hypokalemic periodic paralysis Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_14452)
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Genes

39 genes co-occuring with the disease hypokalemic periodic paralysis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit 2.89721
SCN4A sodium channel, voltage gated, type IV alpha subunit 2.78986
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2 1.90521
KCNE3 potassium channel, voltage gated subfamily E regulatory beta subunit 3 1.87148
CLCN1 chloride channel, voltage-sensitive 1 1.45748
KCNJ12 potassium channel, inwardly rectifying subfamily J, member 12 1.42849
KCNN2 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 2 1.08663
KCNN1 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 1 1.07446
KCNE4 potassium channel, voltage gated subfamily E regulatory beta subunit 4 1.05219
SCN8A sodium channel, voltage gated, type VIII alpha subunit 1.00499
KCNE5 potassium channel, voltage gated subfamily E regulatory beta subunit 5 1.00161
INS insulin 0.906909
RYR1 ryanodine receptor 1 (skeletal) 0.881882
QDPR quinoid dihydropteridine reductase 0.877786
KCNQ5 potassium channel, voltage gated KQT-like subfamily Q, member 5 0.861409
DNAH8 dynein, axonemal, heavy chain 8 0.741923
CST7 cystatin F (leukocystatin) 0.696707
SCN3A sodium channel, voltage gated, type III alpha subunit 0.662387
TRDN triadin 0.635528
LRP4 low density lipoprotein receptor-related protein 4 0.622575
KCNQ3 potassium channel, voltage gated KQT-like subfamily Q, member 3 0.604981
KCNN3 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 3 0.55945
KCNE2 potassium channel, voltage gated subfamily E regulatory beta subunit 2 0.514186
KCNJ8 potassium channel, inwardly rectifying subfamily J, member 8 0.485125
BTNL2 butyrophilin-like 2 0.472982
TBK1 TANK-binding kinase 1 0.466172
KCNN4 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 4 0.452208
CSN3 casein kappa 0.445805
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11 0.413527
CASQ2 calsequestrin 2 (cardiac muscle) 0.396353
CASQ1 calsequestrin 1 (fast-twitch, skeletal muscle) 0.383337
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1 0.371847
KCNMA1 potassium channel, calcium activated large conductance subfamily M alpha, member 1 0.353763
KCNE1 potassium channel, voltage gated subfamily E regulatory beta subunit 1 0.336144
MN1 meningioma (disrupted in balanced translocation) 1 0.334681
THRB thyroid hormone receptor, beta 0.294413
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3 0.292257
GJB1 gap junction protein, beta 1, 32kDa 0.251015
PIK3C2A phosphatidylinositol-4-phosphate 3-kinase, catalytic subunit type 2 alpha 0.247852