Log In|Sign Up
中文
通过体内Cre介导的重组，从Slit1tm1Matl中去除了含有的floxed neo cassette，使得内源性位点被一个包含内质网KDEL保留序列、终止密码子和IRES-tauGFP融合蛋白的 cassette打断。初始插入替换了第二段富含亮氨酸的重复序列的部分编码。使用3'反义探针对E11.5同卵突变胚胎的中脑背根神经节进行的原位杂交未检测到mRNA。(引用：J:73904)
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
