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KCNJ18 gene

Known as: TTPP2, POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 18, KIR2.6 
National Institutes of Health

Papers overview

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2019
2019
Contribution of Asian haplotype of KCNJ18 to susceptibility to and ethnic differences in thyrotoxic periodic paralysis.
CONTEXT AND OBJECTIVES Thyrotoxic periodic paralysis (TPP) is an acute complication of thyrotoxicosis that can be lethal. TPP is… 
2017
2017
Down-regulation of Kir2.6 channel by c-termini mutation D252N and its association with the susceptibility to Thyrotoxic Periodic Paralysis
2016
2016
A novel Kir2.6 mutation associated with hypokalemic periodic paralysis
2016
2016
Whole genome and exome sequencing realignment supports the assignment of KCNJ12, KCNJ17, and KCNJ18 paralogous genes in thyrotoxic periodic paralysis locus: functional characterization of two…
Next-generation sequencing (NGS) has enriched the understanding of the human genome. However, homologous or repetitive sequences… 
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