Log In|Sign Up
中文
这个突变是在Jackson实验室通过电穿孔Cas9蛋白和指导序列GCTTCTGATCCACTGGGGCA、CGTAAGGTGAATGATCCAAA产生，导致了从染色体4的21,686,361bp位置开始，到21,687,063bp后的一个703bp的删除。这个变异删除了ENSMUSE00000563941（第3外显子）以及482bp的内含子序列，包括剪接点的接受者和捐赠者，预测会导致在第66个氨基酸后发生早期截断。（来源：J:188991）
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：
Show/Hide columns
| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
