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中文
Exons 14和15，它们共同编码IIS5跨膜段和重复II中的孔，周围有loxP位点，随后在体外通过Cre介导的重组被剔除，然后传给下一代。尽管RT-PCR检测到13号外显子插入到16号内含子中的异常转录，但 Western blot分析在同卵突变胚胎的心脏中并未发现相应蛋白。(来源：J:66242)
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
