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中文
在exon 7中产生了一个突变，导致第629位的精氨酸被天冬氨酸替换（N629D）。同时，一个由floxed polII驱动的诺卡因筛选 cassette被插入到了intron 7。为了去除诺卡因选择性标记，这些小鼠与Meox2小鼠进行了杂交。（来源：J:155273）
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
