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Cellosaurus iWS780-1.9 (CVCL_EQ40)

[Text version]
Cell line name iWS780-1.9
Synonyms WS iPSC from AG00780 (clone 1.9)
Accession CVCL_EQ40
Resource Identification Initiative To cite this cell line use: iWS780-1.9 (RRID:CVCL_EQ40)
Comments Omics: Transcriptome analysis by microarray.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 12791; WRN; Simple; p.Arg369Ter (c.1105C>T) (c.1336C>T); ClinVar=VCV000005449; Zygosity=Homozygous (PubMed=24749076).
Disease Werner syndrome (NCIt: C3447)
Werner syndrome (ORDO: Orphanet_902)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_U282 (AG00780)
Sex of cell Male
Age at sampling 60Y
Category Induced pluripotent stem cell

PubMed=24749076; DOI=10.1016/j.stemcr.2014.02.006
Cheung H.-H., Liu X.-Z., Canterel-Thouennon L., Li L., Edmonson C., Rennert O.M.
Telomerase protects Werner syndrome lineage-specific stem cells from premature aging.
Stem Cell Reports 2:534-546(2014)

Encyclopedic resources Wikidata; Q54898390
Gene expression databases GEO; GSM1184288
GEO; GSM1184289
Entry history
Entry creation26-Sep-2016
Last entry update29-Jun-2023
Version number10