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Tg(APPSwLon)96Btla
Transgene Detail

Nomenclature
Symbol: Tg(APPSwLon)96Btla
Name: transgene insertion 96, Bruce Lamb
MGI ID: MGI:3693359
Synonyms: APPK670N/M671L and APPV717Im, J1.96, K670N/M671L + V717I
Transgene: Tg(APPSwLon)96Btla   Location: unknown    
Transgene
origin
Germline Transmission: Earliest citation of germline transmission: J:42613
Parent Cell Line: J1 (ES Cell)
Strain of Origin: 129S4/SvJae
Transgene
description
Transgene Type: Transgenic (random, expressed)
Mutation: Insertion
  A 650 kb YAC transgene containing the entire human amyloid beta (A4) precursor protein gene and approximately 250 kb of flanking sequence was altered to include the Familial Alzheimer's Disease- (FAD-) associated "Swedish" double mutation, APPK670N/M671L, and the "London" mutation, APPV717I. RT-PCR analysis shows hemizygous mice express the mutant human and endogenous mouse APP mRNA at similar levels in brain and peripheral tissues; levels of the most common alternative splice variants (encoding human APP-695, -751 and -770) parallel those of the endogenous mouse transcripts. Levels of total amyloid-beta and of longer amyloid-beta peptides (species terminating at amino acids 42/43) are higher than in wildtype mice, but not as high as in a similar strain carrying only the APPK670N/M671L "Swedish" mutant transgene. (J:42613)
Find Mice (IMSR) Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation: Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Phenotype
summary
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Phenotype Summary by Mammalian Phenotype terms

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Genotypes are listed in the next section.

      Key:  
hm homozygous ht heterozygous
cn conditional genotype  cx complex: > 1 genome feature
tg involves transgenes ot other: hemizygous, indeterminate,...
N normal phenotype expected model not found
Affected SystemsGenotypes:
 
tg1
 
tg2
 
tg3
  
nervous system          
  
other phenotype          
 
  
Disease Models          
  
Phenotypic
data by
genotype
Phenotypic Data by Genotype

(show or hide all phenotypic details)

GenotypeAllelic CompositionGenetic Background
  
 tg1   
Tg(APPSwLon)96Btla/Tg(APPSwLon)96Btla involves: 129S4/SvJae
  
 tg2   Disease Model  
Tg(APPSwLon)96Btla/0 involves: 129S4/SvJae
  
 tg3   
Tg(APPSwLon)96Btla/0
Tg(PSEN1H163R)G9Btla/0
involves: 129S4/SvJae
Disease
models
Mouse Models
of Human Disease
NoteGenotypeRef(s)
 
Allelic Composition
Genetic Background
Models involving transgenes or other mutation types.1
Alzheimer Disease; AD
OMIM ID: 104300
 
 
tg2
Tg(APPSwLon)96Btla/0involves: 129S4/SvJaeJ:42613
1Models involving transgenes or other mutation types may also appear in other sections of the table.
Notes The transgene construct was injected into embryonic stem (ES) cells.
References
Original: J:42613 Lamb BT et al., "Altered metabolism of familial Alzheimer's disease-linked amyloid precursor protein variants in yeast artificial chromosome transgenic mice." Hum Mol Genet 1997 Sep;6(9):1535-41
All: 2 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/20/2009
MGI_4.31
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