Homo sapiens potassium inwardly rectifying channel subfamily J member - Nucleotide

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Phenotypic Variability of Andersen-Tawil Syndrome Due to Allelic Mutation c.652C>T in the KCNJ2 Gene-A New Family Case Report. [Biomolecules. 2024]
Phenotypic Variability of Andersen-Tawil Syndrome Due to Allelic Mutation c.652C>T in the KCNJ2 Gene-A New Family Case Report.
Onore ME, Picillo E, D'Ambrosio P, Morra S, Nigro V, Politano L. Biomolecules. 2024 Apr 22; 14(4). Epub 2024 Apr 22.
The Kir2.1E299V mutation increases atrial fibrillation vulnerability while protecting the ventricles against arrhythmias in a mouse model of short QT syndrome type 3. [Cardiovasc Res. 2024]
The Kir2.1E299V mutation increases atrial fibrillation vulnerability while protecting the ventricles against arrhythmias in a mouse model of short QT syndrome type 3.
Moreno-Manuel AI, Macías Á, Cruz FM, Gutiérrez LK, Martínez F, González-Guerra A, Martínez Carrascoso I, Bermúdez-Jimenez FJ, Sánchez-Pérez P, Vera-Pedrosa ML, et al. Cardiovasc Res. 2024 Apr 30; 120(5):490-505.
Activation of Kir2.1 improves myocardial fibrosis by inhibiting Ca (2+) overload and the TGF-β1/Smad signaling pathway. [Acta Biochim Biophys Sin (Shan...]
Activation of Kir2.1 improves myocardial fibrosis by inhibiting Ca (2+) overload and the TGF-β1/Smad signaling pathway.
Rong Y, Zhou X, Guo Z, Zhang Y, Qin W, Li L, Si J, Yang R, Li X, Ma K. Acta Biochim Biophys Sin (Shanghai). 2023 May 15; 55(5):749-757.

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Chromosome neighbors for GEO Profiles (Select 86280034) (20)
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Homo sapiens
Homo sapiens

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Genome Links for Gene (Select 100289095) (1)
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Nucleotide