Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 1-Carboxyglutamic Acid [NCBI]

Gene


 Gene Link Information
Gain		 01
MGP [NCBI] 3.62931e-05
EGF [NCBI] 1.97774e-05
F9 [NCBI] 1.78051e-05
PROC [NCBI] 1.50808e-05
GGCX [NCBI] 1.05751e-05
F10 [NCBI] 7.10274e-06
PRRG2 [NCBI] 4.84962e-06
VKORC1 [NCBI] 4.45048e-06
F7 [NCBI] 2.90378e-06
PRRG3 [NCBI] 2.47241e-06
PRRG1 [NCBI] 2.3815e-06
PRRG4 [NCBI] 2.3815e-06
PTH [NCBI] 2.06928e-06
C4BPB [NCBI] 1.83905e-06
GAS6 [NCBI] 1.71272e-06
BGLAP [NCBI] 1.67195e-06
PROS1 [NCBI] 1.48001e-06
THBD [NCBI] 1.44091e-06
PROCR [NCBI] 1.43197e-06
F3 [NCBI] 1.26572e-06
AMBP [NCBI] 1.06825e-06
BMP7 [NCBI] 1.01435e-06
IBSP [NCBI] 1.00939e-06
BMP4 [NCBI] 9.96736e-07
F2 [NCBI] 9.62067e-07
SERPINE1 [NCBI] 9.51101e-07
TTR [NCBI] 9.22957e-07
CTSG [NCBI] 9.07359e-07
TNFRSF11B [NCBI] 8.61901e-07



OMIM


 OMIM Link Information
gain		 01
BGLAP [NCBI] 0.000228386
AI1G [NCBI] 0.000174453
EGF [NCBI] 0.000159962
OPTA2 [NCBI] 0.000149036
chondrodysplasia punctata, autosomal dominant [NCBI] 0.000129704
vitamin k-dependent clotting factors, combined deficiency of, 1 [NCBI] 0.000125733
OPTB1 [NCBI] 0.000118075
F3 [NCBI] 0.000101295
RA [NCBI] 4.90284e-05
factor x deficiency [NCBI] 4.79893e-05
PRRG3 [NCBI] 4.63982e-05
PRRG1 [NCBI] 4.63982e-05
PRRG4 [NCBI] 4.63982e-05
PRRG2 [NCBI] 3.89756e-05
MGP [NCBI] 3.10307e-05
PROCR [NCBI] 1.93984e-05
HEMB [NCBI] 1.31602e-05
NR1I2 [NCBI] 1.0583e-05
ACPP [NCBI] 9.1236e-06
PTH [NCBI] 6.87468e-06
TFPI [NCBI] 6.70191e-06
TNFRSF11B [NCBI] 5.55569e-06
SPP1 [NCBI] 4.92641e-06
KLK3 [NCBI] 2.62195e-07



Database Center for Life Science