Home  |  Contact

Cellosaurus UKWMPi012-A (CVCL_B0PF)

[Text version]
Cell line name UKWMPi012-A
Synonyms bCJ14cl1
Accession CVCL_B0PF
Resource Identification Initiative To cite this cell line use: UKWMPi012-A (RRID:CVCL_B0PF)
Comments From: Division of Molecular Psychiatry, Center of Mental Health, University of Wurzburg; Wurzburg; Germany.
Population: Caucasian.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Gene amplification; 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_B0PG ! UKWMPi012-B
Sex of cell Male
Age at sampling 54Y
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; UKWMPi012-A
Encyclopedic resources Wikidata; Q108821449
Entry history
Entry creation23-Sep-2021
Last entry update29-Jun-2023
Version number4