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中文
这个等位基因是在表观基因组学中心通过电穿孔，将Cas9核糖核酸复合物与单链引物RNA配对，其中5'端的序列是GAAAAGCAAATACCGCCGGG，3'端的为AAACATTAAACTAGGCGGTC，目标区域是ENSMUSE00000520605。同时，伴随一个单链Bxb1 attB座的短链核酸。这导致了1292bp的chr11染色体从77,465,754到77,467,045（GRCm39）位置的缺失，插入了一个Bxb1 attB序列（GGCTTGTCGACGACGGCGGTCTCCGTCGTCAGGATCATACACCGG）。(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
