Neurolex is being transitioned to a new system and is currently not accepting new additions. If you have additions or questions please contact us at [email protected], or submit an issue to the github issue tracker at


From NeuroLex

Jump to: navigation, search


Name: TgN(APPSWE)2576
Description: Mutant mouse with a mutation in the APPSWE gene, beta amyloid precursor protein.
Synonym(s): APP695swe, APPK670N, M671L, APPSw, APPswe Tg2576, hAPP, K670N/M671L, Tg(APPSWE)2576HKahs, Tg(APPSWE)2576Kahs, Tg(HuAPP695.K670-M671L)2576, Tg2576, TgN(APPSWE)2576
Super-category: Mutant mouse strain
Related to: Alzheimers disease
Link to OWL / RDF: Download this content as OWL/RDF



Pages in category "TgN(APPSWE)2576"

The following 2 pages are in this category, out of 2 total.



*Note: Neurolex imports many terms and their ids from existing community ontologies, e.g., the Gene Ontology. Neurolex, however, is a dynamic site and any content beyond the identifier should not be presumed to reflect the content or views of the source ontology. Users should consult with the authoritative source for each ontology for current information.

Facts about TgN(APPSWE)2576RDF feed
CurationStatusuncurated  +
DefiningCitation  +
DefinitionMutant mouse with a mutation in the APPSWE gene, beta amyloid precursor protein.
LabelTgN(APPSWE)2576  +
ModifiedDate17 June 2010  +
RelatedToAlzheimers disease  +
SuperCategoryMutant mouse strain  +
SynonymAPP695swe  +, APPK670N  +, M671L  +, APPSw  +, APPswe Tg2576  +, hAPP  +, K670N/M671L  +, Tg(APPSWE)2576HKahs  +, Tg(APPSWE)2576Kahs  +, Tg(HuAPP695.K670-M671L)2576  +, Tg2576  +, and TgN(APPSWE)2576  +