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中文
在Pofut1tm2Pst中，通过同源重组和体外Cre介导的剪切后，保留了一个loxP位点，替代了exon 2。据推测，exon 2的缺失可能导致exon 3的终止密码突变。在同卵双胞胎胚胎中，通过全基因组印迹检测未检测到转录本。(来源：J:83299)
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
