ID   TRI13-iPS-C1
AC   CVCL_UG54
DR   Wikidata; Q98133539
RX   PubMed=21949351;
CC   Population: Caucasian.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): PubMed=21949351
ST   Amelogenin: X,Y
ST   CSF1PO: 10,11
ST   D13S317: 11,12
ST   D16S539: 10,13
ST   D18S51: 12,16
ST   D21S11: 29
ST   D3S1358: 14,16
ST   D5S818: 12,13
ST   D7S820: 8,9
ST   D8S1179: 11,14
ST   FGA: 20.2,25
ST   Penta D: 9,13
ST   Penta E: 12,17
ST   TH01: 6,8
ST   TPOX: 8
ST   vWA: 14,17
DI   NCIt; C36529; Trisomy 13
DI   ORDO; Orphanet_3378; Trisomy 13
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_X284 ! GM03330
SX   Male
AG   1D
CA   Induced pluripotent stem cell
DT   Created: 13-11-18; Last updated: 29-06-23; Version: 7
//
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).
//