This allele was generated at The Jackson Laboratory by injecting Cas9 RNA and 4 guide sequences TTAGACCCAGATGCAGAACG, TACCCCATAGAGCTCCTCAG, CTGAGCAGCCAGAATCCTGA and AAGCCAATACCCTAGACCAT, which resulted in a 518 bp deletion beginning at Chromosome 9 positive strand position 110,884,771 bp and ending after 110,885,288 bp (GRCm38/mm10). This mutation deletes ENSMUSE00000332740 (exon 4) and 319 bp of flanking intronic sequence including the splice acceptor and donor and is predicted to cause a change of amino acid sequence after residue 35 and early truncation 31 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