This allele was generated at The Jackson Laboratory by electroporating Cas9 protein and 2 guide sequences CTAGCCTGGGAACAAGTGAG and ACTCTCCATGCTTTACTGCT, which resulted in a 3865 bp deletion beginning at Chromosome 8 position 83,434,286 bp and ending after 83,438,150 bp (GRCm38/mm10). This mutation deletes ENSMUSE00001247660 through ENSMUSE00001393187 (exons 2-4) and 2163 bp of flanking intronic sequence including the splice acceptor and donor and is predicted to cause a change of amino acid sequence after residue 26 and early truncation 16 amino acids later. (J:188991)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count