ID EW-12 AC CVCL_1210 SY EW12; IARC-EW12; IARC-EW-12; IARC-EW 12 DR ArrayExpress; E-MTAB-783 DR ArrayExpress; E-MTAB-3610 DR cancercelllines; CVCL_1210 DR Cell_Model_Passport; SIDM00200 DR ChEMBL-Cells; CHEMBL3308528 DR ChEMBL-Targets; CHEMBL2366255 DR Cosmic; 684063 DR Cosmic; 949162 DR Cosmic; 2804872 DR Cosmic-CLP; 949162 DR DepMap; ACH-002112 DR EGA; EGAS00001000978 DR GDSC; 949162 DR GEO; GSM1669783 DR IARC_TP53; 27163 DR PharmacoDB; EW12_352_2019 DR PRIDE; PXD030304 DR PubChem_Cell_line; CVCL_1210 DR Wikidata; Q54832991 RX PubMed=8108117; RX PubMed=20164919; RX PubMed=27397505; RX PubMed=30894373; RX PubMed=35839778; CC Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE). CC Part of: COSMIC cell lines project. CC Microsatellite instability: Stable (MSS) (Sanger). CC Sequence variation: Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg273Cys (c.817C>T); ClinVar=VCV000043594; Zygosity=Homozygous (Cosmic-CLP=949162). CC Omics: Genomics; DNA methylation analysis. CC Omics: Genomics; Whole exome sequencing. CC Omics: Phenotyping; Drug screening. CC Omics: Proteomics; Quantitative. CC Omics: Transcriptomics; Microarray. CC Omics: Variations; SNP array analysis. CC Genome ancestry: African=21.92%; Native American=0%; East Asian, North=2.41%; East Asian, South=0.17%; South Asian=6.25%; European, North=15.31%; European, South=53.94% (PubMed=30894373). ST Source(s): Cosmic-CLP=949162 ST Amelogenin: X ST CSF1PO: 12 ST D13S317: 11 ST D16S539: 12 ST D5S818: 12 ST D7S820: 10 ST TH01: 9 ST TPOX: 8 ST vWA: 15,20 DI NCIt; C4817; Ewing sarcoma DI ORDO; Orphanet_319; Ewing sarcoma OX NCBI_TaxID=9606; ! Homo sapiens (Human) SX Female AG Age unspecified CA Cancer cell line DT Created: 04-04-12; Last updated: 10-04-25; Version: 32 // RX PubMed=8108117; RA Albert T., Urlbauer B., Kohlhuber F., Hammersen B., Eick D.; RT "Ongoing mutations in the N-terminal domain of c-Myc affect RT transactivation in Burkitt's lymphoma cell lines."; RL Oncogene 9:759-763(1994). // RX PubMed=20164919; DOI=10.1038/nature08768; PMCID=PMC3145113; RA Bignell G.R., Greenman C.D., Davies H.R., Butler A.P., Edkins S., RA Andrews J.M., Buck G., Chen L., Beare D., Latimer C., Widaa S., RA Hinton J., Fahey C., Fu B.-Y., Swamy S., Dalgliesh G.L., Teh B.T., RA Deloukas P., Yang F.-T., Campbell P.J., Futreal P.A., Stratton M.R.; RT "Signatures of mutation and selection in the cancer genome."; RL Nature 463:893-898(2010). // RX PubMed=27397505; DOI=10.1016/j.cell.2016.06.017; PMCID=PMC4967469; RA Iorio F., Knijnenburg T.A., Vis D.J., Bignell G.R., Menden M.P., RA Schubert M., Aben N., Goncalves E., Barthorpe S., Lightfoot H., RA Cokelaer T., Greninger P., van Dyk E., Chang H., de Silva H., Heyn H., RA Deng X.-M., Egan R.K., Liu Q.-S., Mironenko T., Mitropoulos X., RA Richardson L., Wang J.-H., Zhang T.-H., Moran S., Sayols S., RA Soleimani M., Tamborero D., Lopez-Bigas N., Ross-Macdonald P., RA Esteller M., Gray N.S., Haber D.A., Stratton M.R., Benes C.H., RA Wessels L.F.A., Saez-Rodriguez J., McDermott U., Garnett M.J.; RT "A landscape of pharmacogenomic interactions in cancer."; RL Cell 166:740-754(2016). // RX PubMed=30894373; DOI=10.1158/0008-5472.CAN-18-2747; PMCID=PMC6445675; RA Dutil J., Chen Z.-H., Monteiro A.N.A., Teer J.K., Eschrich S.A.; RT "An interactive resource to probe genetic diversity and estimated RT ancestry in cancer cell lines."; RL Cancer Res. 79:1263-1273(2019). // RX PubMed=35839778; DOI=10.1016/j.ccell.2022.06.010; PMCID=PMC9387775; RA Goncalves E., Poulos R.C., Cai Z.-X., Barthorpe S., Manda S.S., Lucas N., RA Beck A., Bucio-Noble D., Dausmann M., Hall C., Hecker M., Koh J., RA Lightfoot H., Mahboob S., Mali I., Morris J., Richardson L., RA Seneviratne A.J., Shepherd R., Sykes E., Thomas F., Valentini S., RA Williams S.G., Wu Y.-X., Xavier D., MacKenzie K.L., Hains P.G., Tully B., RA Robinson P.J., Zhong Q., Garnett M.J., Reddel R.R.; RT "Pan-cancer proteomic map of 949 human cell lines."; RL Cancer Cell 40:835-849.e8(2022). //