Abstract
We report that the Disc1 gene in all extant 129 mouse inbred substrains has a deletion, previously considered specific to the 129S6/SvEv substrain, which is predicted to abolish production of the full-length protein. This finding has implications for the study of knockout mice generated from 129-derived embryonic stem cells. Copyright © 2006 by the Genetics Society of America.
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CITATION STYLE
Clapcote, S. J., & Roder, J. C. (2006). Deletion polymorphism of Disc1 is common to all 129 mouse substrains: Implications for gene-targeting studies of brain function. Genetics, 173(4), 2407–2410. https://doi.org/10.1534/genetics.106.060749
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