TWIK-related individual K+ channel [Homo sapiens]

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Further evidence of biallelic variants in KCNK18 as a cause of intellectual disability and epilepsy with febrile seizure plus. [Clin Dysmorphol. 2023]
Further evidence of biallelic variants in KCNK18 as a cause of intellectual disability and epilepsy with febrile seizure plus.
Majethia P, Harish R, Narayanan DL, B L Y, Sharma S, Shukla A. Clin Dysmorphol. 2023 Oct 1; 32(4):147-150. Epub 2023 May 5.
KCNK18 Biallelic Variants Associated with Intellectual Disability and Neurodevelopmental Disorders Alter TRESK Channel Activity. [Int J Mol Sci. 2021]
KCNK18 Biallelic Variants Associated with Intellectual Disability and Neurodevelopmental Disorders Alter TRESK Channel Activity.
Pavinato L, Nematian-Ardestani E, Zonta A, De Rubeis S, Buxbaum J, Mancini C, Bruselles A, Tartaglia M, Pessia M, Tucker SJ, et al. Int J Mol Sci. 2021 Jun 4; 22(11). Epub 2021 Jun 4.
The Background K(+) Channel TRESK in Sensory Physiology and Pain. [Int J Mol Sci. 2020]
The Background K(+) Channel TRESK in Sensory Physiology and Pain.
Andres-Bilbe A, Castellanos A, Pujol-Coma A, Callejo G, Comes N, Gasull X. Int J Mol Sci. 2020 Jul 23; 21(15). Epub 2020 Jul 23.

RefSeq genomic sequence
See the genomic reference sequence for the KCNK18 gene (NG_028085.1).
RefSeq protein
See the reference protein sequence for potassium channel subfamily K member 18 (NP_862823.1).

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)
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

TWIK-related individual K+ channel [Homo sapiens]
TWIK-related individual K+ channel [Homo sapiens]
gi|32351876|dbj|BAC78527.1|

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