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中文
在exon1的5'端插入了loxP位点，然后在exon1的3'末端插入了loxP和FRT标记的neo cassette。通过Cre介导的重组，neo cassette和exon1的N端区域被去除。 Western blot结果显示RUNX3(P1)蛋白，其有19个独特的N端氨基酸，没有表达。来源：(J:319454)
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
