Cellosaurus cell line WS0101 (CVCL

Cross-references
Cell line name	WS0101
Accession	CVCL_A7BT
Resource Identification Initiative	To cite this cell line use: WS0101 (RRID:CVCL_A7BT)
Comments	Population: Japanese. Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV). Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations	Mutation; HGNC; HGNC:12791; WRN; Simple; p.Lys1046fs*14 (c.3139-1G>C) (IVS25-1G>C); ClinVar=VCV000005447; Zygosity=Heterozygous (PubMed=9365237). Mutation; HGNC; HGNC:12791; WRN; Simple; p.Arg1305Ter (c.3913C>T) (c.4144C>T); ClinVar=VCV000005444; Zygosity=Heterozygous (PubMed=9365237).
Disease	Werner syndrome (NCIt: C3447) Werner syndrome (ORDO: Orphanet_902)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell	Male
Age at sampling	30Y
Category	Transformed cell line
Publications	PubMed=9365237; DOI=10.1038/sj.onc.1201377 Hidetoshi Tahara, Yoshiki Tokutake, Shizuko Maeda, Hiroshi Kataoka, Taro Watanabe, Misako Satoh, Takehisa Matsumoto, Minoru Sugawara, Toshinori Ide, Makoto Goto, Yasuhiro Furuichi, Masanobu Sugimoto; Abnormal telomere dynamics of B-lymphoblastoid cell strains from Werner's syndrome patients transformed by Epstein-Barr virus. Oncogene 15:1911-1920(1997)
Encyclopedic resources	Wikidata; Q107117487
Entry history
Entry creation	20-May-2021
Last entry update	19-Dec-2024
Version number	5