Bos taurus Gene: HAMP
Summary
InnateDB Gene IDBG-635586.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol HAMP
Gene Name hepcidin precursor
Synonyms hepcidin
Species Bos taurus
Ensembl Gene ENSBTAG00000017042
Encoded Proteins
hepcidin
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
InnateDB Annotation from Orthologs
Summary
[Homo sapiens] 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)
[Homo sapiens] HAMP expression in LPS or TNFA-stimulated peripheral blood leukocytes is dependent on the NFkB signalling pathway.
[Homo sapiens] 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)
[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 This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000105697:
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 18:46177091-46178535
Strand Forward strand
Band
Transcripts
ENSBTAT00000022658 ENSBTAP00000022658
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 6 interaction(s) predicted by orthology.
Predicted by orthology
Total 6 [view]
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
GO:0006879 cellular iron ion homeostasis
Cellular Component
GO:0005576 extracellular region
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Cross-References
SwissProt
TrEMBL C5NN20 Q2NKT0
UniProt Splice Variant
Entrez Gene 512301
UniGene Bt.19804
RefSeq NM_001114508
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL AB445457 BC111658 DAAA02046935
GenPept AAI11659 BAH84759
RNA Seq Atlas 512301