Fig. 1
From: Epileptic encephalopathy in a young Bengal cat caused by CAD deficiency
Details of the XP_006930506.2:p.(Ser2015Asn) variant are presented. (A) Sanger electropherograms derived from the genomic DNA of a wildtype control, a carrier, and the affected cat, highlighting the presence of the Ser2015Asn variant. The electropherograms show the wildtype (G/G), carrier (G/A), and affected (A/A) genotypes at the XM_011281284.3:c.6044G>A variant. (B) A multiple species alignment shows the high evolutionary sequence conservation surrounding the Ser2015Asn variant. The secondary structure motifs are indicated, with the α3 helix and β4 sheet highlighted to provide structural context for the position of the variant.
