|Application:||aCGH data analysis, SNP array data analysis|
|Number of samples:||12|
|Release date:||Feb 12 2013|
|Last update date:||May 14 2013|
|Dataset link||To map a potential locus corresponding to the CD23low phenotype|
To map a potential mutation, male LxT1 mice were crossed to female BALB/c mice to generate F1 mice. Two females from the F1 litters were backcrossed to the parental male LxT1 to generate N2 mice for analysis of phenotype and genetic mapping. N2 mice with (n=6) and without (n=5) CD23low surface level and (n=1) BALB/c were used to map putative genetic alteration that may cause the CD23low phenotype.
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