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| Nomenclature |
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Symbol:
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Tg(PDGFB-APPInd)H6Lms
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Name:
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transgene insertion H6, Lennart Mucke
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MGI ID: |
MGI:3717672 |
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Synonyms: |
APPInd, PDGF-hAPP line 6, PDGF-hAPP line H6, Tg(PDGFB-APP*V717F)H6Lms |
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Transgene:
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Tg(PDGFB-APPInd)H6Lms
Location:
unknown
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Transgene description |
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Transgene
Type: | |
Transgenic (random, expressed) |
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Mutation: | |
Insertion |
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Mutation details: The transgene contains a human APP minigene encoding the Indiana mutation (V717F) which is associated with familial Alzheimer disease. The construct contained APP introns 6-8, allowing alternative splicing of exons 7 and 8. The human PDGF beta-chain promoter drives expression, and the construct also contains the SV40 polyadenylation signal. Amyloid-beta ELISA on whole brain homogenates indicates higher cerebral beta-amyloid production than in Tg(APPV717F)109Ili mice expressing the same construct. (J:100980, J:102272)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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| References |
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Original: |
J:102272
Wyss-Coray T et al.,
"Amyloidogenic role of cytokine TGF-beta1 in transgenic mice and in Alzheimer's disease."
Nature 1997 Oct 9;389(6651):603-6
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All: |
4 reference(s)
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