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Cellosaurus GM06056 (CVCL_V822)

[Text version]
Cell line name GM06056
Synonyms GM6056
Accession CVCL_V822
Resource Identification Initiative To cite this cell line use: GM06056 (RRID:CVCL_V822)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Pyruvate carboxylase deficiency (NCIt: C85040)
Pyruvate carboxylase deficiency (ORDO: Orphanet_3008)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 4M
Category Finite cell line
Publications

PubMed=6705569; DOI=10.1159/000132035
Oizumi J., Donnell G.N., Ng W.G., Mulivor R.A., Greene A.E., Coriell L.L.
Congenital lactic acidosis associated with pyruvate carboxylase deficiency. Repository identification No. GM6056.
Cytogenet. Cell Genet. 38:80-80(1984)

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; GM06056
Cell line databases/resources CLO; CLO_0023540
Encyclopedic resources Wikidata; Q54842140
Entry history
Entry creation16-Apr-2014
Last entry update29-Jun-2023
Version number10