FTH1 gene

ferritin heavy chain 1

The information on this page was automatically extracted from online scientific databases.

From NCBI Gene:

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. [provided by RefSeq, Jul 2008]

From UniProt:

Stores iron in a soluble, non-toxic, readily available form. Important for iron homeostasis. Has ferroxidase activity. Iron is taken up in the ferrous form and deposited as ferric hydroxides after oxidation. Also plays a role in delivery of iron to cells. Mediates iron uptake in capsule cells of the developing kidney.

From NCBI Gene:

  • Hemochromatosis type 5

From UniProt:

Hemochromatosis 5 (HFE5): A disorder of iron metabolism characterized by iron overload. Excess iron is deposited in a variety of organs leading to their failure, and resulting in serious illnesses including cirrhosis, hepatomas, diabetes, cardiomyopathy, arthritis, and hypogonadotropic hypogonadism. Severe effects of the disease usually do not appear until after decades of progressive iron loading. [MIM:615517]

Cytogenetic Location: 11q13, which is the long (q) arm of chromosome 11 at position 13

Molecular Location: base pairs 61,964,285 to 61,967,660 on chromosome 11 (Homo sapiens Annotation Release 108, GRCh38.p7) (NCBI)

Cytogenetic Location: 11q13, which is the long (q) arm of chromosome 11 at position 13
  • FHC
  • FTH
  • FTHL6
  • HFE5
  • PIG15
  • PLIF