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中文
限制长度多态性和简单序列变异被用来确定这个等位基因包含的缺失片段的边界。缺失的近端 breakpoints位于D17Leh66EI和D17Leh66EII之间，而远端的则靠近D17Mit122，但不包括D17Leh66D。Qk基因位于这个缺失内。(来源：J:62654)
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：
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| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
