Cell line name |
GM00057 |
Synonyms |
GM-57; GM00057A; GM0057A |
Accession |
CVCL_2N23 |
Resource Identification Initiative |
To cite this cell line use: GM00057 (RRID:CVCL_2N23) |
Comments |
Population: Caucasian. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
Disease |
Propionic acidemia (NCIt: C85030) Propionic acidemia (ORDO: Orphanet_35) |
Species of origin |
Homo sapiens (Human)
(NCBI Taxonomy: 9606) |
Sex of cell |
Female |
Age at sampling |
6Y |
Category |
Finite cell line |
Publications | PubMed=5101292; DOI=10.1172/JCI106466; PMCID=PMC291900 Hsia Y.E., Scully K.J., Rosenberg L.E. Inherited propionyl-Coa carboxylase deficiency in 'ketotic hyperglycinemia'. J. Clin. Invest. 50:127-130(1971) 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) CLPUB00720 Greene A.E., Mulivor R.A. 1986/1987 catalog of cell lines. NIGMS human genetic mutant cell repository. 13th edition. October 1986. (In misc. document) Institute for Medical Research (Camden, N.J.) NIH 87-2011; pp.1-549; National Institutes of Health; Bethesda; USA (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 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; GM00057
|
Cell line databases/resources |
CLO; CLO_0025161
|
Encyclopedic resources |
Wikidata; Q54836008
|
Entry history |
Entry creation | 22-Sep-2015 |
Last entry update | 29-Jun-2023 |
Version number | 10 |
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