DNA variants in or close to the human and genes have been repeatedly associated with facial morphology in independent genome-wide association studies, while their functional roles in determining facial morphology remain to be understood. We generated knockout ( ) and knockout ( ) mice by applying the one-step CRISPR/Cas9 method. A total of 75 adult mice were used for subsequent phenotype analysis, including 38 mice (10 homozygous , 18 heterozygous , 10 wild-type littermates) and 37 mice (12 homozygous , 15 heterozygous , 10 littermates). Facial and other physical morphological phenotypes were obtained from three-dimensional (3D) images acquired with the HandySCAN BLACK scanner. Compared to littermates, the mutant mice had significantly shorter faces ( = 1.08E-8, R = 0.61) and their ears were in a significantly lower position ( = 3.54E-8, R = 0.62) manifesting a "droopy ear" characteristic. Besides these face alternations, mutant mice displayed significantly lower weight as well as shorter body and limb length. mutant mice showed significantly longer noses ( = 1.14E-5, R = 0.46) relative to littermates, but otherwise displayed less obvious morphological alterations than mutant mice did. We provide the first direct functional evidence that two well-known and replicated human face genes, and , impact facial and other body morphology in mice. The general agreement between our findings in knock-out mice with those from previous GWASs suggests that the functional evidence we established here in mice may also be relevant in humans.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8664010PMC
http://dx.doi.org/10.1096/fba.2021-00094DOI Listing

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