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Cellosaurus GENEA089 (CVCL_M240)

[Text version]

Cell line name GENEA089
Synonyms Genea089; SIVF089; GENEAe013-A
Accession CVCL_M240
Resource Identification Initiative To cite this cell line use: GENEA089 (RRID:CVCL_M240)
Comments From: Genea Biocells, Ltd; Australia.
Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-14-0247.
Registration: UK Stem Cell Bank (UKSCB); Steering comm. appl. SCSC14-47.
Miscellaneous: Sibling to GENEA090 (CVCL_M241) and GENEA091 (CVCL_M242).
Sequence variations HTT p.Gln18[41]; has 41 CAG repeats (Genea).
Disease Huntington's disease (NCIt: C82342)
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=27346008

Markers:
AmelogeninX
CSF1PO11,15
D2S133817,19
D3S135817,18
D5S81810,12
D7S82010
D8S117914,15
D13S3178,11
D16S53912
D18S5115
D19S43313,14
D21S1129,31
FGA23,24
TH016,9
TPOX8,11
vWA18,19

Run an STR similarity search on this cell line
Web pages http://geneabiocells.com/services/shelf-products/human-embryonic-stem-cells/
https://grants.nih.gov/stem_cells/registry/current.htm?id=621
Publications

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=27346008; DOI=10.1016/j.scr.2016.02.013
Dumevska B., McKernan R., Hu J., Schmidt U.
Derivation of Huntington disease affected Genea089 human embryonic stem cell line.
Stem Cell Res. 16:434-436(2016)

Cross-references
Cell line databases/resources hPSCreg; GENEAe013-A
ISCR; 2047
Biological sample resources BioSamples; SAMEA104012530
Other Wikidata; Q54835661
Entry history
Entry creation05-Nov-2013
Last entry updated13-Nov-2018
Version number13