This allele was generated at The Jackson Laboratory by electroporating Cas9 protein and 2 guide sequences CTGGCTTTCTAGGGACAAAA and GGAGTTTCGATGATGCAGAA, which resulted in a 142 bp deletion beginning at Chromosome 17 position 65,717,444 bp and ending after 65,717,585 bp (GRCm38/mm10). This mutation deletes ENSMUSE00000657070 (exon 3) and 60 bp of flanking intronic sequence including the splice acceptor and donor and is predicted to cause a change of amino acid sequence after residue 40 and early truncation 29 amino acids later. There is a 5 bp insertion (TAAAG) 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