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Cellosaurus NCBSi001-A (CVCL_UL57)

[Text version]

Cell line name NCBSi001-A
Synonyms AD3
Accession CVCL_UL57
Resource Identification Initiative To cite this cell line use: NCBSi001-A (RRID:CVCL_UL57)
Comments From: Tata Institute of Fundamental Research, National Centre for Biological Sciences; Bangalore; India.
Population: Indian.
Derived from sampling site: Peripheral blood.
Sequence variations Mutation; HGNC; 9508; PSEN1; Simple; p.Trp165Cys (c.495G>C); ClinVar=VCV000098036; Zygosity=Heterozygous (PubMed=30605839).
Disease Familial Alzheimer's disease, type 3 (NCIt: C123412)
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 49Y
Category Induced pluripotent stem cell
STR profile Source(s): PubMed=30605839

Markers:
AmelogeninX
CSF1PO10,11
D5S8189,12
D7S8208,12
D13S31710,13
D16S5398,15
D21S1129,30
TH018
TPOX9,11
vWA17

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Publications

PubMed=30605839; DOI=10.1016/j.scr.2018.101370
Najar A.H., Sneha K.M., Ashok A., Babu S., Subramaniam A.G., Kannan R., Viswanath B., Purushottam M., Varghese M., Parvez S., Panicker M.M., Mukherjee O., Jain S.
Derivation of iPSC lines from two patients with familial Alzheimer's disease from India.
Stem Cell Res. 34:101370-101370(2019)

Cross-references
Cell line databases/resources hPSCreg; NCBSi001-A
Encyclopedic resources Wikidata; Q95992482
Entry history
Entry creation25-Feb-2019
Last entry update20-May-2021
Version number4