Log In|Sign Up
中文
第17外显子被替换为一个经过修改的版本，其中的核苷酸替换导致第744位和第748位的氨基酸由丝氨酸替换为 Alanine(苏氨酸)，即S744A和S748A。下游插入的含neo cassette的克隆通过Cre介导的重组被去除了。(来源：J:166867)
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
