This allele has a spontaneous insertion (duplication) of a C in the CCCCC sequence between chromosome 11 positions 68,988,141-45 (GRCm38), which is in exon 28. This leads to a frameshift and premature stop codon. (J:223062)
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This allele has a spontaneous insertion (duplication) of a C in the CCCCC sequence between chromosome 11 positions 68,988,141-45 (GRCm38), which is in exon 28. This leads to a frameshift and premature stop codon. (J:223062)