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Cellosaurus XWHNi001-A (CVCL_B5GR)

[Text version]
Cell line name XWHNi001-A
Accession CVCL_B5GR
Resource Identification Initiative To cite this cell line use: XWHNi001-A (RRID:CVCL_B5GR)
Comments From: Department of Neurology, Xuan Wu Hospital; Beijing; China.
Population: Chinese.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 620; APP; Simple; p.Val717Ile (c.2149G>A); ClinVar=VCV000018088; Zygosity=Homozygous (PubMed=35149456).
Disease Familial Alzheimer's disease, type 1 (NCIt: C146894)
Early-onset autosomal dominant Alzheimer disease (ORDO: Orphanet_1020)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 58Y
Category Induced pluripotent stem cell
STR profile Source(s): PubMed=35149456

Markers:
AmelogeninX
CSF1PO12
D2S44111
D2S133823,24
D3S135816
D5S81811
D6S104317,19
D7S82011,13
D8S117912,13
D12S39115,18
D13S3178,11
D16S5399
D18S5115,22
D19S43314,15.2
D21S1129,30
FGA20,23
Penta D6,9
Penta E12,20
TH019
TPOX8
vWA16,18

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Publications

PubMed=35149456; DOI=10.1016/j.scr.2022.102690
Wei C.-B., Lu X.-L., Zou Q., Gong S.-T., Chen Y.-F., Lyu J.-H., Jia J.-P.
Generation and characterization of a human induced pluripotent stem cell line (XWHNi001-A) derived from an Alzheimer's disease patient with mutation in the APP gene.
Stem Cell Res. 60:102690-102690(2022)

Cross-references
Cell line databases/resources hPSCreg; XWHNi001-A
Biological sample resources BioSamples; SAMEA10329923
Encyclopedic resources Wikidata; Q110434432
Entry history
Entry creation16-Dec-2021
Last entry update29-Jun-2023
Version number4