hemosiderosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An iron metabolism disease that has_material_basis_in an accumulation of hemosiderin, an iron-storage complex, resulting in iron overload. (Human Disease Ontology, DOID_12119)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005639
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Genes

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

Symbol Name
ANK1 ankyrin 1, erythrocytic
CBS cystathionine-beta-synthase
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
EPO erythropoietin
FOXP3 forkhead box P3
HAMP hepcidin antimicrobial peptide
PICALM phosphatidylinositol binding clathrin assembly protein
PKLR pyruvate kinase, liver and RBC
PRDX2 peroxiredoxin 2
SPTA1 spectrin, alpha, erythrocytic 1
TK1 thymidine kinase 1, soluble