ID   GM02859
AC   CVCL_M932
SY   GM-2859; GM 2859; GM2859; GM02859A; GM2859A; GM17312
DR   CLO; CLO_0012780
DR   CLO; CLO_0013353
DR   BioSample; SAMN00808154
DR   Coriell; GM02859
DR   Coriell; GM17312
DR   Wikidata; Q54837734
RX   CelloPub=CLPUB00447;
RX   PubMed=2498246;
RX   PubMed=6293786;
RX   PubMed=6617268;
RX   PubMed=6661932;
RX   PubMed=6947233;
RX   PubMed=10377420;
RX   PubMed=23665875;
CC   Part of: Human variation panel.
CC   Population: South American (Brazil, Guyana, Venezuela).
CC   Karyotypic information: 46,X,t(X;11)(q11.1;p13) (PubMed=10377420).
CC   Sequence variation: Mutation; HGNC; 2623; CYP2C9; Simple; p.Arg144Cys (c.430C>T) (416C>T); ClinVar=VCV000008409; Zygosity=Heterozygous; Note=CYP2C9*2 allele (Coriell=GM17312).
CC   Omics: CNV analysis.
CC   Cell type: Fibroblast; CL=CL_0000057.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_M933 ! GM03316
SX   Female
AG   3Y
CA   Finite cell line
DT   Created: 05-11-13; Last updated: 30-01-24; Version: 16
//
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   PubMed=2498246; DOI=10.1111/j.1349-7006.1989.tb02278.x;
RA   Koi M., Morita H., Shimizu M., Oshimura M.;
RT   "Construction of mouse A9 clones containing a single human chromosome
RT   (X/autosome translocation) via micro-cell fusion.";
RL   Jpn. J. Cancer Res. 80:122-125(1989).
//
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=6617268; DOI=10.1159/000131883;
RA   Aronson M.M., Nichols W.W., Mulivor R.A., Greene A.E., Coriell L.L.;
RT   "Breakpoint map of chromosomal inversion and deletion cell cultures in
RT   the NIGMS Human Genetic Mutant Cell Repository.";
RL   Cytogenet. Cell Genet. 35:298-302(1983).
//
RX   PubMed=6661932; DOI=10.1159/000131990;
RA   Aronson M.M., Nichols W.W., Mulivor R.A., Greene A.E., Coriell L.L.;
RT   "Chromosome maps of cell lines with specific monosomic or trisomic
RT   portions of the genome in the NIGMS Human Genetic Mutant Cell
RT   Repository.";
RL   Cytogenet. Cell Genet. 36:652-658(1983).
//
RX   PubMed=6947233; DOI=10.1073/pnas.78.10.6339;
RA   Migeon B.R., Brown T.R., Axelman J., Migeon C.J.;
RT   "Studies of the locus for androgen receptor: localization on the human
RT   X chromosome and evidence for homology with the Tfm locus in the
RT   mouse.";
RL   Proc. Natl. Acad. Sci. U.S.A. 78:6339-6343(1981).
//
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).
//
RX   PubMed=23665875; DOI=10.1534/g3.113.006577;
RA   Tang Z.-Y., Berlin D.S., Toji L.H., Toruner G.A., Beiswanger C.M.,
RA   Kulkarni S., Martin C.L., Emanuel B.S., Christman M., Gerry N.P.;
RT   "A dynamic database of microarray-characterized cell lines with
RT   various cytogenetic and genomic backgrounds.";
RL   G3 (Bethesda) 3:1143-1149(2013).
//