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Cellosaurus GM00317 (CVCL_1Y43)

[Text version]
Cell line name GM00317
Synonyms GM-317; GM 317; GM00317A
Accession CVCL_1Y43
Resource Identification Initiative To cite this cell line use: GM00317 (RRID:CVCL_1Y43)
Comments Population: African American.
Cell type: Fibroblast; CL=CL_0000057.
Disease Sandhoff disease (NCIt: C85052)
Sandhoff disease (ORDO: Orphanet_796)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 1Y
Category Finite cell line
Publications

PubMed=817596
Rattazzi M.C., Brown J.A., Davidson R.G., Shows T.B.
Studies on complementation of beta hexosaminidase deficiency in human GM2 gangliosidosis.
Am. J. Hum. Genet. 28:143-154(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)

PubMed=3017984; DOI=10.1016/S0021-9258(18)67145-5
O'Dowd B.F., Klavins M.H., Willard H.F., Gravel R.A., Lowden J.A., Mahuran D.J.
Molecular heterogeneity in the infantile and juvenile forms of Sandhoff disease (O-variant GM2 gangliosidosis).
J. Biol. Chem. 261:12680-12685(1986)

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; GM00317
Cell line databases/resources CLO; CLO_0025542
Encyclopedic resources Wikidata; Q54836155
Entry history
Entry creation22-Sep-2015
Last entry update29-Jun-2023
Version number9