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中文
L1L2_gt2 cassette被插入到染色体1的179,250,641位点，位于关键exon2(使用GRCm39构建)的上游。该 cassette包含FRT引导的lacZ/诺卡因序列，后面跟着一个loxP位点。在exon2下游，再插入一个loxP位点，位置是179,251,462。关键exons被loxP位点前后环绕。通过在携带该等位基因的 mice中表达flp和cre重组酶，产生了一个无lacZ序列、neo选择性 cassette以及loxP引导的exon2的缺失/敲除等位基因。(来源：J:240508)
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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References Literature
Title
PMID
Journal
Year
IF
