This allele was generated at The Jackson Laboratory by electroporating Cas9 protein and 2 guide sequences CAGAGAGGGGCACAACAGTG and CACTTGGTGCCAGAGCCACA, which resulted in a 438 bp deletion beginning at Chromosome 10 position 81,490,901 bp and ending after 81,491,338 bp (GRCm38/mm10). This mutation deletes ENSMUSE00000102265 (exon 6) and 334 bp of flanking intronic sequence including the splice acceptor and donor and is predicted to cause a change of amino acid sequence after residue 232 and early truncation 22 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