ID   XPCS1LV SV40
AC   CVCL_F622
SY   GM14931
DR   CLO; CLO_0030502
DR   BioSample; SAMN00803961
DR   Coriell; GM14931
DR   Wikidata; Q54847525
RX   PubMed=18079351;
CC   Population: Caucasian; Flemish.
CC   Sequence variation: Mutation; HGNC; HGNC:3437; ERCC5; Simple; p.Ser659Valfs*1 (c.1975delA) (2172delA); ClinVar=VCV001696064; Zygosity=Homozygous (from parent cell line).
CC   Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C156031; Xeroderma pigmentosum-Cockayne syndrome complex
DI   ORDO; Orphanet_220295; Xeroderma pigmentosum-Cockayne syndrome complex
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_F620 ! XPCS1LV
SX   Female
AG   5Y
CA   Transformed cell line
DT   Created: 11-02-13; Last updated: 19-12-24; Version: 17
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RX   PubMed=18079351; DOI=10.1259/bjr/27072321;
RA   Arlett C.F., Green M.H.L., Rogers P.B., Lehmann A.R., Plowman P.N.;
RT   "Minimal ionizing radiation sensitivity in a large cohort of xeroderma
RT   pigmentosum fibroblasts.";
RL   Br. J. Radiol. 81:51-58(2008).
//