ID   GM02064
AC   CVCL_M994
SY   GM-2064; GM 2064; GM2064; GM02064A; GM17342
DR   CLO; CLO_0013747
DR   CLO; CLO_0032529
DR   BioSample; SAMN00807450
DR   Coriell; GM02064
DR   Coriell; GM17342
DR   Wikidata; Q54837281
RX   CelloPub=CLPUB00447;
RX   PubMed=6196781;
RX   PubMed=7313555;
CC   Part of: Human variation panel.
CC   Population: Africans south of the Sahara.
CC   Sequence variation: Gene deletion; HGNC; 4827; HBB; Zygosity=Homozygous (Coriell=GM02064).
CC   Sequence variation: Gene deletion; HGNC; 4829; HBD; Zygosity=Homozygous (Coriell=GM02064).
CC   Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C129072; Hereditary persistence of fetal hemoglobin
DI   ORDO; Orphanet_46532; Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   53Y
CA   Transformed cell line
DT   Created: 05-11-13; Last updated: 30-01-24; Version: 16
//
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) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992).
//
RX   PubMed=6196781; DOI=10.1073/pnas.80.22.6937;
RA   Tuan D., Feingold E., Newman M., Weissman S.M., Forget B.G.;
RT   "Different 3' end points of deletions causing delta beta-thalassemia
RT   and hereditary persistence of fetal hemoglobin: implications for the
RT   control of gamma-globin gene expression in man.";
RL   Proc. Natl. Acad. Sci. U.S.A. 80:6937-6941(1983).
//
RX   PubMed=7313555; DOI=10.1111/j.1365-3083.1981.tb00178.x;
RA   Simmons J.G., Fuller C.R., Buchanan P.D., Yount W.J.;
RT   "Distribution of surface, cytoplasmic and secreted IgG subclasses in
RT   human lymphoblastoid cell lines and normal peripheral blood
RT   lymphocytes.";
RL   Scand. J. Immunol. 14:1-13(1981).
//