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Cellosaurus GM02595 (CVCL_X268)

[Text version]
Cell line name GM02595
Synonyms GM 2595; GM2595
Accession CVCL_X268
Resource Identification Initiative To cite this cell line use: GM02595 (RRID:CVCL_X268)
Comments Population: Caucasian.
Karyotypic information: 46,X,i(X)(q10) (PubMed=10377420).
Cell type: Fibroblast; CL=CL_0000057.
Disease Turner syndrome (NCIt: C26900)
Turner syndrome (ORDO: Orphanet_881)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 33Y
Category Finite cell line
Publications

PubMed=6661932; DOI=10.1159/000131990
Aronson M.M., Nichols W.W., Mulivor R.A., Greene A.E., Coriell L.L.
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
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=10377420; DOI=10.1073/pnas.96.13.7364; PMCID=PMC22091
Carrel L., Willard H.F.
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; GM02595
Cell line databases/resources CLO; CLO_0033385
Encyclopedic resources Wikidata; Q54837566
Entry history
Entry creation17-Jul-2014
Last entry update29-Jun-2023
Version number12