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Dickinson, M.E.* ; Flenniken, A.M.* ; Ji, X.* ; Teboul, L.* ; Wong, M.D.* ; White, J.K.* ; Meehan, T.F.* ; Weninger, W.J.* ; Westerberg, H.* ; Adissu, H.A.* ; Baker, C.N.* ; Bower, L.* ; Brown, J.M.* ; Caddle, L.B.* ; Chiani, F.* ; Clary, D.* ; Cleak, J.* ; Daly, M.J.* ; Denegre, J.M.* ; Doe, B.* ; Dolan, M.E.* ; Edie, S.M.* ; Fuchs, H. ; Gailus-Durner, V. ; Galli, A.* ; Gambadoro, A.* ; Gallegos, J.* ; Guo, S.* ; Horner, N.R.* ; Hsu, C.W.* ; Johnson, S.J.* ; Kalaga, S.* ; Keith, L.C.* ; Lanoue, L.* ; Lawson, T.N.* ; Lek, M.* ; Mark, M.* ; Marschall, S. ; Mason, J.* ; McElwee, M.L.* ; Newbigging, S.* ; Nutter, L.M.* ; Peterson, K.A.* ; Ramirez-Solis, R.* ; Rowland, D.J.* ; Ryder, E.* ; Samocha, K.E.* ; Seavitt, J.R.* ; Selloum, M.* ; Szoke-Kovacs, Z.* ; Tamura, M.* ; Trainor, A.G.* ; Tudose, I.* ; Wakana, S.* ; Warren, J.* ; Wendling, O.* ; West, D.B.* ; Wong, L.J.* ; Yoshiki, A.* ; MacArthur, D.G.* ; Tocchini-Valentini, G.P.* ; Gao, X.* ; Flicek, P.* ; Bradley, A.* ; Skarnes, W.C.* ; Justice, M.J.* ; Parkinson, H.E.* ; Moore, M.* ; Wells, S.* ; Braun, R.E.* ; Svenson, K.L.* ; Hrabě de Angelis, M. ; Herault, Y.* ; Mohun, T.* ; Mallon, A.M.* ; Henkelman, R.M.* ; Brown, S.D.* ; Adams, D.J.* ; Lloyd, K.C.K.* ; McKerlie, C.* ; Beaudet, A.L.* ; Bucan, M.* ; Murray, S.A.*

High-throughput discovery of novel developmental phenotypes.

Nature 537, 508-514 (2016)
Postprint Forschungsdaten DOI PMC
Open Access Green
Approximately one-third of all mammalian genes are essential for life. Phenotypes resulting from knockouts of these genes in mice have provided tremendous insight into gene function and congenital disorders. As part of the International Mouse Phenotyping Consortium effort to generate and phenotypically characterize 5,000 knockout mouse lines, here we identify 410 lethal genes during the production of the first 1,751 unique gene knockouts. Using a standardized phenotyping platform that incorporates high-resolution 3D imaging, we identify phenotypes at multiple time points for previously uncharacterized genes and additional phenotypes for genes with previously reported mutant phenotypes. Unexpectedly, our analysis reveals that incomplete penetrance and variable expressivity are common even on a defined genetic background. In addition, we show that human disease genes are enriched for essential genes, thus providing a dataset that facilitates the prioritization and validation of mutations identified in clinical sequencing efforts.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Mammalian Gene-function; Mouse Embryo; Glycogenin-1 Deficiency; Genome-wide; Micro-ct; Screens; Disease; Expression; Resource; Identification
Sprache deutsch
Veröffentlichungsjahr 2016
HGF-Berichtsjahr 2016
ISSN (print) / ISBN 0028-0836
e-ISSN 1476-4687
Zeitschrift Nature
Quellenangaben Band: 537, Heft: 7621, Seiten: 508-514 Artikelnummer: , Supplement: ,
Verlag Nature Publishing Group
Verlagsort London
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Experimental Genetics (IEG)
Institute of Developmental Genetics (IDG)
POF Topic(s) 30201 - Metabolic Health
30204 - Cell Programming and Repair
Forschungsfeld(er) Genetics and Epidemiology
PSP-Element(e) G-500600-001
G-500500-001
DOI 10.1038/nature19356
WOS ID WOS:000383545900047
Scopus ID 84989204804
PubMed ID 27626380
Erfassungsdatum 2016-09-30
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