ID   SJG-6
AC   CVCL_WV08
SY   SJG-006
DR   cancercelllines; CVCL_WV08
DR   Wikidata; Q98132636
RX   CelloPub=CLPUB00517;
RX   CelloPub=CLPUB00518;
RX   PubMed=27693639;
CC   Sequence variation: Mutation; HGNC; HGNC:1509; CASP8; Simple; p.His278Tyr (c.832C>T); Zygosity=Unspecified (PubMed=27693639).
CC   Sequence variation: Mutation; HGNC; HGNC:3595; FAT1; Simple; p.Glu833Ter (c.2497G>T); Zygosity=Unspecified (PubMed=27693639).
CC   Sequence variation: Mutation; HGNC; HGNC:3595; FAT1; Simple; p.Ser3065Ter (c.9194C>G); Zygosity=Unspecified (PubMed=27693639).
CC   Sequence variation: Mutation; HGNC; HGNC:3595; FAT1; Simple; p.Gln3524Ter (c.10570C>T); Zygosity=Unspecified (PubMed=27693639).
CC   Sequence variation: Mutation; HGNC; HGNC:7881; NOTCH1; Simple; p.Cys312Ter (c.936C>A); Zygosity=Heterozygous (CelloPub=CLPUB00517; PubMed=27693639).
CC   Sequence variation: Mutation; HGNC; HGNC:7881; NOTCH1; Simple; p.Trp1843Ter (c.5529G>A); Zygosity=Heterozygous (CelloPub=CLPUB00517; PubMed=27693639).
CC   Sequence variation: Mutation; HGNC; HGNC:9588; PTEN; Simple; p.Gln171Ter (c.511C>T); ClinVar=VCV000189411; Zygosity=Unspecified (PubMed=27693639).
CC   Sequence variation: Mutation; HGNC; HGNC:9588; PTEN; Simple; p.Glu201Gln (c.601G>C); Zygosity=Unspecified (PubMed=27693639).
CC   Sequence variation: Mutation; HGNC; HGNC:9588; PTEN; Simple; p.Gly209Glu (c.626G>A); Zygosity=Unspecified (PubMed=27693639).
CC   Omics: Genomics; Whole exome sequencing.
CC   Miscellaneous: STR profile from personal communication of Broad, Simon.
CC   Derived from site: In situ; Oral cavity, alveolar ridge; UBERON=UBERON_0004103.
ST   Source(s): Direct_author_submission
ST   Amelogenin: X
ST   CSF1PO: 10
ST   D13S317: 12
ST   D16S539: 12
ST   D18S51: 15,16
ST   D21S11: 29,30
ST   D3S1358: 14,15
ST   D5S818: 12,13
ST   D7S820: 10
ST   D8S1179: 13
ST   FGA: 19,24
ST   Penta D: 10,12
ST   Penta E: 7,13
ST   TH01: 6,9.3
ST   TPOX: 10,11
ST   vWA: 17,19
DI   NCIt; C170774; Alveolar ridge squamous cell carcinoma
DI   ORDO; Orphanet_502363; Squamous cell carcinoma of the oral cavity
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   63Y
CA   Cancer cell line
DT   Created: 05-07-19; Last updated: 10-04-25; Version: 11
//
RX   CelloPub=CLPUB00517;
RA   Pritchard, Ashley Jane
RT   "Correlating genetic change with changes in cell behaviour in squamous
RT   cell carcinoma of the head and neck (SCCHN). Focus on inactivating
RT   NOTCH1 mutations.";
RL   Thesis PhD (2018); King's College London; London; United Kingdom.
//
RX   CelloPub=CLPUB00518;
RA   Goldie, Stephen J.
RT   "Studies of FRMD4A in two models of squamous cell carcinoma.";
RL   Thesis PhD (2011); University of Cambridge; Cambridge; United Kingdom.
//
RX   PubMed=27693639; DOI=10.1016/j.canlet.2016.09.014; PMCID=PMC5090049;
RA   Hayes, Tyler F.
RA   Benaich, Nathan
RA   Goldie, Stephen J.
RA   Sipila, Kalle
RA   Ames-Draycott, Ashley
RA   Cai, Wen-Jun
RA   Yin, Guang-Liang
RA   Watt, Fiona Mary
RT   "Integrative genomic and functional analysis of human oral squamous
RT   cell carcinoma cell lines reveals synergistic effects of FAT1 and
RT   CASP8 inactivation.";
RL   Cancer Lett. 383:106-114(2016).
//