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中文
来自项目Zfyve26-5939J-1816的这个等位基因是在Jackson实验室通过向细胞注射Cas9 RNA和引导序列GGAGGACATACTACAGGCGC产生的，导致11个碱基对（ATACTACAGGC）的缺失，位置在12号染色体负链79,295,514bp（GRCm38）。这个变异预测会导致第52位氨基酸之后的序列改变，以及一个在第57个氨基酸后的早期截断。(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
