ID   iWS780-2.10
AC   CVCL_EQ41
SY   WS iPSC from AG00780 (clone 2.10)
DR   GEO; GSM1184290
DR   GEO; GSM1184291
DR   Wikidata; Q54898391
RX   PubMed=24749076;
CC   Sequence variation: Mutation; HGNC; HGNC:12791; WRN; Simple; p.Arg369Ter (c.1105C>T) (c.1336C>T); ClinVar=VCV000005449; Zygosity=Homozygous (PubMed=24749076).
CC   Omics: Transcriptomics; Microarray.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C3447; Werner syndrome
DI   ORDO; Orphanet_902; Werner syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_U282 ! AG00780
SX   Male
AG   60Y
CA   Induced pluripotent stem cell
DT   Created: 26-09-16; Last updated: 10-04-25; Version: 12
//
RX   PubMed=24749076; DOI=10.1016/j.stemcr.2014.02.006; PMCID=PMC3986587;
RA   Cheung H.-H., Liu X.-Z., Canterel-Thouennon L., Li L., Edmonson C.,
RA   Rennert O.M.;
RT   "Telomerase protects Werner syndrome lineage-specific stem cells from
RT   premature aging.";
RL   Stem Cell Reports 2:534-546(2014).
//