A reverse-genetics approach to understanding gene families associated with human disease is presented, using mouse as a model system, and the subsequent mouse phenotyping schedule is described. Because mice defective in a gene of interest, HtrA2, manifested Parkinsonian symptoms, the phenotyping regimen is focused on identifying neurological defects.
Patterson, V. L., Thompson, B. S., Cherry, C., Wang, S., Chen, B., Hoh, J. A Phenotyping Regimen for Genetically Modified Mice Used to Study Genes Implicated in Human Diseases of Aging. J. Vis. Exp. (113), e54136, doi:10.3791/54136 (2016).