ID   WM1789
AC   CVCL_6792
SY   WM-1789; WM 1789; WC00080
DR   cancercelllines; CVCL_6792
DR   Coriell; WC00080
DR   Cosmic; 686395
DR   Cosmic; 1477416
DR   GEO; GSM186475
DR   GEO; GSM186476
DR   Progenetix; CVCL_6792
DR   Rockland; WM1789-01-0001
DR   Wikidata; Q54994194
WW   Info; Wistar; -; https://www.wistar.org/our-scientists/meenhard-herlyn
CC   Part of: Wistar Institute melanoma cell line collection.
CC   Sequence variation: Gene deletion; HGNC; HGNC:9588; PTEN; Zygosity=Hemizygous (Wistar).
CC   Sequence variation: Mutation; HGNC; HGNC:1097; BRAF; Simple; p.Ser363Phe (c.1088C>T); Zygosity=Unspecified (Wistar).
CC   Sequence variation: Mutation; HGNC; HGNC:1097; BRAF; Simple; p.Lys601Glu (c.1801A>G); ClinVar=VCV000013966; Zygosity=Homozygous (Wistar).
CC   Omics: Transcriptomics; Microarray.
CC   Discontinued: Coriell; WC00080; probable.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
ST   Source(s): Wistar
ST   Amelogenin: X,Y
ST   CSF1PO: 11,12
ST   D13S317: 9,11
ST   D16S539: 11,13
ST   D18S51: 12,17
ST   D19S433: 13,14
ST   D21S11: 29,30
ST   D2S1338: 20,24
ST   D3S1358: 15,16
ST   D5S818: 9,13
ST   D7S820: 8,9
ST   D8S1179: 10,15
ST   FGA: 19,22
ST   TH01: 7
ST   TPOX: 10,11
ST   vWA: 17,19
DI   NCIt; C3224; Melanoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   58Y
CA   Cancer cell line
DT   Created: 04-04-12; Last updated: 10-04-25; Version: 24
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