ID   GM03561
AC   CVCL_AX22
DR   CLO; CLO_0017280
DR   BioSample; SAMN00808452
DR   Coriell; GM03561
DR   Wikidata; Q54838131
RX   CelloPub=CLPUB00447;
CC   Population: African American.
CC   Sequence variation: Mutation; HGNC; 10560; ATXN7; Repeat_expansion; CAG[62] (g.53130CAG[(38_130)]); ClinVar=VCV000562100; Zygosity=Heterozygous (Coriell=GM03561).
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C126562; Spinocerebellar ataxia type 7
DI   ORDO; Orphanet_94147; Spinocerebellar ataxia type 7
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_AX23 ! GM03562
SX   Female
AG   22Y
CA   Finite cell line
DT   Created: 02-05-16; Last updated: 30-01-24; Version: 13
//
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) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992).
//