FIGURE

Fig. 1

ID

ZDB-FIG-251022-48

Publication

Fan et al., 2025 - Do variants in the CDH23 gene cause non-syndromic retinitis pigmentosa? Dual validation using whole exome sequencing and a zebrafish model

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Fig. 1

Mutation sequence analysis and clinical examination of the family. (A) Fundus photographs, OCT scans and perimetry results of both eyes of the patient. (B) Pedigree of the family: The filled black symbol represents the affected member, and the arrow denotes the proband. (C) ERG: Significant impairment of cone and rod cell function in both eyes. (D) Pure tone audiometry results of the patient. (E) The homology of amino acid sequences between human CDH23 and other species; the amino acid at positions 858 and 2783 are highly conserved among species, and the mutated residues 858 and 2783 are boxed and indicated. (F) The change in the interaction distance between wild type and mutant proteins further indicates spatial changes. ERG, electroretinography; OCT, optical coherence tomography.

Expression Data

Expression Detail

Antibody Labeling

Phenotype Data

Phenotype Detail

Acknowledgments

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