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Cellosaurus UKWMPi002-A-1 (CVCL_A4YD)

[Text version]
Cell line name UKWMPi002-A-1
Synonyms CDH13+/- iPSC
Accession CVCL_A4YD
Resource Identification Initiative To cite this cell line use: UKWMPi002-A-1 (RRID:CVCL_A4YD)
Comments From: Division of Molecular Psychiatry, Center of Mental Health, University of Wurzburg; Wurzburg; Germany.
Population: Caucasian.
Knockout cell: Method=CRISPR/Cas9; HGNC; HGNC:1753; CDH13 (Note=1 of 2 alleles).
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_A4YC (UKWMPi002-A)
Sex of cell Female
Age at sampling 46Y
Category Induced pluripotent stem cell
Publications

PubMed=33486346; DOI=10.1016/j.scr.2021.102169
Maria Rosaria Vitale, Johanna Eva Maria Zoller, Charline Jansch, Anna Janz, Frank Edenhofer, Eva Klopocki, Daniel van den Hove, Tim Vanmierlo, Olga Rivero, Nael Nadif Kasri, Georg Christoph Ziegler, Klaus-Peter Lesch;
Generation of induced pluripotent stem cell (iPSC) lines carrying a heterozygous (UKWMPi002-A-1) and null mutant knockout (UKWMPi002-A-2) of cadherin 13 associated with neurodevelopmental disorders using CRISPR/Cas9.
Stem Cell Res. 51:102169-102169(2021)

Cross-references
Cell line databases/resources hPSCreg; UKWMPi002-A-1
Encyclopedic resources Wikidata; Q107117238
Entry history
Entry creation20-May-2021
Last entry update19-Dec-2024
Version number7