RecName: Full=Chloride channel protein ClC-Kb; Short=Chloride channel - Protein

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Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions. [Genome Med. 2023]
Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions.
Tschernoster N, Erger F, Kohl S, Reusch B, Wenzel A, Walsh S, Thiele H, Becker C, Franitza M, Bartram MP, et al. Genome Med. 2023 Aug 23; 15(1):62. Epub 2023 Aug 23.
A novel CLCNKB variant in a Chinese family with classic Bartter syndrome and prenatal genetic diagnosis. [Mol Genet Genomic Med. 2022]
A novel CLCNKB variant in a Chinese family with classic Bartter syndrome and prenatal genetic diagnosis.
Zhao Q, Xiang Q, Tan Y, Xiao X, Xie H, Wang H, Yang M, Liu S. Mol Genet Genomic Med. 2022 Oct; 10(10):e2027. Epub 2022 Aug 1.
Thirteen novel CLCNKB variants and genotype/phenotype association study in 42 Chinese patients with Bartter syndrome type 3. [Endocrine. 2020]
Thirteen novel CLCNKB variants and genotype/phenotype association study in 42 Chinese patients with Bartter syndrome type 3.
Han Y, Cheng H, Shao S, Lang Y, Zhao X, Lin Y, Wang S, Shi X, Liu Z, Shao L. Endocrine. 2020 Apr; 68(1):192-202. Epub 2019 Dec 13.

RefSeq genomic sequence
See the genomic reference sequence for the CLCNKB gene (NG_013079.2).

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P51801 [Domain Mapping of Disease Mut...]
P51801
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
Reactome [Reactome]
Reactome
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

chloride channel (putative) [Homo sapiens]
chloride channel (putative) [Homo sapiens]
gi|521074|emb|CAA83121.1|

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