Cellosaurus STBCi019-B (CVCL_RB72)
Cell line name | STBCi019-B |
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Synonyms | SFC828-03-09 |
Accession | CVCL_RB72 |
Resource Identification Initiative | To cite this cell line use: STBCi019-B (RRID:CVCL_RB72) |
Comments | From: StemBANCC; Oxford; United Kingdom. Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067. Cell type: Fibroblast of skin; CL=CL_0002620. |
Sequence variations |
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Disease | Parkinson disease 1, autosomal dominant (NCIt: C198602) Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602) |
Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
Hierarchy | Parent: CVCL_A8X7 (SF828) |
Sex of cell | Female |
Age at sampling | 51Y |
Category | Induced pluripotent stem cell |
Cross-references | |
Cell line collections (Providers) | EBiSC; STBCi019-B - Discontinued
ECACC; 66540677 - Discontinued |
Cell line databases/resources | hPSCreg; STBCi019-B |
Biological sample resources | BioSamples; SAMEA104493639 |
Encyclopedic resources | Wikidata; Q54956389 |
Entry history | |
Entry creation | 05-Mar-2018 |
Last entry update | 19-Dec-2024 |
Version number | 13 |