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Cellosaurus GM09811 (CVCL_IN25)

[Text version]
Cell line name GM09811
Synonyms GM 09811
Accession CVCL_IN25
Resource Identification Initiative To cite this cell line use: GM09811 (RRID:CVCL_IN25)
Comments Population: Caucasian; Portuguese.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
HLA typing Source: PubMed=2916654
Class I
HLA-AA*02,03
HLA-BB*07,44
Disease Neonatal hemochromatosis (NCIt: C129980)
Neonatal hemochromatosis (ORDO: Orphanet_446)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 75D
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; GM09811
Cell line databases/resources CLO; CLO_0030458
Encyclopedic resources Wikidata; Q54844066
Entry history
Entry creation01-Dec-2016
Last entry update29-Jun-2023
Version number8