Cellosaurus HPSI0816i-neow_5 (CVCL_LF17)
Cell line name | HPSI0816i-neow_5 |
---|---|
Synonyms | WTSIi611-A |
Accession | CVCL_LF17 |
Resource Identification Initiative | To cite this cell line use: HPSI0816i-neow_5 (RRID:CVCL_LF17) |
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_LF18 ! HPSI0816i-neow_7 |
Sex of cell | Male |
Age at sampling | 55-59Y |
Category | Induced pluripotent stem cell |
Cross-references | |
Cell line collections (Providers) | ECACC; 77650705 |
Cell line databases/resources | HipSci; HPSI0816i-neow_5
hPSCreg; WTSIi611-A |
Biological sample resources | BioSamples; SAMEA104011308 |
Encyclopedic resources | Wikidata; Q54891432 |
Entry history | |
Entry creation | 22-Aug-2017 |
Last entry update | 29-Jun-2023 |
Version number | 10 |