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中文
选择座、LoxP位点以及HPRT的5'端被插入。这个特定的等位基因仅在10号染色体上与Prmt2tm1Yah这一突变体同源存在。构建这个等位基因是为了实现对10号染色体上Del(10Prmt2-Cstb)4Yah的目标缺失突变。(引用信息：J:167505, J:181132)
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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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
