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. 2020 Oct 16;216(4):905–930. doi: 10.1534/genetics.120.303596

Table 4. Dating the origin and fixation of diagnostic SNPs in five mouse inbred strains.

Substrain Cohort Year Number of samples Range of alleles sampled Diagnostic allele
Absent Segregating Fixed
C57BL/6J BXD E1 1971 22 11 156 0 0
BXD E2 1996 4 0–4 84 72 0
BXD E3 2001–2009 24 (23) 11.5 50 31 75
CC 2004–2007 483 (72) 4–18 8 30 118
Consensusa 2010–2016 15 (1) 15 0 20 136
DBA/2J BXD E1 1971 22 11 105 7 0
BXD E2 1996 4 0–4 37 62 13
BXD E3 2001–2009 24 (23) 11.5 24 75 13
Consensusa 2010–2016 3 (1) 3 0 0 112
A/J CC 2004–2007 483 (72) 2–22 2 11 47
Consensusa 2010–2016 10 (1) 10 0 5 55
129S1/SvImJ CC 2004–2007 483 (72) 3–42 1 6 81
Consensusa 2010–2016 10 (1) 10 0 4 84
NOD/ShiLtJ CC 2004–2007 483 (72) 4–43 1 2 34
Consensusa 2010–2016 8 (1) 8 0 1 36

This table lists the name of the substrain, the cohorts used for dating the diagnostic SNPs, the approximate year(s) when these cohorts were derived from the main stock, the number of samples genotyped, and the range of alleles sampled. When the number of samples does not match the number of strains, the number of strains is shown in parentheses. Diagnostic alleles are classified as absent, segregating, and fixed for each substrain and cohort, and the table provides the total number in each category.

a

In this analysis, we excluded samples purchased from The Jackson Laboratory (the sample names include the suffix jaxDNA) over a decade ago in the consensus cohorts. Details are provided in the text. CC, Collaborative Cross; BXD, recombinant inbred BXD panel