| Cell line name |
AG08807 |
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| Synonyms |
AG8807 |
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| Accession |
CVCL_0N74 |
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| Resource Identification Initiative |
To cite this cell line use: AG08807 (RRID:CVCL_0N74) |
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| Comments |
Population: Caucasian.
Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
Cell type: Fibroblast of skin; CL=CL_0002620. |
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| Sequence variations |
- Mutation; HGNC; HGNC:3437; ERCC5; Simple; p.Glu11Ter (c.31G>T); Zygosity=Heterozygous (from autologous cell line AG08806).
|
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| Species of origin |
Homo sapiens (Human)
(NCBI Taxonomy: 9606) |
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| Originate from same individual |
CVCL_0N73 ! AG08806 |
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| Sex of cell |
Male |
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| Age at sampling |
37Y |
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| Category |
Finite cell line |
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| Publications | CLPUB00597
National Institute on Aging
1994 catalog of cell lines. NIA Aging Cell Repository.
(In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-351; National Institutes of Health; Bethesda; USA (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) |
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| Cross-references |
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| Cell line collections (Providers) |
Coriell; AG08807
|
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| Cell line databases/resources |
CLO; CLO_0031385
|
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| Encyclopedic resources |
Wikidata; Q54742539
|
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| Entry history |
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| Entry creation | 10-Apr-2015 |
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| Last entry update | 19-Dec-2024 |
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| Version number | 12 |
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