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Cellosaurus XP7BR (CVCL_ZQ01)

[Text version]
Cell line name XP7BR
Synonyms Xeroderma Pigmentosum 7 BRighton
Accession CVCL_ZQ01
Resource Identification Initiative To cite this cell line use: XP7BR (RRID:CVCL_ZQ01)
Comments Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:9181; POLH; Simple; p.Leu77del (c.222_224TCT[1]) (c.225_227delTCT) (L75del); ClinVar=VCV000005893; Zygosity=Heterozygous (PubMed=11773631).
  • Mutation; HGNC; HGNC:9181; POLH; Simple; p.Ile255fs (Fs255); Zygosity=Heterozygous (PubMed=11773631).
Disease Xeroderma pigmentosum variant type (NCIt: C141367)
Xeroderma pigmentosum variant (ORDO: Orphanet_90342)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Sex unspecified
Age at sampling 60Y
Category Finite cell line
Publications

PubMed=10022907; DOI=10.1128/mcb.19.3.2206; PMCID=PMC84013
Cordonnier A.M., Lehmann A.R., Fuchs R.P.P.
Impaired translesion synthesis in xeroderma pigmentosum variant extracts.
Mol. Cell. Biol. 19:2206-2211(1999)

PubMed=11773631; DOI=10.1073/pnas.022473899; PMCID=PMC117388
Broughton B.C., Cordonnier A.M., Kleijer W.J., Jaspers N.G.J., Fawcett H., Raams A., Garritsen V.H., Stary A., Avril M.-F., Boudsocq F., Masutani C., Hanaoka F., Fuchs R.P.P., Sarasin A., Lehmann A.R.
Molecular analysis of mutations in DNA polymerase eta in xeroderma pigmentosum-variant patients.
Proc. Natl. Acad. Sci. U.S.A. 99:815-820(2002)

Cross-references
Encyclopedic resources Wikidata; Q98136104
Entry history
Entry creation02-Jul-2020
Last entry update19-Dec-2024
Version number9