ID   GM06927
AC   CVCL_T904
DR   CLO; CLO_0036470
DR   Coriell; GM06927
DR   Wikidata; Q54842393
RX   CelloPub=CLPUB00447;
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; HGNC:10548; ATXN1; Repeat_expansion; CAG[52]; Zygosity=Heterozygous; Note=The other allele has 29 repeats (Coriell=GM06927).
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C129982; Spinocerebellar ataxia type 1
DI   ORDO; Orphanet_98755; Spinocerebellar ataxia type 1
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_T903 ! GM06926
SX   Male
AG   29Y
CA   Finite cell line
DT   Created: 03-02-14; Last updated: 19-12-24; 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).
//