ID   GM03116
AC   CVCL_F064
SY   GM-3116; GM03116A
DR   CLO; CLO_0013556
DR   BioSample; SAMN00808254
DR   Coriell; GM03116
DR   Wikidata; Q54837878
RX   CelloPub=CLPUB00447;
RX   PubMed=477417;
CC   Population: Caucasian.
CC   Derived from site: In situ; Fetal kidney; UBERON=UBERON_0002113.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C61255; Lesch-Nyhan syndrome
DI   ORDO; Orphanet_510; Lesch-Nyhan syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_V745 ! GM03115
OI   CVCL_F065 ! GM03117
SX   Male
AG   19FW
CA   Finite cell line
DT   Created: 22-10-12; Last updated: 29-06-23; Version: 15
//
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=477417; DOI=10.1159/000131379;
RA   Tischfield J.A., Schafer I.A., Dickerman L.H., Trill J.J., Mulivor R.A.,
RA   Greene A.E., Coriell L.L.;
RT   "Lesch-Nyhan syndrome. Repository identification Nos. GM-2290, 2291,
RT   2292, 2338, 3115, 3116, and 3117.";
RL   Cytogenet. Cell Genet. 24:199-200(1979).
//