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中文
CRISPR/Cas9介导的重组去除了LRR9域的21个氨基酸残基，但保留了基因的开放阅读框。 Western blot结果显示，该基因的整体表达没有改变。免疫沉淀分析证实了这种突变导致对Nlgn2的结合被干扰。(来源：256117)
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
