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在chr7大约1.2MB的区域，从chrna7到fan1，包括这两个基因（chrna7和fan1）的编码区域，以及mtmr10, trpm1, klf13和otud7a，通过flp介导的重组，chrna7tm1mima和fan1tm1mima产生了这个缺失。这个区域内的基因表达在杂合子小鼠的脑组织中有所降低。(来源：J:227984)
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
