ID   Der(22)-iPS-C2
AC   CVCL_UG56
DR   Wikidata; Q93525645
RX   PubMed=21949351;
CC   Population: Caucasian.
CC   Cell type: Fibroblast; CL=CL_0000057.
ST   Source(s): PubMed=21949351
ST   Amelogenin: X,Y
ST   CSF1PO: 10,12
ST   D13S317: 12
ST   D16S539: 12
ST   D18S51: 13,16
ST   D21S11: 28,29
ST   D3S1358: 16,17
ST   D5S818: 12
ST   D7S820: 9
ST   D8S1179: 12
ST   FGA: 21,22.2
ST   Penta D: 13
ST   Penta E: 12,15
ST   TH01: 9.3,10
ST   TPOX: 8,12
ST   vWA: 16
DI   NCIt; C114765; Trisomy 22
DI   ORDO; Orphanet_98131; Total autosomal trisomy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_V547 ! GM00084
SX   Male
AG   1M
CA   Induced pluripotent stem cell
DT   Created: 13-11-18; Last updated: 29-06-23; Version: 6
//
RX   PubMed=21949351; DOI=10.1093/hmg/ddr435;
RA   Li W., Wang X.-M., Fan W.-X., Zhao P., Chan Y.-C., Chen S.,
RA   Zhang S.-Q., Guo X.-P., Zhang Y., Li Y.-H., Cai J.-L., Qin D.-J.,
RA   Li X.-Y., Yang J.-Y., Peng T.-R., Zychlinski D., Hoffmann D.,
RA   Zhang R.-S., Deng K., Ng K.-M., Menten B., Zhong M., Wu J.-Y., Li Z.-Y.,
RA   Chen Y.-L., Schambach A., Tse H.-F., Pei D.-Q., Esteban M.A.;
RT   "Modeling abnormal early development with induced pluripotent stem
RT   cells from aneuploid syndromes.";
RL   Hum. Mol. Genet. 21:32-45(2012).
//