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Tg(PDGFB-APPSwInd)20Lms
Transgene Detail

Nomenclature
Symbol: Tg(PDGFB-APPSwInd)20Lms
Name: transgene insertion 20, Lennart Mucke
MGI ID: MGI:3057148
Synonyms: APP Tg, J20, PDGF-APPSwInd, PDGF-hAPP695,751,770V171F, KM670/671NL
Transgene: Tg(PDGFB-APPSwInd)20Lms   Location: unknown    
Transgene
origin
Strain of Origin: (C57BL/6 x DBA/2)F2
Transgene
description
Transgene Type: Transgenic (random, expressed)
Mutation: Insertion
  The transgene expresses the mutant human amyloid protein precursor APPSwInd, which bears both the Swedish (K670N/M671L) and the Indiana (V717F) mutations, under the control of the human platelet derived growth factor, B polypeptide (PDGFB) promoter. Hemizygous transgenic mice express immunodetectable transgene product in cerebral neurons, with the highest level of expression occurring in the neocortex and hippocampus. ELISA analysis reveals approximate total amyloid beta peptides and 42 amino acid length amyloid beta peptides in neocortical and hippocampal tissue from transgenic mice. (J:62290)
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

(show or hide all annotated terms)

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
 
tg4
 
tg5
 
tg6
 
tg7
 
tg8
 
tg9
  
behavior/neurological          
    
  
life span/aging          
  NN  
  
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(PDGFB-APPSwInd)20Lms/0 B6.Cg-Tg(PDGFB-APPSwInd)20Lms
  
 tg2   
Tg(PDGFB-APPSwInd)20Lms/0 B6.D2-Tg(PDGFB-APPSwInd)20Lms
  
 tg3   Disease Model  
Tg(PDGFB-APPSwInd)20Lms/0 involves: C57BL/6 * DBA/2
  
 tg4   
Pla2g4atm1Jvb/Pla2g4a+
Tg(PDGFB-APPSwInd)20Lms/0
involves: 129S4/SvJae * C57BL/6 * DBA/2
  
 tg5   
Pla2g4atm1Jvb/Pla2g4atm1Jvb
Tg(PDGFB-APPSwInd)20Lms/0
involves: 129S4/SvJae * C57BL/6 * DBA/2
  
 tg6   
Mapttm1Hnd/Mapttm1Hnd
Tg(PDGFB-APPSwInd)20Lms/0
involves: C57BL/6 * DBA/2
  
 tg7   
Mapttm1Hnd/Mapt+
Tg(PDGFB-APPSwInd)20Lms/0
involves: C57BL/6 * DBA/2
  
 tg8   
Tg(Camk2a-IDE)1Selk/0
Tg(PDGFB-APPSwInd)20Lms/0
involves: C57BL/6 * DBA/2
  
 tg9   
Tg(Camk2a-MME)3Selk/0
Tg(PDGFB-APPSwInd)20Lms/0
involves: C57BL/6 * DBA/2
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
 
 
tg3
Tg(PDGFB-APPSwInd)20Lms/0involves: C57BL/6 * DBA/2J:62290
1Models involving transgenes or other mutation types may also appear in other sections of the table.
Notes This line is also called line J20.

Diffuse amyloid beta peptides deposition forms in the dendate gyrus and neocortex at 5 to 7 months of age. Amyloid deposition is progressive, with all transgenic mice exhibiting plaques by age 8 to 10 months.

References
Original: J:62290 Mucke L et al., "High-level neuronal expression of abeta 1-42 in wild-type human amyloid protein precursor transgenic mice: synaptotoxicity without plaque formation." J Neurosci 2000 Jun 1;20(11):4050-8
All: 43 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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