Cellosaurus T21-KC-K4DT (CVCL_B3M3)
Cell line name | T21-KC-K4DT |
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Accession | CVCL_B3M3 |
Resource Identification Initiative | To cite this cell line use: T21-KC-K4DT (RRID:CVCL_B3M3) |
Comments | Genetic integration: Method=Transduction; Gene=HGNC; HGNC:1582; CCND1. Genetic integration: Method=Transduction; Gene=HGNC; HGNC:1773; CDK4 (Note=With p.Arg24Cys). Genetic integration: Method=Transduction; Gene=HGNC; HGNC:11730; TERT. Derived from site: In situ; Amniotic fluid; UBERON=UBERON_0000173. Cell type: Keratinocyte; CL=CL_0000312. |
Disease | Down syndrome (NCIt: C2993) Down syndrome (ORDO: Orphanet_870) |
Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
Hierarchy | Parent: CVCL_B3M2 (T21-iPSC#12) |
Sex of cell | Female |
Age at sampling | Fetus |
Category | Telomerase immortalized cell line |
Publications | PubMed=30760866; DOI=10.1038/s41374-019-0230-0; PMCID=PMC6760570 |
Cross-references | |
Encyclopedic resources | Wikidata; Q110433284 |
Entry history | |
Entry creation | 16-Dec-2021 |
Last entry update | 19-Dec-2024 |
Version number | 6 |