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Cellosaurus WG0308 (CVCL_B3W1)

[Text version]
Cell line name WG0308
Synonyms WG308
Accession CVCL_B3W1
Resource Identification Initiative To cite this cell line use: WG0308 (RRID:CVCL_B3W1)
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
Disease Neuronal ceroid lipofuscinosis type 2 (NCIt: C85864)
Congenital neuronal ceroid lipofuscinosis (ORDO: Orphanet_168486)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Category Finite cell line
Publications

PubMed=9295267; DOI=10.1126/science.277.5333.1802
Sleat D.E., Donnelly R.J., Lackland H., Liu C.-G., Sohar I., Pullarkat R.K., Lobel P.
Association of mutations in a lysosomal protein with classical late-infantile neuronal ceroid lipofuscinosis.
Science 277:1802-1805(1997)

Cross-references
Encyclopedic resources Wikidata; Q110433997
Entry history
Entry creation16-Dec-2021
Last entry update19-Dec-2024
Version number6