Cellosaurus logo
expasy logo

Cellosaurus XPCS1LV SV40 (CVCL_F622)

[Text version]
Cell line name XPCS1LV SV40
Synonyms GM14931
Accession CVCL_F622
Resource Identification Initiative To cite this cell line use: XPCS1LV SV40 (RRID:CVCL_F622)
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; HGNC:3437; ERCC5; Simple; p.Ser659Valfs*1 (c.1975delA) (2172delA); ClinVar=VCV001696064; Zygosity=Homozygous (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_F620 (XPCS1LV)
Sex of cell Female
Age at sampling 5Y
Category Transformed cell line
Publications

PubMed=18079351; DOI=10.1259/bjr/27072321
Arlett C.F., Green M.H.L., Rogers P.B., Lehmann A.R., Plowman P.N.
Minimal ionizing radiation sensitivity in a large cohort of xeroderma pigmentosum fibroblasts.
Br. J. Radiol. 81:51-58(2008)

Cross-references
Cell line collections (Providers) Coriell; GM14931
Cell line databases/resources CLO; CLO_0030502
Biological sample resources BioSample; SAMN00803961
Encyclopedic resources Wikidata; Q54847525
Entry history
Entry creation11-Feb-2013
Last entry update19-Dec-2024
Version number17