ID   GM00097
AC   CVCL_V747
SY   GM-97; GM0097; GM 0097; GM00097A
DR   CLO; CLO_0025819
DR   Coriell; GM00097
DR   Wikidata; Q54836039
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=1679663;
RX   PubMed=2498246;
RX   PubMed=4139001;
RX   PubMed=10377420;
CC   Population: Caucasian.
CC   Karyotypic information: 46,X,t(X;1)(q26;q21) (PubMed=10377420).
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C118787; Simpson Golabi Behmel syndrome type 1
DI   ORDO; Orphanet_373; Simpson-Golabi-Behmel syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   1Y
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 29-06-23; 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).
//
RX   PubMed=1679663;
RA   Bader S.A., Fasching C., Brodeur G.M., Stanbridge E.J.;
RT   "Dissociation of suppression of tumorigenicity and differentiation in
RT   vitro effected by transfer of single human chromosomes into human
RT   neuroblastoma cells.";
RL   Cell Growth Differ. 2:245-255(1991).
//
RX   PubMed=2498246; DOI=10.1111/j.1349-7006.1989.tb02278.x;
RA   Koi M., Morita H., Shimizu M., Oshimura M.;
RT   "Construction of mouse A9 clones containing a single human chromosome
RT   (X/autosome translocation) via micro-cell fusion.";
RL   Jpn. J. Cancer Res. 80:122-125(1989).
//
RX   PubMed=4139001; DOI=10.1159/000130291;
RA   Punnett H.H., Kistenmacher M.L., Greene A.E., Coriell L.L.;
RT   "An (X;1) translocation, balanced, 46 chromosomes. Repository
RT   identification No. GM-97.";
RL   Cytogenet. Cell Genet. 13:406-407(1974).
//
RX   PubMed=10377420; DOI=10.1073/pnas.96.13.7364;
RA   Carrel L., Willard H.F.;
RT   "Heterogeneous gene expression from the inactive X chromosome: an
RT   X-linked gene that escapes X inactivation in some human cell lines but
RT   is inactivated in others.";
RL   Proc. Natl. Acad. Sci. U.S.A. 96:7364-7369(1999).
//