ID   PWS SD 2-9 iPSC
AC   CVCL_ZJ55
SY   PWS SD 2-9; PWS2.9; PWS small atypical deletion clone 9
DR   Wikidata; Q98128731
RX   PubMed=24363065;
WW   Provider; FPWR; -; https://www.fpwr.org/hubfs/Research%20Docs/PWS2.9%20Validation%20QC%20Package.pdf
WW   Provider; FPWR; -; https://www.fpwr.org/ipsc-biobank
CC   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).
CC   Cell type: Fibroblast; CL=CL_0000057.
ST   Source(s): FPWR
ST   Amelogenin: X,Y
ST   CSF1PO: 11
ST   D13S317: 11,13
ST   D16S539: 10,12
ST   D5S818: 12,13
ST   D7S820: 8
ST   TH01: 9,9.3
ST   TPOX: 8
ST   vWA: 17,18
DI   NCIt; C75463; Prader-Willi syndrome
DI   ORDO; Orphanet_739; Prader-Willi syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_ZJ46 ! PWS SD fibroblast
SX   Male
AG   19Y
CA   Induced pluripotent stem cell
DT   Created: 02-07-20; Last updated: 10-04-25; Version: 7
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RX   PubMed=24363065; DOI=10.1093/hmg/ddt628; PMCID=PMC3976333;
RA   Martins-Taylor K., Hsiao J.S., Chen I.P.-F., Glatt-Deeley H.R.,
RA   De Smith A.J., Blakemore A.I.F., Lalande M.E., Chamberlain S.J.;
RT   "Imprinted expression of UBE3A in non-neuronal cells from a
RT   Prader-Willi syndrome patient with an atypical deletion.";
RL   Hum. Mol. Genet. 23:2364-2373(2014).
//