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中文
这个等位基因来自TCPR0420项目，由位于表观基因组学中心的实验产生，通过向细胞注入Cas9 mRNA和四种引导RNA（含spacer序列ATAATTCCGTCTCACCTATG、ATTCCCTCCAGAGCTGACCT、CTAAATAGATGGATAAGCTC和CGCATGGCGGCCTCGCAGAA）来实现。这导致了16号染色体（Chr19）上一个601bp的缺失，起始位置在38,069,489，结束于38,070,089（GRCm38参考构建）。(来源：J:237616)
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
