Log In|Sign Up
中文
在c.1086位置插入了胸腺嘧啶，这个发生在exon 5，同时在intron 4插入了一个FRT标记的PGK-neomycin选择座。这个变异等同于人类家族性心律失常中观察到的c.1212InsT变异。随后，通过flp介导的重组移除了neomycin座。来源：(J:339263)
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
