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Cellosaurus PWS-iPSC-2-B (CVCL_5I51)

[Text version]
Cell line name PWS-iPSC-2-B
Accession CVCL_5I51
Resource Identification Initiative To cite this cell line use: PWS-iPSC-2-B (RRID:CVCL_5I51)
Comments Population: African American.
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 Parent: CVCL_U542 (GM21889)
Sex of cell Male
Age at sampling 8Y
Category Induced pluripotent stem cell
Publications

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
Encyclopedic resources Wikidata; Q54948736
Entry history
Entry creation14-Dec-2015
Last entry update29-Jun-2023
Version number8