Varaico: Literature-Extracted Genetic Variants

Gene:ABCA4
Variant:p.R1820_T1821Splc
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ABCA4

NM_000350.3:p.R1820_T1821Splc

Associated Papers

A framework for individualized splice-switching oligonucleotide therapy.

Kim J et al.

Nature, 2023

37438524 (PubMed )
Supplement: 41586_2023_6277_MOESM4_ESM.xlsx › S_Table_16

SpliceVault predicts the precise nature of variant-associated mis-splicing.

Dawes R et al.

Nature Genetics, 2023

36747048 (PubMed )
Supplement: 41588_2022_1293_MOESM3_ESM.xlsx › Table_3_Minigene_studies__n_61_

Compendium of Clinical Variant Classification for 2,246 Unique ABCA4 Variants to Clarify Variant Pathogenicity in Stargardt Disease Using a Modified ACMG/AMP Framework.

Cornelis SS et al.

Human Mutation, 2023

40225145 (PubMed )
Supplement: 6815504.f1.zip › S10_PS3_BS3.xlsx › Functional_data_overview

Impact of Next Generation Sequencing in Unraveling the Genetics of 1036 Spanish Families With Inherited Macular Dystrophies.

Del Pozo-Valero M et al.

Investigative Ophthalmology & Visual Science, 2022

35119454 (PubMed )
Supplement: iovs-63-2-11_s003.pdf

Benchmarking deep learning splice prediction tools using functional splice assays.

Riepe TV et al.

Human Mutation, 2021

33942434 (PubMed )
Supplement: HUMU-42-799-s001.xlsx › ABCA4_NCSS

Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations.

Cremers FPM et al.

Progress in Retinal and Eye Research, 2020

Association of Sex With Frequent and Mild ABCA4 Alleles in Stargardt Disease.

Runhart EH et al.

Jama Ophthalmology, 2020

ABCA4 midigenes reveal the full splice spectrum of all reported noncanonical splice site variants in Stargardt disease.

Sangermano R et al.

Genome Research, 2018

Outcome of ABCA4 disease-associated alleles in autosomal recessive retinal dystrophies: retrospective analysis in 420 Spanish families.

Riveiro-Alvarez R et al.

Ophthalmology, 2013

Comparison of high-resolution melting analysis with denaturing high-performance liquid chromatography for mutation scanning in the ABCA4 gene.

Aguirre-Lamban J et al.

Investigative Ophthalmology & Visual Science, 2010

Novel human pathological mutations. Gene symbol: ABCA4. Disease: macular dystrophy.

Aguirre-Lamban J et al.

Human Genetics, 2009

Molecular analysis of the ABCA4 gene for reliable detection of allelic variations in Spanish patients: identification of 21 novel variants.

Aguirre-Lamban J et al.

The British Journal of Ophthalmology, 2009

Gene symbol: ABCA4. Disease: Macular dystrophy.

Aguirre-Lambán J et al.

Human Genetics, 2008

Gene symbol: ABCA4. Disease: Macular dystrophy.

Aguirre-Lamban J et al.

Human Genetics, 2008

Gene symbol: ABCA4. Disease: Macular dystrophy.

Aguirre-Lamban J et al.

Human Genetics, 2008

Gene symbol: ABCA4. Disease: Macular dystrophy.

Aguirre J et al.

Human Genetics, 2008

Gene symbol: ABCA4. Disease: Macular dystrophy.

Aguirre-Lamban J et al.

Human Genetics, 2008

Gene symbol: ABCA4. Disease: Macular dystrophy.

Aguirre-Lamban J et al.

Human Genetics, 2008

Gene symbol: ABCA4. Disease: Macular dystrophy.

Aguirre-Lambán J et al.

Human Genetics, 2008

Gene symbol: ABCA4. Disease: Macular dystrophy.

Aguirre-Lamban J et al.

Human Genetics, 2008

Gene symbol: ABCA4. Disease: Macular dystrophy.

Maia-Lopes S et al.

Human Genetics, 2008

Gene symbol: ABCA4. Disease: Macular dystrophy.

Maia-Lopes S et al.

Human Genetics, 2008

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