This allele was generated at The Jackson Laboratory by electroporating Cas9 protein and 2 guide sequences GCTGCTTTGTGGTTTTATAT and AAACACTTAGTGGAACACAA, which resulted in a 216 bp deletion beginning at Chromosome 2 position 5,886,393 bp and ending after 5,886,608 bp (GRCm38/mm10). This mutation deletes ENSMUSE00000570184 (exon 4) and 137 bp of flanking intronic sequence including the splice acceptor and donor and is predicted to cause a change of amino acid sequence after residue 47 and early truncation 2 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