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Cellosaurus WISCi005-C (CVCL_EJ82)

[Text version]
Cell line name WISCi005-C
Synonyms UWWC1-DS2U; DS2U
Accession CVCL_EJ82
Resource Identification Initiative To cite this cell line use: WISCi005-C (RRID:CVCL_EJ82)
Comments From: University of Wisconsin; Madison; USA.
Population: Caucasian.
Karyotypic information: Lost the third copy of chromosome 21.
Derived from site: In situ; Chest, skin; UBERON=UBERON_0001868.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Down syndrome (NCIt: C2993)
Down syndrome (ORDO: Orphanet_870)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_L780 (AG05397)
Sex of cell Male
Age at sampling 1Y
Category Induced pluripotent stem cell
STR profile Source(s): PubMed=23716668

Markers:
AmelogeninX,Y
CSF1PO10,11
D5S81810,12
D7S82010,12
D13S31711
D16S53911,13
TH016,9
TPOX8,10
vWA15,17

Run an STR similarity search on this cell line
Publications

PubMed=23716668; DOI=10.1073/pnas.1216575110; PMCID=PMC3683748
Weick J.P., Held D.L., Bonadurer G.F. 3rd, Doers M.E., Liu Y., Maguire C., Clark A., Knackert J.A., Molinarolo K., Musser M.T., Yao L., Yin Y.-N., Lu J.-F., Zhang X.-Q., Zhang S.-C., Bhattacharyya A.
Deficits in human trisomy 21 iPSCs and neurons.
Proc. Natl. Acad. Sci. U.S.A. 110:9962-9967(2013)

Cross-references
Cell line collections (Providers) WiCell; uwwc1-ds2u
Cell line databases/resources hPSCreg; WISCi005-C
Biological sample resources BioSamples; SAMEA104388690
Encyclopedic resources Wikidata; Q54994099
Entry history
Entry creation26-Sep-2016
Last entry update29-Jun-2023
Version number13