ID   GM02066
AC   CVCL_CW97
SY   GM2066; GM-2066; GM 2066
DR   CLO; CLO_0032516
DR   BioSample; SAMN00807454
DR   Coriell; GM02066
DR   Wikidata; Q54837283
RX   CelloPub=CLPUB00387;
RX   CelloPub=CLPUB00447;
RX   CelloPub=CLPUB00720;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=9792862;
RX   PubMed=28649545;
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; 2518; CTNS; Simple; p.Pro48Leufs*7 (c.225+5G>A); Zygosity=Heterozygous (PubMed=28649545).
CC   Sequence variation: Mutation; HGNC; 2518; CTNS; Simple; p.Gly339Arg (c.1015G>A); ClinVar=VCV000004455; Zygosity=Heterozygous (PubMed=28649545).
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C129932; Nephropathic cystinosis
DI   ORDO; Orphanet_411629; Nephropathic infantile cystinosis
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   1Y
CA   Finite cell line
DT   Created: 13-07-16; Last updated: 29-06-23; Version: 14
//
RX   CelloPub=CLPUB00387;
RA   Coriell L.L., Greene A.E., Mulivor R.A.;
RT   "The human genetic mutant cell repository: list of genetic variants,
RT   chromosomal aberrations and normal cell cultures submitted to the
RT   repository. 7th edition. October 1980.";
RL   (In) Institute for Medical Research (Camden, N.J.) NIH 80-2011; pp.1-254; National Institutes of Health; Bethesda (1980).
//
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   CelloPub=CLPUB00720;
RA   Greene A.E., Mulivor R.A.;
RT   "1986/1987 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 13th edition. October 1986.";
RL   (In) Institute for Medical Research (Camden, N.J.) NIH 87-2011; pp.1-549; National Institutes of Health; Bethesda (1986).
//
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=9792862; DOI=10.1086/302118;
RA   Shotelersuk V., Larson D., Anikster Y., McDowell G., Lemons R.,
RA   Bernardini I., Guo J.-R., Thoene J., Gahl W.A.;
RT   "CTNS mutations in an American-based population of cystinosis
RT   patients.";
RL   Am. J. Hum. Genet. 63:1352-1362(1998).
//
RX   PubMed=28649545; DOI=10.1016/j.ymgmr.2015.10.007;
RA   Zykovich A., Kinkade R., Royal G., Zankel T.;
RT   "CTNS mutations in publicly-available human cystinosis cell lines.";
RL   Mol. Genet. Metab. Rep. 5:63-66(2015).
//