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Cellosaurus A0031 iPS#34 (CVCL_IN38)

[Text version]

Cell line name A0031 iPS#34
Synonyms A0031 #34; A0031-derived iPSC clone 34; WS iPSC #34
Accession CVCL_IN38
Resource Identification Initiative To cite this cell line use: A0031 iPS#34 (RRID:CVCL_IN38)
Comments Population: Japanese.
Omics: Transcriptome analysis.
Derived from sampling site: Skin.
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
Publications

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)

Cross-references
Encyclopedic resources Wikidata; Q54606195
Gene expression databases GEO; GSM1519866
Entry history
Entry creation01-Dec-2016
Last entry update20-May-2021
Version number9