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Cellosaurus WG1886 (CVCL_B3VX)

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Cell line name WG1886
Synonyms WG 1886
Accession CVCL_B3VX
Resource Identification Initiative To cite this cell line use: WG1886 (RRID:CVCL_B3VX)
Comments From: Montreal Children's Hospital cell repository; Montreal; Canada.
Population: Japanese.
Miscellaneous: Cell line no longer available.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease 5' 10' methylenetetrahydrofolate reductase deficiency (NCIt: C84524)
Homocystinuria due to methylene tetrahydrofolate reductase deficiency (ORDO: Orphanet_395)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling Children
Category Finite cell line
Publications

PubMed=1627352; DOI=10.1016/0885-4505(92)90029-x
David S. Rosenblatt, Helena Lue-Shing, A. Arzoumanian, Lawrence Low-Nang, Nora V. Matiaszuk;
Methylenetetrahydrofolate reductase (MR) deficiency: thermolability of residual MR activity, methionine synthase activity, and methylcobalamin levels in cultured fibroblasts.
Biochem. Med. Metab. Biol. 47:221-225(1992)

Cross-references
Encyclopedic resources Wikidata; Q110434071
Entry history
Entry creation16-Dec-2021
Last entry update29-Jun-2023
Version number4