Log In|Sign Up
中文
染色体工程在GRCm38的17号染色体上产生了从36,283,667bp到26,815,764bp，长度为532,098bp的缺失，这个变异通过构建了两个独立的融合体得到，Line A被赋予了这个缺失的符号表示，而Line C则标记为Del(17)5Mom(来源：J:207447)。
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
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
