Homo sapiens gap junction protein beta 2 (GJB2), RefSeqGene (LRG_1350) - Nucleotide

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Interactions of genetic variations in FAS, GJB2 and PTPRN2 are associated with noise-induced hearing loss: a case-control study in China. [BMC Med Genomics. 2024]
Interactions of genetic variations in FAS, GJB2 and PTPRN2 are associated with noise-induced hearing loss: a case-control study in China.
Wu S, Wu Z, Chen M, Zhong X, Gu H, Du W, Liu W, Lang L, Wang J. BMC Med Genomics. 2024 Jan 11; 17(1):18. Epub 2024 Jan 11.
Hearing and Hearing Loss Progression in Patients with GJB2 Gene Mutations: A Long-Term Follow-Up. [Int J Mol Sci. 2023]
Hearing and Hearing Loss Progression in Patients with GJB2 Gene Mutations: A Long-Term Follow-Up.
Sakata A, Kashio A, Koyama M, Urata S, Koyama H, Yamasoba T. Int J Mol Sci. 2023 Nov 25; 24(23). Epub 2023 Nov 25.
Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China. [Int J Pediatr Otorhinolaryngol...]
Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China.
Xiong Y, Chen M, Wang H, Chen L, Huang H, Xu L. Int J Pediatr Otorhinolaryngol. 2024 Jan; 176:111777. Epub 2023 Nov 21.

RefSeq alternative splicing
See 3 reference mRNA sequence splice variants for the GJB2 gene.

Protein
Protein sequence from Nucleotide coding region
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RNA
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Nucleotide