ID   GM03808
AC   CVCL_JE12
SY   GM3808; 3808
DR   CLO; CLO_0015562
DR   BioSample; SAMN00808541
DR   Coriell; GM03808
DR   Wikidata; Q54838245
RX   CelloPub=CLPUB00447;
RX   PubMed=2559742;
CC   Population: Caucasian.
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)
SX   Male
AG   9Y
CA   Finite cell line
DT   Created: 15-05-17; 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 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).
//