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Cellosaurus WG1534 (CVCL_5I47)

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Cell line name WG1534
Synonyms PWSdel1; PWS-1
Accession CVCL_5I47
Resource Identification Initiative To cite this cell line use: WG1534 (RRID:CVCL_5I47)
Comments From: Montreal Children's Hospital cell repository; Montreal; Canada.
Miscellaneous: Cell line no longer available.
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_U523 (PWS iPS del 1-1)CVCL_U524 (PWS iPS del 1-2)CVCL_U525 (PWS iPS del 1-3)
CVCL_U526 (PWS iPS del 1-4)CVCL_U527 (PWS iPS del 1-5)CVCL_U528 (PWS iPS del 1-6)
CVCL_U529 (PWS iPS del 1-7)CVCL_U530 (PWS iPS del 1-8)CVCL_U531 (PWS iPS del 1-9)
CVCL_5I48 (PWS-iPSC-1-A)CVCL_5I49 (PWS-iPSC-1-B)
Sex of cell Female
Category Finite cell line
Publications

PubMed=20876107; DOI=10.1073/pnas.1004487107; PMCID=PMC2955112
Stormy J. Chamberlain, Ivy Pin-Fang Chen, Khong Y. Ng, Fany Bourgois-Rocha, Fouad Lemtiri-Chlieh, Eric S. Levine, Marc E. Lalande;
Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes.
Proc. Natl. Acad. Sci. U.S.A. 107:17668-17673(2010)

PubMed=24816254; DOI=10.1038/ng.2968
Yonatan Stelzer, Ido Sagi, Ofra Yanuka, Rachel Eiges, Nissim Benvenisty;
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; Q54993885
Entry history
Entry creation14-Dec-2015
Last entry update29-Jun-2023
Version number8