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Cellosaurus GM23675 (CVCL_5S97)

[Text version]
Cell line name GM23675
Accession CVCL_5S97
Resource Identification Initiative To cite this cell line use: GM23675 (RRID:CVCL_5S97)
Comments Part of: Genetic Testing Reference Material (GeT-RM) samples.
Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
Omics: CNV analysis.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Gene amplification; HGNC; HGNC:6990; MECP2; Duplication; Zygosity=Hemizygous (PubMed=24508304).
Disease Lubs X-linked mental retardation syndrome (NCIt: C126747)
Proximal Xq28 duplication syndrome (ORDO: Orphanet_1762)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 25Y
Category Transformed cell line
Publications

PubMed=23665875; DOI=10.1534/g3.113.006577; PMCID=PMC3704242
Tang Z.-Y., Berlin D.S., Toji L.H., Toruner G.A., Beiswanger C.M., Kulkarni S., Martin C.L., Emanuel B.S., Christman M., Gerry N.P.
A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds.
G3 (Bethesda) 3:1143-1149(2013)

PubMed=24508304; DOI=10.1016/j.jmoldx.2013.11.004; PMCID=PMC3937532
Kalman L.V., Tarleton J.C., Percy A.K., Aradhya S., Bale S., Barker S.D., Bayrak-Toydemir P., Bridges C., Buller-Burckle A.M., Das S., Iyer R.K., Vo T.D., Zvereff V.V., Toji L.H.
Development of a genomic DNA reference material panel for Rett syndrome (MECP2-related disorders) genetic testing.
J. Mol. Diagn. 16:273-279(2014)

Cross-references
Cell line collections (Providers) Coriell; GM23675
Encyclopedic resources Wikidata; Q54853218
Entry history
Entry creation23-Feb-2016
Last entry update19-Dec-2024
Version number12