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The Vsx2 CTCF-binding site, located in intron 3, was targeted with sgRNAs (targeting GAGTCTCTAAAAGTAGGAAA and ACCTAATCAAGCAATCAAGT) using CRISPR/Cas9 technology, resulting in a 485 bp deletion (chr12:84636509-84636993 (GRCm39)). (J:333875)
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
