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Cellosaurus B-LCL-CDG3 (CVCL_C0VC)

[Text version]
Cell line name B-LCL-CDG3
Synonyms CDG-LCL3; CDG-LCL III; LCL-3
Accession CVCL_C0VC
Resource Identification Initiative To cite this cell line use: B-LCL-CDG3 (RRID:CVCL_C0VC)
Comments Population: Caucasian.
Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Cell type: B-cell; CL=CL_0000236.
Sequence variations
Disease Congenital disorder of glycosylation type Ia (NCIt: C126868)
PMM2-CDG (ORDO: Orphanet_79318)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling Children
Category Transformed cell line
STR profile Source(s): CLS=302014

Markers:
AmelogeninX
CSF1PO11,12
D3S135816
D5S81811,12
D7S82010,12
D8S117913,16
D13S3178,12
D16S53910,11
D18S5112,14
D21S1128,32.2
FGA21,23
Penta D10,11
Penta E11,18
TH017,9.3
TPOX8,9
vWA16,18

Run an STR similarity search on this cell line
Publications

PubMed=9719677; DOI=10.1093/glycob/8.10.963
Bergmann M., Gross H.-J., Abdelatty F., Moller P., Jaeken J., Schwartz-Albiez R.
Abnormal surface expression of sialoglycans on B lymphocyte cell lines from patients with carbohydrate deficient glycoprotein syndrome I A (CDGS I A).
Glycobiology 8:963-972(1998)

PubMed=34420056; DOI=10.1093/glycob/cwab087
Parrado A., Rubio-Pedraza G., Serrano M., De la Morena-Barrio M.E., Ibanez-Mico S., Ruiz-Lafuente N., Schwartz-Albiez R., Esteve-Sole A., Alsina L., Corral J., Hernandez-Caselles T.
Dissecting the transcriptional program of phosphomannomutase 2-deficient cells: lymphoblastoide B cell lines as a valuable model for congenital disorders of glycosylation studies.
Glycobiology 32:84-100(2022)

Cross-references
Cell line collections (Providers) CLS; 302014
Encyclopedic resources Wikidata; Q112929256
Entry history
Entry creation23-Jun-2022
Last entry update19-Dec-2024
Version number7