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中文
这种小鼠的表型归因于一个7厘米的染色体易位突变，标记为Del(19)TgN8052Mm，它包含了Pax2和Pkd2l1基因。这个转基因插入了19号染色体远端的LINE元件。Del(19)TgN8052Mm小鼠还缺失了Scd1和pale ear Hps1基因，以及多个D19Mit标记（来源：J:20807, J:50327, J:54055）。
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
