Cellosaurus GM847/hTERT-6 (CVCL_C1HF)
Cell line name | GM847/hTERT-6 | |
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Accession | CVCL_C1HF | |
Resource Identification Initiative | To cite this cell line use: GM847/hTERT-6 (RRID:CVCL_C1HF) | |
Comments | Population: African American. Genetic integration: Method=Transfection; Gene=HGNC; HGNC:11730; TERT. Genetic integration: Method=Transfection; Gene=UniProtKB; P00552; Transposon Tn5 neo. Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40). Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. | |
Disease | Lesch-Nyhan syndrome (NCIt: C61255) Lesch-Nyhan syndrome (ORDO: Orphanet_510) | |
Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) | |
Hierarchy | Parent: CVCL_7908 (GM00847) Children:
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Sex of cell | Male | |
Age at sampling | 5Y6M | |
Category | Transformed cell line | |
Publications | PubMed=11359895; DOI=10.1128/mcb.21.12.3862-3875.2001; PMCID=PMC87050 PubMed=19935656; DOI=10.1038/nbt.1587 | |
Cross-references | ||
Encyclopedic resources | Wikidata; Q114311537 | |
Entry history | ||
Entry creation | 22-Sep-2022 | |
Last entry update | 19-Dec-2024 | |
Version number | 6 |