ID   WM3928
AC   CVCL_6802
SY   WM-3928; WM 3928; WM3928F; WC00115
DR   cancercelllines; CVCL_6802
DR   Coriell; WC00115
DR   GEO; GSM952609
DR   Progenetix; CVCL_6802
DR   Rockland; WM3928-01-0001
DR   Wikidata; Q54994304
WW   https://www.wistar.org/our-scientists/meenhard-herlyn
CC   Part of: Wistar Institute melanoma cell line collection.
CC   Sequence variation: Gene deletion; HGNC; 1788; CDKN2B; Zygosity=Homozygous (Wistar).
CC   Sequence variation: Mutation; HGNC; 9588; PTEN; Simple; p.Tyr177Ter (c.531T>G); ClinVar=VCV000235334; Zygosity=Unspecified (Wistar).
CC   Omics: Transcriptome analysis by microarray.
CC   Discontinued: Coriell; WC00115; probable.
CC   Derived from site: Metastatic; Left inguinal lymph node; UBERON=UBERON_0001542.
ST   Source(s): Wistar
ST   Amelogenin: X,Y
ST   CSF1PO: 12,13
ST   D13S317: 8,9
ST   D16S539: 10
ST   D18S51: 14,19
ST   D19S433: 12,17
ST   D21S11: 28,30
ST   D2S1338: 17,24
ST   D3S1358: 14,15
ST   D5S818: 11,12
ST   D7S820: 10,11
ST   D8S1179: 10,13
ST   FGA: 21
ST   TH01: 7,8
ST   TPOX: 8,11
ST   vWA: 17,18
DI   NCIt; C3224; Melanoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   Age unspecified
CA   Cancer cell line
DT   Created: 04-04-12; Last updated: 05-10-23; Version: 20
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