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中文
这个来自TCPR1158项目的等位基因是在表观基因组学中心通过电穿孔，使用了带有TTATAAGGCTTATTGCCATT、CACGGGACAACCACACAAAC和AGGAAGTTAAAGTTACCCGT的单导RNA同源序列，针对一个关键区域进行的生成。这导致了1638bp的chr1:66473206到66473669（GRCm38）位置的缺失。（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
