The transgene encodes a soluble, dimerizing fusion protein comprising the normal mouse prion protein, without the carboxyl terminal GPI attachment signal, joined to the Fc region of the human immunoglobulin heavy chain gamma 1 constant region (Fcgamma). The construct includes ~6 kb of 5' flanking sequence, exon 1, intron 1 and a fused exon 2/3 from the mouse prion protein gene (Prnp). The Fcgamma coding sequence is modified to eliminate the binding sites for the Fcgamma receptor and complement. A loxP-flanked translation termination (STOP) cassette has been inserted upstream of the open reading frame, blocking expression of the fusion protein until the cassette is excised by Cre recombinase. (J:82734)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
Related Disease
Reference
B6;129S7-Prnptm1Cwe
--
Insertion
--
1
--
1

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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