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中文
在exon 76中引入了一种突变，将Valine的3598位点替换为Lysine(即p.V3598K)，并在内含子76附近插入了含诺卡因抗性基因座的loxP序列。随后通过Cre介导的重组移除了这个neo cassette。这种CaM结合域的突变显著增强了编码肽与钙调素的结合亲和力。(来源：J:308964)
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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References Literature
Title
PMID
Journal
Year
IF
