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Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts

Authors :
Bret A. Moore
Brian C. Leonard
Lionel Sebbag
Sydney G. Edwards
Ann Cooper
Denise M. Imai
Ewan Straiton
Luis Santos
Christopher Reilly
Stephen M. Griffey
Lynette Bower
David Clary
Jeremy Mason
Michel J. Roux
Hamid Meziane
Yann Herault
International Mouse Phenotyping Consortium
Colin McKerlie
Ann M. Flenniken
Lauryl M. J. Nutter
Zorana Berberovic
Celeste Owen
Susan Newbigging
Hibret Adissu
Mohammed Eskandarian
Chih-Wei Hsu
Sowmya Kalaga
Uchechukwu Udensi
Chinwe Asomugha
Ritu Bohat
Juan J. Gallegos
John R. Seavitt
Jason D. Heaney
Arthur L. Beaudet
Mary E. Dickinson
Monica J. Justice
Vivek Philip
Vivek Kumar
Karen L. Svenson
Robert E. Braun
Sara Wells
Heather Cater
Michelle Stewart
Sharon Clementson-Mobbs
Russell Joynson
Xiang Gao
Tomohiro Suzuki
Shigeharu Wakana
Damian Smedley
J. K. Seong
Glauco Tocchini-Valentini
Mark Moore
Colin Fletcher
Natasha Karp
Ramiro Ramirez-Solis
Jacqueline K. White
Martin Hrabe de Angelis
Wolfgang Wurst
Sara M. Thomasy
Paul Flicek
Helen Parkinson
Steve D. M. Brown
Terrence F. Meehan
Patsy M. Nishina
Stephen A. Murray
Mark P. Krebs
Ann-Marie Mallon
K. C. Kent Lloyd
Christopher J. Murphy
Ala Moshiri
Source :
Communications Biology, Communications Biology, Vol 2, Iss 1, Pp 1-2 (2019)
Publication Year :
2019
Publisher :
Nature Publishing Group UK, 2019.

Abstract

Despite advances in next generation sequencing technologies, determining the genetic basis of ocular disease remains a major challenge due to the limited access and prohibitive cost of human forward genetics. Thus, less than 4,000 genes currently have available phenotype information for any organ system. Here we report the ophthalmic findings from the International Mouse Phenotyping Consortium, a large-scale functional genetic screen with the goal of generating and phenotyping a null mutant for every mouse gene. Of 4364 genes evaluated, 347 were identified to influence ocular phenotypes, 75% of which are entirely novel in ocular pathology. This discovery greatly increases the current number of genes known to contribute to ophthalmic disease, and it is likely that many of the genes will subsequently prove to be important in human ocular development and disease.

Details

Language :
English
ISSN :
23993642
Volume :
2
Database :
OpenAIRE
Journal :
Communications Biology
Accession number :
edsair.doi.dedup.....eac9d202796b61bf63deadeee8af041c