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Cellosaurus PWS SD fibroblast (CVCL_ZJ46)

[Text version]
Cell line name PWS SD fibroblast
Synonyms PWS Small atypical Deletion fibroblast
Accession CVCL_ZJ46
Resource Identification Initiative To cite this cell line use: PWS SD fibroblast (RRID:CVCL_ZJ46)
Comments Cell type: Fibroblast; CL=CL_0000057.
Disease Prader-Willi syndrome (NCIt: C75463)
Prader-Willi syndrome (ORDO: Orphanet_739)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_ZJ47 (PWS SD 2-1 iPSC)CVCL_ZJ48 (PWS SD 2-2 iPSC)CVCL_ZJ49 (PWS SD 2-3 iPSC)
CVCL_ZJ50 (PWS SD 2-4 iPSC)CVCL_ZJ51 (PWS SD 2-5 iPSC)CVCL_ZJ52 (PWS SD 2-6 iPSC)
CVCL_ZJ53 (PWS SD 2-7 iPSC)CVCL_ZJ54 (PWS SD 2-8 iPSC)CVCL_ZJ55 (PWS SD 2-9 iPSC)
Sex of cell Male
Age at sampling 19Y
Category Finite cell line
Publications

PubMed=24363065; DOI=10.1093/hmg/ddt628; PMCID=PMC3976333
Martins-Taylor K., Hsiao J.S., Chen I.P.-F., Glatt-Deeley H.R., De Smith A.J., Blakemore A.I.F., Lalande M.E., Chamberlain S.J.
Imprinted expression of UBE3A in non-neuronal cells from a Prader-Willi syndrome patient with an atypical deletion.
Hum. Mol. Genet. 23:2364-2373(2014)

Cross-references
Encyclopedic resources Wikidata; Q98128722
Entry history
Entry creation02-Jul-2020
Last entry update29-Jun-2023
Version number5