这项研究通过CRISPR/Cas9技术对基因进行了靶向。使用了四条sgRNA,两条针对基因编码区域上游,两条针对下游,再加上Cas9 mRNA,注射到了(B6 x D2)F1的卵母细胞的核中。十个候选小鼠品系中,选用了线5进行后续实验。这些小鼠的等位基因在基因上有一个912bp的缺失。(来源:J:274740)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
(C57BL/6J x DBA/2J)F1
Endonuclease-mediated
基因内删除
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1
1
1

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

References Literature

Title
PMID
Journal
Year
IF
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