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中文
这项T(4;11)(Mllt3;9Mll)1Thr的基因重排被设计用来模拟人类的T(9;11)(p22;q23)染色体易位，这种易位是引发白血病关联的。通过同染色体Cre介导的重组，单个loxP位点在Mlltm1Thr和Mllt3tm2Thr基因内产生了这一重排。在突变小鼠的多种组织中，通过RT-PCR分析，我们检测到了包含Mll第8个外显子和Mllt3第b个外显子的融合转录本。(来源：J:68500)
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
