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中文
为了模拟人类遗传性胰腺炎中与之相关的突变(p.K23R)，在第2外显子的第24位，赖氨酸密码子(AAA)被替换为 arginine(AGA)，变异为(c.71A>G, p.K24R)。随后，插入了一个由loxP序列引导的诺卡因抗性基因座，并通过Cre介导的重组手段去除。参考文献：(J:320409)
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
