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Cellosaurus GM03388 (CVCL_1F13)

[Text version]
Cell line name GM03388
Accession CVCL_1F13
Resource Identification Initiative To cite this cell line use: GM03388 (RRID:CVCL_1F13)
Comments Population: Iranian; Arab.
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)
Sex of cell Male
Age at sampling 1Y6M
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) 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)

Cross-references
Cell line collections (Providers) Coriell; GM03388
Cell line databases/resources CLO; CLO_0016628
Biological sample resources BioSample; SAMN00808384
Encyclopedic resources Wikidata; Q54838041
Entry history
Entry creation08-Jul-2015
Last entry update29-Jun-2023
Version number10