Cellosaurus GM847/hTERT-3 subclone 9 (CVCL_C1HG)
| Cell line name | GM847/hTERT-3 subclone 9 |
|---|---|
| Accession | CVCL_C1HG |
| Resource Identification Initiative | To cite this cell line use: GM847/hTERT-3 subclone 9 (RRID:CVCL_C1HG) |
| 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_C1HE (GM847/hTERT-3) |
| 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 |
| Cross-references | |
| Encyclopedic resources | Wikidata; Q114311536 |
| Entry history | |
| Entry creation | 22-Sep-2022 |
| Last entry update | 19-Dec-2024 |
| Version number | 6 |