cyclic nucleotide-gated cation channel beta-3 isoform X1 [Homo sapiens - Protein

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A deep intronic substitution in CNGB3 is one of the major causes of achromatopsia among Jewish patients. [Mol Vis. 2021]
A deep intronic substitution in CNGB3 is one of the major causes of achromatopsia among Jewish patients.
Aweidah H, Salameh M, Yahalom C, Blumenfeld A, Macarov M, Weisschuh N, Kohl S, Banin E, Sharon D. Mol Vis. 2021; 27:588-600. Epub 2021 Sep 22.
Ametropia and Emmetropization in CNGB3 Achromatopsia. [Invest Ophthalmol Vis Sci. 2021]
Ametropia and Emmetropization in CNGB3 Achromatopsia.
Andersen MKG, Kessel L. Invest Ophthalmol Vis Sci. 2021 Feb 1; 62(2):10.
Molecular genetic cause of achromatopsia in two patients of Czech origin. [Cesk Slov Oftalmol. 2019]
Molecular genetic cause of achromatopsia in two patients of Czech origin.
Hlavatá L, Ďuďáková Ľ, Moravíková J, Zobanová A, Kousal B, Lišková P. Cesk Slov Oftalmol. 2019 Winter; 75(5):272-276.

RefSeq genomic sequence
See the genomic reference sequence for the CNGB3 gene (NG_016980.1).
RefSeq mRNA
See reference mRNA sequence for the CNGB3 gene (XM_011517138.3).
RefSeq protein isoforms
See 3 reference sequence protein isoforms for the CNGB3 gene.

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Protein