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)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
129S/SvEvBrd
Targeted
Intragenic deletion
--
1
--
4

Phenotypes

Legend:
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes:
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Phenotypes

References Literature

Title
PMID
Journal
Year
IF
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