Cellosaurus logo
expasy logo

Cellosaurus WG4152 (CVCL_B4K6)

[Text][XML][JSON]
Cell line name WG4152
Synonyms WG-4152
Accession CVCL_B4K6
Resource Identification Initiative To cite this cell line use: WG4152 (RRID:CVCL_B4K6)
Comments From: Montreal Children's Hospital cell repository; Montreal; Canada.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Methylmalonic aciduria and homocystinuria, cblC type (NCIt: C142174)
Methylmalonic acidemia with homocystinuria, type cblC (ORDO: Orphanet_79282)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 59Y
Category Finite cell line
Publications

PubMed=29302025; DOI=10.1038/s41467-017-02306-5; PMCID=PMC5754367
Jean-Louis Gueant, Celine Chery, Abderrahim Oussalah, Javad Nadaf, David Coelho, Thomas Josse, Justine Flayac, Aurelie Robert, Isabelle Koscinski, Isabelle Gastin, Pierre Filhine-Tresarrieu ...Show all 31 authors... , Mihaela Pupavac, Alison Brebner, David Watkins, Tomi Pastinen, Alexandre Montpetit, Fadi Hariri, David-Alexandre Tregouet, Benjamin A. Raby, Wendy Kay Chung, Pierre-Emmanuel Morange, D. Sean Froese, Matthias R. Baumgartner, Jean-Francois Benoist, Can Ficicioglu, Virginie Marchand, Yuri Motorin, Chrystele Bonnemains, Francois Feillet, Jacek Majewski, David S. Rosenblatt; Show fewer authors
A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.
Nat. Commun. 9:67.1-67.12(2018)

Cross-references
Encyclopedic resources Wikidata; Q110434404
Entry history
Entry creation16-Dec-2021
Last entry update29-Jun-2023
Version number4