ID   GENEA022
AC   CVCL_9031
SY   Genea022; GEN022; SIVF022; SIVF-022; GENEAe016-A
DR   BioSamples; SAMEA104130951
DR   hPSCreg; GENEAe016-A
DR   ISCR; 1184
DR   Wikidata; Q54835585
RX   PubMed=25316320;
RX   PubMed=25645121;
RX   PubMed=27346017;
WW   https://web.archive.org/web/20180912205435/http://geneabiocells.com/services/shelf-products/human-embryonic-stem-cells/
CC   From: Genea Biocells, Ltd; Sydney; Australia.
CC   Registration: Swiss research registry; BAG-hES-IMP-0028.
CC   Registration: UK Stem Cell Bank (UKSCB); Steering comm. appl. SCSC14-60.
CC   Omics: SNP array analysis.
CC   Omics: Transcriptome analysis by RNAseq.
CC   Donor information: Embryo is sibling to those giving rise to GENEA021 (Cellosaurus=CVCL_9030) and GENEA023 (Cellosaurus=CVCL_9032).
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
ST   Source(s): PubMed=27346017
ST   Amelogenin: X,Y
ST   CSF1PO: 11,13
ST   D13S317: 12
ST   D16S539: 10,13
ST   D18S51: 14,16
ST   D19S433: 13,14
ST   D21S11: 28,29
ST   D2S1338: 17,18
ST   D3S1358: 15
ST   D5S818: 11
ST   D7S820: 10,13
ST   D8S1179: 12,13
ST   FGA: 20,22
ST   TH01: 6
ST   TPOX: 8,11
ST   vWA: 15,19
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 06-06-12; Last updated: 29-06-23; Version: 17
//
RX   PubMed=25316320; DOI=10.1021/pr500649m;
RA   McQuade L.R., Balachandran A., Scott H.A., Khaira S., Baker M.S.,
RA   Schmidt U.;
RT   "Proteomics of Huntington's disease-affected human embryonic stem
RT   cells reveals an evolving pathology involving mitochondrial
RT   dysfunction and metabolic disturbances.";
RL   J. Proteome Res. 13:5648-5659(2014).
//
RX   PubMed=25645121; DOI=10.1002/stem.1961;
RA   Bosman A.G., Letourneau A., Sartiani L., Del Lungo M., Ronzoni F.,
RA   Kuziakiv R., Tohonen V., Zucchelli M., Santoni F.A., Guipponi M.,
RA   Dumevska B., Hovatta O., Antonarakis S.E., Jaconi Devaud M.E.E.;
RT   "Perturbations of heart development and function in cardiomyocytes
RT   from human embryonic stem cells with trisomy 21.";
RL   Stem Cells 33:1434-1446(2015).
//
RX   PubMed=27346017; DOI=10.1016/j.scr.2016.02.011;
RA   Dumevska B., Bosman A.G., McKernan R., Schmidt U., Peura T.T.;
RT   "Derivation of human embryonic stem cell line Genea022.";
RL   Stem Cell Res. 16:472-475(2016).
//