Homo sapiens cDNA FLJ77596 complete cds, highly similar to Homo sapien - 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.

reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome
Order full-length cDNA clone [GeneCopoeia Inc.]
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Human cDNA clones used in NEDO Project [NITE Biological Resource Cent...]
Human cDNA clones used in NEDO Project
NITE Biological Resource Center

Homo sapiens cDNA FLJ77596 complete cds, highly similar to Homo sapiens chloride...
Homo sapiens cDNA FLJ77596 complete cds, highly similar to Homo sapiens chloride channel Kb (CLCNKB), mRNA
gi|158258101|dbj|AK292335.1|

Nucleotide

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Nucleotide