This allele is defined by a noncomplementation test with C57BL/6JHamSlc-Lystbg. This mutation is the result of a 4 bp deletion in Lyst exon 29 that produced frameshift mutations resulting in 3 amino-acid substitutions and creation of 6 new stop codons. The sequence data was deposited in DDBJ under Accession number LC508235. (J:281218)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count