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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GCCTACAGTTGTGAGATTTG和AATATGGAAAAGTTTTTGAG产生，导致了1775bp的缺失，起点在13号染色体67,592,123bp，终点在67,593,897bp（GRCm38/mm10建库）。这个变异删除了ENSMUSE00000465644（第4外显子）的1775bp，预测会导致第82位氨基酸序列改变以及随后的6个早期终止密码子。（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：
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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
