Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 100134444
Gene Symbol: KCNJ18
KCNJ18
CUI: C2750473
Disease: THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2
THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2 		0.700 GeneticVariation UNIPROT A novel Kir2.6 mutation associated with hypokalemic periodic paralysis. 27178871

2016
Entrez Id: 100134444
Gene Symbol: KCNJ18
KCNJ18
CUI: C2750473
Disease: THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2
THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2 		0.700 GeneticVariation UNIPROT The clinical and genetic features in a cohort of mainland Chinese patients with thyrotoxic periodic paralysis. 25885757

2015
Entrez Id: 100134444
Gene Symbol: KCNJ18
KCNJ18
CUI: C2750473
Disease: THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2
THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2 		0.700 GeneticVariation UNIPROT Identification and functional characterization of Kir2.6 mutations associated with non-familial hypokalemic periodic paralysis. 21665951

2011
Entrez Id: 100134444
Gene Symbol: KCNJ18
KCNJ18
CUI: C2750473
Disease: THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2
THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2 		0.700 GeneticVariation UNIPROT Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis. 20074522

2010