This allele was generated at The Jackson Laboratory by electroporating Cas9 protein and 2 guide sequences TAAGCGGCAAAAGATCACAG and CTCCACAGCCTACTTCCTGG, which resulted in a 227 bp deletion beginning at Chromosome 4 position 74,119,755 bp and ending after 74,119,981 bp (GRCm38/mm10). This mutation deletes ENSMUSE00000398544 (exon 4) and 148 bp of flanking intronic sequence including the splice acceptor and donor and is predicted to cause a change of amino acid sequence after residue 98 and early truncation 73 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