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Cellosaurus Ma-Mel-05 (CVCL_A118)

Cell line name Ma-Mel-05
Synonyms Ma-Mel-5; MaMel-05; MaMel05; MaMel5
Accession CVCL_A118
Resource Identification Initiative To cite this cell line use: Ma-Mel-05 (RRID:CVCL_A118)
Comments Omics: SNP array analysis.
Derived from site: Metastatic; Hypodermis; UBERON=UBERON_0002072.
Derived from site: Metastatic; Skin; UBERON=UBERON_0002097.
Sequence variations
  • Gene deletion; HGNC; 1787; CDKN2A; Zygosity=Homozygous (PubMed=26909863).
  • Gene deletion; HGNC; 1788; CDKN2B; Zygosity=Homozygous (PubMed=26909863).
  • Mutation; HGNC; 5382; IDH1; Simple; p.Arg132Cys (c.394C>T); ClinVar=VCV000375891; Zygosity=Unspecified (PubMed=23851445).
  • Mutation; HGNC; 7989; NRAS; Simple; p.Gln61Arg (c.182A>G); ClinVar=VCV000013900; Zygosity=Unspecified (PubMed=17311103; PubMed=23348503; PubMed=23851445).
  • Mutation; HGNC; 9588; PTEN; Simple; p.Lys128Asn (c.384G>T); Zygosity=Unspecified (PubMed=23851445).
  • Mutation; HGNC; 11730; TERT; Simple; c.1-146C>T (c.250C>T) (C250T); Zygosity=Unspecified; Note=In promoter (PubMed=23348503).
Disease Melanoma (NCIt: C3224)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 49Y
Category Cancer cell line
STR profile Source(s): ECACC; ESTDAB

Markers:
AmelogeninX
CSF1PO11,12
D3S135815,17
D5S8189,11
D7S82011
D13S31711,13
D16S5398,13
FGA20,21
TH019.3
TPOX8
vWA15,17

Run an STR similarity search on this cell line
Publications

PubMed=17311103; DOI=10.1371/journal.pone.0000236
Ugurel S., Thirumaran R.K., Bloethner S., Gast A., Sucker A., Mueller-Berghaus J., Rittgen W., Hemminki K., Becker J.C., Kumar R., Schadendorf D.
B-RAF and N-RAS mutations are preserved during short time in vitro propagation and differentially impact prognosis.
PLoS ONE 2:E236-E236(2007)

PubMed=20544847; DOI=10.1002/gcc.20785
Gast A., Scherer D., Chen B.-W., Bloethner S., Melchert S., Sucker A., Hemminki K., Schadendorf D., Kumar R.
Somatic alterations in the melanoma genome: a high-resolution array-based comparative genomic hybridization study.
Genes Chromosomes Cancer 49:733-745(2010)

PubMed=23348503; DOI=10.1126/science.1230062
Horn S., Figl A., Rachakonda P.S., Fischer C., Sucker A., Gast A., Kadel S., Moll I., Nagore E., Hemminki K., Schadendorf D., Kumar R.
TERT promoter mutations in familial and sporadic melanoma.
Science 339:959-961(2013)

PubMed=23851445; DOI=10.1158/1541-7786.MCR-13-0006
Dahl C., Christensen C., Jonsson G., Lorentzen A., Skjodt M.L., Borg A., Pawelec G., Guldberg P.
Mutual exclusivity analysis of genetic and epigenetic drivers in melanoma identifies a link between p14 ARF and RARbeta signaling.
Mol. Cancer Res. 11:1166-1178(2013)

PubMed=26909863; DOI=10.18632/oncotarget.7503
Xie H.-P., Rachakonda P.S., Heidenreich B., Nagore E., Sucker A., Hemminki K., Schadendorf D., Kumar R.
Mapping of deletion breakpoints at the CDKN2A locus in melanoma: detection of MTAP-ANRIL fusion transcripts.
Oncotarget 7:16490-16504(2016)

Cross-references
Cell line collections (Providers) ECACC; 13012461
Cell line databases/resources cancercelllines; CVCL_A118
ESTDAB; ESTDAB-149
Anatomy/cell type resources BTO; BTO:0005338
Encyclopedic resources Wikidata; Q54903727
Gene expression databases GEO; GSM436987
Polymorphism and mutation databases Cosmic; 1181768
Cosmic; 1467736
Cosmic; 1846563
Cosmic; 2163838
Cosmic; 2686324
Progenetix; CVCL_A118
Entry history
Entry creation06-Jun-2012
Last entry update05-Oct-2023
Version number21