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Cellosaurus T101-iPSC (CVCL_DD61)

[Text version]
Cell line name T101-iPSC
Accession CVCL_DD61
Resource Identification Initiative To cite this cell line use: T101-iPSC (RRID:CVCL_DD61)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:4177; GBA1; Simple; p.Asn409Ser (c.1226A>G) (N370S); ClinVar=VCV000004290; Zygosity=Unspecified (from parent cell line).
Disease Parkinson's disease (NCIt: C26845)
Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_DD53 (ND31630)
Sex of cell Male
Age at sampling 69Y
Category Induced pluripotent stem cell
STR profile Source(s): PubMed=27191603

Markers:
AmelogeninX,Y
CSF1PO10,14
D5S81811,12
D7S82010,11
D13S3179,11
D16S53912
D21S1128,31
TH017,8
TPOX8
vWA16,17

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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; Q54971408
Entry history
Entry creation13-Jul-2016
Last entry update19-Dec-2024
Version number12