e-07
CASP3 [NCBI] 4.73367e-07
EGF [NCBI] 3.06128e-07



OMIM


 OMIM Link Information
gain		 01
succinic acidemia [NCBI] 0.003491
argininosuccinic aciduria [NCBI] 0.000647246
methylmalonic aciduria, cbla type [NCBI] 0.000406976
methylmalonic aciduria due to methylmalonyl-coa mutase deficiency [NCBI] 0.000321731
encephalopathy, ethylmalonic [NCBI] 0.000276019
acyl-coa dehydrogenase, short-chain, deficiency of [NCBI] 0.000217453
SNDI [NCBI] 0.000129757
mitochondrial myopathy with diabetes [NCBI] 0.00011236
succinyl-coa:3-oxoacid coa transferase deficiency [NCBI] 0.000102641
MADD [NCBI] 7.71381e-05
mitochondrial complex i deficiency [NCBI] 7.53131e-05
porphyria, acute intermittent [NCBI] 6.59374e-05
maple syrup urine disease [NCBI] 6.27477e-05
ornithine transcarbamylase deficiency, hyperammonemia due to [NCBI] 5.93945e-05
PC [NCBI] 4.66253e-05
RA [NCBI] 4.36477e-05
MTTL2 [NCBI] 3.84856e-05
SLC16A5 [NCBI] 3.84856e-05
CPZ [NCBI] 3.51589e-05
polycystic kidneys [NCBI] 3.39071e-05
SDHC [NCBI] 3.12439e-05
CAT [NCBI] 3.08682e-05
transcobalamin ii deficiency [NCBI] 2.45202e-05
CPE [NCBI] 2.02211e-05
CPB2 [NCBI] 1.99775e-05
SPINK1 [NCBI] 1.67683e-05
JAK2 [NCBI] 1.63005e-05
PCNA [NCBI] 1.13791e-05
ALB [NCBI] 1.07974e-05
XDH [NCBI] 9.33636e-06
TG [NCBI] 6.97289e-06
MBP [NCBI] 4.24294e-06
CCK [NCBI] 2.67253e-06
NPY [NCBI] 1.66451e-06
EGF [NCBI] 2.0439e-08



Database Center for Life Science