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Cellosaurus GM09564 (CVCL_UR76)

[Text version]
Cell line name GM09564
Synonyms GM 09564
Accession CVCL_UR76
Resource Identification Initiative To cite this cell line use: GM09564 (RRID:CVCL_UR76)
Comments Cell type: Fibroblast; CL=CL_0000057.
HLA typing Source: PubMed=2916654
Class I
HLA-AA*01,02
HLA-BB*51,w57
Disease Neonatal hemochromatosis (NCIt: C129980)
Neonatal hemochromatosis (ORDO: Orphanet_446)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 20D
Category Finite cell line
Publications

PubMed=2916654; PMCID=PMC1879596
Knisely A.S., Harford J.B., Klausner R.D., Taylor S.R.
Neonatal hemochromatosis. The regulation of transferrin-receptor and ferritin synthesis by iron in cultured fibroblastic-line cells.
Am. J. Pathol. 134:439-445(1989)

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; GM09564 - Discontinued
Encyclopedic resources Wikidata; Q93804212
Entry history
Entry creation25-Feb-2019
Last entry update29-Jun-2023
Version number6