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Cellosaurus AG08807 (CVCL_0N74)

[Text version]
Cell line name AG08807
Synonyms AG8807
Accession CVCL_0N74
Resource Identification Initiative To cite this cell line use: AG08807 (RRID:CVCL_0N74)
Comments Population: Caucasian.
Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 3437; ERCC5; Simple; p.Glu11Ter (c.31G>T); Zygosity=Heterozygous (from autologous cell line AG08806).
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_0N73 ! AG08806
Sex of cell Male
Age at sampling 37Y
Category Finite cell line
Publications

CLPUB00597
National Institute on Aging
1994 catalog of cell lines. NIA Aging Cell Repository.
(In) Institute for Medical Research (Camden, N.J.); pp.1-351; National Institutes of Health; Bethesda (1994)

PubMed=8823375; DOI=10.1111/1523-1747.ep12584287
Moriwaki S.-i., Stefanini M., Lehmann A.R., Hoeijmakers J.H.J., Robbins J.H., Rapin I., Botta E., Tanganelli B., Vermeulen W., Broughton B.C., Kraemer K.H.
DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and Cockayne syndrome resemble xeroderma pigmentosum cells.
J. Invest. Dermatol. 107:647-653(1996)

PubMed=9447232; DOI=10.1016/S0921-8777(97)00031-1
Okinaka R.T., Perez-Castro A.V., Sena A., Laubscher K., Strniste G.F., Park M.S., Hernandez R., MacInnes M.A., Kraemer K.H.
Heritable genetic alterations in a xeroderma pigmentosum group G/Cockayne syndrome pedigree.
Mutat. Res. 385:107-114(1997)

Cross-references
Cell line collections (Providers) Coriell; AG08807
Cell line databases/resources CLO; CLO_0031385
Encyclopedic resources Wikidata; Q54742539
Entry history
Entry creation10-Apr-2015
Last entry update29-Jun-2023
Version number11