ID   GM01695
AC   CVCL_V811
SY   GM-1695; GM1695; GM01695A; GM1695A
DR   CLO; CLO_0030959
DR   BioSample; SAMN00807081
DR   Coriell; GM01695
DR   Wikidata; Q54837018
RX   CelloPub=CLPUB00447;
RX   PubMed=2498246;
RX   PubMed=7438786;
RX   PubMed=10377420;
CC   Population: Caucasian.
CC   Karyotypic information: 46,X,t(X;11)(p21;q13) (PubMed=10377420).
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C75482; Duchenne muscular dystrophy
DI   ORDO; Orphanet_98896; Duchenne muscular dystrophy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   26Y
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 29-06-23; Version: 14
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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   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=7438786; DOI=10.1159/000131496;
RA   Greenstein R.M., Reardon M.P., Chan T.-S., Middleton A.B.,
RA   Mulivor R.A., Greene A.E., Coriell L.L.;
RT   "An (X;11) translocation in a girl with Duchenne muscular dystrophy.
RT   Repository identification No. GM1695.";
RL   Cytogenet. Cell Genet. 27:268-268(1980).
//
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).
//