Multiple copies of a transgenic construct, consisting of the Roux Sarcoma Virus promoter adjoined to the entire coding region of the human placental alkaline phosphatase gene, inserted in tandem array in the middle of chromosome 5. Phenotypic characteristics segregated with transgene and were not observed in a different line with similar levels of expression, indicating the phenotype was largely due to the site of insertion. A non-complementation test demonstrated that the insertional mutation is allelic to pirouette. Further molecular analysis showed that the insertion is located in intron 1, 32 kb upstream of exon 2. (J:86585, J:93174, J:156811)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
(C57BL/6J x CBA/Ca)F2
--
Insertion
Recessive
1
3
4

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

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PMID
Journal
Year
IF
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