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Cellosaurus GM02523 (CVCL_1F10)

[Text version]
Cell line name GM02523
Synonyms GM2523
Accession CVCL_1F10
Resource Identification Initiative To cite this cell line use: GM02523 (RRID:CVCL_1F10)
Comments Population: African American.
Omics: Metabolome analysis.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Glycogen storage disease type III (NCIt: C84736)
Glycogen storage disease due to glycogen debranching enzyme deficiency (ORDO: Orphanet_366)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
Sex of cell Male
Age at sampling 1Y
Category Finite cell line

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)

PubMed=33329388; DOI=10.3389/fendo.2020.579981
Hannibal L., Theimer J., Wingert V., Klotz K., Bierschenk I., Nitschke R., Spiekerkoetter U., Grunert S.C.
Metabolic profiling in human fibroblasts enables subtype clustering in glycogen storage disease.
Front. Endocrinol. 11:579981.1-579981.14(2020)

Cell line collections (Providers) Coriell; GM02523
Cell line databases/resources CLO; CLO_0033414
Encyclopedic resources Wikidata; Q54837528
Entry history
Entry creation08-Jul-2015
Last entry update29-Jun-2023
Version number9