Cellosaurus cell line MW [Human melanoma] (CVCL

Cross-references
Cell line name	MW [Human melanoma]
Accession	CVCL_U799
Resource Identification Initiative	To cite this cell line use: MW [Human melanoma] (RRID:CVCL_U799)
Comments	Omics: CNV analysis. Omics: SNP array analysis.
Sequence variations	Gene deletion; HGNC; HGNC:1787; CDKN2A; Zygosity=Homozygous (PubMed=9354451; PubMed=17363583). Mutation; HGNC; HGNC:1097; BRAF; Simple; p.Val600Arg (c.1798_1799delGTinsAG); ClinVar=VCV000375940; Zygosity=Unspecified (PubMed=17363583).
Disease	Melanoma (NCIt: C3224)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell	Sex unspecified
Age at sampling	Age unspecified
Category	Cancer cell line
Publications	PubMed=9354451 Castellano M., Pollock P.M., Walters M.K., Sparrow L.E., Down L.M., Gabrielli B.G., Parsons P.G., Hayward N.K. CDKN2A/p16 is inactivated in most melanoma cell lines. Cancer Res. 57:4868-4875(1997) PubMed=17363583; DOI=10.1158/0008-5472.CAN-06-4152 Stark M.S., Hayward N.K. Genome-wide loss of heterozygosity and copy number analysis in melanoma using high-density single-nucleotide polymorphism arrays. Cancer Res. 67:2632-2642(2007)
Cell line databases/resources	cancercelllines; CVCL_U799
Encyclopedic resources	Wikidata; Q54907127
Gene expression databases	GEO; GSM226864
Polymorphism and mutation databases	Cosmic; 928721 Progenetix; CVCL_U799
Entry history
Entry creation	16-Apr-2014
Last entry update	19-Dec-2024
Version number	14