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Exon 23被替换为一个含有A>C突变的版本，这个突变将丝氨酸密码子933替换为异亮氨酸密码子(等同于p.D993A)。随后，通过Cre介导的重组，随附在内含子22的诺卡因抗性基因座被移除。(来源：J:249307)
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
