ID   NBsusSR
AC   CVCL_1450
DR   CLO; CLO_0050117
DR   ArrayExpress; E-MTAB-783
DR   BioSample; SAMN03472240
DR   Cell_Model_Passport; SIDM00002
DR   ChEMBL-Cells; CHEMBL3308847
DR   ChEMBL-Targets; CHEMBL2366150
DR   Cosmic; 925342
DR   Cosmic-CLP; 925342
DR   DepMap; ACH-002340
DR   GDSC; 925342
DR   GEO; GSM1670156
DR   IARC_TP53; 27185
DR   PharmacoDB; NBsusSR_995_2019
DR   RCB; RCB0803
DR   Wikidata; Q54907560
RX   PubMed=20164919;
RX   PubMed=30894373;
CC   Part of: Cancer Cell Line Encyclopedia (CCLE) project.
CC   Part of: COSMIC cell lines project.
CC   Population: Japanese.
CC   Microsatellite instability: Stable (MSS) (Sanger).
CC   Sequence variation: Mutation; HGNC; 11998; TP53; Simple; p.Arg213Ter (c.637C>T); ClinVar=VCV000043590; Zygosity=Homozygous (CCLE; Cosmic-CLP).
CC   Omics: Deep exome analysis.
CC   Omics: DNA methylation analysis.
CC   Omics: SNP array analysis.
CC   Omics: Transcriptome analysis.
CC   Genome ancestry: African=1.34%; Native American=0%; East Asian, North=75.7%; East Asian, South=20.79%; South Asian=0.62%; European, North=0.87%; European, South=0.68% (PubMed=30894373).
ST   Source(s): Cosmic-CLP; RCB
ST   Amelogenin: X,Y
ST   CSF1PO: 12,13
ST   D13S317: 8,10
ST   D16S539: 10,12
ST   D5S818: 10,12
ST   D7S820: 10,12
ST   TH01: 9
ST   TPOX: 8,11
ST   vWA: 15,18
DI   NCIt; C3270; Neuroblastoma
DI   ORDO; Orphanet_635; Neuroblastoma
OX   NCBI_TaxID=9606; ! Homo sapiens
SX   Male
AG   18Y
CA   Cancer cell line
DT   Created: 04-04-12; Last updated: 20-05-21; Version: 29
RX   PubMed=20164919; DOI=10.1038/nature08768;
RA   Bignell G.R., Greenman C.D., Davies H., 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., Swamy S., Dalgliesh G.L., Teh B.T.,
RA   Deloukas P., Yang F., 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=30894373; DOI=10.1158/0008-5472.CAN-18-2747;
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).