abnormal circulating transferrin level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description deviation from the normal concentration in the blood of a plasma protein that reversibly binds and transports iron and other metal ions through the blood to the liver, spleen and bone marrow (Mammalian Phenotype Ontology, MP_0011892)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011892
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5 gene mutations causing the abnormal circulating transferrin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CCKBR cholecystokinin B receptor
CP ceruloplasmin (ferroxidase)
GAST gastrin
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
UMOD uromodulin