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Cellosaurus CNS1-hiPSC9 (CVCL_C012)

[Text version]
Cell line name CNS1-hiPSC9
Synonyms CNS.1.H.iPSC.9
Accession CVCL_C012
Resource Identification Initiative To cite this cell line use: CNS1-hiPSC9 (RRID:CVCL_C012)
Comments From: Royan Institute; Theran; Iran.
Population: Iranian.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 12530; UGT1A1; Simple; p.Leu413Pro; Zygosity=Unspecified (PubMed=20821352).
Disease Crigler-Najjar syndrome (NCIt: C84656)
Crigler-Najjar syndrome (ORDO: Orphanet_205)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_C004 ! CNS1-hiPSC1
CVCL_C006 ! CNS1-hiPSC2
CVCL_C007 ! CNS1-hiPSC4
CVCL_C008 ! CNS1-hiPSC5
CVCL_C009 ! CNS1-hiPSC6
CVCL_C010 ! CNS1-hiPSC7
CVCL_C011 ! CNS1-hiPSC8
CVCL_C005 ! CNS1-hiPSC10
Sex of cell Female
Age at sampling 19Y
Category Induced pluripotent stem cell
Publications

PubMed=20821352; DOI=10.1007/s12015-010-9189-3
Ghodsizadeh A., Taei A., Totonchi M., Seifinejad A., Gourabi H., Pournasr B., Aghdami N., Malekzadeh R., Almadani N., Salekdeh G.H., Baharvand H.
Generation of liver disease-specific induced pluripotent stem cells along with efficient differentiation to functional hepatocyte-like cells.
Stem Cell Rev. Rep. 6:622-632(2010)

Cross-references
Cell line collections (Providers) RSCB; RSCB0138
Encyclopedic resources Wikidata; Q54813904
Entry history
Entry creation06-Jun-2012
Last entry update29-Jun-2023
Version number13