ID   LN-382T
AC   CVCL_6839
SY   LN 382T; LN382T
DR   cancercelllines; CVCL_6839
DR   Cosmic; 849866
DR   Cosmic; 2367495
DR   Wikidata; Q54902779
RX   PubMed=10416987;
RX   PubMed=22570425;
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; 9884; RB1; Simple; p.Arg320Ter (c.958C>T); ClinVar=VCV000126824; Zygosity=Unspecified (from parent cell line).
CC   Sequence variation: Mutation; HGNC; 11998; TP53; Simple; p.Val197Leu (c.589G>T); ClinVar=VCV000216468; Zygosity=Homozygous (PubMed=10416987).
CC   Derived from site: In situ; Brain, right fronto-parietal lobe.
ST   Source(s): PubMed=22570425
ST   Amelogenin: X
ST   CSF1PO: 10,11
ST   D13S317: 13
ST   D16S539: 9,12
ST   D18S51: 15,16
ST   D21S11: 30,31.2
ST   D3S1358: 14,18
ST   D5S818: 11
ST   D7S820: 8,11
ST   D8S1179: 9,13
ST   FGA: 24,25
ST   Penta D: 12
ST   Penta E: 10
ST   TH01: 9,9.3
ST   TPOX: 8
ST   vWA: 16,18
DI   NCIt; C3058; Glioblastoma
DI   ORDO; Orphanet_360; Glioblastoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_3956 ! LN-382
SX   Male
AG   67Y
CA   Cancer cell line
DT   Created: 04-04-12; Last updated: 05-10-23; Version: 17
RX   PubMed=10416987; DOI=10.1111/j.1750-3639.1999.tb00536.x;
RA   Ishii N., Maier D., Merlo A., Tada M., Sawamura Y., Diserens A.-C.,
RA   Van Meir E.G.;
RT   "Frequent co-alterations of TP53, p16/CDKN2A, p14ARF, PTEN tumor
RT   suppressor genes in human glioma cell lines.";
RL   Brain Pathol. 9:469-479(1999).
RX   PubMed=22570425; DOI=10.1093/neuonc/nos072;
RA   Bady P., Diserens A.-C., Castella V., Kalt S., Heinimann K.,
RA   Hamou M.-F., Delorenzi M., Hegi M.E.;
RT   "DNA fingerprinting of glioma cell lines and considerations on
RT   similarity measurements.";
RL   Neuro-oncol. 14:701-711(2012).