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中文
CRISPR对位于chrX:93,309,594-93,311,455(人染色体10)的1862bp缺失区域进行靶向，该区域包含zygotes中Rr41em1Axvi的增强子。这些等位基因在体细胞内是同源的。(来源：J:254531)
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 |
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References Literature
Title
PMID
Journal
Year
IF
