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Cellosaurus CRICKi012-A (CVCL_C5T4)

[Text version]
Cell line name CRICKi012-A
Synonyms iFCI017
Accession CVCL_C5T4
Resource Identification Initiative To cite this cell line use: CRICKi012-A (RRID:CVCL_C5T4)
Comments From: The Francis Crick Institute Limited; London; United Kingdom.
Donor information: At sampling donor was not affected with Parkinson disease but at risk for disease.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
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)
Sex of cell Female
Age at sampling 57Y
Category Induced pluripotent stem cell

PubMed=37336145; DOI=10.1016/j.scr.2023.103134
Devito L.G., Zanjani Z.S., Evans J.R., Scardamaglia A., Houlden H., Gandhi S., Healy L.
Generation of two G51D SNCA missense mutation iPSC lines (CRICKi011-A, CRICKi012-A) from two individuals at risk of Parkinson's disease.
Stem Cell Res. 71:103134-103134(2023)

Cell line databases/resources hPSCreg; CRICKi012-A
Biological sample resources BioSamples; SAMEA112233748
Encyclopedic resources Wikidata; Q116048795
Entry history
Entry creation15-Dec-2022
Last entry update05-Oct-2023
Version number3