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Cellosaurus WG1575 (CVCL_QZ30)

[Text version]
Cell line name WG1575
Accession CVCL_QZ30
Resource Identification Initiative To cite this cell line use: WG1575 (RRID:CVCL_QZ30)
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.
Sequence variations
  • Mutation; HGNC; HGNC:7473; MTRR; Simple; p.Cys405Arg (c.1213T>C); Zygosity=Heterozygous (PubMed=10484769).
Disease Homocystinuria-megaloblastic anemia, cblE complementation type (NCIt: C142173)
Methylcobalamin deficiency type cblE (ORDO: Orphanet_2169)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling <1Y
Category Finite cell line
Publications

PubMed=1627355; DOI=10.1016/0885-4505(92)90032-T
Susan Linda Sillaots, Charles A. Hall, Valerie Hurteloup, David S. Rosenblatt;
Heterogeneity in cblG: differential retention of cobalamin on methionine synthase.
Biochem. Med. Metab. Biol. 47:242-249(1992)

PubMed=9235907; DOI=10.1074/jbc.272.31.19171
Sumedha Gulati, Zhi-Qiang Chen, Lawrence C. Brody, David S. Rosenblatt, Ruma Banerjee;
Defects in auxiliary redox proteins lead to functional methionine synthase deficiency.
J. Biol. Chem. 272:19171-19175(1997)

PubMed=10484769; DOI=10.1093/hmg/8.11.2009
Aaron Wilson, Daniel Leclerc, David S. Rosenblatt, Roy A. Gravel;
Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism.
Hum. Mol. Genet. 8:2009-2016(1999)

Cross-references
Encyclopedic resources Wikidata; Q54993887
Entry history
Entry creation05-Mar-2018
Last entry update19-Dec-2024
Version number10