ID   GM06199
AC   CVCL_4D89
DR   CLO; CLO_0023142
DR   Coriell; GM06199
DR   Wikidata; Q54842216
RX   CelloPub=CLPUB00447;
CC   Population: African American.
CC   Karyotypic information: 46,XY,r(21)(p13->q22) (Coriell=GM06199).
CC   Derived from site: In situ; Foreskin, skin; UBERON=UBERON_0001471.
CC   Cell type: Fibroblast of foreskin; CL=CL_1001608.
DI   NCIt; C186278; Ring chromosome 21 syndrome
DI   ORDO; Orphanet_1445; Ring chromosome 21 syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   <1M
CA   Finite cell line
DT   Created: 22-09-15; Last updated: 29-06-23; Version: 8
//
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).
//