Log In|Sign Up
中文
这个t<9>补体组成员是一个罕见的重组事件导致的结果，发生在一条完整单倍体和一条野生型染色体之间。tw18缺失覆盖了17号染色体大约4300万个碱基对。缺失的3'端位于17号染色体位置236,000,000，而5'端大约在19.19到19.33 Mb的染色体区间内。（参考文献：J:8922, J:10105, J:14421, J:34878, J:244157）
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
