Cellosaurus WG1302 (CVCL_QY99)
| Cell line name | WG1302 |
|---|---|
| Accession | CVCL_QY99 |
| Resource Identification Initiative | To cite this cell line use: WG1302 (RRID:CVCL_QY99) |
| 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 | Hyperphenylalaninemia, BH4-deficient A (NCIt: C138171) 6-pyruvoyl-tetrahydropterin synthase deficiency (ORDO: Orphanet_13) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Male |
| Age at sampling | 9M |
| Category | Finite cell line |
| Cross-references | |
| Encyclopedic resources | Wikidata; Q54993867 |
| Entry history | |
| Entry creation | 05-Mar-2018 |
| Last entry update | 29-Jun-2023 |
| Version number | 8 |