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中文
这个来自TCPR1524项目的等位基因是在表观基因组学中心通过电穿孔，用带有CTCTCAAAGGTTCTCCTGCG和TTATTATACCATAGTACAGT这两条特定引物RNA的Cas9核糖核酸复合物生成的。这些引物设计针对关键区域的5'和3'端。这导致了chr14:7629190-57629711位置一个522bp的缺失（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
