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AGAATCATGTCATTTCTAAG和CACCACAATTTAAGGCACAA产生的，导致了9号染色体53,595,192到53,595,539处一个348bp的缺失。这个变异删除了ENSMUSE00000276320（第3外显子）以及230bp的内含子序列，包括剪接点和起始点，预测会导致第37位氨基酸序列改变以及随后的6个早期终止。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
