A resource of targeted mutant mouse lines for 5,061 genes

作者：Marie‐Christine Birling, Atsushi Yoshiki, David J. Adams, Shinya Ayabe, Arthur L. Beaudet, Joanna Bottomley, Allan Bradley, Steve D. M. Brown, Antje Bürger, Wendy Bushell, Francesco Chiani, Hsian‐Jean Chin, Skevoulla Christou, Gemma Codner, Francesco J. DeMayo, Mary E. Dickinson, Brendan Doe, Leah Rae Donahue, Martin Fray, Alessia Gambadoro, Xiang Gao, Marina Gertsenstein, Alba Gomez-Segura, Leslie O. Goodwin, Jason D. Heaney, Yann Hérault, Martin Hrabě de Angelis, Si‐Tse Jiang, Monica J. Justice, Petr Kašpárek, Ruairidh King, Ralf Kühn, Ho Lee, Young Jae Lee, Zhiwei Liu, K. C. Kent Lloyd, Isabel Lorenzo, Ann‐Marie Mallon, Colin McKerlie, Terrence F. Meehan, Stuart Newman, Lauryl Mj Nutter, Goo Taeg Oh, Guillaume Pavlovic, Ramiro Ramírez‐Solis, Barry P. Rosen, Edward J. Ryder, Luís Santos, Joel Schick, John R. Seavitt, Radislav Sedláček, Claudia Seisenberger, Je Kyung Seong, William C. Skarnes, Tania Sorg, Karen P. Steel, Masaru Tamura, Glauco P. Tocchini‐Valentini, Chi‐Kuang Leo Wang, Hannah Wardle‐Jones, Marie Wattenhofer‐Donzé, Sara Wells, Brandon Willis, Joshua A. Wood, Wolfgang Wurst, Ying Xu, Lydia Teboul, Stephen A. Murray · 发表于：bioRxiv (Cold Spring Harbor Laboratory) · 年份：2019 · DOI：10.1101/844092 · 被引用次数：10 · 研究领域：Animal Genetics and Reproduction、CRISPR and Genetic Engineering、Molecular Biology Techniques and Applications

Abstract The International Mouse Phenotyping Consortium reports the generation of new mouse mutant strains for over 5,000 genes from targeted embryonic stem cells on the C57BL/6N genetic background. This includes 2,850 null alleles for which no equivalent mutant mouse line exists, 2,987 novel conditional-ready alleles, and 4,433 novel reporter alleles. This nearly triples the number of genes with reporter alleles and almost doubles the number of conditional alleles available to the scientific community. When combined with more than 30 years of community effort, the total mutant allele mouse resource covers more than half of the genome. The extensively validated collection is archived and distributed through public repositories, facilitating availability to the worldwide biomedical research community, and expanding our understanding of gene function and human disease.