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中文
(条件等位基因)(Dchs2)最初通过在Dchs2编码区域的最后一个外显子周围插入loxP位点实现，该区域包括其跨膜和细胞内部分。通过与一种能激活germline的删除-Cre小鼠品系[Tg(CMV-cre)1Cgn]杂交，产生了携带这种遗传性缺失(Dchs2)的实验鼠。(来源：J:226938)
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 |
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References Literature
Title
PMID
Journal
Year
IF
