Hepcidin

Hepcidin is a protein that in humans is encoded by the HAMP gene. Hepcidin is a key regulator of the entry of iron into the circulation in mammals.

HAMP
Available structures
PDBHuman UniProt search: PDBe RCSB
Identifiers
AliasesHAMP, HEPC, HFE2B, LEAP1, PLTR, hepcidin antimicrobial peptide
External IDsOMIM: 606464 HomoloGene: 81623 GeneCards: HAMP
Orthologs
SpeciesHumanMouse
Entrez

57817

n/a

Ensembl

ENSG00000105697

n/a

UniProt

P81172

n/a

RefSeq (mRNA)

NM_021175

n/a

RefSeq (protein)

NP_066998

n/a

Location (UCSC)Chr 19: 35.28 – 35.29 Mbn/a
PubMed searchn/a
Wikidata
View/Edit Human
Hepcidin
Solution structure of hepcidin-25.
Identifiers
SymbolHepcidin
PfamPF06446
InterProIPR010500
SCOP21m4f / SCOPe / SUPFAM
OPM superfamily153
OPM protein1m4e
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary
hepcidin antimicrobial peptide
Identifiers
SymbolHAMP
NCBI gene57817
HGNC15598
OMIM606464
RefSeqNM_021175
UniProtP81172
Other data
LocusChr. 19 q13.1
Search for
StructuresSwiss-model
DomainsInterPro

During conditions in which the hepcidin level is abnormally high, such as inflammation, serum iron falls due to iron trapping within macrophages and liver cells and decreased gut iron absorption. This typically leads to anemia due to an inadequate amount of serum iron being available for developing red blood cells. When the hepcidin level is abnormally low such as in hemochromatosis, iron overload occurs due to increased ferroportin mediated iron efflux from storage and increased gut iron absorption.

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