ABCA4 c.2345G>A ;(p.W782*)

Variant ID: 1-94522194-C-T

NM_000350.2(ABCA4):c.2345G>A;(p.W782*)

This variant was identified in 13 publications

View GRCh38 version.




Publications:


The genetic landscape of inherited retinal dystrophies in Arabs.

Bmc Medical Genomics
Jaffal, Lama L; Joumaa, Hawraa H; Noureldine, Jinane J; Banjak, Malak M; Ibrahim, Mariam M; Mrad, Zamzam Z; Salami, Ali A; Shamieh, Said El SE
Publication Date: 2023-05-01

Variant appearance in text: ABCA4: 2345G>A
PubMed Link: 37127645
Variant Present in the following documents:
  • Main text
  • 12920_2023_Article_1518.pdf
  • 12920_2023_1518_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy.

Scientific Reports
Karali, Marianthi M; Testa, Francesco F; Di Iorio, Valentina V; Torella, Annalaura A; Zeuli, Roberta R; Scarpato, Margherita M; Romano, Francesca F; Onore, Maria Elena ME; Pizzo, Mariateresa M; Melillo, Paolo P; Brunetti-Pierri, Raffaella R; Passerini, Ilaria I; Pelo, Elisabetta E; Cremers, Frans P M FPM; Esposito, Gabriella G; Nigro, Vincenzo V; Simonelli, Francesca F; Banfi, Sandro S
Publication Date: 2022-12-02

Variant appearance in text: ABCA4: 2345G>A; Trp782*
PubMed Link: 36460718
Variant Present in the following documents:
  • 41598_2022_24636_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Phenotyping of ABCA4 Retinopathy by Machine Learning Analysis of Full-Field Electroretinography.

Translational Vision Science & Technology
Glinton, Sophie L SL; Calcagni, Antonio A; Lilaonitkul, Watjana W; Pontikos, Nikolas N; Vermeirsch, Sandra S; Zhang, Gongyu G; Arno, Gavin G; Wagner, Siegfried K SK; Michaelides, Michel M; Keane, Pearse A PA; Webster, Andrew R AR; Mahroo, Omar A OA; Robson, Anthony G AG
Publication Date: 2022-09-01

Variant appearance in text: ABCA4: 2345G>A; Trp782*
PubMed Link: 36178783
Variant Present in the following documents:
  • tvst-11-9-34_s002.pdf
View BVdb publication page



Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies.

Orphanet Journal Of Rare Diseases
Bouzidi, Aymane A; Charoute, Hicham H; Charif, Majida M; Amalou, Ghita G; Kandil, Mostafa M; Barakat, Abdelhamid A; Lenaers, Guy G
Publication Date: 2022-05-12

Variant appearance in text: ABCA4: 2345G>A; Trp782Ter
PubMed Link: 35551639
Variant Present in the following documents:
  • 13023_2022_2340_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Choroidal Caverns in Stargardt Disease.

Investigative Ophthalmology & Visual Science
Mucciolo, Dario Pasquale DP; Giorgio, Dario D; Lippera, Myrta M; Dattilo, Valeria V; Passerini, Ilaria I; Pelo, Elisabetta E; Sodi, Andrea A; Virgili, Gianni G; Giansanti, Fabrizio F; Murro, Vittoria V
Publication Date: 2022-02-01

Variant appearance in text: ABCA4: 2345G>A
PubMed Link: 35156991
Variant Present in the following documents:
  • Main text
  • iovs-63-2-25.pdf
View BVdb publication page



A novel statistical method for interpreting the pathogenicity of rare variants.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Wang, Jun J; Liu, Hehe H; Bertrand, Renae Elaine RE; Sarrion-Perdigones, Alejandro A; Gonzalez, Yezabel Y; Venken, Koen J T KJT; Chen, Rui R
Publication Date: 2021-01

Variant appearance in text: ABCA4: W782X
PubMed Link: 32884132
Variant Present in the following documents:
  • NIHMS1630822-supplement-Supplementary_Tables.xlsx, sheet 6
View BVdb publication page



Genetic spectrum of retinal dystrophies in Tunisia.

Scientific Reports
Habibi, Imen I; Falfoul, Yosra Y; Turki, Ahmed A; Hassairi, Asma A; El Matri, Khaled K; Chebil, Ahmed A; Schorderet, Daniel F DF; El Matri, Leila L
Publication Date: 2020-07-08

Variant appearance in text: ABCA4: W782*
PubMed Link: 32641690
Variant Present in the following documents:
  • Main text
  • 41598_2020_Article_67792.pdf
View BVdb publication page



Variants in the ABCA4 gene in a Brazilian population with Stargardt disease.

Molecular Vision
Salles, Mariana Vallim MV; Motta, Fabiana Louise FL; Martin, Renan R; Filippelli-Silva, Rafael R; Dias da Silva, Elton E; Varela, Patricia P; Costa, Kárita Antunes KA; Chiang, John PeiWen JP; Pesquero, João Bosco JB; Sallum, Juliana-Maria Ferraz JF
Publication Date: 2018

Variant appearance in text: ABCA4: 2345G>A
PubMed Link: 30093795
Variant Present in the following documents:
  • Main text
  • mv-v24-546.pdf
View BVdb publication page



Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.

Nature Genetics
Jin, Sheng Chih SC; Homsy, Jason J; Zaidi, Samir S; Lu, Qiongshi Q; Morton, Sarah S; DePalma, Steven R SR; Zeng, Xue X; Qi, Hongjian H; Chang, Weni W; Sierant, Michael C MC; Hung, Wei-Chien WC; Haider, Shozeb S; Zhang, Junhui J; Knight, James J; Bjornson, Robert D RD; Castaldi, Christopher C; Tikhonoa, Irina R IR; Bilguvar, Kaya K; Mane, Shrikant M SM; Sanders, Stephan J SJ; Mital, Seema S; Russell, Mark W MW; Gaynor, J William JW; Deanfield, John J; Giardini, Alessandro A; Porter, George A GA; Srivastava, Deepak D; Lo, Cecelia W CW; Shen, Yufeng Y; Watkins, W Scott WS; Yandell, Mark M; Yost, H Joseph HJ; Tristani-Firouzi, Martin M; Newburger, Jane W JW; Roberts, Amy E AE; Kim, Richard R; Zhao, Hongyu H; Kaltman, Jonathan R JR; Goldmuntz, Elizabeth E; Chung, Wendy K WK; Seidman, Jonathan G JG; Gelb, Bruce D BD; Seidman, Christine E CE; Lifton, Richard P RP; Brueckner, Martina M
Publication Date: 2017-11

Variant appearance in text: ABCA4: W782X
PubMed Link: 28991257
Variant Present in the following documents:
  • NIHMS906719-supplement-supp_datasets.xlsx, sheet 8
View BVdb publication page



Multimodal analysis of the Preferred Retinal Location and the Transition Zone in patients with Stargardt Disease.

Graefe'S Archive For Clinical And Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie
Verdina, Tommaso T; Greenstein, Vivienne C VC; Sodi, Andrea A; Tsang, Stephen H SH; Burke, Tomas R TR; Passerini, Ilaria I; Allikmets, Rando R; Virgili, Gianni G; Cavallini, Gian Maria GM; Rizzo, Stanislao S
Publication Date: 2017-07

Variant appearance in text: ABCA4: 2345G>A
PubMed Link: 28365912
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identifying mutations in Tunisian families with retinal dystrophy.

Scientific Reports
Habibi, Imen I; Chebil, Ahmed A; Falfoul, Yosra Y; Allaman-Pillet, Nathalie N; Kort, Fedra F; Schorderet, Daniel F DF; El Matri, Leila L
Publication Date: 2016-11-22

Variant appearance in text: ABCA4: W782*
PubMed Link: 27874104
Variant Present in the following documents:
  • Main text
  • srep37455.pdf
View BVdb publication page



Functional Analysis of Retinal Flecks in Stargardt Disease.

Journal Of Clinical & Experimental Ophthalmology
Verdina, Tommaso T; Tsang, Stephen H SH; Greenstein, Vivienne C VC; Zernant, Jana J; Sodi, Andrea A; Lima, Luiz H LH; Chang, Stanley S; Allikmets, Rando R; Menchini, Ugo U
Publication Date: 2012-07-30

Variant appearance in text: ABCA4: 2345G>A
PubMed Link: 24409374
Variant Present in the following documents:
  • Main text
  • nihms535866.pdf
View BVdb publication page



ABCA4 gene screening by next-generation sequencing in a British cohort.

Investigative Ophthalmology & Visual Science
Fujinami, Kaoru K; Zernant, Jana J; Chana, Ravinder K RK; Wright, Genevieve A GA; Tsunoda, Kazushige K; Ozawa, Yoko Y; Tsubota, Kazuo K; Webster, Andrew R AR; Moore, Anthony T AT; Allikmets, Rando R; Michaelides, Michel M
Publication Date: 2013-10-11

Variant appearance in text: ABCA4: 2345G>A; W782*
PubMed Link: 23982839
Variant Present in the following documents:
  • Main text
View BVdb publication page