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中文
这种表型突变是在针对Del(13)39H缺失区段进行的ENU诱变筛选中发现的，该区段大约占据了小鼠染色体13的20%。这个区域与人类染色体6p22.1-6p22.3/6p25有同源的保守序列一致性。(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：
Show/Hide columns
| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
