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Cellosaurus XP14BR.1 (CVCL_ZN23)

[Text version]
Cell line name XP14BR.1
Synonyms Xeroderma Pigmentosum 14 BRighton 1; 86/0029
Accession CVCL_ZN23
Resource Identification Initiative To cite this cell line use: XP14BR.1 (RRID:CVCL_ZN23)
Comments Population: Pakistani.
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 autologous cell line XP14BR.2).
Disease Xeroderma pigmentosum, complementation group C (NCIt: C114770)
Xeroderma pigmentosum (ORDO: Orphanet_910)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_F629 ! XP14BR.2
Sex of cell Female
Age at sampling 9Y
Category Finite cell line
Publications

PubMed=1571258; DOI=10.1111/j.1365-2133.1992.tb00681.x
Salob S.P., Webb D.K.H., Atherton D.J.
A child with xeroderma pigmentosum and bone marrow failure.
Br. J. Dermatol. 126:372-374(1992)

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)

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
Encyclopedic resources Wikidata; Q98135315
Entry history
Entry creation02-Jul-2020
Last entry update19-Dec-2024
Version number8