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Cellosaurus W1799 (CVCL_VL05)

[Text version]
Cell line name W1799
Accession CVCL_VL05
Resource Identification Initiative To cite this cell line use: W1799 (RRID:CVCL_VL05)
Comments Cell type: Fibroblast; CL=CL_0000057.
Sequence variations
  • Mutation; HGNC; 7652; NBN; Simple; p.Lys219Asnfs*16 (c.657_661delACAAA) (657del5); ClinVar=VCV000006940; Zygosity=Homozygous (Coriell=GM16143).
Disease Nijmegen breakage syndrome (NCIt: C4692)
Nijmegen breakage syndrome (ORDO: Orphanet_647)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_VL06 (W1799-hTERT)
Category Finite cell line
Publications

PubMed=9590181; DOI=10.1016/S0092-8674(00)81175-7
Carney J.P., Maser R.S., Olivares H., Davis E.M., Le Beau M.M., Yates J.R. III, Hays L., Morgan W.F., Petrini J.H.J.
The hMre11/hRad50 protein complex and Nijmegen breakage syndrome: linkage of double-strand break repair to the cellular DNA damage response.
Cell 93:477-486(1998)

PubMed=12446774; DOI=10.1128/mcb.22.24.8552-8561.2002
Heffernan T.P., Simpson D.A., Frank A.R., Heinloth A.N., Paules R.S., Cordeiro-Stone M., Kaufmann W.K.
An ATR- and Chk1-dependent S checkpoint inhibits replicon initiation following UVC-induced DNA damage.
Mol. Cell. Biol. 22:8552-8561(2002)

Cross-references
Encyclopedic resources Wikidata; Q98134676
Entry history
Entry creation07-Sep-2018
Last entry update30-Jan-2024
Version number9