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在serine 371位置替换了一个内切终止密码子，随后通过同源重组插入了反向的诺卡因载体，中断了carboxy端激酶域的翻译。 Western和Northern分析证实了全长或较短的Lats2肽缺失，以及较长mRNA的存在。(来源：J:93191)
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 |
|---|
References Literature
Title
PMID
Journal
Year
IF
