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Cellosaurus 2BN (CVCL_8087)

[Text version]
Cell line name 2BN
Accession CVCL_8087
Resource Identification Initiative To cite this cell line use: 2BN (RRID:CVCL_8087)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
Disease Severe combined immunodeficiency due to NHEJ1 deficiency (NCIt: C162695)
Cernunnos-XLF deficiency (ORDO: Orphanet_169079)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_8089 (2BNhTERT)CVCL_8088 (2BNneo)
Sex of cell Female
Category Finite cell line
Publications

PubMed=12604777; DOI=10.1073/pnas.0437964100; PMCID=PMC151363
Dai Y., Kysela B., Hanakahi L.A., Manolis K., Riballo E., Stumm M., Harville T.O., West S.C., Oettinger M.A., Jeggo P.A.
Nonhomologous end joining and V(D)J recombination require an additional factor.
Proc. Natl. Acad. Sci. U.S.A. 100:2462-2467(2003)

PubMed=19056826; DOI=10.1093/nar/gkn957; PMCID=PMC2632933
Riballo E., Woodbine L., Stiff T., Walker S.A., Goodarzi A.A., Jeggo P.A.
XLF-Cernunnos promotes DNA ligase IV-XRCC4 re-adenylation following ligation.
Nucleic Acids Res. 37:482-492(2009)

Cross-references
Anatomy/cell type resources BTO; BTO_0004321
Encyclopedic resources Wikidata; Q54584316
Entry history
Entry creation04-Apr-2012
Last entry update19-Dec-2024
Version number15