Homo sapiens potassium calcium-activated channel subfamily N member 2 - Nucleotide

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A Novel KCNN2 Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico Analysis. [Genes (Basel). 2023]
A Novel KCNN2 Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico Analysis.
d'Apolito M, Ceccarini C, Savino R, Adipietro I, di Bari I, Santacroce R, Curcetti M, D'Andrea G, Croce AI, Cesarano C, et al. Genes (Basel). 2023 Jun 29; 14(7). Epub 2023 Jun 29.
Loss-of-function K(Ca)2.2 mutations abolish channel activity. [Am J Physiol Cell Physiol. 2023]
Loss-of-function K(Ca)2.2 mutations abolish channel activity.
Nam YW, Rahman MA, Yang G, Orfali R, Cui M, Zhang M. Am J Physiol Cell Physiol. 2023 Mar 1; 324(3):C658-C664. Epub 2023 Jan 30.
The CRL4(DCAF6) E3 ligase ubiquitinates CtBP1/2 to induce apoptotic signalling and promote intervertebral disc degeneration. [J Mol Med (Berl). 2023]
The CRL4(DCAF6) E3 ligase ubiquitinates CtBP1/2 to induce apoptotic signalling and promote intervertebral disc degeneration.
Tseng C, Han Y, Lv Z, Song Q, Wang K, Shen H, Chen Z. J Mol Med (Berl). 2023 Feb; 101(1-2):171-181. Epub 2023 Jan 23.

RefSeq alternative splicing
See 9 reference mRNA sequence splice variants for the KCNN2 gene.
RefSeq protein product
See the reference protein sequence for small conductance calcium-activated potassium channel protein 2 isoform c (NP_001359162.1).

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Protein sequence from Nucleotide coding region
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txid691052[Organism:noexp] (18)
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Nucleotide