ID   GM00705
AC   CVCL_0P86
SY   GM-705; GM0705; GM00705A; GM0705A; GMO 705; AnLy
DR   CLO; CLO_0028893
DR   Coriell; GM00705
DR   Wikidata; Q54836399
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=113895;
RX   PubMed=559490;
RX   PubMed=1056018;
RX   PubMed=2338345;
RX   PubMed=8268921;
RX   PubMed=10377420;
RX   PubMed=23665875;
CC   Population: Caucasian.
CC   Karyotypic information: 46,X,t(X;9)(q13.1;p24) (PubMed=10377420).
CC   Omics: CNV analysis.
CC   Cell type: Fibroblast; CL=CL_0000057.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   10M
CA   Finite cell line
DT   Created: 10-04-15; 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) 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=113895; DOI=10.1007/BF01539157;
RA   Shows T.B., Scrafford-Wolff L.R., Brown J.A., Meisler M.H.;
RT   "GM1-gangliosidosis: chromosome 3 assignment of the
RT   beta-galactosidase-A gene (beta GALA).";
RL   Somatic Cell Genet. 5:147-158(1979).
//
RX   PubMed=559490; DOI=10.1007/BF00484467;
RA   Lalley P.A., Brown J.A., Eddy R.L., Haley L.L., Byers M.G.,
RA   Goggin A.P., Shows T.B.;
RT   "Human beta-glucuronidase: assignment of the structural gene to
RT   chromosome 7 using somatic cell hybrids.";
RL   Biochem. Genet. 15:367-382(1977).
//
RX   PubMed=1056018; DOI=10.1073/pnas.72.6.2125;
RA   Shows T.B., Brown J.A.;
RT   "Human X-Linked genes regionally mapped utilizing X-autosome
RT   translocations and somatic cell hybrids.";
RL   Proc. Natl. Acad. Sci. U.S.A. 72:2125-2129(1975).
//
RX   PubMed=2338345; DOI=10.1007/BF00210814;
RA   MacDermot K.D., Hulten M.A.;
RT   "Female with hypohidrotic ectodermal dysplasia and de novo (X;9)
RT   translocation. Clinical documentation of the AnLy cell line case.";
RL   Hum. Genet. 84:577-579(1990).
//
RX   PubMed=8268921; DOI=10.1093/hmg/2.10.1679;
RA   Thomas N.S.T., Chelly J., Zonana J., Davies K.J.P., Morgan S.,
RA   Gault J.M., Rack K.A., Buckle V.J., Brockdorff N., Clarke A.,
RA   Monaco A.P.;
RT   "Characterisation of molecular DNA rearrangements within the
RT   Xq12-q13.1 region, in three patients with X-linked hypohidrotic
RT   ectodermal dysplasia (EDA).";
RL   Hum. Mol. Genet. 2:1679-1685(1993).
//
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).
//
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).
//