visual system homeobox 2, partial [Homo sapiens]

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Association of Missense Variants in VSX2 With a Peculiar Form of Congenital Stationary Night Blindness Affecting All Bipolar Cells. [JAMA Ophthalmol. 2022]
Association of Missense Variants in VSX2 With a Peculiar Form of Congenital Stationary Night Blindness Affecting All Bipolar Cells.
Smirnov VM, Robert MP, Condroyer C, Navarro J, Antonio A, Rozet JM, Sahel JA, Perrault I, Audo I, Zeitz C. JAMA Ophthalmol. 2022 Dec 1; 140(12):1163-1173.
Sequence characterization of RET in 117 Chinese Hirschsprung disease families identifies a large burden of de novo and parental mosaic mutations. [Orphanet J Rare Dis. 2019]
Sequence characterization of RET in 117 Chinese Hirschsprung disease families identifies a large burden of de novo and parental mosaic mutations.
Jiang Q, Wang Y, Li Q, Zhang Z, Xiao P, Wang H, Liu N, Wu J, Zhang F, Chakravarti A, et al. Orphanet J Rare Dis. 2019 Oct 30; 14(1):237. Epub 2019 Oct 30.
Modeling human retinal development with patient-specific induced pluripotent stem cells reveals multiple roles for visual system homeobox 2. [Stem Cells. 2014]
Modeling human retinal development with patient-specific induced pluripotent stem cells reveals multiple roles for visual system homeobox 2.
Phillips MJ, Perez ET, Martin JM, Reshel ST, Wallace KA, Capowski EE, Singh R, Wright LS, Clark EM, Barney PM, et al. Stem Cells. 2014 Jun; 32(6):1480-92.

RefSeq genomic sequence
See the genomic reference sequence for the VSX2 gene (NG_013092.1).
RefSeq protein
See the reference protein sequence for visual system homeobox 2 (NP_878314.1).

Nucleotide
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Protein