MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Tetrahydrofolates
[NCBI]
Gene
Gene
Link
Information
Gain
01
FOLR1
[NCBI]
0.000166277
MTHFR
[NCBI]
1.85641e-05
SLC19A2
[NCBI]
1.65877e-05
DHFR
[NCBI]
1.22663e-05
GNMT
[NCBI]
7.45768e-06
FPGS
[NCBI]
5.88625e-06
ATIC
[NCBI]
3.80086e-06
MTHFD1
[NCBI]
3.39619e-06
SHMT1
[NCBI]
3.32478e-06
RFC1
[NCBI]
3.02559e-06
ABCG2
[NCBI]
1.99151e-06
MTHFD2
[NCBI]
1.92384e-06
SARDH
[NCBI]
1.80289e-06
MAT1A
[NCBI]
1.74483e-06
SHMT2
[NCBI]
1.73209e-06
GGH
[NCBI]
1.598e-06
MTAP
[NCBI]
1.45998e-06
BHMT
[NCBI]
1.4072e-06
CUBN
[NCBI]
1.2177e-06
MTR
[NCBI]
1.16539e-06
SLC4A1
[NCBI]
1.1552e-06
MTRR
[NCBI]
1.13994e-06
PAX3
[NCBI]
1.03373e-06
CYP2E1
[NCBI]
1.01629e-06
PRKACA
[NCBI]
1.0121e-06
NQO1
[NCBI]
9.44403e-07
APC
[NCBI]
7.1728e-07
ACP5
[NCBI]
6.8623e-07
CDK2
[NCBI]
5.8778e-07
CHAT
[NCBI]
5.05422e-07
MBP
[NCBI]
4.64997e-07
TP53
[NCBI]
4.07167e-07
APOE
[NCBI]
3.87119e-07
PCNA
[NCBI]
3.6869e-07
CDKN1A
[NCBI]
3.11794e-07
EGFR
[NCBI]
2.83088e-07
OMIM
OMIM
Link
Information
gain
01
TYMS
[NCBI]
0.000810293
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity
[NCBI]
0.000421259
FPGS
[NCBI]
0.000261579
homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cble complementation type
[NCBI]
0.000152301
methionine adenosyltransferase deficiency
[NCBI]
0.000129728
DHFR
[NCBI]
0.000125081
MTR
[NCBI]
0.000117804
GNMT
[NCBI]
7.34708e-05
MTHFR
[NCBI]
6.24871e-05
SLC19A1
[NCBI]
5.50143e-05
FOLR1
[NCBI]
2.46744e-05
MAT1A
[NCBI]
2.36038e-05
GGH
[NCBI]
2.36038e-05
MTAP
[NCBI]
1.73576e-05
homocystinuria
[NCBI]
1.34171e-05
XDH
[NCBI]
3.64598e-06
CHAT
[NCBI]
5.74595e-07
APOE
[NCBI]
3.07841e-07
MBP
[NCBI]
3.06567e-07
EGFR
[NCBI]
1.55581e-07
PCNA
[NCBI]
2.66616e-09
Database Center for Life Science