ID   PA055
AC   CVCL_1G13
DR   cancercelllines; CVCL_1G13
DR   Cosmic; 1820261
DR   Wikidata; Q54937342
RX   PubMed=22156295;
CC   Population: Japanese.
CC   Microsatellite instability: Stable (MSS) (PubMed=22156295).
CC   Sequence variation: Gene deletion; HGNC; HGNC:6770; SMAD4; Zygosity=Homozygous (PubMed=22156295).
CC   Sequence variation: Mutation; HGNC; HGNC:6407; KRAS; Simple; p.Gly12Asp (c.35G>A); ClinVar=VCV000012582; Zygosity=Unspecified (PubMed=22156295).
CC   Sequence variation: Mutation; HGNC; HGNC:11998; TP53; Simple; p.Ser149fs; Zygosity=Unspecified (PubMed=22156295).
CC   Omics: Deep exome analysis.
CC   Omics: SNP array analysis.
CC   Derived from site: In situ; Pancreas; UBERON=UBERON_0001264.
DI   NCIt; C9120; Pancreatic ductal adenocarcinoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Sex unspecified
AG   Age unspecified
CA   Cancer cell line
DT   Created: 08-07-15; Last updated: 19-12-24; Version: 12
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RX   PubMed=22156295; DOI=10.1101/gr.123109.111; PMCID=PMC3266029;
RA   Wang L.-H., Tsutsumi S., Kawaguchi T., Nagasaki K., Tatsuno K.,
RA   Yamamoto S., Sang F., Sonoda K., Sugawara M., Saiura A., Hirono S.,
RA   Yamaue H., Miki Y., Isomura M., Totoki Y., Nagae G., Isagawa T.,
RA   Ueda H., Murayama-Hosokawa S., Shibata T., Sakamoto H., Kanai Y.,
RA   Kaneda A., Noda T., Aburatani H.;
RT   "Whole-exome sequencing of human pancreatic cancers and
RT   characterization of genomic instability caused by MLH1
RT   haploinsufficiency and complete deficiency.";
RL   Genome Res. 22:208-219(2012).
//