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中文
这个来自TCPR1135项目的等位基因是在表型遗传学中心通过电穿孔，使用了带有AGTTTGGAACTGATTGTATA和GAGTCATACTAAATCAAAGC这两条单链RNA指导的Cas9核糖核酸蛋白复合物，目标是关键外显子的5'端和3'端。这导致了一个712bp的染色体3上的缺失，位置在chr3:24432799到24433510（GRCm38建库编号：J:265051）。
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
