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中文
包含Inppl1和Phox2a两个基因C端部分的7.3千碱基基因序列通过单一导向构建的整合被破坏。一个新霉素选择标记被插入，取代了从Inppl1(19-29号外显子)和Phox2a(3号外显子)延伸的序列。(来源：J:96443)
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
