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. 2015 Oct 5;112(42):E5706–E5714. doi: 10.1073/pnas.1515619112

Fig. 4.

Fig. 4.

Kdelr1 mutation is causative for daniel gray phenotype. (A) Schematic of the Cas9/sgRNA targeting site at the Kdelr1 locus. Boxes indicate exons, with dark shading indicating protein-coding sequence. The sgRNA targeting sequence is underlined, and the protospacer-adjacent motif (PAM) is labeled in red. (B) Frequencies and CD44 mean fluorescence intensity (MFI) of CD4+ and CD8+ blood lymphocytes, including those from a CRISPR/Cas9 engineered mutant of Kdelr1 (U2077). CRISPR WT mice represent nonmutant littermates of U2077. (C) Frequencies and CD44 MFI of CD4+ and CD8+ blood lymphocytes, including those from daniel gray mice with a wild-type Kdelr1 transgene [Tg(Kdelr1)]. P values were calculated by unpaired t test. Each symbol in B and C represents an individual mouse (error bars represent SEM).