Cellosaurus cell line MM266 (CVCL

Cross-references
Cell line name	MM266
Accession	CVCL_DH59
Resource Identification Initiative	To cite this cell line use: MM266 (RRID:CVCL_DH59)
Comments	Omics: CNV analysis. Omics: SNP array analysis.
Sequence variations	Mutation; HGNC; 1097; BRAF; Simple; p.Val600Glu (c.1799T>A); ClinVar=VCV000013961; Zygosity=Heterozygous (PubMed=22383533). Mutation; HGNC; 7029; MET; Simple; p.Thr992Ile (c.2975C>T) (p.Thr1010Ile, c.3029C>T); ClinVar=VCV000041624; Zygosity=Heterozygous (PubMed=22383533).
Disease	Melanoma (NCIt: C3224)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Category	Cancer cell line
Publications	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) PubMed=22383533; DOI=10.1158/1535-7163.MCT-11-0676 Dutton-Regester K., Irwin D., Hunt P., Aoude L.G., Tembe V., Pupo G.M., Lanagan C., Carter C.D., O'Connor L., O'Rourke M., Scolyer R.A., Mann G.J., Schmidt C.W., Herington A., Hayward N.K. A high-throughput panel for identifying clinically relevant mutation profiles in melanoma. Mol. Cancer Ther. 11:888-897(2012)
Cell line databases/resources	cancercelllines; CVCL_DH59
Encyclopedic resources	Wikidata; Q54906088
Gene expression databases	GEO; GSM228548
Polymorphism and mutation databases	Progenetix; CVCL_DH59
Entry history
Entry creation	13-Jul-2016
Last entry update	05-Oct-2023
Version number	5