基因组DNA的Southern分析表明,这个等位基因并未包含Thp和TOrl等缺失相邻区域(D17Leh119II和D17RP17)的缺失,这些缺失在其他等位基因中被发现。从开放阅读框测序的基因组DNA中,我们检测到一个19个碱基的缺失,序列是GCACACGGTCTCAGCTGCC,预测会导致一个在羧基端被截短的蛋白质。(来源:J:85398)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
(C3H/HeH x 101/H)F1
Radiation induced
基因内删除
半显性
1
3
13

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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