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中文
这种多位点缺失是由雄性小鼠接受X射线照射后诱导的，它包含了7D3-7E3的G带区域，附近包含Fah（苯甲醛酸乙酰化水解酶）和更远端是Aqp11（之前称为sjds的水通道蛋白11）。缺失的两侧，靠近端是Mesdc2，一个mesoderm发育候选2基因，远端则是Hbb，即β型血红蛋白复合体。（来源：J:54592, J:100221）
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 |
|---|
References Literature
Title
PMID
Journal
Year
IF
