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Cabin1基因的exon6被敲除了。通过Flp介导的重组去除了选择标记。随后，Cre介导的重组导致exon6的缺失，通过产生从exon5到exons7-12的frameshift，导致Cabin1基因功能丧失（exon8出现早终止密码子）。(来源：J:101977)
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
