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Cellosaurus GM01022 (CVCL_V790)

[Text version]
Cell line name GM01022
Synonyms GM-1022; GM01022A
Accession CVCL_V790
Resource Identification Initiative To cite this cell line use: GM01022 (RRID:CVCL_V790)
Comments Population: Caucasian.
Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Disease Maroteaux-Lamy syndrome (NCIt: C61264)
Mucopolysaccharidosis type 6 (ORDO: Orphanet_583)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_V775 ! GM00519
CVCL_V821 ! GM05358
Sex of cell Female
Age at sampling 4Y
Category Transformed cell line
Publications

PubMed=806052; DOI=10.1203/00006450-197505000-00003
Beratis N.G., Turner B.M., Weiss R., Hirschhorn K.
Arylsulfatase B deficiency in Maroteaux-Lamy syndrome: cellular studies and carrier identification.
Pediatr. Res. 9:475-480(1975)

PubMed=826372; DOI=10.1159/000130717
Beratis N.G., Hirschhorn K., Friedman S., Greene A.E., Coriell L.L.
Maroteaux-Lamy syndrome: repository identification Nos. GM-519, 520, 935, 943, and 1022.
Cytogenet. Cell Genet. 17:236-238(1976)

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) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda (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) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992)

Cross-references
Cell line collections (Providers) Coriell; GM01022
Cell line databases/resources CLO; CLO_0029494
Biological sample resources BioSample; SAMN00803567
Encyclopedic resources Wikidata; Q54836607
Entry history
Entry creation16-Apr-2014
Last entry update29-Jun-2023
Version number14