abnormal intestinal iron level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the amount of iron present in the large or small intestinal tissue (Mammalian Phenotype Ontology, MP_0008740)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008740
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4 gene mutations causing the abnormal intestinal iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FBXL5 F-box and leucine-rich repeat protein 5
HEPH hephaestin
IREB2 iron-responsive element binding protein 2
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1