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Cellosaurus GM05396 (CVCL_X323)

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Cell line name GM05396
Synonyms GM 5396; GM5396
Accession CVCL_X323
Resource Identification Initiative To cite this cell line use: GM05396 (RRID:CVCL_X323)
Comments Population: Caucasian.
Karyotypic information: 45,X,dic(X;22)(p11;p12) (PubMed=10377420).
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 2M
Category Finite cell line
Publications

PubMed=6661932; DOI=10.1159/000131990
Margaret M. Aronson, Warren W. Nichols, Richard A. Mulivor, Arthur E. Greene, Lewis Lemon Coriell;
Chromosome maps of cell lines with specific monosomic or trisomic portions of the genome in the NIGMS Human Genetic Mutant Cell Repository.
Cytogenet. Cell Genet. 36:652-658(1983)

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=10377420; DOI=10.1073/pnas.96.13.7364; PMCID=PMC22091
Laura Carrel, Huntington Faxon Willard;
Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others.
Proc. Natl. Acad. Sci. U.S.A. 96:7364-7369(1999)

Cross-references
Cell line collections (Providers) Coriell; GM05396
Cell line databases/resources CLO; CLO_0024812
Encyclopedic resources Wikidata; Q54839003
Entry history
Entry creation17-Jul-2014
Last entry update29-Jun-2023
Version number13