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Pronuclear-stage embryos were targeted with a zinc finger nuclease pair designed to target exon 3. A founder mouse was identified carrying a 19-bp deletion at the targeted site (CTCGGGatggcactgggtacactggCTGGGCAG -> CTCGGGCTGGGCAG), which causes a reading frame shift resulting in a premature stop codon. Absence of the protein in brain, heart and liver of homozygous mutant mice was confirmed by immunoblot analysis. (J:249809)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
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 |
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References Literature
Title
PMID
Journal
Year
IF
