This allele was generated at The Jackson Laboratory by electroporating Cas9 protein and 2 guide sequences AAAACCTTACAGCTTCAAGG and TTCAGGGCAGAGATTCCCCG, which resulted in a 458 bp deletion beginning at Chromosome 5 position 123,040,862 bp and ending after 123,041,319 bp (GRCm38/mm10). This mutation deletes ENSMUSE00000649828 (exon 2) and 300 bp of flanking intronic sequence including the splice acceptor and donor and is predicted to cause a change of amino acid sequence after residue 49 and early truncation 14 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