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Cellosaurus AG27427 (CVCL_WU12)

[Text version]
Cell line name AG27427
Synonyms AG27427*B
Accession CVCL_WU12
Resource Identification Initiative To cite this cell line use: AG27427 (RRID:CVCL_WU12)
Comments Population: Caucasian.
Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:6636; LMNA; Simple; p.Glu578Val (c.1733A>T); ClinVar=VCV000066863; Zygosity=Heterozygous (Coriell=AG27427).
Disease Werner syndrome (NCIt: C3447)
Atypical Werner syndrome (ORDO: Orphanet_79474)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_U311 (AG04110)
Sex of cell Female
Age at sampling 13Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) Coriell; AG27427
Encyclopedic resources Wikidata; Q93323506
Entry history
Entry creation05-Jul-2019
Last entry update19-Dec-2024
Version number10