ID   GM03117
AC   CVCL_F065
SY   GM-3117
DR   CLO; CLO_0013559
DR   BioSample; SAMN00808255
DR   Coriell; GM03117
DR   Wikidata; Q54837879
RX   CelloPub=CLPUB00447;
RX   PubMed=477417;
CC   Population: Caucasian.
CC   Derived from site: In situ; Fetal lung; UBERON=UBERON_0005597.
CC   Cell type: Fibroblast of lung; CL=CL_0002553.
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_F064 ! GM03116
SX   Male
AG   19FW
CA   Finite cell line
DT   Created: 22-10-12; Last updated: 29-06-23; Version: 13
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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).
//