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中文
一个人类的血红蛋白基因转基因引起了这个插入突变，研究表明它与Hmga2等位，并且确定包含一个包括高移动性组蛋白I，C型（Hmga2）基因的缺失区域。（来源：J:28571, J:74548）
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
