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中文
这个等位基因包含一个2.8kb的缺失。缺失区域包含ajIs(17;In2)1Gso等位基因远端断裂点的129bp。在新生儿皮肤中，该转录本以野生型水平存在，但大小减小，与非阿哥尼基因第三外显子缺失一致（J:3523, J:16567）。
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
