ID   GM02290
AC   CVCL_7356
SY   GM-2290; GM 2290 GM02290A
DR   CLO; CLO_0003523
DR   CLO; CLO_0032129
DR   CLDB; cl1490
DR   BioSample; SAMN00807654
DR   Coriell; GM02290
DR   Wikidata; Q54837406
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=477417;
RX   PubMed=6087472;
CC   Population: Caucasian.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C61255; Lesch-Nyhan syndrome
DI   ORDO; Orphanet_510; Lesch-Nyhan syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_7357 ! GM02291
OI   CVCL_D868 ! GM02292
OI   CVCL_D869 ! GM02338
SX   Male
AG   19FW
CA   Finite cell line
DT   Created: 04-04-12; Last updated: 29-06-23; Version: 17
//
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   DOI=10.5962/bhl.title.4090;
RA   Coriell L.L., Greene A.E.;
RT   "The human genetic mutant cell repository: list of genetic variants,
RT   chromosomal aberrations and normal cell cultures submitted to the
RT   repository. 4th edition. October 1977.";
RL   (In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977).
//
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).
//
RX   PubMed=6087472; DOI=10.1007/BF01535631;
RA   Stambrook P.J., Dush M.K., Trill J.J., Tischfield J.A.;
RT   "Cloning of a functional human adenine phosphoribosyltransferase
RT   (APRT) gene: identification of a restriction fragment length
RT   polymorphism and preliminary analysis of DNAs from APRT-deficient
RT   families and cell mutants.";
RL   Somat. Cell Mol. Genet. 10:359-367(1984).
//