Cellosaurus HPSI0916i-vorn_5 (CVCL_LM52)
Cell line name | HPSI0916i-vorn_5 |
---|---|
Synonyms | WTSIi621-A |
Accession | CVCL_LM52 |
Resource Identification Initiative | To cite this cell line use: HPSI0916i-vorn_5 (RRID:CVCL_LM52) |
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 | Hereditary cerebellar ataxia (NCIt: C140268) Rare hereditary ataxia (ORDO: Orphanet_183518) |
Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
Originate from same individual | CVCL_LM51 ! HPSI0916i-vorn_2 |
Sex of cell | Female |
Age at sampling | 70-74Y |
Category | Induced pluripotent stem cell |
Cross-references | |
Cell line collections (Providers) | ECACC; 77650740 |
Cell line databases/resources | HipSci; HPSI0916i-vorn_5
hPSCreg; WTSIi621-A |
Biological sample resources | BioSamples; SAMEA104012397 |
Encyclopedic resources | Wikidata; Q54891534 |
Entry history | |
Entry creation | 15-Nov-2017 |
Last entry update | 29-Jun-2023 |
Version number | 11 |