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Cellosaurus A0031 iPS#23 (CVCL_IN37)

[Text version]

Cell line name A0031 iPS#23
Synonyms A0031 #23; A0031-derived iPSC clone 23
Accession CVCL_IN37
Resource Identification Initiative To cite this cell line use: A0031 iPS#23 (RRID:CVCL_IN37)
Comments Population: Japanese.
Derived from sampling site: Skin. Cell type=Fibroblast.
Sequence variations
  • Mutation; HGNC; 12791; WRN; Simple; p.Arg369Ter (c.1105C>T) (c.1336C>T); ClinVar=VCV000005449; Zygosity=Heterozygous (PubMed=25390333).
  • Mutation; HGNC; 12791; WRN; Simple; p.Lys1046fs*14 (c.3139-1G>C) (IVS25-1G>C); ClinVar=VCV000005447; Zygosity=Heterozygous; Note=Splice acceptor mutation (PubMed=25390333).
Disease Werner syndrome (NCIt: C3447)
Werner syndrome (ORDO: Orphanet_902)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_T338 (A0031)
Sex of cell Male
Age at sampling 37Y
Category Induced pluripotent stem cell

PubMed=25390333; DOI=10.1371/journal.pone.0112900
Shimamoto A., Kagawa H., Zensho K., Sera Y., Kazuki Y., Osaki M., Oshimura M., Ishigaki Y., Hamasaki K., Kodama Y., Yuasa S., Fukuda K., Hirashima K., Seimiya H., Koyama H., Shimizu T., Takemoto M., Yokote K., Goto M., Tahara H.
Reprogramming suppresses premature senescence phenotypes of Werner syndrome cells and maintains chromosomal stability over long-term culture.
PLoS ONE 9:E112900-E112900(2014)

Encyclopedic resources Wikidata; Q54606194
Entry history
Entry creation01-Dec-2016
Last entry update17-Mar-2022
Version number10