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HAMP

The product encoded by this gene is involved in the maintenance of iron homeostasis, and it is necessary for the regulation of iron storage in macrophages, and for intestinal iron absorption. The preproprotein is post-translationally cleaved into mature peptides of 20, 22 and 25 amino acids, and these active peptides are rich in cysteines, which form intramolecular bonds that stabilize their beta-sheet structures. These peptides exhibit antimicrobial activity against bacteria and fungi. Mutations in this gene cause hemochromatosis type 2B, also known as juvenile hemochromatosis, a disease caused by severe iron overload that results in cardiomyopathy, cirrhosis, and endocrine failure.
Protein class

Disease related genes, Human disease related genes, Potential drug targets, Transporters

Predicted location

Secreted

Single cell type specificity

Cell type enriched (Hepatocytes)

Immune cell specificity

Group enriched (plasmacytoid DC, myeloid DC)

Cell line specificity

Cell line enriched (Hep G2)

Interaction

Interacts with SLC40A1; this interaction promotes SLC40A1 rapid ubiquitination.

Molecular function

Antibiotic, Antimicrobial, Fungicide, Hormone

More Types Infomation

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For Research Use Only. Not For Clinical Use.

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