ID   GM01899
AC   CVCL_2448
AS   CVCL_D867
SY   GM-1899; GM 1899; GM1899; GM01899A; GM1899A; GM1899a; GM01899B; RJK 906; RJK906
DR   CLO; CLO_0032370
DR   BioSample; SAMN00807292
DR   Coriell; GM01899
DR   ECACC; 98120701
DR   Wikidata; Q54837170
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
CC   Population: Caucasian.
CC   HLA typing: A*02,11; B*18,35 (Coriell=GM01899).
CC   Sequence variation: Mutation; HGNC; 5157; HPRT1; Simple; c.610-4_610-2delinsTTT (Ex9del partial); ClinVar=VCV000010055; Zygosity=Hemizygous (Coriell=GM01899).
CC   Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C61255; Lesch-Nyhan syndrome
DI   ORDO; Orphanet_510; Lesch-Nyhan syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   10Y
CA   Transformed cell line
DT   Created: 04-04-12; Last updated: 30-01-24; Version: 21
//
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).
//