这项在ENU诱变筛选中发现的突变被证明是p基因的等位基因,因为其未能补足原粉色眼稀释性状的 coat color 表现。
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This mutation, identified in an ENU mutagenesis screen, was shown to be an allele of p by its failure to complement the coat color phenotype of the original pink-eyed dilution allele.