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Cellosaurus GENEA019 (CVCL_9028)

[Text version]
Cell line name GENEA019
Synonyms Genea019; GENEA-019; SIVF019; SIV019; GENEAe020-A
Accession CVCL_9028
Resource Identification Initiative To cite this cell line use: GENEA019 (RRID:CVCL_9028)
Comments From: Genea Biocells, Ltd; Sydney; Australia.
Registration: NIH Human Embryonic Stem Cell Registry; not approved.
Registration: UK Stem Cell Bank (UKSCB); Steering comm. appl. SCSC14-62.
Omics: Array-based CGH.
Omics: Proteome analysis.
Donor information: Embryo is sibling to that giving rise to GENEA020 (Cellosaurus=CVCL_9029).
Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
Cell type: Embryonic stem cell; CL=CL_0002322.
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling Blastocyst stage
Category Embryonic stem cell
STR profile Source(s): PubMed=27346002

Markers:
AmelogeninX
CSF1PO10,11
D2S133818,23
D3S135815
D5S81811,12
D7S8207,8
D8S117912,13
D13S31711,12
D16S53911
D18S5112,18
D19S43313,14
D21S1129,30
FGA22,23
TH019.3,10
TPOX11
vWA17

Run an STR similarity search on this cell line
Web pages https://web.archive.org/web/20180912205435/http://geneabiocells.com/services/shelf-products/human-embryonic-stem-cells/
https://grants.nih.gov/stem_cells/registry/not_approved.htm
Publications

PubMed=20649476; DOI=10.1089/scd.2010.0120
Bradley C.K., Scott H.A., Chami O., Peura T.T., Dumevska B., Schmidt U., Stojanov T.
Derivation of Huntington's disease-affected human embryonic stem cell lines.
Stem Cells Dev. 20:495-502(2011)

PubMed=25316320; DOI=10.1021/pr500649m
McQuade L.R., Balachandran A., Scott H.A., Khaira S., Baker M.S., Schmidt U.
Proteomics of Huntington's disease-affected human embryonic stem cells reveals an evolving pathology involving mitochondrial dysfunction and metabolic disturbances.
J. Proteome Res. 13:5648-5659(2014)

PubMed=27217344; DOI=10.5966/sctm.2015-0224; PMCID=PMC4996435
Caron L., Kher D., Lee K.L., McKernan R., Dumevska B., Hidalgo A., Li J., Yang H.H., Main H., Ferri G., Petek L.M., Poellinger L., Miller D.G., Gabellini D., Schmidt U.
A human pluripotent stem cell model of facioscapulohumeral muscular dystrophy-affected skeletal muscles.
Stem Cells Transl. Med. 5:1145-1161(2016)

PubMed=27346002; DOI=10.1016/j.scr.2016.02.008
Dumevska B., Peura T.T., McKernan R., Goel D., Schmidt U.
Derivation of human embryonic stem cell line Genea019.
Stem Cell Res. 16:397-400(2016)

PubMed=35805069; DOI=10.3390/cells11131984; PMCID=PMC9265327
Molina-Ruiz F.J., Introna C., Bombau G., Galofre M., Canals J.M.
Standardization of cell culture conditions and routine genomic screening under a quality management system leads to reduced genomic instability in hPSCs.
Cells 11:1984.1-1984.25(2022)

Cross-references
Cell line databases/resources hPSCreg; GENEAe020-A
SKIP; SKIP002919
Biological sample resources BioSamples; SAMEA104013010
Encyclopedic resources Wikidata; Q54835581
Entry history
Entry creation06-Jun-2012
Last entry update10-Sep-2024
Version number19