Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Transcobalamins	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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