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GGATTTCGACAGTTTTGTGG和GCGTTTTGTACGATAGTGGA产生的，导致了5个碱基对（611bp）的删除，起始于染色体5的位置115,237,751，结束于115,238,361。这个变异删除了基因ENSMUSE00000519136（第2和3外显子）以及222bp的内含子序列，包括剪接接受体、捐赠点和起始位点，预测会生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
