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Cellosaurus A0031 (CVCL_T338)

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Cell line name A0031
Accession CVCL_T338
Resource Identification Initiative To cite this cell line use: A0031 (RRID:CVCL_T338)
Comments Population: Japanese.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:12791; WRN; Simple; p.Arg369Ter (c.1105C>T) (c.1336C>T); ClinVar=VCV000005449; Zygosity=Heterozygous (PubMed=25390333).
  • Mutation; HGNC; 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 Children:
CVCL_IN37 (A0031 iPS#23)CVCL_IN38 (A0031 iPS#34)CVCL_IN39 (A0031 iPS#64)
Originate from same individual CVCL_T339 ! B0031
Sex of cell Male
Age at sampling 37Y
Category Finite cell line
Publications

PubMed=25390333; DOI=10.1371/journal.pone.0112900; PMCID=PMC4229309
Akira Shimamoto, Harunobu Kagawa, Kazumasa Zensho, Yukihiro Sera, Yasuhiro Kazuki, Mitsuhiko Osaki, Mitsuo Oshimura, Yasuhito Ishigaki, Kanya Hamasaki, Yoshiaki Kodama, Shinsuke Yuasa ...Show all 20 authors... , Keiichi Fukuda, Kyotaro Hirashima, Hiroyuki Seimiya, Hirofumi Koyama, Takahiko Shimizu, Minoru Takemoto, Koutaro Yokote, Makoto Goto, Hidetoshi Tahara; Show fewer authors
Reprogramming suppresses premature senescence phenotypes of Werner syndrome cells and maintains chromosomal stability over long-term culture.
PLoS ONE 9:e112900.1-e112900.13(2014)

Cross-references
Cell line collections (Providers) RCB; GMC0012
Cell line databases/resources CLO; CLO_0050704
Encyclopedic resources Wikidata; Q54606193
Entry history
Entry creation03-Feb-2014
Last entry update19-Dec-2024
Version number14