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Cellosaurus SDQLCHi065-A (CVCL_D4ZN)

[Text version]
Cell line name SDQLCHi065-A
Accession CVCL_D4ZN
Resource Identification Initiative To cite this cell line use: SDQLCHi065-A (RRID:CVCL_D4ZN)
Comments From: Qilu Children's Hospital of Shandong University; Jinan; China.
Population: Chinese; Han.
Karyotypic information: 47,XY,+21,inv(9)(p12;q21),16qh+ (PubMed=38377649).
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Disease Down syndrome (NCIt: C2993)
Down syndrome (ORDO: Orphanet_870)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 8D
Category Induced pluripotent stem cell
Publications

PubMed=38377649; DOI=10.1016/j.scr.2024.103351
Zhang X., Xin H.-M., Liu Y., Gai Z.-T., Li Z.-L.
An integration-free iPSC line SDQLCHi065-A from a patient with down syndrome, possessing a 47, XY,+21, inv(9)(p12q21),16qh + karyotype.
Stem Cell Res. 76:103351-103351(2024)

Cross-references
Cell line databases/resources hPSCreg; SDQLCHi065-A
Biological sample resources BioSamples; SAMEA115174033
Encyclopedic resources Wikidata; Q127384267
Entry history
Entry creation02-May-2024
Last entry update10-Sep-2024
Version number2