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Cellosaurus PS-iPS2 (CVCL_CW47)

[Text version]
Cell line name PS-iPS2
Accession CVCL_CW47
Resource Identification Initiative To cite this cell line use: PS-iPS2 (RRID:CVCL_CW47)
Comments Derived from site: In situ; Bone marrow; UBERON=UBERON_0002371.
Sequence variations
  • Mutation; HGNC; Group_1972; MT-@; Unexplicit; m.10949del2501; Zygosity=Heteroplasmic (PubMed=23400930).
Disease Pearson syndrome (NCIt: C115326)
Pearson syndrome (ORDO: Orphanet_699)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_CW46 ! PS-iPS1
CVCL_CW48 ! PS-iPS3
Sex of cell Female
Age at sampling 3Y
Category Induced pluripotent stem cell
Publications

PubMed=23400930; DOI=10.1002/stem.1354
Cherry A.B.C., Gagne K.E., McLoughlin E.M., Baccei A., Gorman B., Hartung O., Miller J.D., Zhang J., Zon R.L., Ince T.A., Neufeld E.J., Lerou P.H., Fleming M.D., Daley G.Q., Agarwal S.
Induced pluripotent stem cells with a mitochondrial DNA deletion.
Stem Cells 31:1287-1297(2013)

Cross-references
Encyclopedic resources Wikidata; Q54948407
Entry history
Entry creation13-Jul-2016
Last entry update29-Jun-2023
Version number10