ID   D21-iPSC#2
AC   CVCL_B3MC
SY   AF4 iPS #12-2-D
DR   JCRB; JCRB1841
DR   Wikidata; Q110432766
RX   PubMed=30760866;
CC   Characteristics: While originating from a Down syndrome patient, this cell line has lost the extra copy of chromosome 21.
CC   Derived from site: In situ; Amniotic fluid; UBERON=UBERON_0000173.
ST   Source(s): 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)
SX   Female
AG   Fetus
CA   Induced pluripotent stem cell
DT   Created: 16-12-21; Last updated: 29-06-23; Version: 5
//
RX   PubMed=30760866; DOI=10.1038/s41374-019-0230-0; PMCID=PMC6760570;
RA   Inoue, Momoko
RA   Kajiwara, Kazuhiro
RA   Yamaguchi, Ayumi
RA   Kiyono, Tohru
RA   Samura, Osamu
RA   Akutsu, Hidenori
RA   Sago, Haruhiko
RA   Okamoto, Aikou
RA   Umezawa, Akihiro
RT   "Autonomous trisomic rescue of Down syndrome cells.";
RL   Lab. Invest. 99:885-897(2019).
//