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Cellosaurus GM02668 (CVCL_X093)

[Text version]
Cell line name GM02668
Synonyms GM 2668
Accession CVCL_X093
Resource Identification Initiative To cite this cell line use: GM02668 (RRID:CVCL_X093)
Comments Population: Caucasian.
Karyotypic information: 46,X,del(Y)(pter->q11.2) [77%]; 45,X [33%] (Coriell=GM02668).
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 Sex ambiguous
Age at sampling 41Y
Category Finite cell line
Publications

PubMed=6617268; DOI=10.1159/000131883
Aronson M.M., Nichols W.W., Mulivor R.A., Greene A.E., Coriell L.L.
Breakpoint map of chromosomal inversion and deletion cell cultures in the NIGMS Human Genetic Mutant Cell Repository.
Cytogenet. Cell Genet. 35:298-302(1983)

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) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992)

Cross-references
Cell line collections (Providers) Coriell; GM02668
Cell line databases/resources CLO; CLO_0014999
Encyclopedic resources Wikidata; Q54837612
Entry history
Entry creation17-Jul-2014
Last entry update05-Oct-2023
Version number11