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中文
Exon 2被替换为一个修改过的Exon 2，其中包含由TCT GGA替换为GCC GGC的核苷酸变异，导致第212位氨基酸由丝氨酸（Serine, S212）替换为 alanine（Ala）。通过Cre介导的重组，删除了位于Exon 2下游的floxed Neo抗药性 cassette。(来源：J:204196)
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
