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Cellosaurus XPCS2LV SV40 (CVCL_F621)

[Text version]
Cell line name XPCS2LV SV40
Synonyms GM14930
Accession CVCL_F621
Resource Identification Initiative To cite this cell line use: XPCS2LV SV40 (RRID:CVCL_F621)
Comments Population: Caucasian; Flemish.
Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40).
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 3437; ERCC5; Simple; p.Arg263Ter (c.787C>T) (984C>T); ClinVar=VCV000016570; Zygosity=Heterozygous (from parent cell line).
  • Mutation; HGNC; 3437; ERCC5; Simple; p.Ser659Valfs*1 (c.1975delA) (2172delA); ClinVar=VCV001696064; Zygosity=Heterozygous (from parent cell line).
Disease Xeroderma pigmentosum-Cockayne syndrome complex (NCIt: C156031)
Xeroderma pigmentosum-Cockayne syndrome complex (ORDO: Orphanet_220295)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_F619 (XPCS2LV)
Sex of cell Male
Age at sampling 1Y8M
Category Transformed cell line
Cross-references
Cell line collections (Providers) Coriell; GM14930
Cell line databases/resources CLO; CLO_0030505
Biological sample resources BioSample; SAMN00803959
Encyclopedic resources Wikidata; Q54847524
Entry history
Entry creation11-Feb-2013
Last entry update29-Jun-2023
Version number17