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中文
在exon 2的位置替换了一段修饰过的exon 2，其中的AGT被替换成了GCT，导致了第38位氨基酸由丝氨酸(Ser)变为 alanine(Ala)。这个突变预测不会与内源性复制蛋白A发生相互作用。通过Cre介导的重组，去除了位于修改后exon 2上游的floxed Neo抗性基因座。(来源：J:209271)
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
