Homo sapiens chloride channel Kb, mRNA (cDNA clone MGC:24087 IMAGE:460 - Nucleotide

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Expanding Genotype-Phenotype Correlation of CLCNKA and CLCNKB Variants Linked to Hearing Loss. [Int J Mol Sci. 2023]
Expanding Genotype-Phenotype Correlation of CLCNKA and CLCNKB Variants Linked to Hearing Loss.
Yun Y, Park SS, Lee S, Seok H, Park S, Lee SY. Int J Mol Sci. 2023 Dec 3; 24(23). Epub 2023 Dec 3.
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.

RefSeq alternative splicing
See 2 reference mRNA sequence splice variants for the CLCNKB gene.

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K.K. DNAFORM

Acinetobacter baumannii strain 4300STDY7045722, whole genome shotgun sequence
Acinetobacter baumannii strain 4300STDY7045722, whole genome shotgun sequence
gi|1433270994|ref|NZ_UFIX01000051.1

Nucleotide
Homo sapiens radixin, mRNA (cDNA clone MGC:48283 IMAGE:5284438), complete cds
Homo sapiens radixin, mRNA (cDNA clone MGC:48283 IMAGE:5284438), complete cds
gi|28436808|gb|BC047109.1|

Nucleotide

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Nucleotide