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中文
在通过和Tg(ACTB-cre)13Miya小鼠杂交，随后通过Cre介导的删除，Exon 21被移除了，这产生了一个框架错位的缺失。蛋白产物的缺失通过在肺、胸腺、大脑、脾和胰腺的蛋白质提取物中进行 Western blot 来验证。(来源：J:126164)
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
