This allele from project Syt14-8616J-6466M was generated at The Jackson Laboratory by injecting Cas9 RNA and 4 guide sequences GCTCTCCTTGGCAACCACGG, TAAGGTACGAGAAGCTACAA, CTTATTGGATGAGAGGAGAG and TTATGAATTCTACACAGCAT, which resulted in a 544 bp deletion beginning at Chromosome 1 negative strand position 192,933,556 bp, GAGAGTGGAAAGCTAAGGAA, and ending after CAGTGTCTCATCCCTTGTAG at 192,933,013 bp (GRCm38/mm10). This mutation deletes exon 5 and 272 bp of flanking intronic sequence including the splice acceptor and donor and is predicted to cause a change of amino acid sequence after residue 148 and early truncation 11 amino acids later. (J:188991)
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cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count