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Allele : Tg(Prnp-ITM2B/APP695*42)A12Emcg transgene insertion A12, Eileen McGowan

Primary Identifier  MGI:3710689 Allele Type  Transgenic
Attribute String  Humanized sequence, Inserted expressed sequence Gene  Tg(Prnp-ITM2B/APP695*42)A12Emcg
Strain of Origin  (C3H x C57BL/6)F1 x C57BL/6 Is Recombinase  false
Is Wild Type  false
molecularNote  The transgene was generated with a mouse prion promoter upstream of a BRI-Abeta42 fusion construct, containing a cDNA sequence from human type 2 transmembrane protein (BRI or ITM2B) fused in-frame with a "wildtype APP695" cDNA sequence encoding amyloid-beta42 (Abeta42) at the furin-like cleavage site; the C-terminal 23 amino acid ABri peptide of BRI was replaced with the Abeta42 sequence. Mice from the founder with the highest Abeta42 plasma levels, line BRI-Abeta42A (12e) were donated to the Jackson Laboratory. Transgenic fusion protein expression approximates levels of endogenous mouse APP expression and is expressed in patterns characteristic of the Prnp promoter, with highest expression in cerebellar granule cells and hippocampus. Full length Abeta fusion protein is most highly expressed with processed Abeta42 peptide expressed at lower levels
  • mutations:
  • Insertion
  • synonyms:
  • RI-Abeta42A (12e),
  • BRI-Abeta42A,
  • RI-Abeta42A (12e),
  • BRI-Abeta42A line 12e,
  • BRI-Abeta1-42,
  • BRI-Abeta1-42,
  • BRI-Abeta42A line 12e,
  • BRI-Abeta42A
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

Trail: Allele

0 Driven By

11 Publication categories

Trail: Allele