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中文
在exon 11的第343位丝氨酸(serine, Ser)被替换为阿尔法-Alanine(替换为p.S343A)，并且在exon 13的3' UTR区域插入了一个由loxP序列标记的诺卡因抗性基因元件(cassette)。随后通过Cre介导的重组，这个诺卡因元件被去除了。这种改变产生了无活性激酶的产物。(来源：J:154054)
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
