ID   GM00089
AC   CVCL_F600
SY   GM-89; GM0089; GM089
DR   CLO; CLO_0025157
DR   Coriell; GM00089
DR   Wikidata; Q54836030
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=6293786;
RX   PubMed=10377420;
CC   Population: Caucasian.
CC   Karyotypic information: 46,X,t(X;19)(q22;q13.3) (PubMed=10377420).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   Age unspecified
CA   Finite cell line
DT   Created: 11-02-13; Last updated: 29-06-23; Version: 11
//
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=6293786; DOI=10.1002/cyto.990030302;
RA   Lebo R.V.;
RT   "Chromosome sorting and DNA sequence localization.";
RL   Cytometry 3:145-154(1982).
//
RX   PubMed=10377420; DOI=10.1073/pnas.96.13.7364;
RA   Carrel L., Willard H.F.;
RT   "Heterogeneous gene expression from the inactive X chromosome: an
RT   X-linked gene that escapes X inactivation in some human cell lines but
RT   is inactivated in others.";
RL   Proc. Natl. Acad. Sci. U.S.A. 96:7364-7369(1999).
//