potassium inwardly-rectifying channel kir2.2, subfamily J, member 12 [ - Protein

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Kir2.2 p.Thr140Met: a genetic susceptibility to sporadic periodic paralysis. [Acta Myol. 2018]
Kir2.2 p.Thr140Met: a genetic susceptibility to sporadic periodic paralysis.
Fan C, Kuhn M, Mbiol AP, Groome J, Winston V, Biskup S, Lehmann-Horn F, Jurkat-Rott K. Acta Myol. 2018 Sep; 37(3):193-203. Epub 2018 Sep 1.
Whole exome sequencing identifies a KCNJ12 mutation as a cause of familial dilated cardiomyopathy. [Medicine (Baltimore). 2017]
Whole exome sequencing identifies a KCNJ12 mutation as a cause of familial dilated cardiomyopathy.
Yuan HX, Yan K, Hou DY, Zhang ZY, Wang H, Wang X, Zhang J, Xu XR, Liang YH, Zhao WS, et al. Medicine (Baltimore). 2017 Aug; 96(33):e7727.
Rise and Fall of Kir2.2 Current by TLR4 Signaling in Human Monocytes: PKC-Dependent Trafficking and PI3K-Mediated PIP2 Decrease. [J Immunol. 2015]
Rise and Fall of Kir2.2 Current by TLR4 Signaling in Human Monocytes: PKC-Dependent Trafficking and PI3K-Mediated PIP2 Decrease.
Kim KS, Jang JH, Lin H, Choi SW, Kim HR, Shin DH, Nam JH, Zhang YH, Kim SJ. J Immunol. 2015 Oct 1; 195(7):3345-54. Epub 2015 Aug 31.

RefSeq genomic sequence
See the genomic reference sequence for the KCNJ12 gene (NG_042809.1).
RefSeq protein isoforms
See 5 reference sequence protein isoforms for the KCNJ12 gene.

Nucleotide
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MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
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reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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