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中文
这种自发突变是一个从GRCm38染色体17:44240906到17:44247814的6908bp缺失，涉及到了全部的第3外显子以及周边的内含子区域，删除了42个氨基酸但没有改变阅读框(来源：J:276827)
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
