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中文
这个来自TCPR1478项目的等位基因是在表观基因组学中心通过电穿孔，将Cas9核糖核酸蛋白复合物与具有GCTTAGTGACTGATCGCAGT作为5'端引导RNA和CAAAACAACTACGGAGTTAG作为3'端引导RNA的单链RNA，针对一个关键区域的靶标生成的。这导致了chr12:51388915-51390535位置的1621bp缺失（GRCm38建库）。(来源：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
