Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Carbon-Carbon Ligases [NCBI]

Gene


 Gene Link Information
Gain		 01
VKORC1 [NCBI] 0.000102471
GGCX [NCBI] 9.97479e-05
MCCC1 [NCBI] 2.12791e-05
PCCB [NCBI] 1.88107e-05
MCCC2 [NCBI] 1.79394e-05
PCCA [NCBI] 1.35528e-05
MGP [NCBI] 1.32395e-05
CALU [NCBI] 8.29402e-06
CYP2C9 [NCBI] 7.29274e-06
PC [NCBI] 6.67186e-06
SLC5A6 [NCBI] 5.66038e-06
F9 [NCBI] 2.88198e-06
F7 [NCBI] 2.6713e-06
F2 [NCBI] 2.06467e-06
HLCS [NCBI] 1.767e-06
STC2 [NCBI] 1.73352e-06
ATP2A3 [NCBI] 1.63763e-06
BGLAP [NCBI] 1.55618e-06
ABCC6 [NCBI] 1.32529e-06
LMAN1 [NCBI] 1.29934e-06
GDF15 [NCBI] 1.21829e-06
SLC22A5 [NCBI] 1.19504e-06
PRKACA [NCBI] 1.05884e-06
BMP2 [NCBI] 6.47004e-07
APOE [NCBI] 4.30105e-07
CASP3 [NCBI] 3.20017e-07
PTH [NCBI] 3.04779e-07



OMIM


 OMIM Link Information
gain		 01
3-@methylcrotonyl-coa carboxylase 1 deficiency [NCBI] 0.00179936
holocarboxylase synthetase deficiency [NCBI] 0.0014813
3-@methylcrotonyl-coa carboxylase 2 deficiency [NCBI] 0.0013626
propionic acidemia [NCBI] 0.000704352
GGCX [NCBI] 0.000670644
biotinidase deficiency [NCBI] 0.000486972
MCCC2 [NCBI] 0.000371702
vitamin k-dependent clotting factors, combined deficiency of, 1 [NCBI] 0.000346363
MCCC1 [NCBI] 0.000324822
PCCA [NCBI] 0.000212656
PCCB [NCBI] 0.00020905
vitamin k-dependent clotting factors, combined deficiency of, 2 [NCBI] 0.000116949
CALU [NCBI] 0.000116253
chondrodysplasia punctata, autosomal dominant [NCBI] 9.19426e-05
PC [NCBI] 9.0578e-05
VKORC1 [NCBI] 6.81517e-05
maple syrup urine disease [NCBI] 5.0332e-05
BGLAP [NCBI] 3.30467e-05
GPD2 [NCBI] 2.92594e-05
SLC5A6 [NCBI] 2.86642e-05
HLCS [NCBI] 2.6047e-05
ACACA [NCBI] 2.40577e-05
HEMB [NCBI] 1.28366e-05
F3 [NCBI] 2.33596e-06
APOE [NCBI] 1.20419e-06
PTH [NCBI] 2.26924e-08



Database Center for Life Science