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Cellosaurus GM05876 (CVCL_2Y97)

[Text version]
Cell line name GM05876
Accession CVCL_2Y97
Resource Identification Initiative To cite this cell line use: GM05876 (RRID:CVCL_2Y97)
Comments Population: Caucasian.
Omics: CNV analysis.
Cell type: Fibroblast; CL=CL_0000057.
Disease 22q11.2 deletion syndrome (NCIt: C2989)
22q11.2 deletion syndrome (ORDO: Orphanet_567)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_C0HI (BRCi017-A)
Sex of cell Male
Age at sampling Age unspecified
Category Finite cell line
Publications

CLPUB00447
Mulivor R.A., Suchy S.F.
1992/1993 catalog of cell lines. NIGMS human genetic mutant cell repository. 16th edition. October 1992.
(In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992)

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)

Cross-references
Cell line collections (Providers) Coriell; GM05876
Cell line databases/resources CLO; CLO_0024236
Encyclopedic resources Wikidata; Q54841975
Entry history
Entry creation22-Sep-2015
Last entry update29-Jun-2023
Version number10