Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Ferredoxin-NADP Reductase	[NCBI]

Gene	Link	Information Gain
MTRR	[NCBI]	0.000436814
TRNR	[NCBI]	0.000230073
MTHFR	[NCBI]	0.000125929
MTR	[NCBI]	0.000121552
FDXR	[NCBI]	3.45549e-05
MS	[NCBI]	2.40236e-05
CBS	[NCBI]	2.12095e-05
TCN2	[NCBI]	1.38428e-05
FDX1	[NCBI]	1.31769e-05
TYMS	[NCBI]	1.28798e-05
RFC1	[NCBI]	8.48138e-06
SHMT1	[NCBI]	7.14495e-06
BHMT	[NCBI]	6.87172e-06
CYP11A1	[NCBI]	6.85675e-06
MTHFD1	[NCBI]	5.22656e-06
TCN1	[NCBI]	3.62054e-06
SLC19A1	[NCBI]	3.00521e-06
GSTT1	[NCBI]	2.95445e-06
GSTM1	[NCBI]	2.80633e-06
SLC19A2	[NCBI]	2.71898e-06
CYP27A1	[NCBI]	2.36125e-06
FOLH1	[NCBI]	2.2081e-06
NQO1	[NCBI]	2.12442e-06
NAT2	[NCBI]	1.84187e-06
F2	[NCBI]	1.83663e-06
MMAB	[NCBI]	1.83185e-06
F5	[NCBI]	1.82337e-06
MMACHC	[NCBI]	1.78895e-06
ZNF511	[NCBI]	1.78895e-06
FOLR1	[NCBI]	1.72315e-06
CYP24A1	[NCBI]	1.48232e-06
DHFR	[NCBI]	1.45083e-06
DLL4	[NCBI]	1.42083e-06
GSTO1	[NCBI]	1.41103e-06
AKR1C4	[NCBI]	1.22013e-06
F13A1	[NCBI]	1.13119e-06
CYP11B2	[NCBI]	1.11491e-06
SCP2	[NCBI]	9.58695e-07
STAR	[NCBI]	8.99593e-07
XRCC1	[NCBI]	8.98205e-07
CYBA	[NCBI]	8.98205e-07
CKAP4	[NCBI]	8.86033e-07
CYP2D6	[NCBI]	8.60266e-07
ALDH2	[NCBI]	8.47996e-07
CYBB	[NCBI]	8.47426e-07
CYP1A1	[NCBI]	8.23511e-07
TP63	[NCBI]	7.72351e-07
ABCB1	[NCBI]	6.78368e-07
CYP2C19	[NCBI]	6.46638e-07
CYP2C9	[NCBI]	6.2387e-07
NOS3	[NCBI]	4.38461e-07
MPO	[NCBI]	3.60929e-07
CDKN1A	[NCBI]	2.54199e-07

OMIM	Link	Information gain
homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cble complementation type	[NCBI]	0.000545375
MTRR	[NCBI]	0.000384748
MTR	[NCBI]	0.00037895
FDXR	[NCBI]	0.000299723
neural tube defects, folate-sensitive	[NCBI]	0.000125145
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity	[NCBI]	0.000103923
MTHFR	[NCBI]	7.9204e-05
CYP11A1	[NCBI]	6.54095e-05
FDX1	[NCBI]	3.20062e-05
CRC	[NCBI]	3.08006e-05
DLL4	[NCBI]	2.78913e-05
BHMT	[NCBI]	2.76367e-05
CYP17A1	[NCBI]	2.3294e-05
phenylketonuria	[NCBI]	1.54428e-05
MPO	[NCBI]	2.72918e-06