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中文
从17到21号外显子以及22的一部分，编码656到977位氨基酸，包括头部域的末端和杆状域的起始端，被neo替换。通过Southern blot和PCR确认了重组。 Western blot实验中，这些突变体没有检测到蛋白质。(来源：J:91578)
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 |
|---|
References Literature
Title
PMID
Journal
Year
IF
