Log In|Sign Up
中文
这个来自项目Ddx59-6150J-MP92R的等位基因是在Jackson实验室通过注入Cas9 RNA和指导序列GCAGCAAGTGCTTGACGTTT产生的，导致了1号染色体正链位置136,432,352bp处的8个碱基删除，即TTGACGTT，发生在exon 5。这个变异预计会导致第368位氨基酸之后的序列改变，并且早期有5个氨基酸的缺失。(J:188991)
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
