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| Nomenclature |
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Symbol:
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Tg(ACTA1-SMN)69Ahmb
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Name:
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transgene insertion 69, Arthur H M Burghes
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MGI ID: |
MGI:3774944 |
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Synonyms: |
HSA69-SMN |
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Transgene:
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Tg(ACTA1-SMN)69Ahmb
Location:
unknown
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Transgene origin |
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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 HSA-SMN transgene was designed with the human alpha-skeletal actin (HSA or ACTA1) promoter region, splice acceptor site from the SV40 VP1 intron, full-length humsn SMN cDNA (containing exons 1-8), and two SV40 polyA signals. Mice from founder line 69 (HSA69-SMN) were found to have 11 copies of the transgene. (J:97103, J:131663)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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| References |
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Original: |
J:131663
Gavrilina TO et al.,
"Neuronal SMN expression corrects spinal muscular atrophy in severe SMA mice while muscle specific SMN expression has no phenotypic effect."
Hum Mol Genet 2008 Jan 4;():
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All: |
3 reference(s)
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