protein crumbs homolog 1 isoform X3 [Homo sapiens]

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Genotype-phenotype associations in CRB1 bi-allelic patients: a novel mutation, a systematic review and meta-analysis. [BMC Ophthalmol. 2024]
Genotype-phenotype associations in CRB1 bi-allelic patients: a novel mutation, a systematic review and meta-analysis.
Daher A, Banjak M, Noureldine J, Nehme J, El Shamieh S. BMC Ophthalmol. 2024 Apr 15; 24(1):167. Epub 2024 Apr 15.
A novel pathogenic CRB1 variant presenting as Leber Congenital Amaurosis 8 and evaluation of gene editing feasibility. [Doc Ophthalmol. 2023]
A novel pathogenic CRB1 variant presenting as Leber Congenital Amaurosis 8 and evaluation of gene editing feasibility.
Sylla MM, Kolesinkova M, da Costa BL, Maumenee IH, Tsang SH, Quinn PMJ. Doc Ophthalmol. 2023 Dec; 147(3):217-224. Epub 2023 Oct 7.
Foveal Hypoplasia in CRB1-Related Retinopathies. [Int J Mol Sci. 2023]
Foveal Hypoplasia in CRB1-Related Retinopathies.
Rodriguez-Martinez AC, Higgins BE, Tailor-Hamblin V, Malka S, Cheloni R, Collins AM, Bladen J, Henderson R, Moosajee M. Int J Mol Sci. 2023 Sep 11; 24(18). Epub 2023 Sep 11.

RefSeq mRNA
See reference mRNA sequence for the CRB1 gene (XM_011509367.2).
RefSeq protein isoforms
See 20 reference sequence protein isoforms for the CRB1 gene.

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Protein