ID   IMS-M2
AC   CVCL_RL93
SY   IMSM2
DR   cancercelllines; CVCL_RL93
DR   Wikidata; Q54897681
RX   PubMed=19854508;
CC   Population: Japanese.
CC   Sequence variation: Gene fusion; HGNC; 3495; ETV6 + HGNC; 8033; NTRK3; Name(s)=ETV6-NTRK3, TEL-TRKC; Note=In frame (PubMed=19854508).
CC   Sequence variation: Mutation; HGNC; 7910; NPM1; Simple; p.Trp288Cysfs*12 (c.860_863dupTCTG); ClinVar=VCV000013998; Zygosity=Heterozygous (PubMed=19854508).
CC   Derived from site: In situ; Bone marrow; UBERON=UBERON_0002371.
DI   NCIt; C9154; Adult acute myeloid leukemia
DI   ORDO; Orphanet_519; Acute myeloid leukemia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   59Y
CA   Cancer cell line
DT   Created: 05-03-18; Last updated: 05-10-23; Version: 10
//
RX   PubMed=19854508; DOI=10.1016/j.leukres.2009.09.019;
RA   Chi H.T., Vu H.A., Iwasaki R., Nagamura F., Tojo A., Watanabe T.,
RA   Sato Y.;
RT   "Detection of exon 12 type A mutation of NPM1 gene in IMS-M2 cell
RT   line.";
RL   Leuk. Res. 34:261-262(2010).
//