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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GGTCATGCGGTCTATGGATA和CGCACCTCAAGTCACACCTG产生的，导致了10号染色体80,576,763到80,577,206bp位置的444bp缺失。这个变异删除了ENSMUSE00000307925(第1外显子)上的444bp，包括Kozak序列和起始的ATG，剩下16bp的第1外显子和剪接供体。参考文献：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：
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References Literature
Title
PMID
Journal
Year
IF
