Log In|Sign Up
中文
CRISPR修饰导致了5个碱基的删除(5bp deletion, c.77_81delCGGTA)和1个碱基的插入(1bp insertion, insG; T26fsXfsX31)。这个变异位置参考文献为(J:279596)。
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
