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Cellosaurus 7889SA APP(WT/Swe) (CVCL_E7G8)

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Cell line name 7889SA APP(WT/Swe)
Accession CVCL_E7G8
Resource Identification Initiative To cite this cell line use: 7889SA APP(WT/Swe) (RRID:CVCL_E7G8)
Comments Population: Caucasian; Italian.
Donor information: At sampling donor was not affected with Alzheimer disease but has a 25% risk (from parent cell line).
Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:620; APP; Simple_edited; p.Lys670_Met671delinsAsnLeu (c.2010_2011inv) (c.2010_2011delGAinsTC); ClinVar=VCV000018093; Zygosity=Heterozygous; Note=By CRISPR/Cas9 (PubMed=27120160).
Disease Alzheimer's disease 1 (NCIt: C146894)
Early-onset autosomal dominant Alzheimer disease (ORDO: Orphanet_1020)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_AD15 (NYSCF-AD-1019-AG07889-Skin-RV-IPSC1)
Sex of cell Male
Age at sampling 17Y8M
Category Induced pluripotent stem cell
Publications

PubMed=27120160; DOI=10.1038/nature17664
Dominik Paquet, Dylan G. Kwart, Antonia Chen, Andrew A. Sproul, Samson Jacob, Shaun Teo, Kimberly Moore Olsen, Andrew Gregg, Scott A. Noggle, Marc Tessier-Lavigne;
Efficient introduction of specific homozygous and heterozygous mutations using CRISPR/Cas9.
Nature 533:125-129(2016)

Entry history
Entry creation10-Apr-2025
Last entry update10-Apr-2025
Version number1