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MeSH keywords -> Related genes, diseases (OMIM)


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01 Oxalates [NCBI]

Gene


 Gene Link Information
Gain		 01
AGXT2L1 [NCBI] 3.58432e-05
SLC26A6 [NCBI] 1.63229e-05
UMOD [NCBI] 1.04986e-05
PTH [NCBI] 6.48506e-06
PLN [NCBI] 6.39238e-06
GRHPR [NCBI] 5.99677e-06
AGXT [NCBI] 3.833e-06
SLC26A3 [NCBI] 3.68564e-06
SPINT2 [NCBI] 2.88587e-06
AGXT2 [NCBI] 2.26702e-06
SLC26A9 [NCBI] 2.15035e-06
CASP3 [NCBI] 2.1411e-06
TF [NCBI] 2.11099e-06
KHK [NCBI] 1.79145e-06
SLC25A11 [NCBI] 1.65321e-06
ATP2A1 [NCBI] 1.64357e-06
SLC26A2 [NCBI] 1.56256e-06
PTPRN2 [NCBI] 1.55228e-06
SLC22A12 [NCBI] 1.51765e-06
RYR1 [NCBI] 1.43243e-06
SLC4A1 [NCBI] 1.32454e-06
PTPRN [NCBI] 1.26919e-06
CS [NCBI] 1.13448e-06
SLC9A3 [NCBI] 1.05271e-06
ITPR1 [NCBI] 1.03726e-06
EGR1 [NCBI] 9.57666e-07
ALB [NCBI] 9.56952e-07
EGF [NCBI] 8.6478e-07
COMT [NCBI] 8.40842e-07
G6PD [NCBI] 8.29665e-07
ADA [NCBI] 7.99549e-07
CD68 [NCBI] 7.53995e-07
IL6 [NCBI] 7.3469e-07
CASP9 [NCBI] 7.08431e-07
TLR4 [NCBI] 6.98015e-07
TGFB1 [NCBI] 5.77034e-07
CFTR [NCBI] 4.90672e-07
PTGS2 [NCBI] 4.35698e-07



OMIM


 OMIM Link Information
gain		 01
nephrolithiasis, calcium oxalate [NCBI] 0.0219823
hyperoxaluria, primary, type i [NCBI] 0.00305847
hyperoxaluria, primary, type ii [NCBI] 0.000425549
glycinuria with or without oxalate urolithiasis [NCBI] 0.000126032
hydroxyprolinemia [NCBI] 0.000120283
hypouricemia, renal [NCBI] 9.52902e-05
SPP1 [NCBI] 8.42497e-05
solute carrier family 26 (anion transporter), member 6: slc26a6 [NCBI] 8.23205e-05
GCE [NCBI] 7.92037e-05
PTH [NCBI] 6.77324e-05
AGXT [NCBI] 6.7372e-05
wilson disease [NCBI] 5.17003e-05
TF [NCBI] 2.42113e-05
TLR4 [NCBI] 1.06292e-05
ALB [NCBI] 1.03467e-05
COMT [NCBI] 9.26534e-06
CF [NCBI] 8.38977e-06
ADA [NCBI] 6.81652e-06
G6PD [NCBI] 6.79861e-06
EGF [NCBI] 2.18527e-06



Database Center for Life Science