This allele was generated at The Jackson Laboratory by electroporating Cas9 protein and 2 guide sequences CTAACAAGCCTATTAGCACG and TGAGCCCAAGGAATGACACC, which resulted in a 552 bp deletion beginning at Chromosome 19 position 29,027,034 bp and ending after 29,027,585 bp (GRCm38/mm10). This mutation deletes ENSMUSE00000144943 (exon 3) and 379 bp of flanking intronic sequence including the splice acceptor and donor and is predicted to cause a change of amino acid sequence after residue 91 and early truncation 1 amino acid later. (J:188991)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count