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Cellosaurus WG1631 (CVCL_5I46)

[Text version]
Cell line name WG1631
Synonyms ASdel2
Accession CVCL_5I46
Resource Identification Initiative To cite this cell line use: WG1631 (RRID:CVCL_5I46)
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 Angelman syndrome (NCIt: C75462)
Angelman syndrome (ORDO: Orphanet_72)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_U500 (AS iPS del 2-0)CVCL_U501 (AS iPS del 2-3)
Sex of cell Male
Category Finite cell line
Publications

PubMed=20876107; DOI=10.1073/pnas.1004487107; PMCID=PMC2955112
Chamberlain S.J., Chen I.P.-F., Ng K.Y., Bourgois-Rocha F., Lemtiri-Chlieh F., Levine E.S., Lalande M.E.
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)

Cross-references
Encyclopedic resources Wikidata; Q54993908
Entry history
Entry creation14-Dec-2015
Last entry update29-Jun-2023
Version number8