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Cellosaurus GM00151 (CVCL_Y523)

[Text version]
Cell line name GM00151
Synonyms GM-151; GM 151
Accession CVCL_Y523
Resource Identification Initiative To cite this cell line use: GM00151 (RRID:CVCL_Y523)
Comments Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Sly syndrome (NCIt: C84903)
Mucopolysaccharidosis type 7 (ORDO: Orphanet_584)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 4Y
Category Finite cell line
Publications

DOI=10.5962/bhl.title.4090
Coriell L.L., Greene A.E.
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)

PubMed=908752; DOI=10.1172/JCI108860; PMCID=PMC372461
Kaplan A., Fischer D., Achord D., Sly W.S.
Phosphohexosyl recognition is a general characteristic of pinocytosis of lysosomal glycosidases by human fibroblasts.
J. Clin. Invest. 60:1088-1093(1977)

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; GM00151
Cell line databases/resources CLO; CLO_0025852
Encyclopedic resources Wikidata; Q54836066
Entry history
Entry creation10-Apr-2015
Last entry update29-Jun-2023
Version number11