ID   GM00157
AC   CVCL_V753
SY   GM-157; GM-0157; GM 157
DR   CLO; CLO_0025866
DR   Coriell; GM00157
DR   Wikidata; Q54836069
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=1132249;
RX   PubMed=1183238;
RX   PubMed=6661932;
RX   PubMed=23665875;
CC   Population: Caucasian.
CC   Karyotypic information: 49,XXXXY,t(4;11)(q35;q23).arr(X)x4,(Y)x1 (Coriell=GM00157).
CC   Omics: CNV analysis.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C185635; 49,XXXXY syndrome
DI   ORDO; Orphanet_96264; 49,XXXXY syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   28Y
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 29-06-23; 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) 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).
//
RX   PubMed=1132249; DOI=10.1159/000130320;
RA   de la Chapelle A., Miller R.C., Greene A.E., Coriell L.L.;
RT   "A (4;11) translocation, balanced, XXXXp-Y, 49 chromosomes. Repository
RT   identification No. GM-157.";
RL   Cytogenet. Cell Genet. 14:76-77(1975).
//
RX   PubMed=1183238; DOI=10.1159/000130510;
RA   de la Chapelle A., Miller R.C., Greene A.E., Coriell L.L.;
RT   "A (4;11) translocation, balanced, 49 XXXXY karyotype. Repository
RT   identification No. GM-157.";
RL   Cytogenet. Cell Genet. 15:127-128(1975).
//
RX   PubMed=6661932; DOI=10.1159/000131990;
RA   Aronson M.M., Nichols W.W., Mulivor R.A., Greene A.E., Coriell L.L.;
RT   "Chromosome maps of cell lines with specific monosomic or trisomic
RT   portions of the genome in the NIGMS Human Genetic Mutant Cell
RT   Repository.";
RL   Cytogenet. Cell Genet. 36:652-658(1983).
//
RX   PubMed=23665875; DOI=10.1534/g3.113.006577;
RA   Tang Z.-Y., Berlin D.S., Toji L.H., Toruner G.A., Beiswanger C.M.,
RA   Kulkarni S., Martin C.L., Emanuel B.S., Christman M., Gerry N.P.;
RT   "A dynamic database of microarray-characterized cell lines with
RT   various cytogenetic and genomic backgrounds.";
RL   G3 (Bethesda) 3:1143-1149(2013).
//