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Cellosaurus GM10879 (CVCL_AD74)

[Text version]
Cell line name GM10879
Accession CVCL_AD74
Resource Identification Initiative To cite this cell line use: GM10879 (RRID:CVCL_AD74)
Comments Population: Caucasian.
Derived from site: In situ; Fetus; UBERON=UBERON_0000323.
Cell type: Fibroblast; CL=CL_0000057.
Disease Fryns syndrome (NCIt: C98932)
Fryns syndrome (ORDO: Orphanet_2059)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 27FW
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; GM10879
Cell line databases/resources CLO; CLO_0024119
Biological sample resources BioSample; SAMN00800308
Encyclopedic resources Wikidata; Q54844713
Entry history
Entry creation23-Feb-2016
Last entry update29-Jun-2023
Version number8