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Cellosaurus HIHDNDi001-A (CVCL_YR02)

[Text version]
Cell line name HIHDNDi001-A
Synonyms A30P-3; SNCA3; Tue_020_A
Accession CVCL_YR02
Resource Identification Initiative To cite this cell line use: HIHDNDi001-A (RRID:CVCL_YR02)
Comments From: Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tubingen; Tubingen; Germany.
Population: Caucasian.
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)
Originate from same individual CVCL_YR03 ! HIHDNDi001-B
Sex of cell Male
Age at sampling 67Y
Category Induced pluripotent stem cell

PubMed=32798915; DOI=10.1016/j.scr.2020.101951
Barbuti P.A., Santos B.F.R., Dording C.M., Cruciani G., Massart F., Hummel A., Kruger R.
Generation of two iPS cell lines (HIHDNDi001-A and HIHDNDi001-B) from a Parkinson's disease patient carrying the heterozygous p.A30P mutation in SNCA.
Stem Cell Res. 48:101951-101951(2020)

Cell line databases/resources hPSCreg; HIHDNDi001-A
Biological sample resources BioSamples; SAMEA6611426
Encyclopedic resources Wikidata; Q94208315
Entry history
Entry creation12-Mar-2020
Last entry update29-Jun-2023
Version number7