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Cellosaurus A6-iPSC (CVCL_DD59)

[Text version]
Cell line name A6-iPSC
Accession CVCL_DD59
Resource Identification Initiative To cite this cell line use: A6-iPSC (RRID:CVCL_DD59)
Comments Population: Caucasian.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Gene amplification; HGNC; 11138; SNCA; Triplication; Zygosity=Heterozygous (PubMed=27191603).
Disease Parkinson disease 4, autosomal dominant (NCIt: C198604)
Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_F204 (ND27760)
Sex of cell Female
Age at sampling 55Y
Category Induced pluripotent stem cell
STR profile Source(s): PubMed=27191603

Markers:
AmelogeninX
CSF1PO12
D5S81811
D7S8209,11
D13S3179,11
D16S53911,12
D21S1130,31.2
TH017,9.3
TPOX8,11
vWA15,18

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Publications

PubMed=27191603; DOI=10.1371/journal.pone.0154890; PMCID=PMC4871453
Momcilovic O., Sivapatham R., Oron T.R., Meyer M., Mooney S., Rao M.S., Zeng X.-M.
Derivation, characterization, and neural differentiation of integration-free induced pluripotent stem cell lines from Parkinson's disease patients carrying SNCA, LRRK2, PARK2, and GBA mutations.
PLoS ONE 11:E0154890-E0154890(2016)

Cross-references
Encyclopedic resources Wikidata; Q54607167
Entry history
Entry creation13-Jul-2016
Last entry update29-Jun-2023
Version number12