ID   D21-iPSC#1
AC   CVCL_B3LX
SY   AF4 iPS #12-2-C
DR   JCRB; JCRB1836
DR   Wikidata; Q110432765
RX   PubMed=30760866;
CC   Characteristics: While originating from a Down syndrome patient, this cell line has lost the extra copy of chromosome 21.
CC   Karyotypic information: 46,XX [17/20]; 45,X [1/20]; 45,XX,-12 [1/20]; 90,XXXX,-14,-17 [1/20] (JCRB=JCRB1836).
CC   Derived from site: In situ; Amniotic fluid; UBERON=UBERON_0000173.
ST   Source(s): JCRB=JCRB1836; PubMed=30760866
ST   Amelogenin: X
ST   CSF1PO: 10
ST   D13S317: 11,12
ST   D16S539: 9,11
ST   D18S51: 13,15
ST   D21S11: 31,32
ST   D3S1358: 15,16
ST   D5S818: 12
ST   D7S820: 10,12
ST   D8S1179: 12,13
ST   FGA: 22
ST   Penta D: 9,11
ST   Penta E: 12,19
ST   TH01: 6,7
ST   TPOX: 10,12
ST   vWA: 14,19
DI   NCIt; C2993; Down syndrome
DI   ORDO; Orphanet_870; Down syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_B3M2 ! T21-iPSC#12
SX   Female
AG   Fetus
CA   Induced pluripotent stem cell
DT   Created: 16-12-21; Last updated: 02-05-24; Version: 6
//
RX   PubMed=30760866; DOI=10.1038/s41374-019-0230-0; PMCID=PMC6760570;
RA   Inoue M., Kajiwara K., Yamaguchi A., Kiyono T., Samura O., Akutsu H.,
RA   Sago H., Okamoto A., Umezawa A.;
RT   "Autonomous trisomic rescue of Down syndrome cells.";
RL   Lab. Invest. 99:885-897(2019).
//