Four embryonic phenotypes identified in ENU screen.
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*Number of homozygote mutants observed at weaning from a heterozygote intercross established after outcrossing the G1 founder to C57BL/6J for several generations. Expected 25% for viable phenotype.**Sequencing revealed a nonsense mutation at nucleotide 2997G>T (NM_008881) in the Plxna1gene. Recent data suggest that this mutation is likely to cause the msp4 phenotype [44], however additional complementation testing is required.
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2015-12-02
