Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Protein S [NCBI]

Gene


 Gene Link Information
Gain		 01
PROSP [NCBI] 0.000564273
PROS1 [NCBI] 0.000224899
F5 [NCBI] 4.60557e-05
PROC [NCBI] 4.57033e-05
F2 [NCBI] 3.15439e-05
C4BPA [NCBI] 3.12305e-05
TYRO3 [NCBI] 2.98543e-05
TFPI [NCBI] 1.95307e-05
VWF [NCBI] 1.74065e-05
C4BPB [NCBI] 1.47573e-05
EGF [NCBI] 1.29512e-05
PROCR [NCBI] 9.78926e-06
MERTK [NCBI] 8.90715e-06
MTHFR [NCBI] 8.34733e-06
F10 [NCBI] 7.72763e-06
PLG [NCBI] 6.31063e-06
C4B [NCBI] 4.57999e-06
F8 [NCBI] 4.49371e-06
SHBG [NCBI] 3.8839e-06
GGCX [NCBI] 3.13455e-06
OSM [NCBI] 2.97844e-06
SERPINC1 [NCBI] 2.61596e-06
VKORC1 [NCBI] 2.16974e-06
SP1 [NCBI] 1.97999e-06
PF4 [NCBI] 1.79195e-06
SERPINE1 [NCBI] 1.70103e-06
F8A1 [NCBI] 1.69451e-06
LRG1 [NCBI] 1.55111e-06
CALU [NCBI] 1.51354e-06
CST3 [NCBI] 1.47311e-06
PROZ [NCBI] 1.47298e-06
GAS6 [NCBI] 1.4249e-06
HABP2 [NCBI] 1.40668e-06
GLRX [NCBI] 1.25113e-06
MSR1 [NCBI] 1.2232e-06
F11 [NCBI] 1.2232e-06
CPB2 [NCBI] 1.20887e-06
THBD [NCBI] 1.15365e-06
FOXA1 [NCBI] 1.1514e-06
F9 [NCBI] 1.08255e-06
MAN1C1 [NCBI] 1.08255e-06
A2M [NCBI] 1.07911e-06
F2R [NCBI] 1.0774e-06
FOXA2 [NCBI] 1.05935e-06
TFPI2 [NCBI] 1.02799e-06
PIGA [NCBI] 1.01831e-06
ITGAM [NCBI] 9.987e-07
F3 [NCBI] 9.79279e-07
MGP [NCBI] 9.18004e-07
CREB1 [NCBI] 8.93288e-07
EPO [NCBI] 8.8241e-07
SP3 [NCBI] 8.62356e-07
DAG1 [NCBI] 8.50659e-07
ESR2 [NCBI] 8.27429e-07
MPL [NCBI] 7.90927e-07
AMBP [NCBI] 7.83657e-07
CLU [NCBI] 7.61483e-07
ADAMTS13 [NCBI] 7.31456e-07
TNF [NCBI] 7.05668e-07
PGR [NCBI] 6.91205e-07
CTSG [NCBI] 6.25723e-07
CYP2C9 [NCBI] 5.6874e-07
ESR1 [NCBI] 5.58418e-07
PLAUR [NCBI] 4.74734e-07
JAK2 [NCBI] 4.73003e-07
LIF [NCBI] 4.47062e-07
STAT3 [NCBI] 4.02296e-07
VEGFA [NCBI] 2.98858e-07
PTH [NCBI] 1.65097e-07



OMIM


 OMIM Link Information
gain		 01
PROS1 [NCBI] 0.00157511
SLE [NCBI] 0.000551658
protein c deficiency, congenital thrombotic disease due to [NCBI] 0.000170528
legg-calve-perthes disease [NCBI] 0.000134642
TFPI [NCBI] 0.000123636
thrombophilia due to deficiency of activated protein c cofactor [NCBI] 0.000121158
budd-chiari syndrome [NCBI] 0.000116579
afibrinogenemia, congenital [NCBI] 9.98001e-05
vitamin k-dependent clotting factors, combined deficiency of, 1 [NCBI] 9.79079e-05
coumarin resistance [NCBI] 9.30308e-05
PLG [NCBI] 5.79677e-05
factor v deficiency [NCBI] 5.71356e-05
RA [NCBI] 5.41605e-05
MERTK [NCBI] 5.40072e-05
GGCX [NCBI] 5.09292e-05
EGF [NCBI] 5.06718e-05
antithrombin iii deficiency [NCBI] 4.997e-05
F3 [NCBI] 4.05842e-05
OSM [NCBI] 3.2066e-05
PCI [NCBI] 2.84099e-05
CALU [NCBI] 2.74448e-05
C4BPB [NCBI] 2.74448e-05
TYRO3 [NCBI] 2.74448e-05
AXL [NCBI] 2.65502e-05
GAS6 [NCBI] 2.45217e-05
SHBG [NCBI] 1.78312e-05
FGG [NCBI] 1.64443e-05
PF4 [NCBI] 1.36426e-05
HNF1A [NCBI] 1.22902e-05
VEGF [NCBI] 9.6587e-06
STAT3 [NCBI] 5.57214e-06
PTH [NCBI] 2.74079e-06
TNF [NCBI] 1.49541e-06
EPO [NCBI] 5.67601e-07



Database Center for Life Science