RecName: Full=Inward rectifier potassium channel 18; AltName: Full=Inw - Protein

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Contribution of Asian Haplotype of KCNJ18 to Susceptibility to and Ethnic Differences in Thyrotoxic Periodic Paralysis. [J Clin Endocrinol Metab. 2019]
Contribution of Asian Haplotype of KCNJ18 to Susceptibility to and Ethnic Differences in Thyrotoxic Periodic Paralysis.
Noso S, Babaya N, Hiromine Y, Ito H, Taketomo Y, Yoshida S, Niwano F, Monobe K, Minohara T, Okada T, et al. J Clin Endocrinol Metab. 2019 Dec 1; 104(12):6338-6344.
Down-regulation of Kir2.6 channel by c-termini mutation D252N and its association with the susceptibility to Thyrotoxic Periodic Paralysis. [Neuroscience. 2017]
Down-regulation of Kir2.6 channel by c-termini mutation D252N and its association with the susceptibility to Thyrotoxic Periodic Paralysis.
Paninka RM, Carlos-Lima E, Lindsey SC, Kunii IS, Dias-da-Silva MR, Arcisio-Miranda M. Neuroscience. 2017 Mar 27; 346:197-202. Epub 2017 Jan 25.
A novel Kir2.6 mutation associated with hypokalemic periodic paralysis. [Clin Neurophysiol. 2016]
A novel Kir2.6 mutation associated with hypokalemic periodic paralysis.
Zheng J, Liang Z, Hou Y, Liu F, Hu Y, Lin P, Yan C. Clin Neurophysiol. 2016 Jun; 127(6):2503-8. Epub 2016 Mar 17.

RefSeq genomic sequence
See the genomic reference sequence for the KCNJ18 gene (NG_033093.1).
RefSeq protein isoforms
See 3 reference sequence protein isoforms for the KCNJ18 gene.

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B7U540 [Domain Mapping of Disease Mut...]
B7U540
Domain Mapping of Disease Mutations
Reactome [Reactome]
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reagents [ExactAntigen/Labome]
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