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Cellosaurus PWS UPD 1.2 (CVCL_ZJ75)

[Text version]
Cell line name PWS UPD 1.2
Synonyms PWSUPD1.2; PWS maternal UniParental Disomy line 1.2
Accession CVCL_ZJ75
Resource Identification Initiative To cite this cell line use: PWS UPD 1.2 (RRID:CVCL_ZJ75)
Comments 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)
Sex of cell Female
Category Induced pluripotent stem cell
STR profile Source(s): FPWR

Markers:
AmelogeninX
CSF1PO12
D5S81810,12
D7S8208,9
D13S3179,13
D16S53910,12
TH018
TPOX8,9
vWA16,18

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Web pages Provider; FPWR; -; https://www.fpwr.org/hubfs/Research%20Docs/PWS%20UPD1.2%20Validation%20QC%20Package.pdf
Provider; FPWR; -; https://www.fpwr.org/ipsc-biobank
Publications

PubMed=29228278; DOI=10.1093/hmg/ddx420
Langouet M., Glatt-Deeley H.R., Chung M.S., Dupont-Thibert C.M., Mathieux E., Banda E.C., Stoddard C.E., Crandall L.J., Lalande M.E.
Zinc finger protein 274 regulates imprinted expression of transcripts in Prader-Willi syndrome neurons.
Hum. Mol. Genet. 27:505-515(2018)

Cross-references
Encyclopedic resources Wikidata; Q98128732
Entry history
Entry creation02-Jul-2020
Last entry update10-Apr-2025
Version number6