This allele was generated at The Jackson Laboratory by electroporating Cas9 protein and 2 guide sequences CGAGTACCCAGACATCCACG and ACGCTTGCATGGGAGAGCCG, which resulted in a 255 bp deletion beginning at Chromosome 8 position 25,177,885 bp and ending after 25,178,139 bp (GRCm38/mm10). This mutation deletes ENSMUSE00000637671 (exon 2) and 194 bp of flanking intronic sequence including the splice acceptor and donor and is predicted to cause a change of amino acid sequence after residue 55 and early truncation 4 amino acids later. There is a 3 bp insertion (TTA) 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