Cellosaurus HPSI1116i-uacs_3 (CVCL_WK26)
| Cell line name | HPSI1116i-uacs_3 |
|---|---|
| Accession | CVCL_WK26 |
| Resource Identification Initiative | To cite this cell line use: HPSI1116i-uacs_3 (RRID:CVCL_WK26) |
| Comments | From: University College London; London; United Kingdom. From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom. Population: Caucasian; French. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Disease | Genetic macular dystrophy (NCIt: C140264) Rare genetic macular disorder (ORDO: Orphanet_522574) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Male |
| Age at sampling | 50-59Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | ECACC; 77650833 |
| Cell line databases/resources | HipSci; HPSI1116i-uacs_3 |
| Biological sample resources | BioSamples; SAMEA104012374 |
| Encyclopedic resources | Wikidata; Q94236658 |
| Entry history | |
| Entry creation | 24-May-2019 |
| Last entry update | 29-Jun-2023 |
| Version number | 8 |