decreased liver iron level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduction in the amount of iron present in the liver tissue (Mammalian Phenotype Ontology, MP_0008743)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008743
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Genes

7 gene mutations causing the decreased liver iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CYBRD1 cytochrome b reductase 1
FBXL5 F-box and leucine-rich repeat protein 5
SLC11A2 solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2
SLC31A1 solute carrier family 31 (copper transporter), member 1
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
TFRC transferrin receptor
TMPRSS6 transmembrane protease, serine 6