ID   GM01850
AC   CVCL_M988
SY   GM-1850; GM17101
DR   CLO; CLO_0014894
DR   CLO; CLO_0031426
DR   BioSample; SAMN00807223
DR   Coriell; GM01850
DR   Coriell; GM17101
DR   GEO; GSM596169
DR   GEO; GSM924611
DR   IPD-IMGT/HLA; 19227
DR   Wikidata; Q54837125
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
CC   Part of: Human variation panel.
CC   Population: African American.
CC   HLA typing: A*24:CWFP,26:GAX; B*08:XKT,44:WRJ; C*01:02,03:04; DRB1*01:03,13:04 (IPD-IMGT/HLA=19227).
CC   Sequence variation: Mutation; HGNC; 4696; GUSB; Simple; p.Trp627Cys (c.1881G>T); ClinVar=VCV000000907; Zygosity=Heterozygous (Coriell=GM01850).
CC   Omics: DNA methylation analysis.
CC   Cell type: Fibroblast; CL=CL_0000057.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   28Y
CA   Finite cell line
DT   Created: 05-11-13; Last updated: 30-01-24; Version: 15
//
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   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) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda (1977).
//