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(AGAGGAAGAAATCATAATGC, ATTGATTTCCTACATCACGG)产生的，导致了19号染色体26,646,911到26,647,177bp位置的267bp缺失。这个变异删除了ENSMUSE00000146234(第6外显子)以及140bp的内含子序列，包括剪接点的接受者和捐赠者，预测会导致第359位氨基酸之后序列改变，并且有一个早期的1个氨基酸的截断。(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
