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Cellosaurus 851129W (CVCL_WY27)

[Text version]
Cell line name 851129W
Synonyms 1129W
Accession CVCL_WY27
Resource Identification Initiative To cite this cell line use: 851129W (RRID:CVCL_WY27)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:7652; NBN; Simple; p.Lys219Asnfs*16 (c.657_661delACAAA) (657del5); ClinVar=VCV000006940; Zygosity=Homozygous (PubMed=10987302).
Disease Nijmegen breakage syndrome (NCIt: C4692)
Nijmegen breakage syndrome (ORDO: Orphanet_647)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling Age unspecified
Category Finite cell line
Publications

PubMed=3248383; DOI=10.1159/000132673
Nicolaas G.J. Jaspers, Richard A. Gatti, Carla C. Baan, Peter C.M.L. Linssen, Dirk Bootsma;
Genetic complementation analysis of ataxia telangiectasia and Nijmegen breakage syndrome: a survey of 50 patients.
Cytogenet. Cell Genet. 49:259-263(1988)

DOI=10.1007/978-1-4757-5016-4_9
Nicolaas G.J. Jaspers, Len Roza, Wim Vermeulen, Andre P.M. Eker, Rob Desire F.M. Taalman, Jan Hendrik Jozef Hoeijmakers, Dirk Bootsma;
In vitro correction of cells from patients with mutagen hypersensitivity.
(In book chapter) DNA damage and repair; Castellani, Amleto (eds.); pp.73-82; Springer; Boston; USA (1989)

PubMed=10987302
Pierre-Marie Girard, Nicolas Foray, Markus Stumm, Alastair P.W. Waugh, Enriqueta Riballo, Richard S. Maser, William P. Phillips, John H.J. Petrini, Colin Francis Arlett, Penelope Ann Jeggo;
Radiosensitivity in Nijmegen breakage syndrome cells is attributable to a repair defect and not cell cycle checkpoint defects.
Cancer Res. 60:4881-4888(2000)

Cross-references
Encyclopedic resources Wikidata; Q93310329
Entry history
Entry creation06-Sep-2019
Last entry update19-Dec-2024
Version number9