Home  |  Contact

Cellosaurus NCBSi002-A (CVCL_UL58)

[Text version]
Cell line name NCBSi002-A
Synonyms AD5
Accession CVCL_UL58
Resource Identification Initiative To cite this cell line use: NCBSi002-A (RRID:CVCL_UL58)
Comments From: Tata Institute of Fundamental Research, National Centre for Biological Sciences; Bangalore; India.
Population: Indian.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 613; APOE; Simple; p.Cys130Arg (c.388T>C); ClinVar=VCV000017864; Zygosity=Heterozygous; Note=ApoE4 allele (PubMed=30605839).
  • Mutation; HGNC; 4140; GAP43; Simple; p.Ser41Gly (c.121A>G) (p.Ser77Gly, c.229A>G); Zygosity=Heterozygous (PubMed=30605839).
Disease Alzheimer's disease (NCIt: C2866)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 72Y
Category Induced pluripotent stem cell
STR profile Source(s): PubMed=30605839

Markers:
AmelogeninX
CSF1PO11,12
D5S81811,13
D7S8208,9
D13S3179,12
D16S5399,12
D21S1130.2,31.2
TH018,9.3
TPOX10,11
vWA14,18

Run an STR similarity search on this cell line
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; NCBSi002-A
Encyclopedic resources Wikidata; Q95992483
Entry history
Entry creation25-Feb-2019
Last entry update29-Jun-2023
Version number6