abnormal circulating ferritin level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description deviation from the normal concentration of ferritin, a ubiquitous intracellular protein that stores iron and releases it in a controlled fashion; some ferritin is also found in the blood and is measured in tests for overall iron levels, anemia and chronic diseases (Mammalian Phenotype Ontology, MP_0011889)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011889
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11 gene mutations causing the abnormal circulating ferritin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CCKBR cholecystokinin B receptor
CP ceruloplasmin (ferroxidase)
FOXP2 forkhead box P2
FTH1 ferritin, heavy polypeptide 1
HAMP hepcidin antimicrobial peptide
HMOX1 heme oxygenase 1
IREB2 iron-responsive element binding protein 2
PCMT1 protein-L-isoaspartate (D-aspartate) O-methyltransferase
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
TFR2 transferrin receptor 2
UMOD uromodulin