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中文
这个来自项目Arhgap11a-8693J-5061M的等位基因是在Jackson实验室通过注入Cas9 RNA和3个引导序列(ATGGAGAGAATATCTCAAAC, GAATGCGCTAGAGTATCTGA, ATTAGGCAAATAAAGATCTT)产生的，导致了从染色体2正链位置113,845,222bp的TGAGATATTCTCTCCATTTT开始，到113,845,543bp后AGATTAAAACACTGCCTTCA的322bp缺失。这个变异删除了exon 2(ENSMUSE00001066810)以及251bp的上下游内含子序列，包括剪接点的接受者和捐赠者，预测会导致43号残基后的氨基酸序列改变以及随后的3个氨基酸的早期截断。(来源：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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References Literature
Title
PMID
Journal
Year
IF
