Cellosaurus cell line WG0308 (CVCL

Cross-references
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	Mutation; HGNC; HGNC:2073; TPP1; Simple; p.Cys365Arg (c.1093T>C); ClinVar=VCV000002641; Zygosity=Heterozygous (PubMed=9295267).
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 David E. Sleat, Robert J. Donnelly, Henry Lackland, Chang-Gong Liu, Istvan Sohar, Raju K. Pullarkat, Peter Lobel; Association of mutations in a lysosomal protein with classical late-infantile neuronal ceroid lipofuscinosis. Science 277:1802-1805(1997)
Encyclopedic resources	Wikidata; Q110433997
Entry history
Entry creation	16-Dec-2021
Last entry update	19-Dec-2024
Version number	6