Cellosaurus WG1032 (CVCL_RG74)
| Cell line name | WG1032 |
|---|---|
| Accession | CVCL_RG74 |
| Resource Identification Initiative | To cite this cell line use: WG1032 (RRID:CVCL_RG74) |
| Comments | From: Montreal Children's Hospital cell repository; Montreal; Canada. Miscellaneous: Cell line no longer available. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Disease | Albright's hereditary osteodystrophy (NCIt: C118434) Albright hereditary osteodystrophy (ORDO: Orphanet_665) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Female |
| Age at sampling | 34Y |
| Category | Finite cell line |
| Cross-references | |
| Encyclopedic resources | Wikidata; Q54993828 |
| Entry history | |
| Entry creation | 05-Mar-2018 |
| Last entry update | 29-Jun-2023 |
| Version number | 8 |