ID   SNU-2972-1
AC   CVCL_UD98
SY   NMC1
DR   EGA; EGAD00001003117
DR   KCLB; 02972-1
DR   Wikidata; Q98132789
RX   PubMed=28203693;
CC   Part of: Seoul National University (SNU) cell line collection.
CC   Population: Korean.
CC   Sequence variation: Gene fusion; HGNC; HGNC:13575; BRD4 + HGNC; HGNC:29919; NUTM1; Name(s)=BRD4-NUTM1, BRD4-NUT; Note=BRD4 exon 11 fused to NUTM1 exon 2 (PubMed=28203693).
CC   Omics: Genome sequenced.
CC   Omics: Transcriptome analysis by RNAseq.
CC   Derived from site: Metastatic; Pleural effusion; UBERON=UBERON_0000175.
ST   Source(s): KCLB=02972-1
ST   Amelogenin: X,Y
ST   CSF1PO: 10,12
ST   D13S317: 8
ST   D3S1358: 16
ST   D5S818: 12,13
ST   D7S820: 8,10
ST   FGA: 21,25
ST   TH01: 7,9
ST   TPOX: 9,11
ST   vWA: 14,16
DI   NCIt; C45716; NUT carcinoma
DI   ORDO; Orphanet_443167; NUT midline carcinoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   34Y
CA   Cancer cell line
DT   Created: 13-11-18; Last updated: 19-12-24; Version: 9
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RX   PubMed=28203693; DOI=10.1093/annonc/mdw686; PMCID=PMC5378225;
RA   Lee J.-K., Louzada S., An Y., Kim S.Y., Kim S., Youk J., Park S.,
RA   Koo S.H., Keam B., Jeon Y.K., Ku J.-L., Yang F.-T., Kim T.M., Ju Y.S.;
RT   "Complex chromosomal rearrangements by single catastrophic
RT   pathogenesis in NUT midline carcinoma.";
RL   Ann. Oncol. 28:890-897(2017).
//