Exon 3 was flanked with loxP sites to allow disruption of the zinc-binding site and deletion of the conserved "Met-turn." Cre mediated recombination of the flanking loxP sites resulted in the deletion of exon 3 from Adamts5tm1Eam. RT-PCR confirmed absence of exon 3 in mutant spleen and cartilage transcripts. A protein product from the transcript was not found in mutant cartilage. (J:97590)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count