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Cellosaurus UUIGPi005-A (CVCL_WT82)

[Text version]

Cell line name UUIGPi005-A
Synonyms UUIGPi005A; UUIGPi005; MW1; MWS27(7)
Accession CVCL_WT82
Resource Identification Initiative To cite this cell line use: UUIGPi005-A (RRID:CVCL_WT82)
Comments From: Department of Immunology, Genetics and Pathology, Uppsala University; Uppsala; Sweden.
Sequence variations Heterozygous for ZEB2 p.Arg343Ter (c.1027C>T) (PubMed=31376723).
Disease Mowat-Wilson syndrome (NCIt: C74999)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 10Y
Category Induced pluripotent stem cell

PubMed=31376723; DOI=10.1016/j.scr.2019.101518
Schuster J., Sobol M., Fatima A., Khalfallah A., Laan L., Anderlid B.-M., Nordgren A., Dahl N.
Mowat-Wilson syndrome: Generation of two human iPS cell lines (UUIGPi004A and UUIGPi005A) from siblings with a truncating ZEB2 gene variant.
Stem Cell Res. 39:101518-101518(2019)

Cell line databases/resources hPSCreg; UUIGPi005-A
Entry history
Entry creation05-Jul-2019
Last entry updated06-Sep-2019
Version number2