Log In|Sign Up
中文
在exon 10的位置替换了一段经过修改的exon 10，其中由G替换为C的核苷酸变异导致了第572位氨基酸从赖氨酸变为亮氨酸（V572L）。通过Cre介导的重组，去除了位于修改后exon 10下游的floxed neo cassette（来源：J:184315）。
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：
Show/Hide columns
| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
