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Cellosaurus AG24467 (CVCL_UY16)

[Text version]
Cell line name AG24467
Accession CVCL_UY16
Resource Identification Initiative To cite this cell line use: AG24467 (RRID:CVCL_UY16)
Comments Population: Caucasian.
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.Asn1197Thrfs*2 (c.3590delA); ClinVar=VCV000038890; Zygosity=Homozygous (Coriell=AG24467).
Disease Werner syndrome (NCIt: C3447)
Werner syndrome (ORDO: Orphanet_902)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 39Y
Category Finite cell line
Cross-references
Cell line collections (Providers) Coriell; AG24467
Encyclopedic resources Wikidata; Q93323309
Entry history
Entry creation25-Feb-2019
Last entry update19-Dec-2024
Version number10