ID   GM07792
AC   CVCL_2T36
SY   GM7792
DR   CLO; CLO_0010221
DR   Coriell; GM07792
DR   Wikidata; Q54842916
RX   CelloPub=CLPUB00447;
RX   PubMed=10377420;
RX   PubMed=23665875;
CC   Population: Caucasian.
CC   Karyotypic information: 46,X,t(X;20)(p10;q10) (PubMed=10377420).
CC   Omics: CNV analysis.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C84392; Mental retardation
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   14Y
CA   Finite cell line
DT   Created: 22-09-15; Last updated: 29-06-23; Version: 10
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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).
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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).
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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).
//