Homo sapiens potassium channel h-eag

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Phenotypic and genetic analysis of children with unexplained neurodevelopmental delay and neurodevelopmental comorbidities in a Chinese cohort using trio-based whole-exome sequencing. [Orphanet J Rare Dis. 2024]
Phenotypic and genetic analysis of children with unexplained neurodevelopmental delay and neurodevelopmental comorbidities in a Chinese cohort using trio-based whole-exome sequencing.
Wu R, Li X, Meng Z, Li P, He Z, Liang L. Orphanet J Rare Dis. 2024 May 19; 19(1):205. Epub 2024 May 19.
14-3-3 proteins regulate cullin 7-mediated Eag1 degradation. [Cell Biosci. 2023]
14-3-3 proteins regulate cullin 7-mediated Eag1 degradation.
Hsieh CH, Chou CC, Fang YC, Hsu PH, Chiu YH, Yang CS, Jow GM, Tang CY, Jeng CJ. Cell Biosci. 2023 Jan 30; 13(1):18. Epub 2023 Jan 30.
Phenotypic expansion of KCNH1-associated disorders to include isolated epilepsy and its associations with genotypes and molecular sub-regional locations. [CNS Neurosci Ther. 2023]
Phenotypic expansion of KCNH1-associated disorders to include isolated epilepsy and its associations with genotypes and molecular sub-regional locations.
Tian MQ, Li RK, Yang F, Shu XM, Li J, Chen J, Peng LY, Yu XH, Yang CJ. CNS Neurosci Ther. 2023 Jan; 29(1):270-281. Epub 2022 Oct 25.

RefSeq alternative splicing
See 8 reference mRNA sequence splice variants for the KCNH1 gene.

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Nucleotide