Home  |  Contact

Cellosaurus EURACi005-A (CVCL_YC01)

[Text version]
Cell line name EURACi005-A
Synonyms iPS-2011; iPSC-2011
Accession CVCL_YC01
Resource Identification Initiative To cite this cell line use: EURACi005-A (RRID:CVCL_YC01)
Comments From: EURAC Research Institute for Biomedicine; Bolzano; Italy.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 8607; PRKN; Unexplicit; Ex3del; Zygosity=Homozygous (PubMed=31715428).
Disease Parkinson disease 2, autosomal recessive juvenile (NCIt: C198603)
Young-onset Parkinson disease (ORDO: Orphanet_2828)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling Age unspecified
Category Induced pluripotent stem cell
Publications

PubMed=31715428; DOI=10.1016/j.scr.2019.101624
Zanon A., Riekschnitz D.A., von Troyer M., Volpato C.B., Picard A., Cantaloni C., Di Segni M., Silipigni R., Pramstaller P.P., Hicks A.A., Pichler I.
Generation of an induced pluripotent stem cell line (EURACi005-A) from a Parkinson's disease patient carrying a homozygous exon 3 deletion in the PRKN gene.
Stem Cell Res. 41:101624-101624(2019)

Cross-references
Cell line databases/resources hPSCreg; EURACi005-A
Biological sample resources BioSamples; SAMEA5922750
Encyclopedic resources Wikidata; Q93546841
Entry history
Entry creation19-Dec-2019
Last entry update29-Jun-2023
Version number7