abnormal liver 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 liver tissue (Mammalian Phenotype Ontology, MP_0008738)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008738
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29 gene mutations causing the abnormal liver iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADD2 adducin 2 (beta)
ANK1 ankyrin 1, erythrocytic
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like
CCKBR cholecystokinin B receptor
CP ceruloplasmin (ferroxidase)
CYBRD1 cytochrome b reductase 1
EPB41 erythrocyte membrane protein band 4.1
FBXL5 F-box and leucine-rich repeat protein 5
GLMP glycosylated lysosomal membrane protein
HAMP hepcidin antimicrobial peptide
HFE hemochromatosis
HFE2 hemochromatosis type 2 (juvenile)
HK1 hexokinase 1
HYAL2 hyaluronoglucosaminidase 2
IREB2 iron-responsive element binding protein 2
KLF1 Kruppel-like factor 1 (erythroid)
LTF lactotransferrin
NFE2L2 nuclear factor, erythroid 2-like 2
PRKAG1 protein kinase, AMP-activated, gamma 1 non-catalytic subunit
SLC11A2 solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2
SLC31A1 solute carrier family 31 (copper transporter), member 1
SLC39A2 solute carrier family 39 (zinc transporter), member 2
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
SPTA1 spectrin, alpha, erythrocytic 1
STEAP3 STEAP family member 3, metalloreductase
TFR2 transferrin receptor 2
TFRC transferrin receptor
TMPRSS6 transmembrane protease, serine 6
TRIB1 tribbles pseudokinase 1