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This transgene construct consists of the mouse Prnp containing a substitution of a leucine for proline codon at residue 101, corresponding to the Gerstmann-Straussler-Scheinker disease mutation at codon 102 of the human PRNP gene, in the cosSHa.Tet vector. This line overexpresses the transgene about 8-fold. Three lines were generated; 2247, 2866, and 2862. (J:136434)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
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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References Literature
Title
PMID
Journal
Year
IF
