familial periodic paralysis Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

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

Symbol Name Standardized Value
SCN4A sodium channel, voltage gated, type IV alpha subunit 3.24712
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit 2.81153
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2 1.98063
KCNE3 potassium channel, voltage gated subfamily E regulatory beta subunit 3 1.93468
SCN8A sodium channel, voltage gated, type VIII alpha subunit 1.46671
CLCN1 chloride channel, voltage-sensitive 1 1.45616
KCNJ12 potassium channel, inwardly rectifying subfamily J, member 12 1.44035
SCN3A sodium channel, voltage gated, type III alpha subunit 1.39477
PTPRB protein tyrosine phosphatase, receptor type, B 1.0795
KCNJ14 potassium channel, inwardly rectifying subfamily J, member 14 1.01301
NFASC neurofascin 1.01174
KCNN2 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 2 0.996127
KCNN1 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 1 0.9839
KCNE4 potassium channel, voltage gated subfamily E regulatory beta subunit 4 0.961634
INS insulin 0.952438
RYR1 ryanodine receptor 1 (skeletal) 0.918024
KCNE5 potassium channel, voltage gated subfamily E regulatory beta subunit 5 0.911845
PTPRZ1 protein tyrosine phosphatase, receptor-type, Z polypeptide 1 0.901978
DNAH8 dynein, axonemal, heavy chain 8 0.838885
SCN1B sodium channel, voltage gated, type I beta subunit 0.824538
QDPR quinoid dihydropteridine reductase 0.789672
KCNQ5 potassium channel, voltage gated KQT-like subfamily Q, member 5 0.772887
CNBP CCHC-type zinc finger, nucleic acid binding protein 0.662387
KCNE1 potassium channel, voltage gated subfamily E regulatory beta subunit 1 0.635528
CST7 cystatin F (leukocystatin) 0.61162
TRDN triadin 0.551298
LRP4 low density lipoprotein receptor-related protein 4 0.538893
KCNQ3 potassium channel, voltage gated KQT-like subfamily Q, member 3 0.521117
KCNN3 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 3 0.476772
SPTA1 spectrin, alpha, erythrocytic 1 0.459373
KCNE2 potassium channel, voltage gated subfamily E regulatory beta subunit 2 0.43227
GBE1 glucan (1,4-alpha-), branching enzyme 1 0.412031
KCNJ8 potassium channel, inwardly rectifying subfamily J, member 8 0.404184
BTNL2 butyrophilin-like 2 0.392257
TBK1 TANK-binding kinase 1 0.385565
KCNN4 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 4 0.371477
CSN3 casein kappa 0.365562
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11 0.333949
CASQ2 calsequestrin 2 (cardiac muscle) 0.316819
CASQ1 calsequestrin 1 (fast-twitch, skeletal muscle) 0.304503
TK1 thymidine kinase 1, soluble 0.301615
KRT1 keratin 1, type II 0.301254
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1 0.292975
TNC tenascin C 0.292257
KCNMA1 potassium channel, calcium activated large conductance subfamily M alpha, member 1 0.275801
LIPE lipase, hormone-sensitive 0.264431
MN1 meningioma (disrupted in balanced translocation) 1 0.257358
THRB thyroid hormone receptor, beta 0.218715
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3 0.216332
FECH ferrochelatase 0.207578
GJB1 gap junction protein, beta 1, 32kDa 0.179802
PIK3C2A phosphatidylinositol-4-phosphate 3-kinase, catalytic subunit type 2 alpha 0.177029
AVPR2 arginine vasopressin receptor 2 0.170544
MB myoglobin 0.169812
DMPK dystrophia myotonica-protein kinase 0.163111
REN renin 0.161523
FABP3 fatty acid binding protein 3, muscle and heart 0.141438
DMD dystrophin 0.138822
POMC proopiomelanocortin 0.137491