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中文
这个Vsx2增强子通过sgRNAs( GUUAGACCUAGUCAGAACUC和GCAGGCCAUGUGCUCGUCGA)以及ssODN模板(TGTAATACCTGTAGTGGCCAGAAGAGGGCATCAGATCCCCAGGAGCTGGAGTACCTACATCTTTGGTTGGTGGTTCAGTCTCTGAGAGCCCCAGGGGCCCAGGTTTGTTGACTCTGTTGG)使用CRISPR/Cas9技术被定向编辑，产生了998bp的缺失，位置在chr12:84578818-84579815，参照GRCm39。(来源：J:328714)
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
