hemochromatosis Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A metal metabolism disorder characterized by the accumulation of iron in various organs of the body. (Human Disease Ontology, DOID_2352)
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Genes

17 genes associated with the disease hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
BMP2 bone morphogenetic protein 2
BMP4 bone morphogenetic protein 4
HAMP hepcidin antimicrobial peptide
HFE hemochromatosis
HFE2 hemochromatosis type 2 (juvenile)
HLA-A major histocompatibility complex, class I, A
HLA-B major histocompatibility complex, class I, B
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HRES1 HTLV-1 related endogenous sequence
IL6 interleukin 6
SLC11A2 solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
SMAD1 SMAD family member 1
SMAD4 SMAD family member 4
SMAD5 SMAD family member 5
TFR2 transferrin receptor 2
TNF tumor necrosis factor