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Cellosaurus CMY (CVCL_A602)

[Text version]
Cell line name CMY
Accession CVCL_A602
Resource Identification Initiative To cite this cell line use: CMY (RRID:CVCL_A602)
Comments Population: Japanese.
Doubling time: ~46 hours (PubMed=9852262); ~48 hours (DSMZ=ACC-986).
Derived from site: In situ; Bone marrow; UBERON=UBERON_0002371.
Sequence variations
  • Mutation; HGNC; HGNC:9811; RAD21; Simple; p.Tyr3Ter (c.9C>G); Zygosity=Unspecified (PubMed=23955599).
Disease Down syndrome (NCIt: C2993)
Myeloid leukemia associated with Down syndrome (NCIt: C43223)
Down syndrome (ORDO: Orphanet_870)
Acute megakaryoblastic leukemia in Down syndrome (ORDO: Orphanet_99887)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 2Y
Category Cancer cell line
STR profile Source(s): DSMZ=ACC-986

Markers:
AmelogeninX,Y
CSF1PO7,11
D2S133822,23
D3S135815
D5S8189,11
D7S82010,12
D8S117912,13
D13S3178,11
D16S53910,12
D18S5113,16
D19S43313
D21S1129,30
FGA23,24
Penta D10,13
Penta E5,16
TH016,7
TPOX11
vWA14

Run an STR similarity search on this cell line
Publications

PubMed=9852262; DOI=10.3892/ijmm.1.3.559
Nobuyuki Miura, Takeyuki Sato, Akira Fuse, Yuri Okimoto, Naoko Kinugawa, Hiroshi Horie, Setsuo Ota, Harumi Kakuda, Hidetaka Yokoe, Tsuneo Miya, Nobuo Suzuki, Hiroo Niimi;
Establishment of a new human megakaryoblastic cell line, CMY, with chromosome 17p abnormalities.
Int. J. Mol. Med. 1:559-563(1998)

PubMed=10674912; DOI=10.3109/10428190009148861
Takeyuki Sato, Hiromasa Sekine, Harumi Kakuda, Nobuyuki Miura, Masataka Sunohara, Akira Fuse;
HIV infection of megakaryocytic cell lines.
Leuk. Lymphoma 36:397-404(2000)

DOI=10.1016/B978-0-12-221970-2.50457-5
Hans Gunther Drexler;
The leukemia-lymphoma cell line factsbook.
(In book) ISBN 9780122219702; pp.1-733; Academic Press; London; United Kingdom (2001)

PubMed=14504097; DOI=10.1182/blood-2003-02-0418
Takeshi Taketani, Tomohiko Taki, Kanji Sugita, Yoshiyuki Furuichi, Eiichi Ishii, Ryoji Hanada, Masahiro Tsuchida, Kenichi Sugita, Kohmei Ida, Yasuhide Hayashi;
FLT3 mutations in the activation loop of tyrosine kinase domain are frequently found in infant ALL with MLL rearrangements and pediatric ALL with hyperdiploidy.
Blood 103:1085-1088(2004)

PubMed=16408098; DOI=10.1038/sj.leu.2404081
Hilmar Quentmeier, Roderick A.F. MacLeod, Margarete Zaborski, Hans Gunther Drexler;
JAK2 V617F tyrosine kinase mutation in cell lines derived from myeloproliferative disorders.
Leukemia 20:471-476(2006)

PubMed=23955599; DOI=10.1038/ng.2731
Ayana Kon, Lee-Yung Shih, Masashi Minamino, Masashi Sanada, Yuichi Shiraishi, Yasunobu Nagata, Ken-ichi Yoshida, Yusuke Okuno, Masashige Bando, Ryuichiro Nakato, Shumpei Ishikawa ...Show all 41 authors... , Aiko Sato-Otsubo, Genta Nagae, Aiko Nishimoto, Claudia Haferlach, Daniel Nowak, Yusuke Sato, Tamara Alpermann, Masao Nagasaki, Teppei Shimamura, Hiroko Tanaka, Kenichi Chiba, Ryo Yamamoto, Tomoyuki Yamaguchi, Makoto Otsu, Naoshi Obara, Mamiko Sakata-Yanagimoto, Tsuyoshi Nakamaki, Ken Ishiyama, Florian Nolte, Wolf-Karsten Hofmann, Shuichi Miyawaki, Shigeru Chiba, Hiraku Mori, Hiromitsu Nakauchi, Harold Phillip Koeffler, Hiroyuki Aburatani, Torsten Haferlach, Katsuhiko Shirahige, Satoru Miyano, Seishi Ogawa; Show fewer authors
Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms.
Nat. Genet. 45:1232-1237(2013)

Cross-references
Cell line collections (Providers) DSMZ; ACC-986
Encyclopedic resources Wikidata; Q54813866
Polymorphism and mutation databases Cosmic; 787424
Cosmic; 975242
Cosmic; 996323
Cosmic; 1012063
Cosmic; 1037675
Cosmic; 1191082
Cosmic; 1281308
Cosmic; 2089669
Entry history
Entry creation06-Jun-2012
Last entry update19-Dec-2024
Version number18