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中文
这个来自项目Ubn1-6239J-105P8MR的等位基因是在Jackson实验室通过向细胞注射Cas9 RNA和指导序列ACGTAGGAAAGACCGAATAC产生的，导致了16号染色体正链位置5,062,557-5,062,563处的7个碱基缺失，具体为ACCGAAT，这个变异预测会在第121位氨基酸后产生氨基酸序列变化，并导致提前终止1个氨基酸(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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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
