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中文
这个来自项目Rab11fip4-6842J-M9341的等位基因是在Jackson实验室通过注入Cas9 RNA和3个指导序列（CGTCTACAAGTGCGTCTGCA, ATGACATTGGCCCTACCTGA, ACGGGTACTTTCTAGCTCCG）产生的，导致了11号染色体正链位置7,968,0652到7,968,1056的405bp缺失，起始于内含子4的CGTGACTCAGCCACCATGAGAG，终点在内含子5的TTTCTAGCTCCGGGGCCACATGCC之后。这个变异删除了exon 4，预测会导致112号残基后的氨基酸序列变化以及随后的28个早期终止密码子。(J:188991)
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
