Homo sapiens potassium inwardly rectifying channel subfamily J member - Nucleotide

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The unique structural characteristics of the Kir 7.1 inward rectifier potassium channel: a novel player in energy homeostasis control. [Am J Physiol Cell Physiol. 2023]
The unique structural characteristics of the Kir 7.1 inward rectifier potassium channel: a novel player in energy homeostasis control.
Hernandez CC, Gimenez LE, Dahir NS, Peisley A, Cone RD. Am J Physiol Cell Physiol. 2023 Mar 1; 324(3):C694-C706. Epub 2023 Jan 30.
A novel phenotype associated with the R162W variant in the KCNJ13 gene. [Ophthalmic Genet. 2022]
A novel phenotype associated with the R162W variant in the KCNJ13 gene.
Schroeder M, Peter VG, Gränse L, Andréasson S, Rivolta C, Kjellström U. Ophthalmic Genet. 2022 Aug; 43(4):500-507. Epub 2022 Apr 27.
KCNJ13 Gene Deletion Impairs Cell Alignment and Phagocytosis in Retinal Pigment Epithelium Derived from Human-Induced Pluripotent Stem Cells. [Invest Ophthalmol Vis Sci. 2020]
KCNJ13 Gene Deletion Impairs Cell Alignment and Phagocytosis in Retinal Pigment Epithelium Derived from Human-Induced Pluripotent Stem Cells.
Kanzaki Y, Fujita H, Sato K, Hosokawa M, Matsumae H, Shiraga F, Morizane Y, Ohuchi H. Invest Ophthalmol Vis Sci. 2020 May 11; 61(5):38.

RefSeq alternative splicing
See 5 reference mRNA sequence splice variants for the KCNJ13 gene.
RefSeq protein product
See the reference protein sequence for inward rectifier potassium channel 13 isoform 3 (NP_001165888.1).

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Nucleotide