Log In|Sign Up
中文
Exon 3通过CRISPR/Cas9技术用sgRNAs针对CTTACTTGAGCCCACAGGCA和ACAGAACCATTTTGTACTAG设计，产生了44bp的缺失。这个变异在同一条ES细胞系中与MGI:6491613(网址链接)的Ythdf1em1Jhha、Ythdf1em3Jhha和Ythdf3em1Jhha基因座一起存在。(来源：J:299108)
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
