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Cellosaurus WG2292 (CVCL_QZ37)

[Text version]
Cell line name WG2292
Accession CVCL_QZ37
Resource Identification Initiative To cite this cell line use: WG2292 (RRID:CVCL_QZ37)
Comments From: Montreal Children's Hospital cell repository; Montreal; Canada.
Miscellaneous: Cell line no longer available.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Arakawa syndrome II (NCIt: C99081)
Methylcobalamin deficiency type cblG (ORDO: Orphanet_2170)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Category Finite cell line
Publications

PubMed=8968737; DOI=10.1093/hmg/5.12.1867
Leclerc D., Campeau E., Goyette P., Adjalla C.-E., Christensen B., Ross M., Eydoux P., Rosenblatt D.S., Rozen R., Gravel R.A.
Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders.
Hum. Mol. Genet. 5:1867-1874(1996)

PubMed=9235907; DOI=10.1074/jbc.272.31.19171
Gulati S., Chen Z.-Q., Brody L.C., Rosenblatt D.S., Banerjee R.
Defects in auxiliary redox proteins lead to functional methionine synthase deficiency.
J. Biol. Chem. 272:19171-19175(1997)

Cross-references
Encyclopedic resources Wikidata; Q54993976
Entry history
Entry creation05-Mar-2018
Last entry update29-Jun-2023
Version number7