The function of most of our 20,000 genes is currently unknown, and we know even less about what happens if each gene has a mutation. In ‘clinical spotlight’ feature for the Winter edition of Rare Revolution Magazine , the DMDD and IMPC consortia talk about the role mouse embryo phenotyping plays in understanding the genetic basis of rare disease, and the efforts to make their data freely available to all.

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The Rare Revolution Winter 2016 edition.