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在exon 8的位置，替换为经过修改的一个，其中由T到G的点突变导致了第341位氨基酸由valine替换为phenylalanine，即F341V。通过cre介导的重组，去除了上游插入的含neo抗性基因的克隆。(来源：J:226418)
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
