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中文
这个等位基因是通过 shotgun CRISPR/Cas9编辑通过设计针对Pcdhg基因簇每个可变exon的pool sgRNAs产生的，检测到它存在插入或替换，导致了可变exon A7的框架错位或其他变异，以及在可变exon A3的内切突变，还有影响B1到A6的结构重组。(来源：J:285314)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
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 |
|---|
References Literature
Title
PMID
Journal
Year
IF
