hemochromatosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A metal metabolism disorder characterized by the accumulation of iron in various organs of the body. (Human Disease Ontology, DOID_2352)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005638
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Genes

7 gene mutations causing the hemochromatosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
B2M beta-2-microglobulin
CP ceruloplasmin (ferroxidase)
HFE hemochromatosis
HFE2 hemochromatosis type 2 (juvenile)
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
TF transferrin
TFR2 transferrin receptor 2