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中文
这个等位基因来自TCPR0409项目，由中心性表观基因组学通过向细胞注射Cas9 mRNA和四种带有spacer序列的guide RNA（GGGGAGGTCCTCCGTCATCC、TCAGCACTTCAGGCCAGGTC、GTGAGTTGGGATATTCTTGC和GGCCTGCTGCTCTCCCCGTG）生成。这导致了染色体13的三个变异：8569440位置的缺失-T插入CCTCCTCTGA，一个1140bp的染色体13从8569541到8570680的删除；以及85670687位置的插入-T（GRCm38建库版本）。(来源：J:165963)
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
