Abstract:A male mixed breed dog with clinical Hemophilia B was tested with a direct-to-consumer dog genomics service. After being genotyped as “normal” at three previously published Hemophilia B variants, all coding regions of the dog’s F9 gene were sequenced. A single basepair deletion in exon 5 of F9 led to a frameshift mutation leading to a premature truncation of FIX, including loss of the catalytic domain. The dam for this individual is a Great Pyrenees suggesting this X chromosome variant could segregate within t… Show more
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