ID   GM01368
AC   CVCL_GY15
SY   GM-1368
DR   CLO; CLO_0030847
DR   BioSample; SAMN00803826
DR   Coriell; GM01368
DR   Wikidata; Q54836786
RX   CelloPub=CLPUB00447;
CC   Population: African American.
CC   Sequence variation: Gene deletion; HGNC; 4827; HBB; Zygosity=Homozygous (Coriell=GM01368).
CC   Sequence variation: Gene deletion; HGNC; 4829; HBD; Zygosity=Homozygous (Coriell=GM01368).
CC   Cell type: Fibroblast; CL=CL_0000057.
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   15Y
CA   Finite cell line
DT   Created: 26-09-16; Last updated: 30-01-24; Version: 12
//
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).
//