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中文
从粉眼稀释区带分析中，使用来自p基因的cDNA探针表明，这个等位基因包含p基因5'端的重排。靠近Her2羧端的960bp内含子缺失，导致预测蛋白中删除了320个氨基酸，包括HECT域。这个p区域突变的整体缺失大约为8.0kb。（来源：J:2206, J:49046）
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 |
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References Literature
Title
PMID
Journal
Year
IF
