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Cellosaurus GM06199 (CVCL_4D89)

[Text version]
Cell line name GM06199
Accession CVCL_4D89
Resource Identification Initiative To cite this cell line use: GM06199 (RRID:CVCL_4D89)
Comments Population: African American.
Karyotypic information: 46,XY,r(21)(p13->q22) (Coriell=GM06199).
Derived from site: In situ; Foreskin, skin; UBERON=UBERON_0001471.
Cell type: Fibroblast of foreskin; CL=CL_1001608.
Disease Ring chromosome 21 syndrome (NCIt: C186278)
Ring chromosome 21 syndrome (ORDO: Orphanet_1445)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling <1M
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)

Cross-references
Cell line collections (Providers) Coriell; GM06199
Cell line databases/resources CLO; CLO_0023142
Encyclopedic resources Wikidata; Q54842216
Entry history
Entry creation22-Sep-2015
Last entry update29-Jun-2023
Version number8