Homo sapiens isolate S2 crystallin beta A4 (CRYBA4) gene, exon 4 and p - Nucleotide

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A novel missense variant c.71G > T (p.Gly24Val) of the CRYBA4 gene contributes to autosomal-dominant congenital cataract in a Chinese family. [Int Ophthalmol. 2023]
A novel missense variant c.71G > T (p.Gly24Val) of the CRYBA4 gene contributes to autosomal-dominant congenital cataract in a Chinese family.
Zhang X, Liang C, Liu M, Wang Z, Leng X, Xie S, Tan X, Yang Y, Liu Y. Int Ophthalmol. 2023 Jan; 43(1):43-50. Epub 2022 Jul 16.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome. [Cell. 2021]
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Huttlin EL, Bruckner RJ, Navarrete-Perea J, Cannon JR, Baltier K, Gebreab F, Gygi MP, Thornock A, Zarraga G, Tam S, et al. Cell. 2021 May 27; 184(11):3022-3040.e28. Epub 2021 May 6.
In silico analysis and high-risk pathogenic phenotype predictions of non-synonymous single nucleotide polymorphisms in human Crystallin beta A4 gene associated with congenital cataract. [PLoS One. 2020]
In silico analysis and high-risk pathogenic phenotype predictions of non-synonymous single nucleotide polymorphisms in human Crystallin beta A4 gene associated with congenital cataract.
Wang Z, Huang C, Lv H, Zhang M, Li X. PLoS One. 2020; 15(1):e0227859. Epub 2020 Jan 14.

RefSeq alternative splicing
See 3 reference mRNA sequence splice variants for the CRYBA4 gene.

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Nucleotide