abnormal circulating unsaturated transferrin level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the concentration of transferrin that is not saturated (bound) with iron; this represents the reserve capacity of transferrin and is often measured by the Unsaturated Iron Binding Capacity (UIBC) test (Mammalian Phenotype Ontology, MP_0011895)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011895
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Genes

4 gene mutations causing the abnormal circulating unsaturated 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