| Cell line name | HPSI0816i-neow_7 |
|---|---|
| Synonyms | WTSIi611-B; WTSIi631-A |
| Accession | CVCL_LF18 |
| Resource Identification Initiative | To cite this cell line use: HPSI0816i-neow_7 (RRID:CVCL_LF18) |
| 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 | Alport syndrome (NCIt: C34842) Alport syndrome (ORDO: Orphanet_63) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_LF17 ! HPSI0816i-neow_5 |
| Sex of cell | Male |
| Age at sampling | 55-59Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | ECACC; 77650706 |
| Cell line databases/resources | HipSci; HPSI0816i-neow_7
hPSCreg; WTSIi611-B |
| Biological sample resources | BioSamples; SAMEA104011453 |
| Encyclopedic resources | Wikidata; Q54891433 |
| Entry history | |
| Entry creation | 22-Aug-2017 |
| Last entry update | 29-Jun-2023 |
| Version number | 10 |