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中文
这个突变是在Jackson实验室通过电穿孔Cas9蛋白和两个引导序列GAGAGACTAAAATAGTTCAG和GTTCACACGCTATAGGGCAG产生的，导致17号染色体3,162,731bp至3,163,187bp位置的457bp区域缺失。这个变异删除了ENSMUSE00000345755（第5外显子）以及303bp的内含子序列，包括剪接点的接受者和供体，预测会导致第107位氨基酸序列改变以及随后的3个氨基酸早期截断。缺失位置有4bp的插入（CTTC）。(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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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
