This allele was generated at The Jackson Laboratory by electroporating Cas9 protein and 2 guide sequences ACGTGAACGGAGAGAACACA and GTGTTTTGCAGAAAGTACCG, which resulted in a 3917 bp deletion beginning at Chromosome 11 position 113,699,772 bp and ending after 113,703,688 bp (GRCm38/mm10). This mutation deletes ENSMUSE00000108704-ENSMUSE00001266028 (exons 4-6) and 3577 bp of flanking intronic sequence including the splice acceptor and donor and is predicted to cause a change of amino acid sequence after residue 51 and early truncation 17 amino acids later. In addition, there is a 2 bp (TC) insertion at the deletion site. (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