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中文
来自项目Zfp329-7039J-F1199的这个等位基因是在Jackson实验室通过向细胞注射Cas9 RNA和两个引导序列(AGTTGAGTGGCTTCCATGGA和CAAGAGATTTTATAAAGGTA)产生的，导致7号染色体负链位置12,811,259bp的13bp缺失，从'ATGGAAGCCACTC'开始，直到12,811,246bp的exon 2之后。这个变异预计会导致112个氨基酸之后的氨基酸序列变化，并在接下来的两个位置发生早期截断。(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
