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中文
这个t<9>补体组成员是一个罕见的重组事件，发生在一套完整单体型和一个野生型染色体之间，通过微剪和微克隆技术获得的DNA探针显示，它包含D17Leh54,94,180和443的缺失，以及D17Leh89,467和525的重复。这个特定的等位基因属于t<9>补体组，并非在野生种群中发现。(来源：J:8922)
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 |
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References Literature
Title
PMID
Journal
Year
IF
