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中文
这个等位基因是在Jackson实验室通过电穿孔Cas9蛋白和两个引导序列（CGAGAACCTTTTCTAAATCT, GTCTCTCTGAAACACACCGA）产生的，导致了5号染色体（Chr5）100,480,147-100,480,565一段419bp的缺失，具体位置是GRCm38/mm10基因组。这个变异移除了ENSMUSE00001057239的外显子。（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
