MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
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