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Cellosaurus GM05659T (CVCL_ZU51)

[Text version]
Cell line name GM05659T
Accession CVCL_ZU51
Resource Identification Initiative To cite this cell line use: GM05659T (RRID:CVCL_ZU51)
Comments Population: Caucasian.
Genetic integration: Method=Transfection/transduction; Gene=HGNC; 11730; TERT.
Derived from site: In situ; Chest, skin; UBERON=UBERON_0001868.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 4177; GBA1; Simple; p.Thr408Met (c.1223C>T) (T369M); ClinVar=VCV000093447; Zygosity=Heterozygous (from parent cell line).
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_7434 (GM05659)
Sex of cell Male
Age at sampling 1Y2M
Category Telomerase immortalized cell line
Publications

PubMed=27543334; DOI=10.1073/pnas.1610020113; PMCID=PMC5018765
Reid-Bayliss K.S., Arron S.T., Loeb L.A., Bezrookove V., Cleaver J.E.
Why Cockayne syndrome patients do not get cancer despite their DNA repair deficiency.
Proc. Natl. Acad. Sci. U.S.A. 113:10151-10156(2016)

Cross-references
Encyclopedic resources Wikidata; Q98126374
Entry history
Entry creation02-Jul-2020
Last entry update10-Sep-2024
Version number8