Log In|Sign Up
中文
这个转基因构建包含一段完整的人类 dystrophin 基因，通过删除 H2 区域，并去除从 spectrin-like repeat 4 到 repeat 19 和 C-末端的序列，生成了微小的 dystrophin cDNA（DH2-R19）。它在人类骨骼肌 alpha 1 actin（ACTA1）启动子的调控下运作（来源：J:146281）。
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
