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Cellosaurus PWS SD 2-9 iPSC (CVCL_ZJ55)

[Text version]
Cell line name PWS SD 2-9 iPSC
Synonyms PWS SD 2-9; PWS2.9; PWS small atypical deletion clone 9
Accession CVCL_ZJ55
Resource Identification Initiative To cite this cell line use: PWS SD 2-9 iPSC (RRID:CVCL_ZJ55)
Comments Characteristics: Has a high propensities to differentiate into neurons due to the robust expression of neural lineage markers and silencing of the pluripotency genes (PubMed=24363065).
Cell type: Fibroblast; CL=CL_0000057.
Disease Prader-Willi syndrome (NCIt: C75463)
Prader-Willi syndrome (ORDO: Orphanet_739)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_ZJ46 (PWS SD fibroblast)
Sex of cell Male
Age at sampling 19Y
Category Induced pluripotent stem cell
STR profile Source(s): FPWR

Markers:
AmelogeninX,Y
CSF1PO11
D5S81812,13
D7S8208
D13S31711,13
D16S53910,12
TH019,9.3
TPOX8
vWA17,18

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Web pages Provider; FPWR; -; https://www.fpwr.org/hubfs/Research%20Docs/PWS2.9%20Validation%20QC%20Package.pdf
Provider; FPWR; -; https://www.fpwr.org/ipsc-biobank
Publications

PubMed=24363065; DOI=10.1093/hmg/ddt628; PMCID=PMC3976333
Martins-Taylor K., Hsiao J.S., Chen I.P.-F., Glatt-Deeley H.R., De Smith A.J., Blakemore A.I.F., Lalande M.E., Chamberlain S.J.
Imprinted expression of UBE3A in non-neuronal cells from a Prader-Willi syndrome patient with an atypical deletion.
Hum. Mol. Genet. 23:2364-2373(2014)

Cross-references
Encyclopedic resources Wikidata; Q98128731
Entry history
Entry creation02-Jul-2020
Last entry update10-Apr-2025
Version number7