Varaico: Literature-Extracted Genetic Variants

Gene:RPE65
Variant:p.H527R
Back to variants list

RPE65

NM_000329.3:p.H527R

Associated Papers

Higher Throughput Assays for Understanding the Pathogenicity of Variants of Unknown Significance in the RPE65 Gene.

Azizzadeh Pormehr L et al.

Investigative Ophthalmology & Visual Science, 2025

Determination of the Population Frequency of Monoallelic and Biallelic Predicted Pathogenic RPE65 Variants in a Normal Database.

Abdul R et al.

Investigative Ophthalmology & Visual Science, 2025

40879297 (PubMed )
Supplement: iovs-66-11-73_s001.xlsx › Assessment

Structure-based analysis of missense mutations impacting the catalytic and substrate binding sites of hRPE65.

Poli G et al.

Journal of Molecular Graphics & Modelling, 2025

Higher throughput assays for understanding the pathogenicity of variants of unknown significance (VUS) in the RPE65 gene.

Pormehr LA et al.

Biorxiv : the Preprint Server for Biology, 2025

Linking Protein Stability to Pathogenicity: Predicting Clinical Significance of Single-Missense Mutations in Ocular Proteins Using Machine Learning.

Majid I et al.

International Journal of Molecular Sciences, 2024

39519200 (PubMed )
Supplement: ijms-25-11649-s001.zip › ijms-3279427-supplementary.pdf

Pathogenicity reclassification of the RPE65 c.1580A>G (p.His527Arg) - a case report.

Bjeloš M et al.

Ophthalmic Genetics, 2023

Voretigene Neparvovec for the Treatment of RPE65-associated Retinal Dystrophy: Consensus and Recommendations from the Korea RPE65-IRD Consensus Paper Committee.

Han J et al.

Korean Journal of Ophthalmology : Kjo, 2023

Development of a novel prediction model based on protein structure for identifying RPE65-associated inherited retinal disease (IRDs) of missense variants.

Wu J et al.

Peerj, 2023

37547722 (PubMed )
Supplement: peerj-11-15702-s004.xlsx › Table_S2

Rescue of enzymatic function for disease-associated RPE65 proteins containing various missense mutations in non-active sites.

Li S et al.

The Journal of Biological Chemistry, 2014

[Genetic and clinical heterogeneity in LCA patients. The end of uniformity].

Preising MN et al.

Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft, 2007

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."