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Identification of a novel candidate for Cone-Rod dystrophy 8 using cross-species phenotype comparisons at the IMPC portal. A high scoring phenotype match for OMIM:605549 is obtained for an IMPC mouse strain involving disruption of the mouse Arhgef11 gene where abnormalities of the retina are reported in both the disease and the model. In addition, the tool highlights the human orthologue that lies within the previously reported locus at 1q12-24
