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Cellosaurus FM93 (CVCL_9680)

[Text version]
Cell line name FM93
Accession CVCL_9680
Resource Identification Initiative To cite this cell line use: FM93 (RRID:CVCL_9680)
Comments Omics: Array-based CGH.
Sequence variations
  • Gene deletion; HGNC; 1787; CDKN2A; Zygosity=Homozygous (PubMed=17260012).
  • Mutation; HGNC; 1097; BRAF; Simple; p.Val600Glu (c.1799T>A); ClinVar=VCV000013961; Zygosity=Unspecified (PubMed=17260012).
  • Mutation; HGNC; 11998; TP53; Simple; p.Gly266Arg (c.795_796GG>AA); Zygosity=Unspecified (PubMed=17260012).
Disease Cutaneous melanoma (NCIt: C3510)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_C617 (FM93/2)
Sex of cell Sex unspecified
Age at sampling Age unspecified
Category Cancer cell line
Publications

PubMed=9288767
Guldberg P., thor Straten P., Birck A., Ahrenkiel V., Kirkin A.F., Zeuthen J.
Disruption of the MMAC1/PTEN gene by deletion or mutation is a frequent event in malignant melanoma.
Cancer Res. 57:3660-3663(1997)

PubMed=17260012; DOI=10.1038/sj.onc.1210252
Jonsson G., Dahl C., Staaf J., Sandberg T., Bendahl P.-O., Ringner M., Guldberg P., Borg A.
Genomic profiling of malignant melanoma using tiling-resolution arrayCGH.
Oncogene 26:4738-4748(2007)

Cross-references
Cell line databases/resources cancercelllines; CVCL_9680
Encyclopedic resources Wikidata; Q54835075
Gene expression databases GEO; GSM156038
Polymorphism and mutation databases Cosmic; 1047684
IARC_TP53; 26110
Progenetix; CVCL_9680
Entry history
Entry creation06-Jun-2012
Last entry update05-Oct-2023
Version number16