对这种等位基因纯合小鼠的序列分析显示,在起始密码子后363bp的位置,第四外显子的剪接供体位点插入了8个碱基的TTAACTTG,预测会导致框架移位和蛋白质部分缺失。(来源:J:37172)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
(102/El x C3H/El)F1
Chemically and radiation induced
插入
半显性
1
8
1

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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