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Cellosaurus IBMS-iPSC-014-05 (CVCL_QY07)

[Text version]

Cell line name IBMS-iPSC-014-05
Synonyms IBMSi003-A
Accession CVCL_QY07
Resource Identification Initiative To cite this cell line use: IBMS-iPSC-014-05 (RRID:CVCL_QY07)
Comments From: Institute of Biomedical Sciences, Academia Sinica; Taipei; Taiwan.
Population: Chinese; Taiwan.
Derived from sampling site: Peripheral blood.
Sequence variations
  • Mutation; HGNC; 9009; PKD2; Simple; p.Arg803Ter (c.2407C>T); ClinVar=VCV000618321; Zygosity=Heterozygous (PubMed=29055226).
Disease Autosomal dominant polycystic kidney disease (NCIt: C84578)
Autosomal dominant polycystic kidney disease (ORDO: Orphanet_730)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_ZE87 (IBMS-iPSC-014-C )
Sex of cell Female
Age at sampling 63Y
Category Induced pluripotent stem cell
STR profile Source(s): PubMed=29055226

Markers:
AmelogeninX
CSF1PO12,13
D2S133819,24
D3S135815,17
D5S81811
D7S8208
D8S117914,15
D13S31710,11
D16S5399,11
D18S5114
D19S43313
D21S1129,30
FGA21,24
TH018,9
TPOX9,11
vWA14

Run an STR similarity search on this cell line
Publications

PubMed=29055226; DOI=10.1016/j.scr.2017.10.005
Ho M.-C., Huang C.-Y., Lee J.-J., Hsu S.-H., Cheng Y.-C., Hsu Y.-H., Hwang D.-Y., Lu H.-E., Chen H.-C., Hsieh P.C.-H.
Generation of an induced pluripotent stem cell line, IBMS-iPSC-014-05, from a female autosomal dominant polycystic kidney disease patient carrying a common mutation of R803X in PKD2.
Stem Cell Res. 25:38-41(2017)

Cross-references
Cell line collections BCRC; SC81046
BCRC; SC81047
Cell line databases/resources hPSCreg; IBMSi003-A
SKIP; SKIP005633
SKIP; SKIP005634
Biological sample resources BioSamples; SAMEA104387752
Encyclopedic resources Wikidata; Q54897192
Entry history
Entry creation05-Mar-2018
Last entry update20-May-2021
Version number7