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Cellosaurus GM00078 (CVCL_6B30)

[Text version]
Cell line name GM00078
Synonyms GM-78; GM 78
Accession CVCL_6B30
Resource Identification Initiative To cite this cell line use: GM00078 (RRID:CVCL_6B30)
Comments Cell type: Fibroblast; CL=CL_0000057.
Disease Metachromatic leukodystrophy (NCIt: C61251)
Metachromatic leukodystrophy (ORDO: Orphanet_512)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 3Y
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) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda (1977)

PubMed=36611; DOI=10.1073/pnas.76.4.1957
DeLuca C., Brown J.A., Shows T.B.
Lysosomal arylsulfatase deficiencies in humans: chromosome assignments for arylsulfatase A and B.
Proc. Natl. Acad. Sci. U.S.A. 76:1957-1961(1979)

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; GM00078 - Discontinued
Cell line databases/resources CLO; CLO_0025168
Encyclopedic resources Wikidata; Q54836020
Entry history
Entry creation23-Feb-2016
Last entry update29-Jun-2023
Version number9