Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Tachycardia, Ventricular [NCBI]


Gene


Gene Link Information
Gain
01
ARVD3 [NCBI] 0.000438875
CASQ2 [NCBI] 0.000342016
RYR2 [NCBI] 0.000270256
SCN5A [NCBI] 0.000113527
KCNJ2 [NCBI] 7.32506e-05
KCNQ1 [NCBI] 3.33665e-05
ADRB1 [NCBI] 3.23832e-05
KCNH6 [NCBI] 2.59903e-05
FKBP1B [NCBI] 2.35158e-05
KCNE2 [NCBI] 1.69078e-05
DMPK [NCBI] 1.67814e-05
MUC1 [NCBI] 1.44933e-05
KCNIP2 [NCBI] 1.29649e-05
KCNK1 [NCBI] 1.29649e-05
NPPB [NCBI] 1.26877e-05
ERG [NCBI] 1.05483e-05
TRDN [NCBI] 1.04169e-05
CACNB2 [NCBI] 1.04169e-05
ADRB2 [NCBI] 9.92342e-06
KCND3 [NCBI] 9.765e-06
KCNV2 [NCBI] 9.765e-06
KCND2 [NCBI] 9.43713e-06
KCNE1L [NCBI] 9.16209e-06
SP4 [NCBI] 9.03956e-06
ACTN2 [NCBI] 8.81805e-06
RRAD [NCBI] 8.62199e-06
ASPH [NCBI] 8.53179e-06
CACNA2D1 [NCBI] 8.53179e-06
ANK2 [NCBI] 8.36455e-06
CACNA1C [NCBI] 8.21223e-06
PKP2 [NCBI] 7.94318e-06
GNAI2 [NCBI] 7.88207e-06
DSG2 [NCBI] 7.36783e-06
NGF [NCBI] 7.21148e-06
ACE2 [NCBI] 6.90461e-06
REN [NCBI] 6.31222e-06
KCNE1 [NCBI] 6.21964e-06
NKX2-5 [NCBI] 5.78547e-06
GJA1 [NCBI] 5.76817e-06
DSP [NCBI] 5.71733e-06
KCNJ8 [NCBI] 5.5133e-06
KCNH2 [NCBI] 5.25394e-06
EDN1 [NCBI] 4.56229e-06
LMNA [NCBI] 4.14735e-06
CYP2C19 [NCBI] 3.97705e-06
PDE5A [NCBI] 3.77173e-06
CFLAR [NCBI] 3.57218e-06
PLN [NCBI] 3.32913e-06
ABCB1 [NCBI] 3.02301e-06
SERPINE1 [NCBI] 2.88348e-06
AGT [NCBI] 2.86938e-06
ACE [NCBI] 1.89691e-06
IL6 [NCBI] 1.60977e-06
BAX [NCBI] 9.51041e-07
EPO [NCBI] 8.52944e-07




OMIM


OMIM Link Information
gain
01
ARVD3 [NCBI] 0.00102023
CPVT [NCBI] 0.000886515
RYR2 [NCBI] 0.000815017
CASQ2 [NCBI] 0.000550804
andersen cardiodysrhythmic periodic paralysis [NCBI] 0.000240509
ventricular tachycardia, familial [NCBI] 0.00023291
GJA1 [NCBI] 0.000142602
apnea, obstructive sleep [NCBI] 0.000142159
FKBP1B [NCBI] 0.000122892
KCNH2 [NCBI] 0.000108758
cardiac arrhythmia, ankyrin-b-related [NCBI] 9.51693e-05
LVNCX [NCBI] 9.1078e-05
VF [NCBI] 9.1078e-05
LVNC1 [NCBI] 9.1078e-05
cardiomyopathy, dilated, with woolly hair and keratoderma [NCBI] 8.78187e-05
ARVD2 [NCBI] 8.78187e-05
SQT1 [NCBI] 8.5109e-05
cardiac conduction defect [NCBI] 8.279e-05
KCNIP2 [NCBI] 8.21209e-05
gitelman syndrome [NCBI] 7.73439e-05
SP4 [NCBI] 6.83427e-05
ARVD1 [NCBI] 6.65411e-05
brugada syndrome 1 [NCBI] 6.57736e-05
GNAI2 [NCBI] 5.97685e-05
MCOPS7 [NCBI] 5.91268e-05
ANK2 [NCBI] 5.72593e-05
DM2 [NCBI] 5.14471e-05
ADRB1 [NCBI] 4.98282e-05
CLS [NCBI] 4.81669e-05
GJA5 [NCBI] 4.63428e-05
SLC25A20 [NCBI] 4.43549e-05
CMH [NCBI] 3.47368e-05
SCN5A [NCBI] 3.31275e-05
KCNQ1 [NCBI] 3.31275e-05
RYR1 [NCBI] 3.07725e-05
dystrophia myotonica 1 [NCBI] 2.80488e-05
NGFB [NCBI] 2.48659e-05
PD [NCBI] 1.01421e-05
NPPA [NCBI] 7.0761e-06
EPO [NCBI] 1.17994e-06




Database Center for Life Science