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Cellosaurus GM02079 (CVCL_1H41)

[Text version]
Cell line name GM02079
Synonyms GM-2079; GM 2079; GM02079A
Accession CVCL_1H41
Resource Identification Initiative To cite this cell line use: GM02079 (RRID:CVCL_1H41)
Comments Population: Caucasian.
Cell type: Fibroblast; CL=CL_0000057.
Disease Huntington's disease (NCIt: C82342)
Huntington disease (ORDO: Orphanet_399)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_1H42 ! GM02080
Sex of cell Female
Age at sampling 48Y
Category Finite cell line
Publications

DOI=10.5962/bhl.title.4090
Coriell L.L., Greene A.E.
The human genetic mutant cell repository: list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository. 4th edition. October 1977.
(In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977)

PubMed=6220707; DOI=10.1016/0006-291x(83)90361-3
Chua C.C., Geiman D.E., Ladda R.L.
Detection of an Mr 200,000 glycoprotein in the culture medium of skin fibroblasts from patients with Huntington disease.
Biochem. Biophys. Res. Commun. 111:690-699(1983)

CLPUB00447
Mulivor R.A., Suchy S.F.
1992/1993 catalog of cell lines. NIGMS human genetic mutant cell repository. 16th edition. October 1992.
(In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992)

Cross-references
Cell line collections (Providers) Coriell; GM02079
Cell line databases/resources CLO; CLO_0032509
Biological sample resources BioSample; SAMN00807468
Encyclopedic resources Wikidata; Q54837291
Entry history
Entry creation08-Jul-2015
Last entry update29-Jun-2023
Version number12