ID CEM/C2 AC CVCL_3497 SY CCRF-CEM C2; CEM-C2; CEMC2 DR BTO; BTO_0005931 DR CLO; CLO_0002356 DR CLDB; cl5178 DR ATCC; CRL-2264 DR BioSample; SAMN03471853 DR cancercelllines; CVCL_3497 DR Cell_Model_Passport; SIDM01250 DR ChEMBL-Cells; CHEMBL3307952 DR ChEMBL-Targets; CHEMBL612406 DR Cosmic; 683535 DR IZSLER; BS TCL 153 DR LINCS_LDP; LCL-1035 DR PubChem_Cell_line; CVCL_3497 DR Wikidata; Q54809270 RX PubMed=7579731; RX PubMed=12068308; CC Population: Caucasian. CC Doubling time: ~30 hours (ATCC=CRL-2264). CC Selected for resistance to: ChEBI; CHEBI_27656; Camptothecin (CPT). CC Sequence variation: Gene fusion; HGNC; HGNC:13222; BCL11B + HGNC; HGNC:2488; NKX2-5; Name(s)=NKX2.5-BCL11B (from parent cell line). CC Sequence variation: Mutation; HGNC; HGNC:16712; FBXW7; Simple; p.Arg465Cys (c.1393C>T); ClinVar=VCV000376414; Zygosity=Heterozygous (from parent cell line). CC Sequence variation: Mutation; HGNC; HGNC:3765; FLT3; Simple; p.Ala627Thr (c.1879G>A); Zygosity=Heterozygous (from parent cell line). CC Sequence variation: Mutation; HGNC; HGNC:6407; KRAS; Simple; p.Gly12Asp (c.35G>A); ClinVar=VCV000012582; Zygosity=Heterozygous (PubMed=12068308). CC Sequence variation: Mutation; HGNC; HGNC:7881; NOTCH1; Simple; p.Leu1593_Arg1594insProArgLeuProHisAsnSerSerPheHisPheLeu (c.4780_4781ins36); Zygosity=Heterozygous (from parent cell line). CC Sequence variation: Mutation; HGNC; HGNC:7881; NOTCH1; Simple; p.Pro2412Thr (c.7234C>A); Zygosity=Heterozygous (from parent cell line). CC Sequence variation: Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg175His (c.524G>A); ClinVar=VCV000012374; Zygosity=Heterozygous (from parent cell line). CC Sequence variation: Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg248Gln (c.743G>A); ClinVar=VCV000012356; Zygosity=Heterozygous (from parent cell line). CC Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. CC Cell type: T-cell; CL=CL_0000084. ST Source(s): ATCC=CRL-2264; IZSLER=BS TCL 153 ST Amelogenin: X ST CSF1PO: 11 ST D13S317: 11,12 ST D16S539: 10,13 ST D21S11: 31,34.2 ST D5S818: 13 ST D7S820: 8.3,9 (ATCC=CRL-2264) ST D7S820: 9 (IZSLER=BS TCL 153) ST TH01: 6,7 ST TPOX: 8 ST vWA: 17,19 DI NCIt; C7953; Childhood T acute lymphoblastic leukemia DI ORDO; Orphanet_99861; Precursor T-cell acute lymphoblastic leukemia OX NCBI_TaxID=9606; ! Homo sapiens (Human) HI CVCL_0207 ! CCRF-CEM SX Female AG 3Y11M CA Cancer cell line DT Created: 04-04-12; Last updated: 19-12-24; Version: 33 // RX PubMed=12068308; DOI=10.1038/nature00766; RA Davies, Helen R. RA Bignell, Graham Robert RA Cox, Charles RA Stephens, Philip J. RA Edkins, Sarah RA Clegg, Sheila RA Teague, Jon W. RA Woffendin, Hayley RA Garnett, Mathew J. RA Bottomley, William RA Davis, Neil RA Dicks, Ed RA Ewing, Rebecca RA Floyd, Yvonne RA Gray, Kristian RA Hall, Sarah RA Hawes, Rachel RA Hughes, Jaime RA Kosmidou, Vivian RA Menzies, Andrew RA Mould, Catherine RA Parker, Adrian RA Stevens, Claire RA Watt, Stephen RA Hooper, Steven RA Wilson, Rebecca RA Jayatilake, Hiran RA Gusterson, Barry Austin RA Cooper, Colin S. RA Shipley, Janet M. RA Hargrave, Darren RA Pritchard-Jones, Kathryn RA Maitland, Norman J. RA Chenevix-Trench, Georgia RA Riggins, Gregory J. RA Bigner, Darell Doty RA Palmieri, Giuseppe RA Cossu, Antonio RA Flanagan, Adrienne Margaret RA Nicholson, Andrew RA Ho, Judy W.C. RA Leung, Suet Yi RA Yuen, Siu Tsan RA Weber, Barbara L. RA Seigler, Hilliard Foster RA Darrow, Timothy L. RA Paterson, Hugh F. RA Marais, Richard RA Marshall, Christopher John RA Wooster, Richard RA Stratton, Michael Rudolf RA Futreal, P. Andrew RT "Mutations of the BRAF gene in human cancer."; RL Nature 417:949-954(2002). // RX PubMed=7579731; RA Kapoor, Rohit RA Slade, D. Lynn RA Fujimori, Akira RA Pommier, Yves RA Harker, W. Graydon RT "Altered topoisomerase I expression in two subclones of human CEM RT leukemia selected for resistance to camptothecin."; RL Oncol. Res. 7:83-95(1995). //