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Cellosaurus UKWMPi011-A (CVCL_B0PD)

[Text version]
Cell line name UKWMPi011-A
Synonyms bCJ13cl3
Accession CVCL_B0PD
Resource Identification Initiative To cite this cell line use: UKWMPi011-A (RRID:CVCL_B0PD)
Comments From: Department of Neurology, University of Wurzburg; Wurzburg; Germany.
Population: Caucasian.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Gene amplification; HGNC; HGNC:11007; SLC2A3; Duplication; Zygosity=Heterozygous (PubMed=34492570).
Disease Attention deficit hyperactivity disorder (NCIt: C97160)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_B0PE ! UKWMPi011-B
Sex of cell Female
Age at sampling 41Y
Category Induced pluripotent stem cell
Publications

PubMed=34492570; DOI=10.1016/j.scr.2021.102526
Ziegler G.C., Radtke F., Vitale M.R., Preusse A., Klopocki E., Herms S., Lesch K.-P.
Generation of multiple human iPSC lines from peripheral blood mononuclear cells of two SLC2A3 deletion and two SLC2A3 duplication carriers.
Stem Cell Res. 56:102526-102526(2021)

Cross-references
Cell line databases/resources hPSCreg; UKWMPi011-A
Encyclopedic resources Wikidata; Q108821447
Entry history
Entry creation23-Sep-2021
Last entry update19-Dec-2024
Version number5