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中文
这种突变是在针对Del(13)36H缺失区段进行的ENU诱变筛选中被识别的，该区段覆盖了12.66兆碱基，大约占鼠染色体13（Chr13）的20%，包括A3.1到A4带。被删除的区域与人类6p25和6p22区域有同源性，这些区域与6p缺失综合症和6p相关疾病关联。（来源：J:101156）
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
