FTH1

Source: Wikipedia, the free encyclopedia.
FTH1
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl
UniProt
RefSeq (mRNA)

NM_002032

NM_010239

RefSeq (protein)

NP_002023

NP_034369

Location (UCSC)Chr 11: 61.96 – 61.97 MbChr 19: 9.96 – 9.96 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Ferritin heavy chain is a ferroxidase enzyme that in humans is encoded by the FTH1 gene.[5][6] FTH1 gene is located on chromosome 11, and its mutation causes Hemochromatosis type 5.[7]

Function

This gene encodes the heavy subunit of ferritin, the major intracellular iron storage protein in prokaryotes and eukaryotes. It is composed of 24 subunits of the heavy and light ferritin chains. Variation in ferritin subunit composition may affect the rates of iron uptake and release in different tissues. A major function of ferritin is the storage of iron in a soluble and nontoxic state. Defects in ferritin proteins are associated with several neurodegenerative diseases. This gene has multiple pseudogenes. Several alternatively spliced transcript variants have been observed, but their biological validity has not been determined.[6]

Interactions

FTH1 has been shown to

See also

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000167996Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000024661Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. PMID 3020541
    .
  6. ^ a b "Entrez Gene: FTH1 ferritin, heavy polypeptide 1".
  7. ^ "Hemochromatosis type 5 - About the Disease - Genetic and Rare Diseases Information Center".
  8. S2CID 4427026
    .
  9. .

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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