Relationships of skeletal size, SNP markers, IGF1 haplotype, and serum levels of the IGF1 protein in PWDs. (A) A mixed-model test for association between size and genotype. The association of three genotype categories (A1A1, A1A2, and A2A2) with skeletal size measurements was calculated with the use of all pairwise coefficients of consanguinity for 376 dogs. Each point represents a single SNP position on canine chromosome 15 and negative log P value for the association statistic. (B) PWD IGF1 haplotypes and mean skeletal size. Haplotypes were inferred for 20 markers spanning the IGF1 gene (chromosome 15: 44,212,792 to 44,278,140, CanFam1). Out of the 720 chromosomes with successful inference, 96% carry one of just two haplotypes, B and I, identical to haplotypes inferred for small and giant dogs, respectively (Fig. 3). Data are graphed as a histogram for each genotype: B/B (closed triangle, black line), B/I (open square, dashed line), and I/I (closed circle, gray line). (C) Serum levels of IGF1 protein (ng/ml) as a function of haplotype. Serum levels of IGF1 protein were assayed in 31 PWDs carrying haplotypes B and I. Box plots show the median (center line in box), first and third quartile (box ends), and maximum and minimum values (whiskers) obtained for each category: homozygous B/B (n = 15), heterozygous B/I (n = 7), and homozygous I/I (n = 9).