Log In|Sign Up
中文
通过sgRNA和ssODN模板，利用CRISPR/Cas9技术，Serine的第68位(AGC)被替换为Alanine(替换为GCT)，这个变异(记为p.S68A)阻止了该高度保守的残基被MAPK通常磷酸化(来源：J:327336)。
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
