Cellosaurus GR-ST (CVCL_1236)

Cell line name GR-ST
Accession CVCL_1236
Resource Identification Initiative To cite this cell line use: GR-ST (RRID:CVCL_1236)
Comments Part of: COSMIC cell lines project.
Microsatellite instability: Instable (MSI-high) (Sanger).
Transfected with: HGNC; 2439; CSF3R.
Omics: Deep exome analysis.
Omics: DNA methylation analysis.
Derived from sampling site: Peripheral blood.
Disease Childhood B acute lymphoblastic leukemia (NCIt: C9140)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_U347 (ST [Human leukemia])
Sex of cell Male
Age at sampling 11Y
Category Cancer cell line
STR profile Source(s): Cosmic-CLP; RCB

D16S53912,13 (Cosmic-CLP)
12,13,14 (RCB)
D5S81810,12 (Cosmic-CLP)
10,11,12 (RCB)
vWA14,19 (Cosmic-CLP)
14,18,19 (RCB)

PubMed=7538617; DOI=10.1016/0145-2126(94)00156-5
el-Sonbaty S.S., Tsuchiya H., Watanabe M., Hochito K., Kunisada T., Shimosaka A., Matsuda I.
Exogenous expression of human granulocyte colony-stimulating factor receptor in a B-lineage acute lymphoblastic leukemia cell line: a possible model for mixed lineage leukemia.
Leuk. Res. 19:249-256(1995)

PubMed=27397505; DOI=10.1016/j.cell.2016.06.017
Iorio F., Knijnenburg T.A., Vis D.J., Bignell G.R., Menden M.P., Schubert M., Aben N., Goncalves E., Barthorpe S., Lightfoot H., Cokelaer T., Greninger P., van Dyk E., Chang H., de Silva H., Heyn H., Deng X., Egan R.K., Liu Q., Mironenko T., Mitropoulos X., Richardson L., Wang J., Zhang T., Moran S., Sayols S., Soleimani M., Tamborero D., Lopez-Bigas N., Ross-Macdonald P., Esteller M., Gray N.S., Haber D.A., Stratton M.R., Benes C.H., Wessels L.F.A., Saez-Rodriguez J., McDermott U., Garnett M.J.
A landscape of pharmacogenomic interactions in cancer.
Cell 166:740-754(2016)

Cell line collections RCB; RCB1182
Cell line databases/resources Cosmic-CLP; 906877
GDSC; 906877
Ontologies CLO; CLO_0050981
Biological sample resources BioSample; SAMN03472171
Chemistry resources ChEMBL-Cells; CHEMBL3308529
ChEMBL-Targets; CHEMBL2366111
Gene expression databases GEO; GSM1669816
Polymorphism and mutation databases Cosmic; 906877