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Cellosaurus PSADFN542 (CVCL_C3PG)

[Text version]
Cell line name PSADFN542
Accession CVCL_C3PG
Resource Identification Initiative To cite this cell line use: PSADFN542 (RRID:CVCL_C3PG)
Comments Part of: Progeria Research Foundation cell lines.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 6636; LMNA; Simple; p.Arg644Cys (c.1930C>T); ClinVar=VCV000014527; Zygosity=Heterozygous (PRF).
Disease Progeria (NCIt: C34951)
Hutchinson-Gilford progeria syndrome (ORDO: Orphanet_740)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 75Y2M
Category Finite cell line
Web pages https://www.progeriaresearch.org/available-cell-lines/
Cross-references
Encyclopedic resources Wikidata; Q116050131
Entry history
Entry creation15-Dec-2022
Last entry update29-Jun-2023
Version number3