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Cellosaurus WM1789 (CVCL_6792)

[Text version]
Cell line name WM1789
Synonyms WM-1789; WM 1789; WC00080
Accession CVCL_6792
Resource Identification Initiative To cite this cell line use: WM1789 (RRID:CVCL_6792)
Comments Part of: Wistar Institute melanoma cell line collection.
Omics: Transcriptome analysis by microarray.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Sequence variations
  • Gene deletion; HGNC; HGNC:9588; PTEN; Zygosity=Hemizygous (Wistar).
  • Mutation; HGNC; HGNC:1097; BRAF; Simple; p.Ser363Phe (c.1088C>T); Zygosity=Unspecified (Wistar).
  • Mutation; HGNC; HGNC:1097; BRAF; Simple; p.Lys601Glu (c.1801A>G); ClinVar=VCV000013966; Zygosity=Homozygous (Wistar).
Disease Melanoma (NCIt: C3224)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 58Y
Category Cancer cell line
STR profile Source(s): Wistar

Markers:
AmelogeninX,Y
CSF1PO11,12
D2S133820,24
D3S135815,16
D5S8189,13
D7S8208,9
D8S117910,15
D13S3179,11
D16S53911,13
D18S5112,17
D19S43313,14
D21S1129,30
FGA19,22
TH017
TPOX10,11
vWA17,19

Run an STR similarity search on this cell line
Web pages https://www.wistar.org/our-scientists/meenhard-herlyn
Cross-references
Cell line collections (Providers) Coriell; WC00080 - Discontinued
Rockland; WM1789-01-0001
Cell line databases/resources cancercelllines; CVCL_6792
Encyclopedic resources Wikidata; Q54994194
Gene expression databases GEO; GSM186475
GEO; GSM186476
Polymorphism and mutation databases Cosmic; 686395
Cosmic; 1477416
Progenetix; CVCL_6792
Entry history
Entry creation04-Apr-2012
Last entry update19-Dec-2024
Version number23