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中文
将编码人类KCNIP3（DREAM）的cDNA，其中在EFhand2、3和4位点有两处氨基酸替换（EFmDREAM），插入到牛甲状腺素基因的启动子下游，以在甲状腺中驱动表达。这些氨基酸改变使得突变体对钙离子失去敏感性。（来源：J:148712）
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
