ID   GM02052+hTERT
AC   CVCL_VL09
SY   hTERT+ GM02052
DR   Wikidata; Q93575552
RX   PubMed=11313956;
CC   Population: Jewish; Moroccan.
CC   Sequence variation: Mutation; HGNC; HGNC:795; ATM; Simple; p.Arg35Ter (c.103C>T); ClinVar=VCV000003025; Zygosity=Homozygous (from parent cell line).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C2887; Ataxia telangiectasia syndrome
DI   ORDO; Orphanet_100; Ataxia telangiectasia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_7350 ! GM02052
SX   Female
AG   15Y
CA   Telomerase immortalized cell line
DT   Created: 07-09-18; Last updated: 19-12-24; Version: 9
//
RX   PubMed=11313956; DOI=10.1038/sj.onc.1204072;
RA   Wood L.D., Halvorsen T.L., Dhar S., Baur J.A., Pandita R.K.,
RA   Wright W.E., Hande M.P., Calaf G., Hei T.K., Levine F., Shay J.W.,
RA   Wang J.J.Y., Pandita T.K.;
RT   "Characterization of ataxia telangiectasia fibroblasts with extended
RT   life-span through telomerase expression.";
RL   Oncogene 20:278-288(2001).
//