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Cellosaurus GM21889 (CVCL_U542)

[Text version]
Cell line name GM21889
Accession CVCL_U542
Resource Identification Initiative To cite this cell line use: GM21889 (RRID:CVCL_U542)
Comments Population: African American.
Omics: CNV analysis.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Prader-Willi syndrome (NCIt: C75463)
Prader-Willi syndrome (ORDO: Orphanet_739)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_5I50 (PWS-iPSC-2-A)CVCL_5I51 (PWS-iPSC-2-B)
Sex of cell Male
Age at sampling 8Y
Category Finite cell line
Publications

PubMed=23665875; DOI=10.1534/g3.113.006577
Tang Z.-Y., Berlin D.S., Toji L.H., Toruner G.A., Beiswanger C.M., Kulkarni S., Martin C.L., Emanuel B.S., Christman M., Gerry N.P.
A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds.
G3 (Bethesda) 3:1143-1149(2013)

PubMed=24816254; DOI=10.1038/ng.2968
Stelzer Y., Sagi I., Yanuka O., Eiges R., Benvenisty N.
The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader-Willi syndrome.
Nat. Genet. 46:551-557(2014)

Cross-references
Cell line collections (Providers) Coriell; GM21889
Encyclopedic resources Wikidata; Q54852210
Entry history
Entry creation16-Apr-2014
Last entry update29-Jun-2023
Version number10