| Cell line name | UNEWi011-A |
|---|---|
| Synonyms | UNEW011Ai |
| Accession | CVCL_VF32 |
| Resource Identification Initiative | To cite this cell line use: UNEWi011-A (RRID:CVCL_VF32) |
| Comments | From: University of Newcastle; Newcastle; United Kingdom. Miscellaneous: Cell line has been lost (EBiSC=UNEWi011-A). Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Disease | Severe combined immunodeficiency due to NHEJ1 deficiency (NCIt: C162695) Cernunnos-XLF deficiency (ORDO: Orphanet_169079) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Male |
| Age at sampling | 1-4Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | EBiSC; UNEWi011-A - Discontinued
ECACC; 66540041 - Discontinued |
| Cell line databases/resources | hPSCreg; UNEWi011-A |
| Biological sample resources | BioSamples; SAMEA2629624 |
| Encyclopedic resources | Wikidata; Q54991156 |
| Entry history | |
| Entry creation | 14-May-2018 |
| Last entry update | 30-Jan-2024 |
| Version number | 10 |