ID   GM07092
AC   CVCL_L479
SY   GM 7092; RJK 888; RJK888
DR   CLO; CLO_0036822
DR   Coriell; GM07092
DR   Wikidata; Q54842530
RX   CelloPub=CLPUB00447;
CC   Population: Caucasian; Irish/Italian.
CC   Sequence variation: Mutation; HGNC; 5157; HPRT1; Simple; c.609+5G>A (Ex8del); ClinVar=VCV000010054; Zygosity=Hemizygous (Coriell=GM07092).
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   2Y
CA   Transformed cell line
DT   Created: 06-05-13; Last updated: 30-01-24; 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).
//