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. 2018 Mar 5;16(2):154–164. doi: 10.1038/cmi.2017.160

Figure 3.

Figure 3

Missense mutations of Siglece coding region in B6.NZM Sle1/Sle2/Sle3 mice. (a) Sequencing reads were aligned using CLC Main Workbench. Arrows indicate SNP annotations. (b) Sequence alignment of Siglec E from C57BL/6 (WT) and B6.NZM Sle1/Sle2/Sle3 (Sle1–3) mice. Red indicates amino-acid substitutions. (c) Graphical representation of the Siglec E protein, which consists of a leader sequence (LS), a V-set Ig-like domain, C2-set Ig-like-1 and C2-set Ig-like-2 domains, a transmembrane domain (TM) and a cytoplasmic domain. Two amino-acid substitutions were in the V-set Ig-like domain, at positions 24 and 102, and one amino-acid substitution was in the C2-set Ig-like-1 domain at position 227. Siglec, sialic acid-binding immunoglobulin-like lectin; SNP, single-nucleotide polymorphism; WT, wild type.