Cell line name |
MM369 |
Synonyms |
MM 369 |
Accession |
CVCL_C839 |
Resource Identification Initiative |
To cite this cell line use: MM369 (RRID:CVCL_C839) |
Comments |
Omics: CNV analysis. Omics: SNP array analysis. |
Sequence variations |
- Mutation; HGNC; 1097; BRAF; Simple; p.Val600Glu (c.1799T>A); ClinVar=VCV000013961; Zygosity=Unspecified (PubMed=17363583).
- Mutation; HGNC; 1787; CDKN2A; Simple; p.Arg80Ter (c.238C>T) (p.Pro94Leu, c.281C>T); ClinVar=VCV000009409; Zygosity=Unspecified (PubMed=17363583).
|
Disease |
Melanoma (NCIt: C3224) |
Species of origin |
Homo sapiens (Human)
(NCBI Taxonomy: 9606) |
Category |
Cancer cell line |
Publications | PubMed=3756862 Maynard K., Parsons P.G. Cross-sensitivity of methylating agents, hydroxyurea, and methotrexate in human tumor cells of the Mer- phenotype. Cancer Res. 46:5009-5013(1986) 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=10070891; DOI=10.1038/sj.bjc.6690147 Zerp S.F., van Elsas A., Peltenburg L.T.C., Schrier P.I. p53 mutations in human cutaneous melanoma correlate with sun exposure but are not always involved in melanomagenesis. Br. J. Cancer 79:921-926(1999) 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) |
Cross-references |
Cell line databases/resources |
cancercelllines; CVCL_C839
|
Encyclopedic resources |
Wikidata; Q54906110
|
Gene expression databases |
GEO; GSM224861
|
Polymorphism and mutation databases |
Cosmic; 928746
Cosmic; 1211157
Progenetix; CVCL_C839
|
Entry history |
Entry creation | 22-Oct-2012 |
Last entry update | 05-Oct-2023 |
Version number | 14 |
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