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MeSH keywords -> Related genes, diseases (OMIM)


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01 Mitomycins [NCBI]


Gene


Gene Link Information
Gain
01
MS [NCBI] 0.000111788
TNF [NCBI] 6.79563e-06
AFP [NCBI] 6.39028e-06
DNASE2B [NCBI] 3.38086e-06
DHFR [NCBI] 2.38989e-06
AHRR [NCBI] 2.04227e-06
FASLG [NCBI] 1.95445e-06
EPO [NCBI] 1.91264e-06
ERCC3 [NCBI] 1.76654e-06
ERCC4 [NCBI] 1.62995e-06
XDH [NCBI] 1.55946e-06
CDKN1C [NCBI] 1.48786e-06
ARNT [NCBI] 1.37974e-06
CTNNA1 [NCBI] 1.30637e-06
CDH1 [NCBI] 1.23492e-06
PGR [NCBI] 1.21364e-06
IL2 [NCBI] 1.154e-06
AHR [NCBI] 1.09384e-06
GSTP1 [NCBI] 1.08305e-06
CD38 [NCBI] 1.0743e-06
CTNNB1 [NCBI] 8.45608e-07
HGF [NCBI] 8.39372e-07
VWF [NCBI] 7.87732e-07
CCK [NCBI] 7.57666e-07
CDKN1A [NCBI] 6.884e-07




OMIM


OMIM Link Information
gain
01
FA [NCBI] 0.00160985
FANCB [NCBI] 0.000252938
hla modifier [NCBI] 0.000177262
intrauterine growth retardation with increased mitomycin c sensitivity [NCBI] 0.00014568
hla-d histocompatibility type [NCBI] 0.000130726
seckel syndrome 1 [NCBI] 0.000115704
ERCC1 [NCBI] 9.79999e-05
ED1 [NCBI] 7.8399e-05
BLM [NCBI] 6.83941e-05
SDS [NCBI] 6.47015e-05
AFP [NCBI] 4.23788e-05
AT [NCBI] 3.39539e-05
SLE [NCBI] 3.30498e-05
CEACAM5 [NCBI] 3.15392e-05
PEPC [NCBI] 3.02022e-05
XRCC2 [NCBI] 2.81386e-05
TNF [NCBI] 2.60679e-05
IL2 [NCBI] 2.2441e-05
INHBA [NCBI] 2.1865e-05
lymphoma, non-hodgkin, familial [NCBI] 1.81954e-05
DHFR [NCBI] 1.41e-05
PGR [NCBI] 9.00931e-06
CYP1A1 [NCBI] 7.9231e-06
EPO [NCBI] 6.16073e-06
XDH [NCBI] 6.15764e-06
TYMS [NCBI] 4.85039e-06
HGF [NCBI] 1.65742e-06
CCK [NCBI] 6.55548e-07




Database Center for Life Science