chloride channel Kb, isoform CRA_c [Homo sapiens]

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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).
RefSeq protein isoforms
See 2 reference sequence protein isoforms for the CLCNKB gene.

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