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这项删除，大约占据了长臂(MSYq)中大部分(约9/10)的雄性特异性区域，发生在携带11kb Srydl1Rob短臂缺失的鼠中，这个缺失移除了Sry基因。长臂上的删除区域包含了Ssty基因家族的大部分或所有拷贝。短臂上的Rbmy基因家族和同源异型区段保持完好。(来源：J:89616)
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
