abnormal heart 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 heart tissue (Mammalian Phenotype Ontology, MP_0008741)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008741
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5 gene mutations causing the abnormal heart iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
F10 coagulation factor X
FXN frataxin
HFE2 hemochromatosis type 2 (juvenile)
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
TMPRSS6 transmembrane protease, serine 6