metal metabolism disorder Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An inherited metabolic disorder that involves metabolic disturbances in the processing or distribution of dietary minerals. (Human Disease Ontology, DOID_896)
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10 genes involed in the disease metal metabolism disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ATP7A ATPase, Cu++ transporting, alpha polypeptide
ATP7B ATPase, Cu++ transporting, beta polypeptide
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
HAMP hepcidin antimicrobial peptide
HFE hemochromatosis
HFE2 hemochromatosis type 2 (juvenile)
PRNP prion protein
SCN4A sodium channel, voltage gated, type IV alpha subunit
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
TFR2 transferrin receptor 2