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中文
他来自TCPR0921项目的一个等位基因是在phenogenomics中心通过电穿孔，使用了带有ATACCATCCTACACCAGACT和AGGAATGGATCAATCCACGC这两条3'侧导向的单链RNA指导的Cas9核糖核酸蛋白复合物，目标区域是5'端，以及TGATTCAACTTTAAAGACGG和GGAGAACAAGTCAGTGACGA这两条5'侧导向的，产生了一个841bp的缺失，位置在chr1:52640700到52641540（GRCm38）。(引用信息：J:237616)
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
