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中文
在exon 22和exon 24中插入了由ACA变为GCC导致的906位丝氨酸替换为异亮氨酸(Thr906Ala)以及由ACC变为GCC导致的1007位丝氨酸替换为异亮氨酸(Thr1007Ala)的变异。同时，位于22号和23号外显子之间的loxP引导的诺卡因选择性 cassette通过Cre介导的重组被移除。(来源：J:265906)
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
