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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（TCTTGAATCCACACAAGAAT和GTACTTCAGCTTCATTCAAG）产生的，导致了6号染色体40,449,418-40,449,905一段488bp的缺失，具体位置是GRCm38/mm10基因组。这个变异移除了ENSMUSE00000266539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
