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Cellosaurus GM00025 (CVCL_CX21)

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Cell line name GM00025
Synonyms GM-25
Accession CVCL_CX21
Resource Identification Initiative To cite this cell line use: GM00025 (RRID:CVCL_CX21)
Comments Cell type: Fibroblast; CL=CL_0000057.
Disease Glycogen storage disease type IX (NCIt: C122662)
Glycogen storage disease due to phosphorylase kinase deficiency (ORDO: Orphanet_370)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 2Y6M
Category Finite cell line
Publications

DOI=10.5962/bhl.title.4090
Lewis Lemon Coriell, Arthur E. Greene;
The human genetic mutant cell repository: list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository. 4th edition. October 1977.
(In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977)

Cross-references
Cell line collections (Providers) Coriell; GM00025 - Discontinued
Encyclopedic resources Wikidata; Q54835982
Entry history
Entry creation13-Jul-2016
Last entry update29-Jun-2023
Version number7