Homo sapiens Gene: HAMP
Summary
InnateDB Gene IDBG-43921.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol HAMP
Gene Name hepcidin antimicrobial peptide
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000105697
Encoded Proteins
hepcidin antimicrobial peptide
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
InnateDB Annotation
Summary
HAMP (hepcidin), an iron regulatory hormone and antimicrobial peptide, inhibits the liver-stage infection in malarial parasitemia by arresting Plasmodium sporozoites in liver hepatocytes and prevents their development into blood-stage parasites. (Demonstrated in murine model)
HAMP expression in LPS or TNFA-stimulated peripheral blood leukocytes is dependent on the NFkB signalling pathway.
HAMP expression is induced by TLR2/TLR4 ligands and may regulate pro-inflammatory cytokine production through maintenance of iron homeostasis in macrophages. (Demonstrated in mice)
InnateDB Annotation from Orthologs
Summary
[Mus musculus] Hamp is a peptide hormone that regulates iron homeostasis and acts as an antimicrobial peptide, functioning in modulating acute inflammatory responses by mediating transcriptional changes.
[Mus musculus] Hamp (hepcidin), an iron regulatory hormone, inhibits the liver-stage infection in malarial parasitemia by arresting Plasmodium sporozoites in liver hepatocytes and prevents their development into blood-stage parasites.
[Mus musculus] Hamp expression in LPS or Tnfa-stimulated peripheral blood leukocytes is dependent on the NFkB signalling pathway. (Demonstrated in human)
[Mus musculus] Hamp expression is induced by Tlr2/Tlr4 ligands and may regulate pro-inflammatory cytokine production through maintenance of iron homeostasis in macrophages.
Entrez Gene
Summary 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. 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. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 19:35280716-35285143
Strand Forward strand
Band q13.12
Transcripts
ENST00000222304 ENSP00000222304
ENST00000598398 ENSP00000471894
ENST00000593580
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 5 experimentally validated interaction(s) in this database.
They are also associated with 3 interaction(s) predicted by orthology.
Experimentally validated
Total 5 [view]
Protein-Protein 3 [view]
Protein-DNA 2 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 3 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005179 hormone activity
Biological Process
GO:0006879 cellular iron ion homeostasis
GO:0006955 immune response
GO:0031640 killing of cells of other organism
GO:0042742 defense response to bacterium
GO:0045087 innate immune response (InnateDB)
GO:0050832 defense response to fungus
Cellular Component
GO:0005576 extracellular region
GO:0005737 cytoplasm
GO:0045179 apical cortex
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.8821
RefSeq NM_021175
HUGO
OMIM
CCDS CCDS12454
HPRD 05925
IMGT
EMBL
GenPept
RNA Seq Atlas