Log In|Sign Up
中文
这项CRISPR/Cas9介导的突变在染色体6上有一个25,971bp的缺失，位置从6,141,223bp到6,167,193bp（GRCm38.p4）。这个缺失区域包含潜在的hs1642增强子元件和在exon4中的进化保守区域。（来源：J:254776）
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
