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中文
通过比较来自纯合突变体的1.3kb接头片段序列与公共基因组序列，发现这个等位基因包含一个216kb的缺失，从内含子1延伸至polyadenylation序列下游148kb，移除了Tbx15基因除第一个外的所有外显子。
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：
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| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
