MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
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