Cellosaurus cell line GM04222 (CVCL

Cross-references
Cell line name	GM04222
Accession	CVCL_1I08
Resource Identification Initiative	To cite this cell line use: GM04222 (RRID:CVCL_1I08)
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_1I09 ! GM04223
Sex of cell	Male
Age at sampling	59Y
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)
Cell line collections (Providers)	Coriell; GM04222
Cell line databases/resources	CLO; CLO_0019456
Encyclopedic resources	Wikidata; Q54838434
Entry history
Entry creation	08-Jul-2015
Last entry update	29-Jun-2023
Version number	9