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. Author manuscript; available in PMC: 2016 Jul 21.
Published in final edited form as: Calcif Tissue Int. 2012 Dec 22;92(4):362–371. doi: 10.1007/s00223-012-9687-1

Figure 1.

Figure 1

The regions of CAST Chr 1 transferred onto a B6 background for the three congenic sublines used to locate the BMD1-4 locus. The genotyping data for every marker are represented with “B” referring to homozygous b6/b6, “C” referring to cast/cast. We only presented some of the polymorphic markers used for genotyping. The names of the congenic sublines of mice are on the left. We used a letter “C” followed by the proximal and distal limits of CAST alleles carried by the congenic sublines in megabases (NCBI built 36). C180-184 did not show any difference in vBMD between congenic and B6 control mice [25]. C175-185 and C178-185 showed high vBMD in females but not males [24]. Subcongenic C180-184 and C178-185 lines of mice that have been previously generated [25, 24] are used here only to delimit the BMD1-4 QTL region, while C175-185 was used for all experiments in the study.