| 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; PMCID=PMC1684927 Mario Cristiano Rattazzi, Judith A. Brown, Ronald G. Davidson, Thomas Byron Shows; 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 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) PubMed=3017984; DOI=10.1016/S0021-9258(18)67145-5 Brian F. O'Dowd, Maris H. Klavins, Huntington Faxon Willard, Roy A. Gravel, John Alexander Lowden, Don J. Mahuran; Molecular heterogeneity in the infantile and juvenile forms of Sandhoff disease (O-variant GM2 gangliosidosis). J. Biol. Chem. 261:12680-12685(1986) CLPUB00447 Richard A. Mulivor, Sharon F. Suchy; 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; GM00317
|
| Cell line databases/resources |
CLO; CLO_0025542
|
| Encyclopedic resources |
Wikidata; Q54836155
|
| Entry history |
| Entry creation | 22-Sep-2015 |
| Last entry update | 29-Jun-2023 |
| Version number | 9 |
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