ID   GM00084
AC   CVCL_V547
SY   GM-84; GM-0084; GM 84; GM84; GM00084A; Der(22) fibroblast
DR   CLO; CLO_0025153
DR   Coriell; GM00084
DR   Wikidata; Q54836026
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=6661932;
RX   PubMed=7329430;
RX   PubMed=7471105;
RX   PubMed=21949351;
CC   Population: Caucasian.
CC   Karyotypic information: 47,XY,+der(22)(22pter->22q11::11q23->11qter)mat (Coriell=GM00084).
CC   Cell type: Fibroblast; CL=CL_0000057.
ST   Source(s): PubMed=21949351
ST   Amelogenin: X,Y
ST   CSF1PO: 10,12
ST   D13S317: 12
ST   D16S539: 12
ST   D18S51: 13,16
ST   D21S11: 28,29
ST   D3S1358: 16,17
ST   D5S818: 12
ST   D7S820: 9
ST   D8S1179: 12
ST   FGA: 21,22.2
ST   Penta D: 13
ST   Penta E: 12,15
ST   TH01: 9.3,10
ST   TPOX: 8,12
ST   vWA: 16
DI   NCIt; C114765; Trisomy 22
DI   ORDO; Orphanet_98131; Total autosomal trisomy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   1M
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 29-06-23; Version: 13
//
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=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=7329430; DOI=10.1016/0027-5107(81)90059-2;
RA   Nove J., Nichols W.W., Weichselbaum R.R., Little J.B.;
RT   "Abnormalities of human chromosome 13 and in vitro radiosensitivity; a
RT   study of 19 fibroblast strains.";
RL   Mutat. Res. 84:157-167(1981).
//
RX   PubMed=7471105;
RA   Weichselbaum R.R., Nove J., Little J.B.;
RT   "X-ray sensitivity of fifty-three human diploid fibroblast cell
RT   strains from patients with characterized genetic disorders.";
RL   Cancer Res. 40:920-925(1980).
//
RX   PubMed=21949351; DOI=10.1093/hmg/ddr435;
RA   Li W., Wang X.-M., Fan W.-X., Zhao P., Chan Y.-C., Chen S.,
RA   Zhang S.-Q., Guo X.-P., Zhang Y., Li Y.-H., Cai J.-L., Qin D.-J.,
RA   Li X.-Y., Yang J.-Y., Peng T.-R., Zychlinski D., Hoffmann D.,
RA   Zhang R.-S., Deng K., Ng K.-M., Menten B., Zhong M., Wu J.-Y., Li Z.-Y.,
RA   Chen Y.-L., Schambach A., Tse H.-F., Pei D.-Q., Esteban M.A.;
RT   "Modeling abnormal early development with induced pluripotent stem
RT   cells from aneuploid syndromes.";
RL   Hum. Mol. Genet. 21:32-45(2012).
//