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MeSH keywords -> Related genes, diseases (OMIM)


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01 Apoferritins [NCBI]

Gene


 Gene Link Information
Gain		 01
LOC286463 [NCBI] 0.000251681
FTHL16 [NCBI] 0.000216972
FTLL1 [NCBI] 0.000195365
FTH1 [NCBI] 1.9269e-05
FTL [NCBI] 1.8478e-05
MS [NCBI] 1.37638e-05
FTMT [NCBI] 1.30794e-05
TFRC [NCBI] 8.43932e-06
RPL17L1 [NCBI] 3.17051e-06
RPL7AL1 [NCBI] 3.17051e-06
RPS3L1 [NCBI] 3.17051e-06
RPS17L3 [NCBI] 3.17051e-06
NARFL [NCBI] 2.44721e-06
CYBRD1 [NCBI] 2.05834e-06
ACO1 [NCBI] 1.96348e-06
PIAS3 [NCBI] 1.87577e-06
TP53 [NCBI] 1.85203e-06
NFYA [NCBI] 1.81436e-06
CUGBP1 [NCBI] 1.79668e-06
SLC40A1 [NCBI] 1.78825e-06
ATF1 [NCBI] 1.78414e-06
TFR2 [NCBI] 1.58009e-06
DMRT1 [NCBI] 1.56709e-06
CD47 [NCBI] 1.50297e-06
THBS1 [NCBI] 1.48373e-06
SUMO1 [NCBI] 1.4478e-06
RAB11A [NCBI] 1.37966e-06
FXN [NCBI] 1.32325e-06
CP [NCBI] 1.26481e-06
AMBP [NCBI] 1.25452e-06
CIITA [NCBI] 1.23663e-06
ENG [NCBI] 1.19679e-06
MYC [NCBI] 1.13152e-06
HMOX1 [NCBI] 1.10344e-06
TF [NCBI] 1.04837e-06
HFE [NCBI] 9.80436e-07
CXCL12 [NCBI] 9.5361e-07
TLR4 [NCBI] 8.74563e-07
NOS2 [NCBI] 8.27604e-07
TNF [NCBI] 3.91349e-07



OMIM


 OMIM Link Information
gain		 01
hyperferritinemia-cataract syndrome [NCBI] 0.000360322
basal ganglia disease, adult-onset [NCBI] 0.000169613
hemochromatosis, neonatal [NCBI] 0.000165798
FTL [NCBI] 0.000108825
ACO1 [NCBI] 3.42105e-05
FTH1 [NCBI] 3.26246e-05
HAMP [NCBI] 3.21021e-05
SLC40A1 [NCBI] 2.97296e-05
TFRC [NCBI] 2.68418e-05
HFE [NCBI] 2.04843e-05
CP [NCBI] 1.63296e-05
TLR4 [NCBI] 1.43118e-05
TF [NCBI] 1.2103e-05
TNF [NCBI] 1.12121e-06



Database Center for Life Science