ID GM02171 AC CVCL_1H55 SY GM-2171; GM 2171 DR CLO; CLO_0031767 DR BioSample; SAMN00807564 DR Coriell; GM02171 DR GEO; GSM1266971 DR Wikidata; Q54837347 RX CelloPub=CLPUB00447; RX DOI=10.5962/bhl.title.4090; RX PubMed=6220707; RX PubMed=25326100; CC Population: Caucasian. CC Omics: Variations; SNP array analysis. CC Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease. CC Derived from site: In situ; Skin; UBERON=UBERON_0002097. CC Cell type: Fibroblast of skin; CL=CL_0002620. DI NCIt; C82342; Huntington's disease DI ORDO; Orphanet_399; Huntington disease OX NCBI_TaxID=9606; ! Homo sapiens (Human) OI CVCL_1H54 ! GM02170 SX Female AG 22Y CA Finite cell line DT Created: 08-07-15; Last updated: 10-04-25; Version: 17 // 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=6220707; DOI=10.1016/0006-291x(83)90361-3; RA Chua C.C., Geiman D.E., Ladda R.L.; RT "Detection of an Mr 200,000 glycoprotein in the culture medium of skin RT fibroblasts from patients with Huntington disease."; RL Biochem. Biophys. Res. Commun. 111:690-699(1983). // RX PubMed=25326100; DOI=10.15252/msb.20145114; PMCID=PMC4299376; RA Adoue V., Schiavi A., Light N., Almlof J.C., Lundmark P., Ge B., RA Kwan T., Caron M., Ronnblom L., Wang C., Chen S.-H., Goodall A.H., RA Cambien F., Deloukas P., Ouwehand W.H., Syvanen A.-C., Pastinen T.; RT "Allelic expression mapping across cellular lineages to establish RT impact of non-coding SNPs."; RL Mol. Syst. Biol. 10:754-754(2014). //