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Cellosaurus GM07215 (CVCL_2Y98)

[Text version]
Cell line name GM07215
Accession CVCL_2Y98
Resource Identification Initiative To cite this cell line use: GM07215 (RRID:CVCL_2Y98)
Comments Population: Caucasian.
Omics: Variations; 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)
Sex of cell Female
Age at sampling 3D
Category Finite cell line
Publications

CLPUB00447
Richard A. Mulivor, Sharon F. Suchy;
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
Zhen-Ya Tang, Dorit S. Berlin, Lorraine H. Toji, Gokce Altay Toruner, Christine M. Beiswanger, Shashikant Kulkarni, Christa Lese Martin, Beverly S. Emanuel, Michael Christman, Norman P. Gerry;
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; GM07215
Cell line databases/resources CLO; CLO_0036922
Encyclopedic resources Wikidata; Q54842582
Entry history
Entry creation22-Sep-2015
Last entry update10-Apr-2025
Version number11