Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Glycolates [NCBI]


Gene


Gene Link Information
Gain
01
AGXT2L1 [NCBI] 1.84494e-05
TDP1 [NCBI] 6.41122e-06
GRHPR [NCBI] 6.37513e-06
BMP2 [NCBI] 5.06199e-06
PGP [NCBI] 4.21568e-06
CLIC1 [NCBI] 4.10981e-06
PRKDC [NCBI] 2.59831e-06
XRCC5 [NCBI] 2.53718e-06
AGXT2 [NCBI] 2.39101e-06
BPGM [NCBI] 2.08101e-06
TREX1 [NCBI] 1.96008e-06
GSTZ1 [NCBI] 1.9154e-06
AGXT [NCBI] 1.85001e-06
TPI1 [NCBI] 1.83134e-06
APTX [NCBI] 1.74049e-06
DCLRE1C [NCBI] 1.67616e-06
LIG3 [NCBI] 1.62714e-06
CFTR [NCBI] 1.58293e-06
XRCC6 [NCBI] 1.5356e-06
KRT5 [NCBI] 1.48672e-06
ETS2 [NCBI] 1.47697e-06
APEX1 [NCBI] 1.44971e-06
CYP1B1 [NCBI] 1.35801e-06
WRN [NCBI] 1.27013e-06
DCT [NCBI] 1.24696e-06
IBSP [NCBI] 1.13949e-06
BMP4 [NCBI] 1.1268e-06
FOLR1 [NCBI] 1.03492e-06
NFKB1 [NCBI] 1.00907e-06
G6PD [NCBI] 9.51985e-07
CDK2 [NCBI] 8.74117e-07
CASP9 [NCBI] 8.29767e-07
AFP [NCBI] 7.25361e-07
AR [NCBI] 6.89107e-07
AVP [NCBI] 6.72723e-07
PCNA [NCBI] 6.44307e-07
CDKN1A [NCBI] 5.82424e-07
CASP3 [NCBI] 5.46523e-07
PTH [NCBI] 5.29909e-07
TNF [NCBI] 3.40992e-07




OMIM


OMIM Link Information
gain
01
hyperoxaluria, primary, type i [NCBI] 0.000857337
hyperoxaluria, primary, type ii [NCBI] 0.000299241
hydroxyprolinemia [NCBI] 0.000139291
PHA2 [NCBI] 0.000107087
adrenoleukodystrophy, autosomal neonatal form [NCBI] 8.82258e-05
WRN [NCBI] 7.81184e-05
AGXT [NCBI] 7.12602e-05
PGP [NCBI] 6.52657e-05
diphosphoglycerate mutase deficiency of erythrocyte [NCBI] 3.26603e-05
CFTR [NCBI] 2.01972e-05
CDK2 [NCBI] 1.65925e-05
SERPINA6 [NCBI] 1.61529e-05
SPP1 [NCBI] 9.87248e-06
G6PD [NCBI] 8.50765e-06
AR [NCBI] 5.0708e-06
VEGF [NCBI] 5.01227e-06
AFP [NCBI] 5.0046e-06
PCNA [NCBI] 3.71845e-06
AVP [NCBI] 3.27007e-06
PTH [NCBI] 1.99772e-06
TNF [NCBI] 3.15154e-07
CF [NCBI] 7.87444e-08




Database Center for Life Science