ID   GM06938
AC   CVCL_5N52
SY   GM6938; GM06938B; 6938
DR   CLO; CLO_0036455
DR   Coriell; GM06938
DR   Wikidata; Q54842399
RX   CelloPub=CLPUB00447;
RX   PubMed=2559742;
RX   PubMed=23665875;
CC   Population: Caucasian.
CC   Omics: CNV analysis.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C3718; Wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome
DI   ORDO; Orphanet_893; WAGR syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_5N68 ! GM07736
SX   Male
AG   3W
CA   Finite cell line
DT   Created: 23-02-16; Last updated: 29-06-23; Version: 9
//
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 misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992).
//
RX   PubMed=2559742; DOI=10.1002/mc.2940020606;
RA   Kano Y., Little J.B.;
RT   "Efficient immortalization by SV40 T DNA of skin fibroblasts from
RT   patients with Wilms' tumor associated with chromosome 11p deletion.";
RL   Mol. Carcinog. 2:314-321(1989).
//
RX   PubMed=23665875; DOI=10.1534/g3.113.006577; PMCID=PMC3704242;
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).
//