Log In|Sign Up
中文
这个突变是在Jackson实验室通过电穿孔Cas9蛋白和两个引导序列(CATGCGCAGACTTTCCTCAA和TGATTGCAAAGTTTTATGAT)产生的，导致了8号染色体66,511,711到66,513,975bp位置的2265bp缺失。这个变异删除了ENSMUSE00000151364(第1外显子)以及244bp的上下游内含子序列，包括起始点、剪接接受点和捐赠点，预测会形成一个无功能的等位基因。(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
