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MeSH keywords -> Related genes, diseases (OMIM)


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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