ID GM00082 AC CVCL_L495 SY GM-82; GM82 DR CLO; CLO_0025151 DR Coriell; GM00082 DR JCRB; KURB1026 DR Wikidata; Q54836023 RX CelloPub=CLPUB00447; RX DOI=10.5962/bhl.title.4090; RX PubMed=1372102; RX PubMed=1702221; RX PubMed=9671271; CC Population: Caucasian. CC Derived from site: In situ; Skin; UBERON=UBERON_0002097. CC Cell type: Fibroblast of skin; CL=CL_0002620. DI NCIt; C3965; Xeroderma pigmentosum, complementation group A DI ORDO; Orphanet_910; Xeroderma pigmentosum OX NCBI_TaxID=9606; ! Homo sapiens (Human) SX Female AG 12Y CA Finite cell line DT Created: 06-05-13; Last updated: 29-06-23; Version: 15 // RX CelloPub=CLPUB00447; RA Mulivor R.A., Suchy S.F.; RT "1992/1993 catalog of cell lines. NIGMS human genetic mutant cell RT repository. 16th edition. October 1992."; RL (In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992). // RX DOI=10.5962/bhl.title.4090; RA Coriell L.L., Greene A.E.; RT "The human genetic mutant cell repository: list of genetic variants, RT chromosomal aberrations and normal cell cultures submitted to the RT repository. 4th edition. October 1977."; RL (In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977). // RX PubMed=1372102; DOI=10.1016/0921-8777(92)90080-M; RA Satokata I., Tanaka K., Miura N., Narita M., Mimaki T., Satoh Y., RA Kondo S., Okada Y.; RT "Three nonsense mutations responsible for group A xeroderma RT pigmentosum."; RL Mutat. Res. 273:193-202(1992). // RX PubMed=1702221; DOI=10.1073/pnas.87.24.9908; PMCID=PMC55283; RA Satokata I., Tanaka K., Miura N., Miyamoto I., Satoh Y., Kondo S., RA Okada Y.; RT "Characterization of a splicing mutation in group A xeroderma RT pigmentosum."; RL Proc. Natl. Acad. Sci. U.S.A. 87:9908-9912(1990). // RX PubMed=9671271; DOI=10.1002/(SICI)1098-1004(1998)12:2<103::AID-HUMU5>3.0.CO;2-6; RA States J.C., McDuffie E.R., Myrand S.P., McDowell M.L., Cleaver J.E.; RT "Distribution of mutations in the human xeroderma pigmentosum group A RT gene and their relationships to the functional regions of the DNA RT damage recognition protein."; RL Hum. Mutat. 12:103-113(1998). //