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Cellosaurus hIPSC-Di21-C3-1-2 (CVCL_D1FF)

[Text version]
Cell line name hIPSC-Di21-C3-1-2
Synonyms Di C3-1-2; C3-1-2
Accession CVCL_D1FF
Resource Identification Initiative To cite this cell line use: hIPSC-Di21-C3-1-2 (RRID:CVCL_D1FF)
Comments Population: Caucasian.
Characteristics: Using CRISPR/Cas9 a IRES-TK-Neo-polyA site cassette was introduced in one allele of exon 3 of APP on chromosome 21 (PubMed=23084023).
Genetic integration: Method=CRISPR/Cas9; Gene=UniProtKB; Q9QNF7; Human herpesvirus 1 TK.
Genetic integration: Method=CRISPR/Cas9; Gene=UniProtKB; P00552; Transposon Tn5 neo.
Derived from site: In situ; Chest, skin; UBERON=UBERON_0001868.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Down syndrome (NCIt: C2993)
Down syndrome (ORDO: Orphanet_870)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_D1FA (hIPSC-Tri21-C3-1)
Sex of cell Female
Age at sampling 1Y
Category Induced pluripotent stem cell
Publications

PubMed=23084023; DOI=10.1016/j.stem.2012.08.004; PMCID=PMC3705773
Li L.B., Chang K.-H., Wang P.-R., Hirata R.K., Papayannopoulou T., Russell D.W.
Trisomy correction in Down syndrome induced pluripotent stem cells.
Cell Stem Cell 11:615-619(2012)

Cross-references
Encyclopedic resources Wikidata; Q127381762
Entry history
Entry creation30-Jan-2024
Last entry update10-Sep-2024
Version number2