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这个插入到定位点的靶向构建包含了CAG启动子、可删除的诺卡因抗性以及终止子，以及在第12外显子956到959位置带有TCTG重复的人类cDNA（GenBank accession号NM_002520）。这个突变是NPM1基因中急性髓系白血病（AML）患者中最常见的变异（J:196690）。
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 |
|---|
References Literature
Title
PMID
Journal
Year
IF
