ID   GM00589
AC   CVCL_V777
SY   GM-589; GM589
DR   CLO; CLO_0026000
DR   Coriell; GM00589
DR   Wikidata; Q54836325
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=872630;
CC   Population: Caucasian.
CC   Karyotypic information: 46,XY,t(5;14)(5qter->5p14::14q21->14qter;14pter->14q21::5p14->5pter) (Coriell=GM00589).
CC   Cell type: Fibroblast; CL=CL_0000057.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   18Y
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 29-06-23; Version: 10
//
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).
//
RX   DOI=10.5962/bhl.title.4090;
RA   Coriell L.L., Greene A.E.;
RT   "The human genetic mutant cell repository: list of genetic variants,
RT   chromosomal aberrations and normal cell cultures submitted to the
RT   repository. 4th edition. October 1977.";
RL   (In) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda (1977).
//
RX   PubMed=872630; DOI=10.1159/000130767;
RA   Borgaonkar D.S., Aronson M.M., Greene A.E., Coriell L.L.;
RT   "A (5;14) translocation, 46 chromosomes. Repository identification No.
RT   GM-589.";
RL   Cytogenet. Cell Genet. 18:242-242(1977).
//