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中文
染色体16包含一个大约10.0兆碱基的重复，这是通过在ES细胞中通过Cre介导的重组，在Hspa13（之前称为Stch）和App基因上通过Mutagenic Insertion and Chromosome Engineering Resource（MICER）提供的靶向载体进行同源重组后，由loxP座引发的。(来源：J:82809)
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
