ID   GM01251
AC   CVCL_M985
SY   GM-1251; GM17152
DR   CLO; CLO_0013959
DR   CLO; CLO_0030930
DR   BioSample; SAMN00803760
DR   Coriell; GM01251
DR   Coriell; GM17152
DR   GEO; GSM924662
DR   IPD-IMGT/HLA; 23055
DR   Wikidata; Q54836737
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=477407;
CC   Part of: Human variation panel.
CC   Population: African American.
CC   HLA typing: A*03:CVAB,29:02; B*58:02,81:MN; C*06:02,18:AB; DRB1*03:01,08:04 (IPD-IMGT/HLA=23055).
CC   Omics: Genomics; DNA methylation analysis.
CC   Cell type: Fibroblast; CL=CL_0000057.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   4Y
CA   Finite cell line
DT   Created: 05-11-13; Last updated: 10-04-25; Version: 14
//
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).
//
RX   PubMed=477407; DOI=10.1159/000131367;
RA   Pope I.S., Thuline H.C., Aronson M.M., Bozarth B., Greene A.E.,
RA   Coriell L.L.;
RT   "Duplication of a segment of chromosome 3 in a subject with multiple
RT   congenital anomalies and a 47,XYY father, inversion of chromosomes 3
RT   and 9 in the mother, and inversion of chromosome 9 in a brother.
RT   Repository identification Nos. GM-1253, GM-1252, and GM-1251.";
RL   Cytogenet. Cell Genet. 24:127-128(1979).
//