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Cellosaurus GM02052+hTERT (CVCL_VL09)

[Text version]
Cell line name GM02052+hTERT
Synonyms hTERT+ GM02052
Accession CVCL_VL09
Resource Identification Initiative To cite this cell line use: GM02052+hTERT (RRID:CVCL_VL09)
Comments Population: Jewish; Moroccan.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:795; ATM; Simple; p.Arg35Ter (c.103C>T); ClinVar=VCV000003025; Zygosity=Homozygous (from parent cell line).
Disease Ataxia telangiectasia syndrome (NCIt: C2887)
Ataxia telangiectasia (ORDO: Orphanet_100)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_7350 (GM02052)
Sex of cell Female
Age at sampling 15Y
Category Telomerase immortalized cell line
Publications

PubMed=11313956; DOI=10.1038/sj.onc.1204072
Wood L.D., Halvorsen T.L., Dhar S., Baur J.A., Pandita R.K., Wright W.E., Hande M.P., Calaf G., Hei T.K., Levine F., Shay J.W., Wang J.J.Y., Pandita T.K.
Characterization of ataxia telangiectasia fibroblasts with extended life-span through telomerase expression.
Oncogene 20:278-288(2001)

Cross-references
Encyclopedic resources Wikidata; Q93575552
Entry history
Entry creation07-Sep-2018
Last entry update19-Dec-2024
Version number9