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Cellosaurus CCE2.2 (CVCL_HL99)

[Text version]
Cell line name CCE2.2
Synonyms ConCordant Epilepsy 2.2
Accession CVCL_HL99
Resource Identification Initiative To cite this cell line use: CCE2.2 (RRID:CVCL_HL99)
Comments Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
Omics: Transcriptomics; Microarray.
Donor information: Established from monozygotic twin of CCE2.1 (Cellosaurus=CVCL_HL98).
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Disease Childhood absence epilepsy (NCIt: C128189)
Childhood absence epilepsy (ORDO: Orphanet_64280)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 34Y
Category Transformed cell line
Publications

PubMed=18435749; DOI=10.1111/j.1528-1167.2008.01630.x
Helbig I., Matigian N.A., Vadlamudi L., Lawrence K.M., Bayly M.A., Bain S.M., Diyagama D., Scheffer I.E., Mulley J.C., Holloway A.J., Dibbens L.M., Berkovic S.F., Hayward N.K.
Gene expression analysis in absence epilepsy using a monozygotic twin design.
Epilepsia 49:1546-1554(2008)

Cross-references
Encyclopedic resources Wikidata; Q54808948
Gene expression databases GEO; GSM181385
Entry history
Entry creation01-Dec-2016
Last entry update10-Apr-2025
Version number9