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Cellosaurus Der(22)-iPS-C2 (CVCL_UG56)

[Text version]
Cell line name Der(22)-iPS-C2
Accession CVCL_UG56
Resource Identification Initiative To cite this cell line use: Der(22)-iPS-C2 (RRID:CVCL_UG56)
Comments Population: Caucasian.
Cell type: Fibroblast; CL=CL_0000057.
Disease Trisomy 22 (NCIt: C114765)
Total autosomal trisomy (ORDO: Orphanet_98131)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_V547 (GM00084)
Sex of cell Male
Age at sampling 1M
Category Induced pluripotent stem cell
STR profile Source(s): PubMed=21949351

Markers:
AmelogeninX,Y
CSF1PO10,12
D3S135816,17
D5S81812
D7S8209
D8S117912
D13S31712
D16S53912
D18S5113,16
D21S1128,29
FGA21,22.2
Penta D13
Penta E12,15
TH019.3,10
TPOX8,12
vWA16

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Publications

PubMed=21949351; DOI=10.1093/hmg/ddr435
Li W., Wang X.-M., Fan W.-X., Zhao P., Chan Y.-C., Chen S., Zhang S.-Q., Guo X.-P., Zhang Y., Li Y.-H., Cai J.-L., Qin D.-J., Li X.-Y., Yang J.-Y., Peng T.-R., Zychlinski D., Hoffmann D., Zhang R.-S., Deng K., Ng K.-M., Menten B., Zhong M., Wu J.-Y., Li Z.-Y., Chen Y.-L., Schambach A., Tse H.-F., Pei D.-Q., Esteban M.A.
Modeling abnormal early development with induced pluripotent stem cells from aneuploid syndromes.
Hum. Mol. Genet. 21:32-45(2012)

Cross-references
Encyclopedic resources Wikidata; Q93525645
Entry history
Entry creation13-Nov-2018
Last entry update29-Jun-2023
Version number6