Molekulargenetisches Labor
Zentrum für Nephrologie und Stoffwechsel
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Ferritin—schwere Kette

Das FTH1-Gen kodiert die schwere Kette des Ferritin, des wichtigsten intrazellulären Eisenspeicherproteins. Einige Promotormutationen werden mit der autosomal dominanten Hämochromatose Typ 5 in Zusammenhang gebracht.


Klinisch Untersuchungsmethoden Familienuntersuchung
Bearbeitungszeit 5 Tage
Probentyp genomische DNS
Klinisch Untersuchungsmethoden Hochdurchsatz-Sequenzierung
Bearbeitungszeit 25 Tage
Probentyp genomische DNS
Klinisch Untersuchungsmethoden Direkte Sequenzierung der proteinkodierenden Bereiche eines Gens
Bearbeitungszeit 25 Tage
Probentyp genomische DNS

Verknüpfte Erkrankungen:

Hämochromatose 5



Worwood M et al. (1985) Assignment of human ferritin genes to chromosomes 11 and 19q13.3----19qter.

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Wu KJ et al. (1999) Coordinated regulation of iron-controlling genes, H-ferritin and IRP2, by c-MYC.

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Courseaux A et al. (1996) Definition of the minimal MEN1 candidate area based on a 5-Mb integrated map of proximal 11q13. The European Consortium on Men1, (GENEM 1; Groupe d'Etude des Néoplasies Endocriniennes Multiples de type 1).

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Harrison PM et al. (1996) The ferritins: molecular properties, iron storage function and cellular regulation.

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Boyd D et al. (1984) Isolation and characterization of a cDNA clone for human ferritin heavy chain.

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Murray MT et al. (1987) Conservation of ferritin heavy subunit gene structure: implications for the regulation of ferritin gene expression.

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Youssoufian H et al. (1988) Association of a new chromosomal deletion [del(1)(q32q42)] with diaphragmatic hernia: assignment of a human ferritin gene.

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Leibold EA et al. (1988) Cytoplasmic protein binds in vitro to a highly conserved sequence in the 5' untranslated region of ferritin heavy- and light-subunit mRNAs.

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Costanzo F et al. (1986) Structure of gene and pseudogenes of human apoferritin H.

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Gatti RA et al. (1987) Human ferritin genes: chromosomal assignments and polymorphisms.

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Hasegawa S et al. (2013) Growth retardation and hair loss in transgenic mice overexpressing human H-ferritin gene.

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Li L et al. (2010) Binding and uptake of H-ferritin are mediated by human transferrin receptor-1.

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Yachou A et al. (1991) Mouse ferritin H sequences map to chromosomes 3, 6, and 19.

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Faniello MC et al. (2006) Detection and functional analysis of an SNP in the promoter of the human ferritin H gene that modulates the gene expression.

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Yachou AK et al. (1991) Mouse ferritin H multigene family is polymorphic and contains a single multiallelic functional gene located on chromosome 19.

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Pham CG et al. (2004) Ferritin heavy chain upregulation by NF-kappaB inhibits TNFalpha-induced apoptosis by suppressing reactive oxygen species.

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Papadopoulos P et al. (1992) A second human ferritin H locus on chromosome 11.

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Ferreira C et al. (2001) H ferritin knockout mice: a model of hyperferritinemia in the absence of iron overload.

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None (2000) Iron regulatory proteins and the molecular control of mammalian iron metabolism.

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Ferreira C et al. (2000) Early embryonic lethality of H ferritin gene deletion in mice.

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Mancias JD et al. (2014) Quantitative proteomics identifies NCOA4 as the cargo receptor mediating ferritinophagy.

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Shi H et al. (2008) A cytosolic iron chaperone that delivers iron to ferritin.

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Sammarco MC et al. (2008) Ferritin L and H subunits are differentially regulated on a post-transcriptional level.

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Kato J et al. (2001) A mutation, in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload.

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Caskey JH et al. (1983) Human ferritin gene is assigned to chromosome 19.

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Cragg SJ et al. (1985) Genes for the 'H' subunit of human ferritin are present on a number of human chromosomes.

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Hentze MW et al. (1986) Cloning, characterization, expression, and chromosomal localization of a human ferritin heavy-chain gene.

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Orphanet article

Orphanet ID 159608 external link

NCBI article

NCBI 2495 external link

OMIM.ORG article

Omim 134770 external link
Update: 14. August 2020
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