这个靶向构建插入了lox2272位点的第12个内含子,包含导致第495位氨基酸由asp替换为lys的突变核苷酸序列(E495K)。它包含了loxP位点、lox2272位点以及一个由FRT引导的诺卡因抗性基因座。通过Flp酶介导的重组移除了选择性基因座,而Cre介导的重组则恢复了修改后的第12个外显子。来源:(J:309176)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6J
Targeted
插入
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1
4
1

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

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PMID
Journal
Year
IF
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