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中文
这个来自TCPR1460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特定 Spacer 序列（5'侧为GTTTAAGGGCATTCTCACCC，3'侧为GTTGATAGACTGGGCAAGAC）的单链RNA引导物一起制备的。这导致了一个1290bp的染色体3上的缺失，位置在GRCm38的357,890,82-357,903,71。 (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
