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中文
Exon 21被替换为一个修改过的Exon 21，其中的核苷酸变异导致了在位置1060的丝氨酸被天冬氨酸(苏氨酸)替换，即C1060S。通过Cre介导的重组，去除了随修改后的Exon 21一起插入的floxed neo cassette。(来源：J:191998)
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
