Cellosaurus cell line XP226BA (CVCL

Cross-references
Cell line name	XP226BA
Accession	CVCL_ZU53
Resource Identification Initiative	To cite this cell line use: XP226BA (RRID:CVCL_ZU53)
Comments	Population: Guatemalan. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations	Mutation; HGNC; HGNC:12816; XPC; Simple; p.Arg314Glyfs*10 (c.940delC) (C940del-1); ClinVar=VCV003588617; Zygosity=Homozygous (PubMed=27543334).
Disease	Xeroderma pigmentosum, complementation group C (NCIt: C114770) Xeroderma pigmentosum (ORDO: Orphanet_910)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Category	Finite cell line
Publications	PubMed=27543334; DOI=10.1073/pnas.1610020113; PMCID=PMC5018765 Reid-Bayliss K.S., Arron S.T., Loeb L.A., Bezrookove V., Cleaver J.E. Why Cockayne syndrome patients do not get cancer despite their DNA repair deficiency. Proc. Natl. Acad. Sci. U.S.A. 113:10151-10156(2016)
Encyclopedic resources	Wikidata; Q98135542
Entry history
Entry creation	02-Jul-2020
Last entry update	10-Apr-2025
Version number	8