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Cellosaurus WG4095 (CVCL_B4GH)

[Text version]
Cell line name WG4095
Accession CVCL_B4GH
Resource Identification Initiative To cite this cell line use: WG4095 (RRID:CVCL_B4GH)
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 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)
Category Finite cell line
Publications

CLPUB00670
Kim J.C.
Novel inborn error of vitamin B12 metabolism caused by mutations in ABCD4.
Thesis MSc (2012); McGill University Montreal; Montreal; Canada

Cross-references
Encyclopedic resources Wikidata; Q110434400
Entry history
Entry creation16-Dec-2021
Last entry update29-Jun-2023
Version number4