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Cellosaurus XP14BRneo17 (CVCL_F630)

[Text version]
Cell line name XP14BRneo17
Synonyms GM16093
Accession CVCL_F630
Resource Identification Initiative To cite this cell line use: XP14BRneo17 (RRID:CVCL_F630)
Comments Population: Pakistani.
Genetic integration: Method=Transfection; Gene=UniProtKB; P03070; SV40 large T antigen.
Genetic integration: Method=Transfection; Gene=UniProtKB; P00552; Transposon Tn5 neo.
Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40) (Note=pSV3-neo).
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.Arg718Ter (c.2152C>T); ClinVar=VCV000551486; Zygosity=Unspecified (from parent cell line).
Disease Xeroderma pigmentosum, complementation group C (NCIt: C114770)
Xeroderma pigmentosum (ORDO: Orphanet_910)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_F629 (XP14BR.2)
Sex of cell Female
Age at sampling 14-15Y
Category Finite cell line
Publications

PubMed=16714754; DOI=10.1259/bjr/83726649
Arlett C.F., Plowman P.N., Rogers P.B., Parris C.N., Abbaszadeh F., Green M.H.L., McMillan T.J., Bush C., Foray N., Lehmann A.R.
Clinical and cellular ionizing radiation sensitivity in a patient with xeroderma pigmentosum.
Br. J. Radiol. 79:510-517(2006)

Cross-references
Cell line collections (Providers) Coriell; GM16093
Cell line databases/resources CLO; CLO_0018854
Encyclopedic resources Wikidata; Q54848317
Entry history
Entry creation11-Feb-2013
Last entry update19-Dec-2024
Version number16