对突变小鼠的基因组DNA序列分析显示,存在一个7.1kb的LINE 1序列,其两端各被整合位点内编码Reln蛋白第八个EGF样motif的内含子直接重复序列所包覆。核苷酸序列分析表明,LINE插入导致该内含子在转录时被跳过,从而在Reln mRNA中产生一个220bp的缺失。(来源:J:34099)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
BALB/c
Spontaneous
转座子插入
隐性
1
10
24

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

References Literature

Title
PMID
Journal
Year
IF
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