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MeSH keywords -> Related genes, diseases (OMIM)


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01 Bungarotoxins [NCBI]


Gene


Gene Link Information
Gain
01
ACHE [NCBI] 3.77344e-05
CHRNA7 [NCBI] 3.6926e-05
CHAT [NCBI] 1.17925e-05
CHRNA1 [NCBI] 1.04341e-05
CHRNA5 [NCBI] 8.06029e-06
NEFH [NCBI] 6.88572e-06
MUSK [NCBI] 6.20105e-06
COLQ [NCBI] 5.96124e-06
CHRNE [NCBI] 5.82123e-06
CHRNB1 [NCBI] 4.15199e-06
CHRND [NCBI] 4.05432e-06
RIC3 [NCBI] 4.05432e-06
RAPSN [NCBI] 3.78086e-06
CHRNB4 [NCBI] 3.56392e-06
CHRNA3 [NCBI] 3.42817e-06
SLC18A3 [NCBI] 3.21135e-06
MYOD1 [NCBI] 2.43397e-06
BCHE [NCBI] 2.41433e-06
FYN [NCBI] 2.14242e-06
CHRNA10 [NCBI] 2.07481e-06
CNTF [NCBI] 1.99837e-06
LYNX1 [NCBI] 1.91744e-06
CHRNB3 [NCBI] 1.83314e-06
SNTB1 [NCBI] 1.81905e-06
AGRN [NCBI] 1.79294e-06
CHRNA2 [NCBI] 1.78078e-06
NGF [NCBI] 1.73291e-06
SNTA1 [NCBI] 1.67433e-06
MAPK12 [NCBI] 1.66647e-06
FGF13 [NCBI] 1.65883e-06
CAPN2 [NCBI] 1.53937e-06
ABI1 [NCBI] 1.52991e-06
CHRNB2 [NCBI] 1.49106e-06
CHRNA4 [NCBI] 1.48314e-06
CAPN1 [NCBI] 1.43024e-06
SIRPA [NCBI] 1.42706e-06
AR [NCBI] 1.28836e-06
ADAM10 [NCBI] 1.26773e-06
VIP [NCBI] 1.25563e-06
CNTN2 [NCBI] 1.21581e-06
TH [NCBI] 1.17595e-06
PRKCI [NCBI] 1.15708e-06
PIK3R1 [NCBI] 1.08443e-06
KCNJ8 [NCBI] 1.06595e-06
PTN [NCBI] 1.02752e-06
DMPK [NCBI] 1.01452e-06
CASP3 [NCBI] 1.00532e-06
MAPK3 [NCBI] 9.84284e-07
CDK5 [NCBI] 9.50815e-07
PARP1 [NCBI] 9.48728e-07
MARCKS [NCBI] 9.41049e-07
ERBB4 [NCBI] 9.11053e-07
BCL2 [NCBI] 8.93233e-07
MYC [NCBI] 8.45052e-07
APP [NCBI] 8.42966e-07
MAPK1 [NCBI] 8.40554e-07
SLC2A1 [NCBI] 8.23627e-07
MAP2K1 [NCBI] 8.17594e-07
PTPN11 [NCBI] 8.10169e-07
PRKCA [NCBI] 7.90223e-07
BACE1 [NCBI] 7.20911e-07
STAT1 [NCBI] 6.54143e-07
JAK2 [NCBI] 6.50047e-07
CASP9 [NCBI] 6.02957e-07
NOS3 [NCBI] 5.59123e-07
AKT1 [NCBI] 4.87708e-07
GFAP [NCBI] 4.44194e-07
PTGS2 [NCBI] 3.37132e-07
EGF [NCBI] 1.7896e-07




OMIM


OMIM Link Information
gain
01
MG [NCBI] 0.00282514
MEAX [NCBI] 0.00194777
pena-shokeir syndrome, type i [NCBI] 0.00183065
myasthenic syndrome, congenital, fast-channel [NCBI] 0.00037431
ACHE [NCBI] 0.000370031
myasthenic syndrome, congenital, associated with episodic apnea [NCBI] 0.000192242
myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency [NCBI] 0.000183971
CHAT [NCBI] 0.000123526
myotonia congenita, autosomal recessive [NCBI] 9.30365e-05
CHRNA1 [NCBI] 8.55445e-05
AMC [NCBI] 8.43071e-05
danon disease [NCBI] 7.67194e-05
SCCMS [NCBI] 7.67194e-05
SLC18A3 [NCBI] 4.98976e-05
CHRNE [NCBI] 4.97907e-05
LYNX1 [NCBI] 3.69016e-05
SMAX1 [NCBI] 3.6264e-05
CHRNA9 [NCBI] 3.22827e-05
RIC3 [NCBI] 3.09311e-05
ABL2 [NCBI] 3.09311e-05
CHRNG [NCBI] 2.81926e-05
MUSK [NCBI] 2.81926e-05
COLQ [NCBI] 2.75228e-05
CHRNA7 [NCBI] 2.75228e-05
CHRND [NCBI] 2.75228e-05
AGRN [NCBI] 2.69279e-05
ITPR1 [NCBI] 2.59068e-05
RAPSN [NCBI] 2.4313e-05
UTRN [NCBI] 2.33693e-05
BCHE [NCBI] 2.28223e-05
DAG1 [NCBI] 2.12584e-05
CALCA [NCBI] 2.07079e-05
ABL1 [NCBI] 1.82483e-05
AANAT [NCBI] 1.77296e-05
CNTF [NCBI] 1.45601e-05
DMD [NCBI] 1.09563e-05
JAK2 [NCBI] 1.03033e-05
CDK5 [NCBI] 9.19964e-06
SDC2 [NCBI] 8.80583e-06
EGF [NCBI] 4.5305e-06
AR [NCBI] 4.31752e-06
VIP [NCBI] 2.8087e-06
NGFB [NCBI] 2.58059e-06
TH [NCBI] 1.93313e-06
GFAP [NCBI] 2.52522e-08




Database Center for Life Science