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MeSH keywords -> Related genes, diseases (OMIM)


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01 Transcobalamins [NCBI]


Gene


Gene Link Information
Gain
01
TCN2 [NCBI] 8.29609e-05
TCN1 [NCBI] 4.39964e-05
MTHFR [NCBI] 2.32267e-05
MTRR [NCBI] 1.74251e-05
CUBN [NCBI] 1.13926e-05
MTR [NCBI] 8.96955e-06
FOLR1 [NCBI] 6.83387e-06
SLC19A1 [NCBI] 3.51903e-06
SP3 [NCBI] 2.72039e-06
LMBRD1 [NCBI] 2.16868e-06
COMT [NCBI] 2.08868e-06
GIF [NCBI] 2.06542e-06
ADA [NCBI] 2.00528e-06
MNDA [NCBI] 1.80167e-06
MTHFD1 [NCBI] 1.69726e-06
GSTO1 [NCBI] 1.66667e-06
SHMT1 [NCBI] 1.66189e-06
EGF [NCBI] 1.65956e-06
LRP2 [NCBI] 1.63066e-06
BHMT [NCBI] 1.59523e-06
MPO [NCBI] 1.56261e-06
RFC1 [NCBI] 1.51332e-06
USF2 [NCBI] 1.50531e-06
LAMP1 [NCBI] 1.48996e-06
SLC19A2 [NCBI] 1.42812e-06
CBS [NCBI] 1.34283e-06
B2M [NCBI] 1.31693e-06
PMS2 [NCBI] 1.31435e-06
TYMS [NCBI] 1.30057e-06
USF1 [NCBI] 1.24961e-06
FOLH1 [NCBI] 1.17307e-06
GSTM1 [NCBI] 8.96203e-07
DHFR [NCBI] 7.93552e-07
AFP [NCBI] 6.22952e-07
APOE [NCBI] 5.62539e-07




OMIM


OMIM Link Information
gain
01
r binder deficiency with lactoferrin deficiency [NCBI] 0.00541205
transcobalamin ii deficiency [NCBI] 0.00195934
intrinsic factor and r binder, combined congenital deficiency of [NCBI] 0.000200648
methylcobalamin deficiency, cblg type [NCBI] 0.000126597
SGD [NCBI] 0.000116971
TCN1 [NCBI] 9.00669e-05
r binder protein [NCBI] 7.98425e-05
MTR [NCBI] 3.90523e-05
RA [NCBI] 3.09311e-05
GIF [NCBI] 3.05184e-05
BHMT [NCBI] 2.32302e-05
LCN2 [NCBI] 1.66381e-05
B2M [NCBI] 1.62962e-05
ADA [NCBI] 1.13628e-05
COMT [NCBI] 4.79044e-06
MPO [NCBI] 4.55134e-06
SLE [NCBI] 3.93856e-06
TYMS [NCBI] 3.26709e-06
DHFR [NCBI] 2.40335e-06
CF [NCBI] 7.91015e-07
AFP [NCBI] 4.9581e-07
EGF [NCBI] 2.17995e-07




Database Center for Life Science