Cellosaurus logo
expasy logo

Cellosaurus UIi001-A (CVCL_B5RX)

[Text version]
Cell line name UIi001-A
Synonyms SCZ019-A; SCZ019
Accession CVCL_B5RX
Resource Identification Initiative To cite this cell line use: UIi001-A (RRID:CVCL_B5RX)
Comments From: University of Iowa; Iowa City; USA.
Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Chromosome 16p11.2 deletion syndrome (NCIt: C120408)
Schizophrenia (NCIt: C3362)
Proximal 16p11.2 microdeletion syndrome (ORDO: Orphanet_261197)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 33Y
Category Induced pluripotent stem cell
Publications

PubMed=34953327; DOI=10.1016/j.scr.2021.102636
Madencioglu D.A., Kruth K., Shin M., Andreasen N.C., Wassink T.H., Williams A.J.
Generation of a human induced pluripotent stem cell line from a patient diagnosed with schizophrenia carrying a 16p11.2 deletion.
Stem Cell Res. 59:102636-102636(2022)

Cross-references
Cell line databases/resources hPSCreg; UIi001-A
Encyclopedic resources Wikidata; Q112041881
Entry history
Entry creation17-Mar-2022
Last entry update29-Jun-2023
Version number4