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Cellosaurus GM04226 (CVCL_1I11)

[Text version]
Cell line name GM04226
Accession CVCL_1I11
Resource Identification Initiative To cite this cell line use: GM04226 (RRID:CVCL_1I11)
Comments Population: Caucasian.
Donor information: At sampling donor was not affected with Huntington disease but at low risk for disease.
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_1I12 ! GM04227
Sex of cell Male
Age at sampling 74Y
Category Finite cell line
Publications

PubMed=6316146; DOI=10.1038/306234a0
Gusella J.F., Wexler N.S., Conneally P.M., Naylor S.L., Anderson M.A., Tanzi R.E., Watkins P.C., Ottina K., Wallace M.R., Sakaguchi A.Y., Young A.B., Shoulson I., Bonilla E., Martin J.B.
A polymorphic DNA marker genetically linked to Huntington's disease.
Nature 306:234-238(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; GM04226
Cell line databases/resources CLO; CLO_0019461
Encyclopedic resources Wikidata; Q54838437
Entry history
Entry creation08-Jul-2015
Last entry update29-Jun-2023
Version number10