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（GGAGATGGCGTCCTACTGAG和GCAGTCACCCTATTATAGAT）产生的，导致了从7号染色体43,674,889bp起始，至43,678,494bp之后的3606bp区域的缺失。这个变异删除了基因ENSMUSE00000279483（第2和3外显子）以及1191bp的内含子序列，包括起始点、剪接接受体和捐赠位点，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
