uKATP-1 [Homo sapiens]

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A novel mutation in the KCNJ8 gene encoding the Kir6.1 subunit of an ATP-sensitive potassium channel in a Japanese patient with Cantú syndrome. [J Eur Acad Dermatol Venereol. ...]
A novel mutation in the KCNJ8 gene encoding the Kir6.1 subunit of an ATP-sensitive potassium channel in a Japanese patient with Cantú syndrome.
Chihara M, Asahina A, Itoh M. J Eur Acad Dermatol Venereol. 2020 Sep; 34(9):e476-e478. Epub 2020 May 6.
Cantú syndrome resulting from activating mutation in the KCNJ8 gene. [Hum Mutat. 2014]
Cantú syndrome resulting from activating mutation in the KCNJ8 gene.
Cooper PE, Reutter H, Woelfle J, Engels H, Grange DK, van Haaften G, van Bon BW, Hoischen A, Nichols CG. Hum Mutat. 2014 Jul; 35(7):809-13. Epub 2014 May 6.
Mutation of KCNJ8 in a patient with Cantú syndrome with unique vascular abnormalities - support for the role of K(ATP) channels in this condition. [Eur J Med Genet. 2013]
Mutation of KCNJ8 in a patient with Cantú syndrome with unique vascular abnormalities - support for the role of K(ATP) channels in this condition.
Brownstein CA, Towne MC, Luquette LJ, Harris DJ, Marinakis NS, Meinecke P, Kutsche K, Campeau PM, Yu TW, Margulies DM, et al. Eur J Med Genet. 2013 Dec; 56(12):678-82. Epub 2013 Oct 28.

RefSeq genomic sequence
See the genomic reference sequence for the KCNJ8 gene (NG_041794.1).
RefSeq protein
See the reference protein sequence for ATP-sensitive inward rectifier potassium channel 8 (NP_004973.1).

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)
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

uKATP-1 [Homo sapiens]
uKATP-1 [Homo sapiens]
gi|1109634|dbj|BAA08851.1|

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