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Cellosaurus WG2324 (CVCL_B3YP)

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Cell line name WG2324
Accession CVCL_B3YP
Resource Identification Initiative To cite this cell line use: WG2324 (RRID:CVCL_B3YP)
Comments From: Montreal Children's Hospital cell repository; Montreal; Canada.
Population: Caucasian.
Omics: Genomics; Whole genome sequencing.
Omics: Transcriptomics; RNAseq.
Miscellaneous: Cell line no longer available.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Methylmalonic acidemia (NCIt: C98986)
Methylmalonic acidemia without homocystinuria (ORDO: Orphanet_293355)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 13Y
Category Finite cell line
Publications

PubMed=27233228; DOI=10.1016/j.ymgme.2016.05.014
Jordan Chu, Mihaela Pupavac, David Watkins, Xia Tian, Yan-Ming Feng, Stella Chen, Remington Fenter, Victor W. Zhang, Jing Wang, Lee-Jun Wong, David S. Rosenblatt;
Next generation sequencing of patients with mut methylmalonic aciduria: validation of somatic cell studies and identification of 16 novel mutations.
Mol. Genet. Metab. 118:264-271(2016)

CLPUB00669
Jordan Chu;
Investigation of patients diagnosed with mut methylmalonic aciduria.
Thesis MSc (2017); McGill University Montreal; Montreal; Canada

PubMed=31462756; DOI=10.1038/s41436-019-0640-9
Lina Sobhi Abdrabo, David Watkins, Sophie Ran Wang, Joel Lafond-Lapalme, Jean-Baptiste Riviere, David S. Rosenblatt;
Genome and RNA sequencing in patients with methylmalonic aciduria of unknown cause.
Genet. Med. 22:432-436(2020)

Cross-references
Encyclopedic resources Wikidata; Q110434110
Entry history
Entry creation16-Dec-2021
Last entry update10-Apr-2025
Version number5