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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| Similar Terms |
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| Downloads & Tools |
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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
|
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SMAD4
|
SMAD family member 4
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SMAD5
|
SMAD family member 5
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TFR2
|
transferrin receptor 2
|
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TNF
|
tumor necrosis factor
|
