| Cell line name | HPSI0916i-moyn_1 |
|---|---|
| Synonyms | WTSIi657-B; WTSIi711-A |
| Accession | CVCL_LM47 |
| Resource Identification Initiative | To cite this cell line use: HPSI0916i-moyn_1 (RRID:CVCL_LM47) |
| Comments | From: University College London; London; United Kingdom. From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom. Population: Caucasian. 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) |
| Originate from same individual | CVCL_LM48 ! HPSI0916i-moyn_4 |
| Sex of cell | Male |
| Age at sampling | 55-59Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | ECACC; 77650761 |
| Cell line databases/resources | HipSci; HPSI0916i-moyn_1
hPSCreg; WTSIi657-B |
| Biological sample resources | BioSamples; SAMEA104130575 |
| Encyclopedic resources | Wikidata; Q54891529 |
| Entry history | |
| Entry creation | 15-Nov-2017 |
| Last entry update | 29-Jun-2023 |
| Version number | 11 |