| Cell line name | TNGB-78816 | ||
|---|---|---|---|
| Synonyms | 78816 | ||
| Accession | CVCL_A9ZG | ||
| Resource Identification Initiative | To cite this cell line use: TNGB-78816 (RRID:CVCL_A9ZG) | ||
| Comments | Population: Caucasian. Derived from site: In situ; Fetus; UBERON=UBERON_0000323. Cell type: Fibroblast; CL=CL_0000057. | ||
| Disease | Klinefelter syndrome (NCIt: C34752) | ||
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) | ||
| Hierarchy | Children:
| ||
| Sex of cell | Male | ||
| Age at sampling | Fetus | ||
| Category | Finite cell line | ||
| Cross-references | |||
| Cell line collections (Providers) | TNGB; 78816 | ||
| Encyclopedic resources | Wikidata; Q102115000 | ||
| Entry history | |||
| Entry creation | 29-Oct-2020 | ||
| Last entry update | 29-Jun-2023 | ||
| Version number | 5 | ||