KEGG   VARIANT: 57817v1
Entry
57817v1                      Variant                               
Name
HAMP mutation
Type
Loss of function
Gene
HAMP  hepcidin antimicrobial peptide [KO:K23106]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 606464
Network
nt06507  TGFB signaling
Disease
H00211  Hemochromatosis
Reference
PMID:30420953
  Authors
Pantopoulos K
  Title
Inherited Disorders of Iron Overload.
  Journal
Front Nutr 5:103 (2018)
DOI:10.3389/fnut.2018.00103
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