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01 Myasthenic Syndromes, Congenital [NCBI]


Gene


Gene Link Information
Gain
01
RAPSN [NCBI] 0.000205013
CHRNE [NCBI] 0.00018998
DOK7 [NCBI] 0.000104983
COLQ [NCBI] 8.70896e-05
MUSK [NCBI] 7.79577e-05
CHRND [NCBI] 6.67145e-05
ACHE [NCBI] 3.87047e-05
CHRNA1 [NCBI] 3.35646e-05
CHAT [NCBI] 3.0625e-05
CACNA1A [NCBI] 2.94462e-05
SCN4A [NCBI] 2.54949e-05
CHRNG [NCBI] 1.14513e-05
CACNB2 [NCBI] 1.11639e-05
ZBTB33 [NCBI] 1.09179e-05
CNTN1 [NCBI] 8.8865e-06
PRKCG [NCBI] 8.51117e-06
STX1A [NCBI] 8.51117e-06
CHRNA3 [NCBI] 8.51117e-06
SLC18A3 [NCBI] 8.20364e-06
CHRNB2 [NCBI] 7.94316e-06
PRKCZ [NCBI] 7.90337e-06
PLEC1 [NCBI] 6.96119e-06
PRKCE [NCBI] 6.17907e-06
CTNND1 [NCBI] 5.96562e-06
PRKCD [NCBI] 5.34483e-06
DAG1 [NCBI] 4.95419e-06
PRKCA [NCBI] 4.39362e-06
PRKCB [NCBI] 4.25904e-06
CASP9 [NCBI] 2.70441e-06
CASP3 [NCBI] 1.01488e-06




OMIM


OMIM Link Information
gain
01
EMWX [NCBI] 0.00137383
myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency [NCBI] 0.0012178
myasthenia, limb-girdle, with tubular aggregates [NCBI] 0.000948879
CHRNE [NCBI] 0.000730648
RAPSN [NCBI] 0.000687457
SCCMS [NCBI] 0.000495623
myasthenic syndrome, congenital, fast-channel [NCBI] 0.000312924
myasthenic syndrome, congenital, associated with episodic apnea [NCBI] 0.000270336
CHRNA1 [NCBI] 0.000171793
MUSK [NCBI] 0.000162469
CHAT [NCBI] 0.000154858
COLQ [NCBI] 0.000134913
CHRND [NCBI] 0.000129026
ACHE [NCBI] 0.000113922
myasthenia, limb-girdle, familial [NCBI] 9.17009e-05
MG [NCBI] 8.79425e-05
EAD [NCBI] 8.57315e-05
PRPS2 [NCBI] 8.11133e-05
DOK7 [NCBI] 8.11133e-05
opitz syndrome [NCBI] 7.95849e-05
multiple pterygium syndrome, lethal type [NCBI] 7.51466e-05
amelogenesis imperfecta, hypoplastic/hypomaturation, x-linked 1 [NCBI] 7.27487e-05
multiple pterygium syndrome, escobar variant [NCBI] 7.27487e-05
CHRNG [NCBI] 6.21367e-05
MCOPS7 [NCBI] 5.97447e-05
OA1 [NCBI] 3.49895e-05
SCN4A [NCBI] 3.47374e-05
CACNA1A [NCBI] 3.27221e-05




Database Center for Life Science